CClinicalTrials.gg
CompletedNCT07513259Updated Aug 17, 2026Results posted

Pre-Diagnosis GLP-1 Receptor Agonist Use and Post-Cancer Mortality in Adults With Obesity and Type 2 Diabetes

An observational study in Obesity & Overweight, Diabetes Mellitus Type 2 and Neoplasms, sponsored by Chung Shan Medical University. Completed at 1 site in Taiwan. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-17.

Sponsored by Chung Shan Medical University · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
203,424
Ages
18 Years and older
Sex
All
01

Study summary

This study will examine whether the type of diabetes treatment used before cancer diagnosis is associated with survival and serious complications after obesity-associated cancer in adults with obesity and type 2 diabetes. The study focuses on glucagon-like peptide-1 receptor agonists (GLP-1 RA) and compares them with other commonly used glucose-lowering therapies, including SGLT2 inhibitors, DPP-4 inhibitors, sulfonylureas, metformin, and usual care. Using de-identified electronic health record data from the TriNetX US Collaborative Network, the study will assess whether patients who used GLP-1 RA before cancer diagnosis have different risks of death, hospitalization, sepsis, and other major outcomes after cancer diagnosis. This is an observational study designed to evaluate associations in routine clinical care and not to prove a treatment effect.

02

Conditions studied

  • Obesity & Overweight
  • Diabetes Mellitus Type 2
  • Neoplasms
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,695 are open to participants now.

This study's enrollment of 203,424 is above the median of 135 across 1,283 observational studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

Chung Shan Medical University is the lead sponsor of 124 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adults will be selected from the TriNetX US Collaborative Network, a distributed database of de-identified electronic health records contributed by participating healthcare organizations across multiple clinical systems and practice settings. The study population consists of adults with obesity and type 2 diabetes who received routine clinical care in this network and were identified through diagnosis records, body mass index data, and medication prescribing data. The overall study population was classified into two mutually exclusive cohorts according to pre-diagnosis GLP-1 receptor agonist use: participants with pre-diagnosis GLP-1 receptor agonist use and participants without pre-diagnosis GLP-1 receptor agonist use. Comparator-specific propensity score-matched cohorts for GLP-1 RA versus SGLT2 inhibitors, DPP-4 inhibitors, sulfonylureas, metformin, and usual care were defined within this source population for prespecified pairwise outcome analyses.

Inclusion criteria

  • Adults aged 18 years or older
  • BMI ≥27 kg/m2, or diagnosis codes consistent with obesity
  • Type 2 diabetes mellitus
  • Initiation of a glucose-lowering medication before obesity-associated cancer diagnosis
  • Incident obesity-associated cancer diagnosed after medication initiation
  • No dispensing of the study drug class during the 6-month washout period before the first qualifying prescription

Exclusion criteria

Exclusion Criteria:

  • Type 1 diabetes mellitus, Other specified diabetes types that are not type 2 diabetes
  • Human immunodeficiency virus infection
  • End-stage renal disease
  • Prior bariatric surgery
  • Prior organ transplantation
  • Transplant-related complications
  • Any use of tirzepatide before cohort entry
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
203,424 participants (actual)
Patient registry
No

Groups and cohorts

  • GLP-1 RA

    Adults with obesity and type 2 diabetes who developed an obesity-associated cancer after initiating a GLP-1 receptor agonist before cancer diagnosis. This cohort served as the GLP-1 RA exposure cohort in the overall study population and represents the unique participants with pre-diagnosis GLP-1 receptor agonist use.

  • Usual Care Without GLP-1 RA

    Adults with obesity and type 2 diabetes who developed an obesity-associated cancer and had no GLP-1 receptor agonist prescriptions before cancer diagnosis. This cohort served as the non-GLP-1 RA comparator cohort in the overall study population. Participants could receive routine clinical care, including other non-GLP-1 RA glucose-lowering medications. This cohort represents the unique participants without pre-diagnosis GLP-1 receptor agonist use.

