CClinicalTrials.gg
Status unknownNCT03595410Updated Jul 23, 2018

Nomograms to Precisely Predict Conditional Risk of Recurrence for Patients With Laryngeal Cancer

An observational study in Recurrent Laryngeal Cancer, sponsored by First Affiliated Hospital, Sun Yat-Sen University. Status unknown at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2018-07-23.

Sponsored by First Affiliated Hospital, Sun Yat-Sen University · Observational

The sponsor has not verified this record recently (last verified Jul 2018), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
300
Ages
18 Years to 75 Years
Sex
All
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Study summary

Advanced laryngeal squamous cell carcinoma (SCC) remains a highly morbid and fatal disease despite aggressive interventions. Mortality is high in this cohort: laryngeal cancer affects over 13 000 patients in the United States, with over 3500 deaths annually.The results of the Veterans Affairs Cooperative Studies Program Laryngeal Cancer Trial and subsequent studies demonstrated similar overall survival (OS) rates for organ preservation protocols involving radiotherapy (RT) or chemoradiotherapy (CRT) when compared to surgery, with the benefit of preserving the larynx in a large majority of patients. As such, the use of RT or CRT has become the predominant initial intervention for patients with laryngeal SCC.6 However, the prognosis of recurrent and persistent laryngeal SCC is particularly dire.In this study, we sought to identify preoperative predictors of survival for patients with recurrent or persistent laryngeal SCC in order to set patient expectations and address modifiable risk factors. Identification of predictors of survival may also identify patients who could benefit from novel therapeutic agents in a neo/adjuvant fashion. Herein,we examine a cohort of patients with recurrent or persistent laryngeal SCC after definitive RT/CRT who has undergone total laryngectomy in order to identify potential preoperative predictors of clinical outcomes.

Read the detailed description

Demographic, clinical, and survival data were abstracted. Death was verified via medical records and the social security death index. Primary outcome measures were OS (time from salvage laryngectomy to death from any cause), disease-specific survival (DSS; time from salvage laryngectomy to death from recurrent/persistent laryngeal SCC), and DFS (time from salvage laryngectomy to laryngeal SCC recurrence)

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Conditions studied

  • Recurrent Laryngeal Cancer

Keywords

  • risk of recurrence
  • Nomograms
  • Laryngeal cancer
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In context

Laryngeal Neoplasms

244 studies on the registry are indexed under Laryngeal Neoplasms; 63 are open to participants now.

This study's planned enrollment of 300 is above the median of 100 across 54 observational studies indexed under Laryngeal Neoplasms.

Browse Laryngeal Neoplasms studies →

Lead sponsor

First Affiliated Hospital, Sun Yat-Sen University is the lead sponsor of 155 studies on the registry; 51 are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Sampling method
Probability sample

Study population

patients with laryngeal cancer

Inclusion criteria

patients with a diagnosis of laryngeal squamous cell carcinoma

Exclusion criteria

Exclusion Criteria:

multiple primarry malignant neo-plasms

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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
300 participants (estimated)
Patient registry
No

Groups and cohorts

  • Recurrence laryngeal cancer

    Other: Recurrence laryngeal cancer

  • No recurrence laryngeal cancer

    Other: Recurrence laryngeal cancer

Interventions

  • OtherRecurrence laryngeal cancer

    Recurrence laryngeal cancer has a wide range of invasion, rapid progression and poor prognosis.

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What researchers measure

Primary outcomes

  1. Overall survival

    time from salvage laryngectomy to death from any cause

    Time frame: Follow up 5 years

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Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 23, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03595410
Lead sponsor
First Affiliated Hospital, Sun Yat-Sen University
Responsible party
GengLong Liu (Principal Investigator, First Affiliated Hospital, Sun Yat-Sen University) — Principal investigator
First posted
Jul 23, 2018
Start date
Jan 1, 2017
Primary completion
Jan 1, 2020 (estimated)
Completion
Jan 1, 2020 (estimated)
Last update
Jul 23, 2018

Study contacts

Genglong Liu, MD
Contact
lglong3@mail2.sysu.edu.cn
+8615626405844
Genglong Liu
principal investigator · First Affiliated Hospital, Sun Yat-Sen University

Oversight

FDA-regulated drug
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2018. You cannot join it, but the record below documents what was studied.

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