Randomized Phase II Study of PET Response-Adapted Combined Modality Therapy for Esophageal Cancer: Mature Results of the CALGB 80803 (Alliance) Trial

被引:70
作者
Goodman, Karyn A. [1 ]
Ou, Fang-Shu [2 ]
Hall, Nathan C. [3 ]
Bekaii-Saab, Tanios [4 ]
Fruth, Briant [2 ]
Twohy, Erin [2 ]
Meyers, Michael O. [5 ]
Boffa, Daniel J. [6 ]
Mitchell, Kisha [7 ]
Frankel, Wendy L. [8 ]
Niedzwiecki, Donna [9 ]
Noonan, Anne [8 ]
Janjigian, Yelena Y. [10 ]
Thurmes, Paul J. [11 ]
Venook, Alan P. [12 ]
Meyerhardt, Jeffrey A. [13 ]
O'Reilly, Eileen M. [10 ]
Ilson, David H. [10 ]
机构
[1] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[2] Mayo Clin, Alliance Stat & Data Ctr, Rochester, MN USA
[3] Hosp Univ Penn, Philadelphia, PA 19104 USA
[4] Mayo Clin, Canc Ctr, Scottsdale, AZ USA
[5] Univ N Carolina, Chapel Hill, NC 27515 USA
[6] Yale Univ, New Haven, CT USA
[7] Greenwich Hosp, Greenwich, CT USA
[8] Ohio State Univ, Wexner Med Ctr, Columbus, OH 43210 USA
[9] Duke Univ, Durham, NC USA
[10] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[11] Metro Minnesota Community Oncol Res Consortium, Minneapolis, MN USA
[12] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[13] Dana Farber Partners CancerCare, Boston, MA USA
基金
美国国家卫生研究院;
关键词
PREOPERATIVE CHEMORADIATION; ESOPHAGOGASTRIC JUNCTION; INDUCTION CHEMOTHERAPY; NEOADJUVANT CHEMORADIOTHERAPY; TRIMODALITY THERAPY; SURGERY; ADENOCARCINOMAS; FLUOROURACIL; METAANALYSIS; SURVIVAL;
D O I
10.1200/JCO.20.03611
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE To evaluate the use of early assessment of chemotherapy responsiveness by positron emission tomography (PET) imaging to tailor therapy in patients with esophageal and esophagogastric junction adenocarcinoma. METHODS After baseline PET, patients were randomly assigned to an induction chemotherapy regimen: modified oxaliplatin, leucovorin, and fluorouracil (FOLFOX) or carboplatin-paclitaxel (CP). Repeat PET was performed after induction; change in maximum standardized uptake value (SUV) from baseline was assessed. PET nonresponders (< 35% decrease in SUV) crossed over to the alternative chemotherapy during chemoradiation (50.4 Gy/28 fractions). PET responders (>= 35% decrease in SUV) continued on the same chemotherapy during chemoradiation. Patients underwent surgery at 6 weeks postchemoradiation. Primary end point was pathologic complete response (pCR) rate in nonresponders after switching chemotherapy. RESULTS Two hundred forty-one eligible patients received Protocol treatment, of whom 225 had an evaluable repeat PET. The pCR rates for PET nonresponders after induction FOLFOX who crossed over to CP (n = 39) or after induction CP who changed to FOLFOX (n = 50) was 18.0% (95% CI, 7.5 to 33.5) and 20% (95% CI, 10 to 33.7), respectively. The pCR rate in responders who received induction FOLFOX was 40.3% (95% CI, 28.9 to 52.5) and 14.1% (95% CI, 6.6 to 25.0) in responders to CP. With a median follow-up of 5.2 years, median overall survival was 48.8 months (95% CI, 33.2 months to not estimable) for PET responders and 27.4 months (95% CI, 19.4 months to not estimable) for nonresponders. For induction FOLFOX patients who were PET responders, median survival was not reached. CONCLUSION Early response assessment using PET imaging as a biomarker to individualize therapy for patients with esophageal and esophagogastric junction adenocarcinoma was effective, improving pCR rates in PET nonresponders. PET responders to induction FOLFOX who continued on FOLFOX during chemoradiation achieved a promising 5-year overall survival of 53%.
引用
收藏
页码:2803 / +
页数:20
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