06

What researchers measure

Primary outcomes

  1. All-cause Mortality (Comparison 1)

    All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  2. All-cause Mortality (Comparison 2)

    All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  3. All-cause Mortality (Comparison 3)

    All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  4. All-cause Mortality (Comparison 4)

    All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  5. All-cause Mortality (Comparison 5)

    All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

    Time frame: From obesity-associated cancer diagnosis through 36 months

Secondary outcomes

  1. Inpatient (Comparison 1)

    Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  2. Inpatient (Comparison 2)

    Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  3. Inpatient (Comparison 3)

    Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  4. Inpatient (Comparison 4)

    Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  5. Inpatient (Comparison 5)

    Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  6. Pericardial Effusion (Comparison 1)

    Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  7. Pericardial Effusion (Comparison 2)

    Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  8. Pericardial Effusion (Comparison 3)

    Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  9. Pericardial Effusion (Comparison 4)

    Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  10. Pericardial Effusion (Comparison 5)

    Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  11. Pulmonary Embolism (Comparison 1)

    Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  12. Pulmonary Embolism (Comparison 2)

    Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  13. Pulmonary Embolism (Comparison 3)

    Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  14. Pulmonary Embolism (Comparison 4)

    Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  15. Pulmonary Embolism (Comparison 5)

    Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  16. Sepsis (Comparison 1)

    Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  17. Sepsis (Comparison 2)

    Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  18. Sepsis (Comparison 3)

    Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  19. Sepsis (Comparison 4)

    Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

    Time frame: From obesity-associated cancer diagnosis through 36 months

  20. Sepsis (Comparison 5)

    Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

    Time frame: From obesity-associated cancer diagnosis through 36 months

07

Results

Posted Aug 17, 2026
Limitations and caveats
This retrospective observational target-trial emulation is subject to residual confounding, misclassification, and missing or incomplete electronic health record data. Treatment strategies were not randomly assigned, and propensity score matching was performed separately for each pairwise comparison. Outcome ascertainment may have been affected by variable documentation and follow-up in routine clinical practice.

Participant flow

Participants were retrospectively identified from the TriNetX US Collaborative Network using de-identified electronic health records. Eligible adults with obesity and type 2 diabetes who initiated glucose-lowering therapy between January 1, 2018 and October 31, 2025 and subsequently developed an obesity-associated cancer were included based on prespecified eligibility criteria.

Participant flow — Overall Study
MilestoneGLP-1 RAUsual Care Without GLP-1 RA
Started27208176216
Matched into comparison 1 (glp-1 ra without sglt2i vs sglt2i)1219312193
Matched into comparison 2 (glp-1 ra without dpp-4i vs dpp-4i)1115411154
Matched into comparison 3 (glp-1 ra without sulfonylureas vs sulfonylureas)1407214072
Matched into comparison 4 (glp-1 ra without metformin vs metformin)98199819
Matched into comparison 5 (glp-1 ra vs usual care)2643326433
Completed27208176216
Not completed00

Outcome measures

PrimaryAll-cause Mortality (Comparison 1)

All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
All-cause Mortality (Comparison 1)
participants with eventGLP-1 RA Without History of SGLT2i (Comparison 1)SGLT2i (Comparison 1)
All-cause Mortality (Comparison 1)8761233
SecondaryInpatient (Comparison 1)

Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Inpatient (Comparison 1)
participants with eventGLP-1 RA Without History of SGLT2i (Comparison 1)SGLT2i (Comparison 1)
Inpatient (Comparison 1)874952
SecondaryInpatient (Comparison 2)

Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Inpatient (Comparison 2)
participants with eventGLP-1 RA Without History of DPP-4i (Comparison 2)DPP-4i (Comparison 2)
Inpatient (Comparison 2)7841077
SecondaryInpatient (Comparison 3)

Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Inpatient (Comparison 3)
participants with eventGLP-1 RA Without History of Sulfonylureas (Comparison 3)Sulfonylureas (Comparison 3)
Inpatient (Comparison 3)9941477
SecondaryInpatient (Comparison 4)

Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Inpatient (Comparison 4)
participants with eventGLP-1 RA Without History of Metformin (Comparison 4)Metformin (Comparison 4)
Inpatient (Comparison 4)622865
PrimaryAll-cause Mortality (Comparison 2)

All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
All-cause Mortality (Comparison 2)
participants with eventGLP-1 RA Without History of DPP-4i (Comparison 2)DPP-4i (Comparison 2)
All-cause Mortality (Comparison 2)8151364
SecondaryInpatient (Comparison 5)

Inpatient within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Inpatient (Comparison 5)
participants with eventGLP-1 RA (Comparison 5)Usual Care (Comparison 5)
Inpatient (Comparison 5)18962522
SecondaryPericardial Effusion (Comparison 1)

Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pericardial Effusion (Comparison 1)
participants with eventGLP-1 RA Without History of SGLT2i (Comparison 1)SGLT2i (Comparison 1)
Pericardial Effusion (Comparison 1)107128
SecondaryPericardial Effusion (Comparison 2)

Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pericardial Effusion (Comparison 2)
participants with eventGLP-1 RA Without History of DPP-4i (Comparison 2)DPP-4i (Comparison 2)
Pericardial Effusion (Comparison 2)105133
SecondaryPericardial Effusion (Comparison 3)

Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pericardial Effusion (Comparison 3)
participants with eventGLP-1 RA Without History of Sulfonylureas (Comparison 3)Sulfonylureas (Comparison 3)
Pericardial Effusion (Comparison 3)113161
PrimaryAll-cause Mortality (Comparison 3)

All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
All-cause Mortality (Comparison 3)
participants with eventGLP-1 RA Without History of Sulfonylureas (Comparison 3)Sulfonylureas (Comparison 3)
All-cause Mortality (Comparison 3)8831736
SecondaryPericardial Effusion (Comparison 4)

Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pericardial Effusion (Comparison 4)
participants with eventGLP-1 RA Without History of Metformin (Comparison 4)Metformin (Comparison 4)
Pericardial Effusion (Comparison 4)6982
SecondaryPericardial Effusion (Comparison 5)

Pericardial effusion within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pericardial Effusion (Comparison 5)
participants with eventGLP-1 RA (Comparison 5)Usual Care (Comparison 5)
Pericardial Effusion (Comparison 5)218261
SecondaryPulmonary Embolism (Comparison 1)

Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pulmonary Embolism (Comparison 1)
participants with eventGLP-1 RA Without History of SGLT2i (Comparison 1)SGLT2i (Comparison 1)
Pulmonary Embolism (Comparison 1)192217
SecondaryPulmonary Embolism (Comparison 2)

Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pulmonary Embolism (Comparison 2)
participants with eventGLP-1 RA Without History of DPP-4i (Comparison 2)DPP-4i (Comparison 2)
Pulmonary Embolism (Comparison 2)163216
PrimaryAll-cause Mortality (Comparison 4)

All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
All-cause Mortality (Comparison 4)
participants with eventGLP-1 RA Without History of Metformin (Comparison 4)Metformin (Comparison 4)
All-cause Mortality (Comparison 4)631871
SecondaryPulmonary Embolism (Comparison 3)

Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pulmonary Embolism (Comparison 3)
participants with eventGLP-1 RA Without History of Sulfonylureas (Comparison 3)Sulfonylureas (Comparison 3)
Pulmonary Embolism (Comparison 3)220281
SecondaryPulmonary Embolism (Comparison 4)

Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pulmonary Embolism (Comparison 4)
participants with eventGLP-1 RA Without History of Metformin (Comparison 4)Metformin (Comparison 4)
Pulmonary Embolism (Comparison 4)123163
SecondaryPulmonary Embolism (Comparison 5)

Pulmonary embolism within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Pulmonary Embolism (Comparison 5)
participants with eventGLP-1 RA (Comparison 5)Usual Care (Comparison 5)
Pulmonary Embolism (Comparison 5)385506
SecondarySepsis (Comparison 1)

Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 1, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior SGLT2 inhibitor use versus SGLT2 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Sepsis (Comparison 1)
participants with eventGLP-1 RA Without History of SGLT2i (Comparison 1)SGLT2i (Comparison 1)
Sepsis (Comparison 1)453553
PrimaryAll-cause Mortality (Comparison 5)

All-cause mortality within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
All-cause Mortality (Comparison 5)
participants with eventGLP-1 RA (Comparison 5)Usual Care (Comparison 5)
All-cause Mortality (Comparison 5)15842660
SecondarySepsis (Comparison 2)

Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 2, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior DPP-4 inhibitor use versus DPP-4 inhibitor-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Sepsis (Comparison 2)
participants with eventGLP-1 RA Without History of DPP-4i (Comparison 2)DPP-4i (Comparison 2)
Sepsis (Comparison 2)414590
SecondarySepsis (Comparison 3)

Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 3, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior sulfonylurea use versus sulfonylurea-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Sepsis (Comparison 3)
participants with eventGLP-1 RA Without History of Sulfonylureas (Comparison 3)Sulfonylureas (Comparison 3)
Sepsis (Comparison 3)506743
SecondarySepsis (Comparison 4)

Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 4, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist without prior metformin use versus metformin-treated adults.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Sepsis (Comparison 4)
participants with eventGLP-1 RA Without History of Metformin (Comparison 4)Metformin (Comparison 4)
Sepsis (Comparison 4)320406
SecondarySepsis (Comparison 5)

Sepsis within 36 months after obesity-associated cancer diagnosis in the propensity score-matched cohort for Comparison 5, comparing adults with obesity and type 2 diabetes treated with GLP-1 receptor agonist versus adults receiving usual care.

