Phase III Randomized Trial of Induction Chemotherapy in Patients With N2 or N3 Locally Advanced Head and Neck Cancer

被引:410
作者
Cohen, Ezra E. W. [1 ]
Karrison, Theodore G. [1 ]
Kocherginsky, Masha [1 ]
Mueller, Jeffrey [1 ]
Egan, Robyn [1 ]
Huang, Chao H. [4 ,5 ]
Brockstein, Bruce E. [2 ]
Agulnik, Mark B. [3 ]
Mittal, Bharat B. [3 ]
Yunus, Furhan [6 ]
Samant, Sandeep [6 ]
Raez, Luis E. [7 ]
Mehra, Ranee [8 ]
Kumar, Priya [9 ]
Ondrey, Frank [9 ]
Marchand, Patrice [10 ]
Braegas, Bettina [10 ]
Seiwert, Tanguy Y. [1 ]
Villaflor, Victoria M. [1 ]
Haraf, Daniel J. [1 ]
Vokes, Everett E. [1 ]
机构
[1] Univ Chicago, Chicago, IL 60637 USA
[2] North Shore Univ Hlth Syst, Evanston, IL USA
[3] Northwestern Univ, Chicago, IL 60611 USA
[4] Univ Kansas, Kansas City, KS USA
[5] Vet Affairs Med Ctr, Kansas City, KS USA
[6] Univ Tennessee, Memphis, TN USA
[7] Univ Miami, Miami, FL USA
[8] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[9] Univ Minnesota, Minneapolis, MN USA
[10] Nuvisan Oncol, Le Kremlin Bicetre, France
关键词
LOCOREGIONALLY ADVANCED HEAD; STIMULATING FACTOR SUPPORT; CONCOMITANT CHEMORADIOTHERAPY; CONCURRENT CHEMORADIOTHERAPY; DISTANT METASTASIS; CLINICAL-TRIALS; FLUOROURACIL; HYDROXYUREA; PACLITAXEL; DOCETAXEL;
D O I
10.1200/JCO.2013.54.6309
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Induction chemotherapy (IC) before radiotherapy lowers distant failure (DF) rates in locally advanced squamous cell carcinoma of the head and neck (SCCHN). The goal of this phase III trial was to determine whether IC before chemoradiotherapy (CRT) further improves survival compared with CRT alone in patients with N2 or N3 disease. Patients and Methods Treatment-naive patients with nonmetastatic N2 or N3 SCCHN were randomly assigned to CRT alone (CRT arm; docetaxel, fluorouracil, and hydroxyurea plus radiotherapy 0.15 Gy twice per day every other week) versus two 21-day cycles of IC (docetaxel 75 mg/m(2) on day 1, cisplatin 75 mg/m(2) on day 1, and fluorouracil 750 mg/m(2) on days 1 to 5) followed by the same CRT regimen (IC + CRT arm). The primary end point was overall survival (OS). Secondary end points included DF-free survival, failure pattern, and recurrence-free survival (RFS). Results A total of 285 patients were randomly assigned. The most common grade 3 to 4 toxicities during IC were febrile neutropenia (11%) and mucositis (9%); during CRT (both arms combined), they were mucositis (49%), dermatitis (21%), and leukopenia (18%). Serious adverse events were more common in the IC arm (47% v 28%; P = .002). With a minimum follow-up of 30 months, there were no statistically significant differences in OS (hazard ratio, 0.91; 95% CI, 0.59 to 1.41), RFS, or DF-free survival. Conclusion IC did not translate into improved OS compared with CRT alone. However, the study was underpowered because it did not meet the planned accrual target, and OS was higher than predicted in both arms. IC cannot be recommended routinely in patients with N2 or N3 locally advanced SCCHN. (C) 2014 by American Society of Clinical Oncology
引用
收藏
页码:2735 / +
页数:13
相关论文
共 26 条
[1]   Taxane-Cisplatin-Fluorouracil As Induction Chemotherapy in Locally Advanced Head and Neck Cancers: An Individual Patient Data Meta-Analysis of the Meta-Analysis of Chemotherapy in Head and Neck Cancer Group [J].
