Eastern Cooperative Oncology Group and American College of Radiology Imaging Network Randomized Phase 2 Trial of Neoadjuvant Preoperative Paclitaxel/Cisplatin/Radiation Therapy (RT) or Irinotecan/Cisplatin/RT in Esophageal Adenocarcinoma: Long-Term Outcome and Implications for Trial Design

被引:19
作者
Kleinberg, Lawrence R. [1 ]
Catalano, Paul J. [2 ,3 ]
Forastiere, Arlene A. [4 ]
Keller, Steven M. [5 ]
Mitchel, Edith P. [6 ]
Anne, Pramila Rani [7 ]
Benson, Al B., III [8 ]
机构
[1] Johns Hopkins Univ, Dept Radiat Oncol & Mol Radiat Sci, 401 N Broadway,Ste 1440, Baltimore, MD 21231 USA
[2] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
[3] Harvard Univ, TH Chan Sch Publ Hlth, Boston, MA 02115 USA
[4] Johns Hopkins Univ, Dept Oncol, Baltimore, MD 21231 USA
[5] Montefiore Med Ctr, Dept Cardiovasc & Thorac Surg, 111 E 210th St, Bronx, NY 10467 USA
[6] Thomas Jefferson Univ, Dept Med Oncol, Philadelphia, PA 19107 USA
[7] Thomas Jefferson Univ, Dept Radiat Oncol, Philadelphia, PA 19107 USA
[8] Northwestern Univ, Dept Med Hematol Oncol, Lurie Canc Ctr, Chicago, IL 60611 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2016年 / 94卷 / 04期
关键词
CONCURRENT RADIOTHERAPY; II TRIAL; SURGERY; CANCER; CHEMORADIOTHERAPY; CISPLATIN; IRINOTECAN; PET; CHEMORADIATION; FLUOROURACIL;
D O I
10.1016/j.ijrobp.2015.12.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Toxicity, pathologic complete response, and long-term outcomes are reported for the neoadjuvant therapies assessed in a randomized phase 2 Eastern Cooperative Oncology Group and American College of Radiology Imaging Network trial for operable esophageal adenocarcinoma, staged as II-IVa by endoscopy/ultrasonography (EUS). Methods and Materials: A total of 86 eligible patients began treatment. For arm A, preoperative chemotherapy was cisplatin, 30 mg/m(2), and irinotecan, 50 mg/m(2), on day 1, 8, 22, 29 during 45 Gy radiation therapy (RT), 1.8 Gy per day over 5 weeks. Adjuvant therapy was cisplatin, 30 mg/m(2), and irinotecan, 65 mg/m(2) day 1, 8 every 21 days for 3 cycles. Arm B therapy was cisplatin, 30 mg/m(2), and paclitaxel, 50 mg/m(2), day 1, 8, 15, 22, 29 with RT, followed by adjuvant cisplatin, 75 mg/m(2), and paclitaxel, 175 mg/m(2), day 1 every 21 days for 3 cycles. Stratification included EUS stage and performance status. Results: In arm A, median overall survival was 35 months, and 5-, 6-, and 7-year survival rates were 46%, 39%, and 35%, respectively, whereas for arm B, they were 21 months and 27%, 27%, and 23%, respectively. Median progression-or recurrence-free survival (PFS) was 39.8 months with a 3-year PFS of 50% for arm A and 12.4 months (P=. 046) with 3-year PFS of 28% for arm B. Eighty percent of the observed incidents of progression occurred within 19 months. Survival did not differ significantly by EUS and performance status strata. Conclusions: Long-term survival was similar for both arms and did not appear superior to results achieved with other standard regimens. (c) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:738 / 746
页数:9
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