Time frame:
From obesity-associated cancer diagnosis through 36 months
Reported as:
Number · participants with event
Sepsis (Comparison 5)
participants with eventGLP-1 RA (Comparison 5)Usual Care (Comparison 5)
Sepsis (Comparison 5)9041213

Adverse events

Collected over From index date through 36 months of follow-up. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
GLP-1 RA Without History of SGLT2i (Comparison 1)876/12,060 (7.3%)——
SGLT2i (Comparison 1)1,233/12,125 (10.2%)——
GLP-1 RA Without History of DPP-4i (Comparison 2)815/10,922 (7.5%)——
DPP-4i (Comparison 2)1,364/10,984 (12.4%)——
GLP-1 RA Without History of Sulfonylureas (Comparison 3)883/13,801 (6.4%)——
Sulfonylureas (Comparison 3)1,736/13,819 (12.6%)——
GLP-1 RA Without History of Metformin (Comparison 4)631/9,590 (6.6%)——
Metformin (Comparison 4)871/9,645 (9%)——
GLP-1 RA (Comparison 5)1,584/25,910 (6.1%)——
Usual Care (Comparison 5)2,660/25,920 (10.3%)——

Baseline characteristics

Baseline characteristics are reported separately for each prespecified pairwise propensity score-matched comparison. For each baseline measure corresponding to a given comparison, data are provided only for the two arms included in that comparison; the remaining arms are assigned 0 participants analyzed in order to avoid counting participants more than once within a row.

Age, Customized
Age, Customized(Participants)GLP-1 RA Without History of SGLT2i (Comparison 1)SGLT2i (Comparison 1)GLP-1 RA Without History of DPP-4i (Comparison 2)DPP-4i (Comparison 2)GLP-1 RA Without History of Sulfonylureas (Comparison 3)Sulfonylureas (Comparison 3)GLP-1 RA Without History of Metformin (Comparison 4)Metformin (Comparison 4)GLP-1 RA (Comparison 5)Usual Care (Comparison 5)Total
<65 years (Comparison 1)46294636000000009265
≥65 years (Comparison 1)756475570000000015121
<65 years (Comparison 2)00327232840000006556
≥65 years (Comparison 2)007882787000000015752
<65 years (Comparison 3)000051485193000010341
≥65 years (Comparison 3)000089248879000017803
<65 years (Comparison 4)00000041324065008197
≥65 years (Comparison 4)000000568757540011441
<65 years (Comparison 5)00000000120661208524151
≥65 years (Comparison 5)00000000143671434828715
Sex/Gender, Customized
Sex/Gender, Customized(Participants)GLP-1 RA Without History of SGLT2i (Comparison 1)SGLT2i (Comparison 1)GLP-1 RA Without History of DPP-4i (Comparison 2)DPP-4i (Comparison 2)GLP-1 RA Without History of Sulfonylureas (Comparison 3)Sulfonylureas (Comparison 3)GLP-1 RA Without History of Metformin (Comparison 4)Metformin (Comparison 4)GLP-1 RA (Comparison 5)Usual Care (Comparison 5)Total
Male (Comparison 1)35343508000000007042
Female (Comparison 1)865186790000000017330
Unknown or Not Reported (Comparison 1)860000000014
Male (Comparison 2)00354635340000007080
Female (Comparison 2)007605761500000015220
Unknown or Not Reported (Comparison 2)00350000008
Male (Comparison 3)00004205423900008444
Female (Comparison 3)000098639827000019690
Unknown or Not Reported (Comparison 3)000046000010
Male (Comparison 4)00000024842481004965
Female (Comparison 4)000000732773290014656
Unknown or Not Reported (Comparison 4)000000890017
Male (Comparison 5)000000006883710913992
Female (Comparison 5)00000000195321930738839
Unknown or Not Reported (Comparison 5)00000000181735
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)GLP-1 RA Without History of SGLT2i (Comparison 1)SGLT2i (Comparison 1)GLP-1 RA Without History of DPP-4i (Comparison 2)DPP-4i (Comparison 2)GLP-1 RA Without History of Sulfonylureas (Comparison 3)Sulfonylureas (Comparison 3)GLP-1 RA Without History of Metformin (Comparison 4)Metformin (Comparison 4)GLP-1 RA (Comparison 5)Usual Care (Comparison 5)Total
Comparison 1 — Hispanic or Latino10071024000000002031
Comparison 1 — Not Hispanic or Latino924592510000000018496
Comparison 1 — Unknown or Not Reported19411918000000003859
Comparison 2 — Hispanic or Latino00102310120000002035
Comparison 2 — Not Hispanic or Latino008463843400000016897
Comparison 2 — Unknown or Not Reported00166817080000003376
Comparison 3 — Hispanic or Latino00001154114700002301
Comparison 3 — Not Hispanic or Latino00001060510638000021243
Comparison 3 — Unknown or Not Reported00002313228700004600
Comparison 4 — Hispanic or Latino000000687667001354
Comparison 4 — Not Hispanic or Latino000000723973100014549
Comparison 4 — Unknown or Not Reported00000018931842003735
Comparison 5 — Hispanic or Latino00000000229422174511
Comparison 5 — Not Hispanic or Latino00000000197841992639710
Comparison 5 — Unknown or Not Reported00000000435542908645
HbA1c ≥7%
HbA1c ≥7%(Participants)GLP-1 RA Without History of SGLT2i (Comparison 1)SGLT2i (Comparison 1)GLP-1 RA Without History of DPP-4i (Comparison 2)DPP-4i (Comparison 2)GLP-1 RA Without History of Sulfonylureas (Comparison 3)Sulfonylureas (Comparison 3)GLP-1 RA Without History of Metformin (Comparison 4)Metformin (Comparison 4)GLP-1 RA (Comparison 5)Usual Care (Comparison 5)Total
HbA1c ≥7% (Comparison 1)723072320000000014462
HbA1c ≥7% (Comparison 2)007048698100000014029
HbA1c ≥7% (Comparison 3)000087098673000017382
HbA1c ≥7% (Comparison 4)000000530052550010555
HbA1c ≥7% (Comparison 5)00000000168771703633913
08

