Comparative effectiveness of induction chemotherapy for oropharyngeal squamous cell carcinoma: A population-based analysis

被引:19
作者
Sher, David J. [1 ,2 ]
Schwartz, David L. [3 ]
Nedzi, Lucien [3 ]
Khan, Saad [4 ]
Hughes, Randall [4 ]
Fidler, Mary Jo [5 ]
Koshy, Matthew [6 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Radiat Oncol, 5810 Forest Pk Dr, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Div Outcomes & Hlth Serv Res, 5810 Forest Pk Dr, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Radiat Oncol, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Med Oncol, Dallas, TX 75390 USA
[5] Rush Univ, Med Ctr, Dept Med Oncol, Chicago, IL 60612 USA
[6] Univ Chicago, Dept Radiat Oncol, Chicago, IL 60637 USA
关键词
Head and neck cancer; Induction chemotherapy; Combined modality therapy; Outcomes research; Chemoradiotherapy; Oropharyngeal cancer; Human papillomavirus; LOCALLY ADVANCED HEAD; PHASE-III TRIAL; NECK-CANCER; NEOADJUVANT CHEMOTHERAPY; RANDOMIZED-TRIAL; UNITED-STATES; RADIOTHERAPY; CHEMORADIOTHERAPY; COMBINATION; MANAGEMENT;
D O I
10.1016/j.oraloncology.2015.12.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Despite several randomized trials, the optimal chemotherapy paradigm for locally advanced oropharyngeal carcinoma (OPSCC) is controversial. This population-based analysis assessed the overall survival (OS) benefit of induction chemotherapy (IC) for patients with stage III-IVB OPSCC. Materials and Methods: Patients in the National Cancer Database with stage III-IVA-B OPSCC treated with curative-dose radiotherapy and IC or concurrent chemotherapy (CRT) between 2003 and 2011 were eligible. The primary outcome was OS, and secondary endpoints included OS for high-risk (T4 and/or N3 disease) and human papillomavirus (HPV) subsets. Results: Of the 14,856 analyzed patients, 78% and 22% received CRT and IC, respectively. With a median follow-up for surviving patients of 44 months, the 5-year OS probability for the entire cohort was 66% (66% CRT vs. 64% IC, p = 0.022). Multivariable survival analysis showed no significant difference between CRT and IC (hazard ratio, HR, 0.95 for IC, p = 0.255), and sensitivity analyses to adjust for immortal time bias brought the HR to 1.0 (p = 0.859). There was also no OS difference for high-risk patients. There was a trend in favor of CRT for HPV-positive OPSCC (HR 1.63 with IC, p = 0.064), with a significant OS benefit for HPV-negative, high-risk OPSCC (HR 0.63, p = 0.048). Conclusion: For the vast majority of patients, including HPV-positive individuals, there was no difference in OS with IC, arguing for CRT to remain as the standard therapy. Subset analysis revealed a small cohort of aggressive cancer (T4/N3 HPV-negative) which may benefit from from IC, although selection bias could not be ruled out. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:58 / 67
页数:10
相关论文
共 21 条
[1]  
American College of Surgeons, NAT CANC DAT
[2]   Head and neck carcinoma in the United States [J].
Ang, K. Kian ;
Chen, Amy ;
Curran, Walter J., Jr. ;
Garden, Adam S. ;
Harari, Paul M. ;
Murphy, Barbara A. ;
Wong, Stuart J. ;
Bellm, Lisa A. ;
Schwartz, Marc ;
Newman, Jason ;
Adkins, Douglas ;
Hayes, D. Neil ;
Parvathaneni, Upendra ;
Brachman, David ;
Ghabach, Bassam ;
Schneider, Charles J. ;
Greenberg, Michael ;
Anne, Pramila R. .
CANCER, 2012, 118 (23) :5783-5792
[3]   Current Management of Locally Advanced Head and Neck Cancer: The Combination of Chemotherapy With Locoregional Treatments [J].
Bar-Ad, Voichita ;
Palmer, Joshua ;
Yang, Hushan ;
Cognetti, David ;
Curry, Joseph ;
Luginbuhl, Adam ;
Tuluc, Madalina ;
Campling, Barbara ;
Axelrod, Rita .
SEMINARS IN ONCOLOGY, 2014, 41 (06) :798-806
[4]   Hyperfractionated or accelerated radiotherapy in head and neck cancer:: a meta-analysis [J].
Bourhis, Jean ;
Overgaard, Jens ;
Audry, Helene ;
Ang, Kian K. ;
Saunders, Michele ;
Bernier, Jacques ;
Horiot, Jean-Claude ;
Le Maitre, Aurlie ;
Pajak, Thomas F. ;
Paulsen, Michael G. ;
O'Sullivan, Brian ;
Dobrowsky, Werner ;
Hliniak, Andrzej ;
Skladowski, Krzysztof ;
Hay, John H. ;
Pinto, Luiz H. J. ;
Fallai, Carlo ;
Fu, Karen K. ;
Sylvester, Richard ;
Pignon, Jean-Pierre .
LANCET, 2006, 368 (9538) :843-854
[5]  
Coca-Perraillon M., 2006, NE SAS US GROUP C NE
[6]   Phase III Randomized Trial of Induction Chemotherapy in Patients With N2 or N3 Locally Advanced Head and Neck Cancer [J].
Cohen, Ezra E. W. ;
Karrison, Theodore G. ;
Kocherginsky, Masha ;
Mueller, Jeffrey ;
Egan, Robyn ;
Huang, Chao H. ;
Brockstein, Bruce E. ;
Agulnik, Mark B. ;
Mittal, Bharat B. ;
Yunus, Furhan ;
Samant, Sandeep ;
Raez, Luis E. ;
Mehra, Ranee ;
Kumar, Priya ;
Ondrey, Frank ;
Marchand, Patrice ;
Braegas, Bettina ;
Seiwert, Tanguy Y. ;
Villaflor, Victoria M. ;
Haraf, Daniel J. ;
Vokes, Everett E. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (25) :2735-+
[7]   Randomized trial of neoadjuvant chemotherapy in oropharyngeal carcinoma [J].
Domenge, C ;
Hill, C ;
Lefebvre, JL ;
De Raucourt, D ;
Rhein, B ;
Wibault, P ;
Marandas, P ;
Coche-Dequeant, B ;
Stromboni-Luboinski, M ;
Sancho-Garnier, H ;
Luboinski, B .
BRITISH JOURNAL OF CANCER, 2000, 83 (12) :1594-1598
[8]   The Never-Ending Story: Finding a Role for Neoadjuvant Chemotherapy in the Management of Head and Neck Cancer [J].
Garden, Adam S. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (25) :2685-2686
[9]   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
[10]   Why has induction chemotherapy for advanced head and neck cancer become a United States community standard of practice? [J].
Harari, PM .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (05) :2050-2055