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Recurrent Laryngeal CancerNCT03595410

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

An observational study of Recurrent Laryngeal Cancer, run by First Affiliated Hospital, Sun Yat-Sen University at 1 site in China.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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… Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Recurrent Laryngeal Cancer
What is being tested?
Recurrence laryngeal cancer
How many people
300 participants
Where
1 siteChina
Study dates
1 Jan 2017to 1 Jan 2020
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • Adult, Older adult

Study population: patients with laryngeal cancer

Who may be able to join

  • patients with a diagnosis of laryngeal squamous cell carcinoma

Who cannot join

  • multiple primarry malignant neo-plasms

Trial locations and contacts

1 site in 1 country.

China1 site, 1 recruiting
  • Genglong Liu

    Guangzhou, Guangdong

    Genglong Liu, MD, +8615626405844, lglong3@mail2.sysu.edu.cn

    Recruiting

Other trials in China

About this study

Official title: Development and Validation of Nomograms to Precisely Predict Conditional Risk of Recurrence for Patients With Laryngeal Cancer: a Single-institutional Study

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)

Being tested
Recurrence laryngeal cancer
Keywords
risk of recurrence, Nomograms, Laryngeal cancer
Medical subject headings
Laryngeal Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Recurrence laryngeal cancerOther

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

Study groups in NCT03595410
Study groupRoleWhat they receive
Recurrence laryngeal cancerNot described
Receives: Other: Recurrence laryngeal cancer
No recurrence laryngeal cancerNot described
Receives: Other: Recurrence laryngeal cancer

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Overall survival

    time from salvage laryngectomy to death from any cause

    Measured: Follow up 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Jul 2018
  2. Study start1 Jan 2017
  3. Primary completion1 Jan 2020 (estimated)
  4. Study completion1 Jan 2020 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03595410
Sponsor's protocol ID
Laryngeal carcinoma
Status last verified
Jul 2018
First submitted
13 Jul 2018
Last updated
23 Jul 2018
Results posted
No
FDA-regulated drug
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Recurrent Laryngeal Cancer, run by First Affiliated Hospital, Sun Yat-Sen University at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 23 Jul 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Genglong Liu, MD (+8615626405844, lglong3@mail2.sysu.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall survival (time frame: Follow up 5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jul 2018.

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