Study locations

1 site
  • Chung Shan Medical University Hospital
    Taichung, Taichung City 402, Taiwan
09

References and documents

Publications

  • Kim C, Dinan MA, Robinson TJ, Ross JS, Jastreboff AM, Krumholz HM, Lu Y. Semaglutide and Tirzepatide Prescribing for Obesity in Patients With Preexisting Comorbid Cancers. JAMA Oncol. 2025 Nov 6;12(1):101-4. doi: 10.1001/jamaoncol.2025.4560. Online ahead of print. PubMed 41196576 ↗
  • Tsujimoto T, Kajio H, Sugiyama T. Association between hyperinsulinemia and increased risk of cancer death in nonobese and obese people: A population-based observational study. Int J Cancer. 2017 Jul 1;141(1):102-111. doi: 10.1002/ijc.30729. Epub 2017 Apr 22. PubMed 28390156 ↗
  • Zhang AMY, Wellberg EA, Kopp JL, Johnson JD. Hyperinsulinemia in Obesity, Inflammation, and Cancer. Diabetes Metab J. 2021 May;45(3):285-311. doi: 10.4093/dmj.2020.0250. Epub 2021 Mar 29. PubMed 33775061 ↗
  • Perkovic V, Tuttle KR, Rossing P, Mahaffey KW, Mann JFE, Bakris G, Baeres FMM, Idorn T, Bosch-Traberg H, Lausvig NL, Pratley R; FLOW Trial Committees and Investigators. Effects of Semaglutide on Chronic Kidney Disease in Patients with Type 2 Diabetes. N Engl J Med. 2024 Jul 11;391(2):109-121. doi: 10.1056/NEJMoa2403347. Epub 2024 May 24. PubMed 38785209 ↗
  • Wong CK, McLean BA, Baggio LL, Koehler JA, Hammoud R, Rittig N, Yabut JM, Seeley RJ, Brown TJ, Drucker DJ. Central glucagon-like peptide 1 receptor activation inhibits Toll-like receptor agonist-induced inflammation. Cell Metab. 2024 Jan 2;36(1):130-143.e5. doi: 10.1016/j.cmet.2023.11.009. Epub 2023 Dec 18. PubMed 38113888 ↗
  • Rohm TV, Meier DT, Olefsky JM, Donath MY. Inflammation in obesity, diabetes, and related disorders. Immunity. 2022 Jan 11;55(1):31-55. doi: 10.1016/j.immuni.2021.12.013. PubMed 35021057 ↗
  • Wong CK, Drucker DJ. Antiinflammatory actions of glucagon-like peptide-1-based therapies beyond metabolic benefits. J Clin Invest. 2025 Nov 3;135(21):e194751. doi: 10.1172/JCI194751. eCollection 2025 Nov 3. PubMed 41178710 ↗
  • Zheng Z, Zong Y, Ma Y, Tian Y, Pang Y, Zhang C, Gao J. Glucagon-like peptide-1 receptor: mechanisms and advances in therapy. Signal Transduct Target Ther. 2024 Sep 18;9(1):234. doi: 10.1038/s41392-024-01931-z. PubMed 39289339 ↗
  • Chen B, Yu X, Horvath-Diano C, Ortuno MJ, Tschop MH, Jastreboff AM, Schneeberger M. GLP-1 programs the neurovascular landscape. Cell Metab. 2024 Oct 1;36(10):2173-2189. doi: 10.1016/j.cmet.2024.09.003. PubMed 39357509 ↗
  • Pfaffenlehner M, Behrens M, Zoller D, Ungethum K, Gunther K, Rucker V, Reese JP, Heuschmann P, Kesselmeier M, Remo F, Scherag A, Binder H, Binder N; EVA4MII project. Methodological challenges using routine clinical care data for real-world evidence: a rapid review utilizing a systematic literature search and focus group discussion. BMC Med Res Methodol. 2025 Jan 14;25(1):8. doi: 10.1186/s12874-024-02440-x. PubMed 39810151 ↗
