CClinicalTrials.gg
Status unknownNCT05170256HERESUpdated Aug 12, 2022

Trastuzumab and Standard Treatment With Chemo- and Immunotherapy as First Line Treatment for HER2 Positive Esophageal Squamous Cell Carcinoma Patients

A Phase 2 interventional study of Trastuzumab in Esophageal Squamous Cell Carcinoma, HER-2 Protein Overexpression and HER-2 Gene Amplification, sponsored by Morten Mau-Sørensen. Status unknown at 2 sites in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-08-12.

Sponsored by Morten Mau-Sørensen · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Aug 2022), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
24
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The study aims to determine the efficacy of trastuzumab added to standard treatment (fluoropyrimidine/platinum doublet with pembrolizumab) in patients with HER2 positive Esophageal squamous cell carcinoma (ESCC) determined by 6 months progression free survival (PFS) (RECIST 1.1).

02

Conditions studied

  • Esophageal Squamous Cell Carcinoma
  • HER-2 Protein Overexpression
  • HER-2 Gene Amplification
03

In context

Carcinoma

6,741 studies on the registry are indexed under Carcinoma; 1,161 are open to participants now.

This study's planned enrollment of 24 is below the median of 45 across 5,170 interventional studies indexed under Carcinoma.

Browse Carcinoma studies →

Lead sponsor

This is the only study on the registry with Morten Mau-Sørensen as lead sponsor.

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

Inclusion criteria

  1. Signed informed consent
  2. Age ≥18 years
  3. Inoperable locally advanced or metastatic squamous cell carcinoma of the esophagus not amenable for curative intended therapy
  4. HER2 positive defined as IHC2+ and FISH amplification ratio ≥2 or IHC3+
  5. ECOG PS \<2
  6. Baseline left ventricular ejection fraction > 50% measured by echocardiography or MUGA
  7. Adequate bone marrow function and organ function:

    1. Hematopoietic function:
    2. Leucocytes > 3.0 x 109/l, neutrocytes > 1.5 x 109/l and thrombocytes > 100 x 109/l
    3. Serum bilirubin \< 1.5 × upper limit of normal (ULN); and AST/ALT \< 2.5 × ULN (or \< 5 × ULN in patients with liver metastases).
  8. Creatinine clearance > 30 ml/min

Exclusion criteria

Exclusion Criteria:

  1. Prior systemic treatment with non-curative intent including HER2-targeting drugs. Prior neoadjuvant and adjuvant therapies as well as palliative radiotherapy are allowed
  2. Significant medical illness that in the investigator's opinion cannot be adequately controlled with appropriate therapy or would compromise the patient's ability to tolerate study treatment
  3. Congestive heart failure (New York Heart Association (NYHA) class 3+4); uncontrolled angina pectoris; poorly controlled hypertension (systolic BP > 180 mmHg or diastolic BP > 100 mmHg); or high-risk uncontrollable arrhythmias.
  4. Patients with severe dyspnoea at rest due to complications of advanced malignancy or requiring supplementary oxygen therapy.
  5. Patients with known hypersensitivity to trastuzumab or any of the study drugs, murine proteins, or to any of the excipients
  6. Symptomatic brain metastases uncontrolled by corticosteroids or carcinomatous meningitis
  7. Homozygosity or compound heterozygosity for more than one gene variant of dihydropyrimidine dehydrogenase (DPD) known to cause major reduced metabolism of 5-FU derivates OR plasma uracil > 150 ng/ml are not eligible. Patients with minor DPD insufficiency are allowed provided that local guidelines for administration of 5-FU are followed.
  8. Any other cancer (excluding low risk prostate cancer, carcinoma in situ and radically operated localised squamous skin cancer) with clinical activity within the last 2 years
  9. Other current cancer treatments except for anti-hormone and anti-resorptive treatment of bone metastasis.
  10. Allopurinol, phenytoin, warfarin treatment is not allowed. Non vitamin K oral anticoagulants (NOAK) and low molecular weight (LMW) heparin is allowed
  11. Pregnancy or breast-feeding
  12. Positive serum pregnancy test in women of childbearing potential.
  13. Subjects with reproductive potential not willing to use an effective method of contraception under and 3 months after participation in this study
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
24 participants (estimated)

Study arms

  • Experimental
    Treatment arm

    Drug: Trastuzumab

Interventions

  • DrugTrastuzumab

    Addition of trastuzumab to standard treatment (fluoropyrimidine/platinum doublet with pembrolizumab)

06

What researchers measure

Primary outcomes

  1. Progression free survival (PFS) .

    PFS according to RECIST 1.1

    Time frame: 6 months

Secondary outcomes

  1. Response rate according to RECIST 1.1

    Partial, complete and overall response rate according to RECIST 1.1

    Time frame: Best response during 6 months follow-up

  2. Frequency of AEs assessed by NCI CTCAE, v. 5.0

    Safety and tolerability of trastuzumab, pembrolizumab and a fluoropyrimidine/platinum assessed by NCI CTCAE, v. 5.0

    Time frame: During minimum 6 months follow-up

  3. Overall survival

    Time to death of all causes

    Time frame: 6 months

Other outcomes

  1. Change in amplified HER2 in ctDNA during treatment

    Clinical utility of measurements of amplified HER2 in ctDNA as a monitoring tool of treatment with 5-FU platinum, trastuzumab and pembrolizumab

    Time frame: During mininum 6 months follow-up

  2. Frequency of germeline Fc Gamma Receptor polymorphisms

    Predictive value of Fc Gamma Receptor polymorphisms in ESCC patients receiving

    Time frame: During minimum 6 months follow-up

  3. Frequency of PD-L1 status by CPS score

    PD-L1 status by CPS score

    Time frame: During minimum 6 months follow-up

07

Study locations

2 of 2 sites recruiting
  • Dept of Oncology, Rigshospitalet
    Copenhagen, Region H DK-2100, Denmark
    Recruiting
  • Onkologisk Afdeling R, Odense University Hospital
    Odense, Region Syd 5000, Denmark
    • Mette Falbe-Hansen, Nurse · Contact · +45 29658926
    • Per Pfeiffer, MD PhD · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 12, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05170256
Lead sponsor
Morten Mau-Sørensen
Collaborators
Odense University Hospital, Aalborg University Hospital, Aarhus University Hospital
Responsible party
Morten Mau-Sørensen (MD PhD, Rigshospitalet, Denmark) — Sponsor-investigator
First posted
Dec 27, 2021
Start date
Feb 4, 2022
Primary completion
Jan 2025 (estimated)
Completion
Jan 2025 (estimated)
Last update
Aug 12, 2022

Study contacts

Morten Mau-Sørensen, MD PhD
Contact
paul.morten.mau-soerensen@regionh.dk
35450879 ext. 0045
Kristian Egebjerg, MD
Contact
kristian.egebjerg.02@regionh.dk
Lene Baeksgaard, MD PhD
principal investigator · Rigshospitalet, Denmark

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Aug 2022. 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