International Journal of Radiation Oncology * Biology * Physics
Volume 73, Issue 5 , Pages 1293-1303, 1 April 2009

Larynx Preservation Clinical Trial Design: Key Issues and Recommendations—A Consensus Panel Summary

  • Jean-Louis Lefebvre, M.D.

      Affiliations

    • Département de Cancérologie Cervico-Faciale, Centre Oscar Lambret, Lille, France
    • Corresponding Author InformationReprint requests to: Jean-Louis Lefebvre, M.D., Département de Cancérologie Cervico–Faciale, Centre Oscar Lambret, 3 rue Frédéric Combemale, B.P. 307, F-59020, Lille, France. Tel: +33 3 2029 5531; Fax: +33 3 2029 5961
  • ,
  • K. Kian Ang, M.D.

      Affiliations

    • University of Texas MD Anderson Cancer Center, Houston, TX
  • ,
  • Larynx Preservation Consensus Panel

Received 7 August 2008; received in revised form 24 October 2008; accepted 30 October 2008.

Purpose

To develop guidelines for the conduct of Phase III clinical trials of larynx preservation in patients with locally advanced laryngeal and hypopharyngeal cancer.

Methods and Materials

A multidisciplinary international consensus panel developed recommendations after reviewing results from completed Phase III randomized trials, meta-analyses, and published clinical reports with updates available through November, 2007. The guidelines were reviewed and approved by the panel.

Results

According to the recommendations, the trial population should include patients with T2 or T3 laryngeal or hypopharyngeal squamous cell carcinoma not considered for partial laryngectomy and exclude those with laryngeal dysfunction or age greater than 70 years. Functional assessments should include speech and swallowing. Voice should be routinely assessed with a simple, validated instrument. The primary endpoint should capture survival and function. The panel created a new endpoint: laryngo-esophageal dysfunction–free survival. Events are death, local relapse, total or partial laryngectomy, tracheotomy at 2 years or later, or feeding tube at 2 years or later. Recommended secondary endpoints are overall survival, progression-free survival, locoregional control, time to tracheotomy, time to laryngectomy, time to discontinuation of feeding tube, and quality of life/patient-reported outcomes. Correlative biomarker studies for near-term trials should include estimated glomerular filtration rate, excision repair cross-complementary-1 gene, E-cadherin and β-catenin, epiregulin and amphiregulin, and TP53 mutation.

Conclusions

Revised trial designs in several key areas are needed to advance the study of larynx preservation. With consistent methodologies, clinical trials can more effectively evaluate and quantify the therapeutic benefit of novel treatment options for patients with locally advanced laryngeal and hypopharyngeal cancer.

Head and neck carcinoma, Larynx preservation, Guidelines, Laryngeal carcinoma, Hypopharyngeal carcinoma

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 Sources of support: Sanofi-Aventis.

 Conflict of interest: Jean-Louis Lefebvre has potential conflicts of interest with Sanofi-Aventis, Merck Serono, IRX Therapeutics, and Genmab. K. Kian Ang has served on Advisory Boards of AstraZeneca, BMS, Imclone Systems Inc., Merck Serono, and Sanofi-Aventis. These commitments do not interfere with performing the task presented in the manuscript.

 To be published simultaneously in Head & Neck.

PII: S0360-3016(08)03693-6

doi:10.1016/j.ijrobp.2008.10.047

International Journal of Radiation Oncology * Biology * Physics
Volume 73, Issue 5 , Pages 1293-1303, 1 April 2009