  • Zhou L, Duanmu W, Tan F, Gu X, Che H, Yin W. Information pharmacists assist in the construction of GLP-1RA prescription review rules in a tertiary hospital in China. BMC Health Serv Res. 2025 Oct 1;25(1):1276. doi: 10.1186/s12913-025-13377-2. PubMed 41034888 ↗
  • Arroyo V, Angeli P, Moreau R, Jalan R, Claria J, Trebicka J, Fernandez J, Gustot T, Caraceni P, Bernardi M; investigators from the EASL-CLIF Consortium, Grifols Chair and European Foundation for the Study of Chronic Liver Failure (EF-Clif). The systemic inflammation hypothesis: Towards a new paradigm of acute decompensation and multiorgan failure in cirrhosis. J Hepatol. 2021 Mar;74(3):670-685. doi: 10.1016/j.jhep.2020.11.048. Epub 2020 Dec 7. PubMed 33301825 ↗
  • Liu C, Liu T, Zhang Q, Song M, Zhang Q, Shi J, Deng L, Chen Y, Zheng X, Lin S, Wang Z, Xie H, Chen S, Wu S, Shi H. Temporal relationship between inflammation and metabolic disorders and their impact on cancer risk. J Glob Health. 2024 Feb 16;14:04041. doi: 10.7189/jogh.14.04041. PubMed 38386717 ↗
  • Silverii GA, Marinelli C, Bettarini C, Del Vescovo GG, Monami M, Mannucci E. GLP-1 receptor agonists and the risk for cancer: A meta-analysis of randomized controlled trials. Diabetes Obes Metab. 2025 Aug;27(8):4454-4468. doi: 10.1111/dom.16489. Epub 2025 May 29. PubMed 40437949 ↗
  • Valencia-Rincon E, Rai R, Chandra V, Wellberg EA. GLP-1 receptor agonists and cancer: current clinical evidence and translational opportunities for preclinical research. J Clin Invest. 2025 Nov 3;135(21):e194743. doi: 10.1172/JCI194743. eCollection 2025 Nov 3. PubMed 41178720 ↗
  • Wang L, Xu R, Kaelber DC, Berger NA. Glucagon-Like Peptide 1 Receptor Agonists and 13 Obesity-Associated Cancers in Patients With Type 2 Diabetes. JAMA Netw Open. 2024 Jul 1;7(7):e2421305. doi: 10.1001/jamanetworkopen.2024.21305. PubMed 38967919 ↗
  • Ko A, Chang YC, Bahar F, Wang TH, Xanthavanij N, Yu CC, Hsieh RJ, See XY, Lo SW, Song J, Hsia YP, Chiang CH, Xu X, Lin S, Chiang CH. Risk for Cancer With Glucagon-Like Peptide-1 Receptor Agonists and Dual Agonists : A Systematic Review and Meta-analysis. Ann Intern Med. 2026 Feb;179(2):216-229. doi: 10.7326/ANNALS-25-02237. Epub 2025 Dec 9. PubMed 41359966 ↗
  • Huang YN, Tsou MY, Li PH, Chen JC, Liu YL, Meyerowitz-Katz G, Tsai TH, Su PH. Effectiveness of Pre-Transplant Dual GLP-1 Receptor Agonist and SGLT2 Inhibitor Therapy on All-Cause Mortality in Organ Transplantation Candidates with Obesity and Type 2 Diabetes: a Target-Trial Emulation. Adv Sci (Weinh). 2026 Feb;13(11):e18813. doi: 10.1002/advs.202518813. Epub 2025 Dec 12. PubMed 41387113 ↗
  • Dib BN, Swanson SA. Emulating a Target Trial Using Observational Data. JAMA Intern Med. 2025 Apr 1;185(4):459-460. doi: 10.1001/jamainternmed.2024.8129. PubMed 39992643 ↗
  • Hernan MA, Robins JM. Using Big Data to Emulate a Target Trial When a Randomized Trial Is Not Available. Am J Epidemiol. 2016 Apr 15;183(8):758-64. doi: 10.1093/aje/kwv254. Epub 2016 Mar 18. PubMed 26994063 ↗
