E1308: Phase II Trial of Induction Chemotherapy Followed by Reduced-Dose Radiation and Weekly Cetuximab in Patients With HPV-Associated Resectable Squamous Cell Carcinoma of the Oropharynx-ECOG-ACRIN Cancer Research Group

被引:348
作者
Marur, Shanthi [1 ]
Li, Shuli [2 ]
Cmelak, Anthony J. [3 ]
Gillison, Maura L. [4 ]
Zhao, Weiqiang J. [4 ]
Ferris, Robert L. [5 ]
Westra, William H. [1 ]
Gilbert, Jill [3 ]
Bauman, Julie E. [5 ]
Wagner, Lynne I. [6 ]
Trevarthen, David R. [7 ]
Balkrishna, Jahagirdar [8 ]
Murphy, Barbara A. [3 ]
Agrawal, Nishant [9 ]
Colevas, A. Dimitrios [10 ]
Chung, Christine H. [11 ]
Burtness, Barbara [12 ]
机构
[1] Johns Hopkins Univ, Baltimore, MD USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Vanderbilt Univ, 221 Kirkland Hall, Nashville, TN 37235 USA
[4] Ohio State Univ, Columbus, OH 43210 USA
[5] Univ Pittsburgh, Pittsburgh, PA USA
[6] Wake Forest Sch Med, Winston Salem, NC USA
[7] Colorado Canc Res Program, Denver, CO USA
[8] Univ Minnesota, St Paul, MN 55108 USA
[9] Univ Chicago Med, Chicago, IL USA
[10] Stanford Univ, Stanford, CA 94305 USA
[11] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[12] Yale Univ, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
LOCALLY-ADVANCED HEAD; COOPERATIVE-ONCOLOGY-GROUP; NECK-CANCER; HUMAN-PAPILLOMAVIRUS; PLUS CETUXIMAB; STANDARD FRACTIONATION; ORGAN PRESERVATION; RADIOTHERAPY; CISPLATIN; THERAPY;
D O I
10.1200/JCO.2016.68.3300
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Human papillomavirus (HPV)-associated oropharyngeal squamous cell carcinoma (OPSCC) is treatment-responsive. Definitive chemoradiation results in high cure rates but causes long-term toxicity andZ may represent overtreatment of some patients. This phase II trial evaluated whether complete clinical response (cCR) to induction chemotherapy (IC) could select patients with HPV-associated OPSCC for reduced radiation dose as a means of sparing late sequelae. Methods Patients with HPV16 and/or p16-positive, stage III-IV OPSCC received three cycles of IC with cisplatin, paclitaxel, and cetuximab. Patients with primary-site cCR to IC received intensity-modulated radiation therapy (IMRT) 54 Gy with weekly cetuximab; those with less than cCR to IC at the primary site or nodes received 69.3 Gy and cetuximab to those regions. The primary end point was 2-year progression-free survival. Results Of the 90 patients enrolled, 80 were evaluable. Their median age was 57 years (range, 35 to 73 years), with the majority having stage T1-3N0-N2b OPSCC and a history of <= 10 pack-years of cigarette smoking. Three cycles of IC were delivered to 77 of the 80 patients. Fifty-six patients (70%) achieved a primary-site cCR to IC and 51 patients continued to cetuximab with IMRT 54 Gy. After median follow-up of 35.4 months, 2-year progression-free survival and overall survival rates were 80% and 94%, respectively, for patients with primary-site cCR treated with 54 Gy of radiation (n = 51); 96% and 96%, respectively, for patients with < T4, < N2c, and <= 10 pack-year smoking history who were treated with <= 54 Gy of radiation (n = 27). At 12 months, significantly fewer patients treated with a radiation dose <= 54 Gy had difficulty swallowing solids (40% v 89%; P =.011) or had impaired nutrition (10% v 44%; P =.025). Conclusion For IC responders, reduced-dose IMRT with concurrent cetuximab is worthy of further study in favorable-risk patients with HPV-associated OPSCC. Radiation dose reduction resulted in significantly improved swallowing and nutritional status.
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页码:490 / +
页数:12
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