医学
福克斯
危险系数
结直肠癌
全直肠系膜切除术
新辅助治疗
外科
卡培他滨
人口
临床终点
养生
中期分析
内科学
奥沙利铂
随机对照试验
肿瘤科
置信区间
癌症
乳腺癌
环境卫生
作者
Deborah Schrag,Qian Shi,Martin R. Weiser,Marc J. Gollub,Leonard B. Saltz,Benjamin Musher,Joel E. Goldberg,Tareq Al Baghdadi,Karyn A. Goodman,Robert R. McWilliams,Jeffrey M. Farma,Thomas J. George,Hagen F. Kennecke,Alan P. Venook,Eileen M. O’Reilly,Jeffrey A. Meyerhardt,Amylou C. Dueck,Ethan Basch,George J. Chang,Harvey J. Mamon
标识
DOI:10.1200/jco.2023.41.17_suppl.lba2
摘要
LBA2 Background: Radiation with sensitizing fluoropyrimidine (5FUCRT) is a standard curative intent treatment for LARC. It improves disease-free survival (DFS) by decreasing pelvic recurrence but has short- and long-term toxicity. The PROSPECT trial compares FOLFOX chemotherapy with selective use of 5FUCRT (intervention) to 5FUCRT (control) for neoadjuvant treatment prior to TME for LARC. Methods: Eligible patients (pts) had cT2N+, cT3N-, cT3N+ rectal cancers deemed appropriate for neoadjuvant therapy prior to low anterior resection with TME. Pts with distal, T4 tumors, threatened radial margins or > 4 enlarged lymph nodes were ineligible. Pts were randomized 1:1 without blinding. Pts in the control group received 5FUCRT with 5040 cGy over 5.5 weeks with either capecitabine or 5FU. Pts in the intervention group had 6 cycles of mFOLFOX6 followed by restaging. If tumor regression was > 20%, then TME was performed without radiation; if < 20%, 5FUCRT was given before TME. DFS was the 1°outcome, defined as time from randomization to any recurrence or death, analyzed in the per-protocol population. One interim analysis was conducted with α spending = 0.001. Noninferiority (NI) of the intervention could be claimed if the upper limit of the 2-sided 90.2% confidence interval (CI) of the DFS hazard ratio did not exceed 1.29 (NI margin). Secondary endpoints included overall survival (OS), local recurrence free survival, R0 resection, pathologic complete response (CR), and toxicity. Results: From June 2012 to December 2018, 1194, pts were randomized and 1128 initiated protocol-assigned treatment. Median age was 57, 34.5% were women and 61.9% had clinically positive nodes. 53 of 585 pts in the intervention group (9%) received preop 5FUCRT. DFS was analyzed after 227 events and median follow-up of 58 months. Conclusions: FOLFOX chemotherapy with selective use of 5FUCRT is non-inferior to 5FUCRT for neoadjuvant treatment of LARC prior to low anterior resection with TME. Patients and physicians have alternative strategies for management of LARC. Clinical trial information: NCT01515787 . [Table: see text]
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