  • Cashin AG, Hansford HJ, Hernan MA, Swanson SA, Lee H, Jones MD, Dahabreh IJ, Dickerman BA, Egger M, Garcia-Albeniz X, Golub RM, Islam N, Lodi S, Moreno-Betancur M, Pearson SA, Schneeweiss S, Sharp MK, Sterne JAC, Stuart EA, McAuley JH. Transparent reporting of observational studies emulating a target trial: the TARGET Statement. BMJ. 2025 Sep 3;390:e087179. doi: 10.1136/bmj-2025-087179. PubMed 40903028 ↗
  • Yadav K, Lewis RJ. Immortal Time Bias in Observational Studies. JAMA. 2021 Feb 16;325(7):686-687. doi: 10.1001/jama.2020.9151. No abstract available. PubMed 33591334 ↗
  • Hicks B, Kaye JA, Azoulay L, Kristensen KB, Habel LA, Pottegard A. The application of lag times in cancer pharmacoepidemiology: a narrative review. Ann Epidemiol. 2023 Aug;84:25-32. doi: 10.1016/j.annepidem.2023.05.004. Epub 2023 May 9. PubMed 37169040 ↗
  • Zuo H, Yu L, Campbell SM, Yamamoto SS, Yuan Y. The implementation of target trial emulation for causal inference: a scoping review. J Clin Epidemiol. 2023 Oct;162:29-37. doi: 10.1016/j.jclinepi.2023.08.003. Epub 2023 Aug 9. PubMed 37562726 ↗
  • Enserro DM, Gunn HJ, Elsaid MI, Duan F, Pugh SL. Challenges to and considerations of designing cancer prevention trials. J Natl Cancer Inst Monogr. 2025 Mar 1;2025(68):49-55. doi: 10.1093/jncimonographs/lgae044. PubMed 39989045 ↗
  • Hernan MA, Dahabreh IJ, Dickerman BA, Swanson SA. The Target Trial Framework for Causal Inference From Observational Data: Why and When Is It Helpful? Ann Intern Med. 2025 Mar;178(3):402-407. doi: 10.7326/ANNALS-24-01871. Epub 2025 Feb 18. PubMed 39961105 ↗
  • Soni PD, Hartman HE, Dess RT, Abugharib A, Allen SG, Feng FY, Zietman AL, Jagsi R, Schipper MJ, Spratt DE. Comparison of Population-Based Observational Studies With Randomized Trials in Oncology. J Clin Oncol. 2019 May 10;37(14):1209-1216. doi: 10.1200/JCO.18.01074. Epub 2019 Mar 21. PubMed 30897037 ↗
  • Chan SH, Li PY, Li PH, Lin YJ, Wang WH, Huang YN, Chen JY. GLP-1 receptor agonist use during immune checkpoint inhibitor therapy is associated with mortality and Immune-Related adverse events across cancer types in People with type 2 Diabetes: A Target-Trial emulation. Diabetes Res Clin Pract. 2026 Jan;231:113073. doi: 10.1016/j.diabres.2025.113073. Epub 2025 Dec 24. PubMed 41453566 ↗
  • Dai H, Li Y, Lee YA, Lu Y, George TJ, Donahoo WT, Lee KP, Nakshatri H, Allen J, Guo Y, Sun RC, Guo J, Bian J. GLP-1 Receptor Agonists and Cancer Risk in Adults With Obesity. JAMA Oncol. 2025 Oct 1;11(10):1186-1193. doi: 10.1001/jamaoncol.2025.2681. PubMed 40839273 ↗
  • Drucker DJ. GLP-1-based therapies for diabetes, obesity and beyond. Nat Rev Drug Discov. 2025 Aug;24(8):631-650. doi: 10.1038/s41573-025-01183-8. Epub 2025 Apr 25. PubMed 40281304 ↗
  • Huang YN, Liao WL, Huang JY, Lin YJ, Yang SF, Huang CC, Wang CH, Su PH. Long-term safety and efficacy of glucagon-like peptide-1 receptor agonists in individuals with obesity and without type 2 diabetes: A global retrospective cohort study. Diabetes Obes Metab. 2024 Nov;26(11):5222-5232. doi: 10.1111/dom.15869. Epub 2024 Aug 22. PubMed 39171569 ↗
  • Luconi M, Cantini G, Crescioli C. Repurposing glucose-lowering drugs for cancer therapy. Trends Cancer. 2025 Jul;11(7):691-710. doi: 10.1016/j.trecan.2025.04.010. Epub 2025 May 15. PubMed 40374399 ↗