Blanchard, Pierre ;
Bourhis, Jean ;
Lacas, Benjamin ;
Posner, Marshall R. ;
Vermorken, Jan B. ;
Cruz Hernandez, Juan J. ;
Bourredjem, Abderrahmane ;
Calais, Gilles ;
Paccagnella, Adriano ;
Hitt, Ricardo ;
Pignon, Jean-Pierre .
JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (23) :2854-+
[2]   Phase I study of concomitant chemoradiotherapy with paclitaxel, fluorouracil, and hydroxyurea with granulocyte colony-stimulating factor support for patients with poor-prognosis cancer of the head and neck [J].
Brockstein, B ;
Haraf, DJ ;
Stenson, K ;
Fasanmade, A ;
Stupp, R ;
Glisson, B ;
Lippman, SM ;
Ratain, MJ ;
Sulzen, L ;
Klepsch, A ;
Weichselbaum, RR ;
Vokes, EE .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) :735-744
[3]   A phase I-II study of concomitant chemoradiotherapy with paclitaxel (one-hour infusion), 5-fluorouracil and hydroxyurea with granulocyte colony stimulating factor support for patients with poor prognosis head and neck cancer [J].
Brockstein, B ;
Haraf, DJ ;
Stenson, K ;
Sulzen, L ;
Witt, ME ;
Weichselbaum, RW ;
Vokes, EE .
ANNALS OF ONCOLOGY, 2000, 11 (06) :721-728
[4]   Patterns of failure, prognostic factors and survival in locoregionally advanced head and neck cancer treated with concomitant chemoradiotherapy: a 9-year, 337-patient, multi-institutional experience [J].
Brockstein, B ;
Haraf, DJ ;
Rademaker, AW ;
Kies, MS ;
Stenson, KM ;
Rosen, F ;
Mittal, BB ;
Pelzer, H ;
Fung, BB ;
Witt, ME ;
Wenig, B ;
Portugal, L ;
Weichselbaum, RW ;
Vokes, EE .
ANNALS OF ONCOLOGY, 2004, 15 (08) :1179-1186
[5]   Epidermal Growth Factor Receptor Inhibitor Gefitinib Added to Chemoradiotherapy in Locally Advanced Head and Neck Cancer [J].
Cohen, Ezra E. W. ;
Haraf, Daniel J. ;
Kunnavakkam, Rangesh ;
Stenson, Kerstin M. ;
Blair, Elizabeth A. ;
Brockstein, Bruce ;
Lester, Eric P. ;
Salama, Joseph K. ;
Dekker, Allison ;
Williams, Rosalyn ;
Witt, Mary Ellyn ;
Grushko, Tatyana A. ;
Dignam, James J. ;
Lingen, Mark W. ;
Olopade, Olufunmilayo I. ;
Vokes, Everett E. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (20) :3336-3343
[6]  
COX DR, 1972, J R STAT SOC B, V34, P187
[7]   A proportional hazards model for the subdistribution of a competing risk [J].
Fine, JP ;
Gray, RJ .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1999, 94 (446) :496-509
[8]  
Gooley TA, 1999, STAT MED, V18, P695, DOI 10.1002/(SICI)1097-0258(19990330)18:6<695::AID-SIM60>3.3.CO
[9]  
2-F
[10]   Induction chemotherapy followed by concurrent chemoradiotherapy (sequential chemoradiotherapy) versus concurrent chemoradiotherapy alone in locally advanced head and neck cancer (PARADIGM): a randomised phase 3 trial [J].
Haddad, Robert ;
O'Neill, Anne ;
Rabinowits, Guilherme ;
Tishler, Roy ;
Khuri, Fadlo ;
Adkins, Douglas ;
Clark, Joseph ;
Sarlis, Nicholas ;
Lorch, Jochen ;
Beitler, Jonathan J. ;
Limaye, Sewanti ;
Riley, Sarah ;
Posner, Marshall .
LANCET ONCOLOGY, 2013, 14 (03) :257-264