  • Chan JCN, Lim LL, Wareham NJ, Shaw JE, Orchard TJ, Zhang P, Lau ESH, Eliasson B, Kong APS, Ezzati M, Aguilar-Salinas CA, McGill M, Levitt NS, Ning G, So WY, Adams J, Bracco P, Forouhi NG, Gregory GA, Guo J, Hua X, Klatman EL, Magliano DJ, Ng BP, Ogilvie D, Panter J, Pavkov M, Shao H, Unwin N, White M, Wou C, Ma RCW, Schmidt MI, Ramachandran A, Seino Y, Bennett PH, Oldenburg B, Gagliardino JJ, Luk AOY, Clarke PM, Ogle GD, Davies MJ, Holman RR, Gregg EW. The Lancet Commission on diabetes: using data to transform diabetes care and patient lives. Lancet. 2021 Dec 19;396(10267):2019-2082. doi: 10.1016/S0140-6736(20)32374-6. Epub 2020 Nov 12. No abstract available. PubMed 33189186 ↗
  • Kang C, LeRoith D, Gallagher EJ. Diabetes, Obesity, and Breast Cancer. Endocrinology. 2018 Nov 1;159(11):3801-3812. doi: 10.1210/en.2018-00574. PubMed 30215698 ↗
  • Perry RJ, Shulman GI. Mechanistic Links between Obesity, Insulin, and Cancer. Trends Cancer. 2020 Feb;6(2):75-78. doi: 10.1016/j.trecan.2019.12.003. Epub 2020 Jan 14. PubMed 32061306 ↗
  • Zullig LL, Sung AD, Khouri MG, Jazowski S, Shah NP, Sitlinger A, Blalock DV, Whitney C, Kikuchi R, Bosworth HB, Crowley MJ, Goldstein KM, Klem I, Oeffinger KC, Dent S. Cardiometabolic Comorbidities in Cancer Survivors: JACC: CardioOncology State-of-the-Art Review. JACC CardioOncol. 2022 Jun 21;4(2):149-165. doi: 10.1016/j.jaccao.2022.03.005. eCollection 2022 Jun. PubMed 35818559 ↗
  • Rask-Andersen M, Ivansson E, Hoglund J, Ek WE, Karlsson T, Johansson A. Adiposity and sex-specific cancer risk. Cancer Cell. 2023 Jun 12;41(6):1186-1197.e4. doi: 10.1016/j.ccell.2023.05.010. PubMed 37311415 ↗
  • GBD 2019 Cancer Risk Factors Collaborators. The global burden of cancer attributable to risk factors, 2010-19: a systematic analysis for the Global Burden of Disease Study 2019. Lancet. 2022 Aug 20;400(10352):563-591. doi: 10.1016/S0140-6736(22)01438-6. PubMed 35988567 ↗

Study documents

  • Protocol and statistical analysis plan · Apr 6, 2026

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No — Individual participant data will not be shared. This retrospective observational study uses de-identified electronic health record data from the TriNetX US Collaborative Network. Access to individual-level data is restricted by data use agreements, institutional policies, and privacy protections. Researchers who meet eligibility requirements may obtain access to similar de-identified data through a TriNetX license or through participating institutions.

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT07513259
Lead sponsor
Chung Shan Medical University
Collaborators
National Science and Technology Council, Taiwan
Responsible party
Yu-Nan Huang (Assistant Professor/Research Fellow, Chung Shan Medical University) — Principal investigator
First posted
Apr 7, 2026
Start date
Jan 1, 2018
Primary completion
Oct 31, 2025
Completion
Oct 31, 2025
Results posted
Aug 17, 2026
Last update
Aug 17, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion