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术前卡培他滨和奥沙利铂强化放化疗联合或不联合诱导化疗用于局部晚期直肠癌合并同步肝局限性可切除转移患者的II期研究

Phase II Study of Preoperative Capecitabine and Oxaliplatin-based Intensified Chemoradiotherapy With or Without Induction Chemotherapy in Patients With Locally Advanced Rectal Cancer and Synchronous Liver-limited Resectable Metastases.

作者信息

Cho Hyungwoo, Kim Jeong Eun, Kim Kyu-Pyo, Yu Chang Sik, Kim Jin Cheon, Kim Jong Hoon, Lee Myung Ah, Jang Hong Seok, Oh Seong Taek, Kim Sun Young, Oh Jae Hwan, Kim Dae Yong, Hong Yong Sang, Kim Tae Won

机构信息

*Department of Internal Medicine, Asan Medical Center Departments of †Oncology ‡Surgery §Radiation Oncology, Asan Medical Center, University of Ulsan College of Medicine Departments of ∥Medical Oncology ¶Radiation Oncology #Colorectal Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul **Center for Colorectal Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Korea.

出版信息

Am J Clin Oncol. 2016 Dec;39(6):623-629. doi: 10.1097/COC.0000000000000315.

Abstract

OBJECTIVES

Controversy surrounds the management of patients with locally advanced rectal cancer with synchronous resectable liver metastases (LMs). This study was designed to improve both systemic and local control in these patients.

METHODS

Patients with locally advanced rectal cancer (cT3-4N0 or cTanyN1-2) and synchronous resectable liver-limited metastases (cM1a) were randomly assigned to receive either preoperative treatments of induction CapeOx, followed by chemoradiotherapy with CapeOx (CapeOx-RT) (arm A) or CapeOx-RT alone (arm B). Induction CapeOx consisted of oxaliplatin 130 mg/m on day 1 and capecitabine 1000 mg/m twice daily on days 1 to 14, every 3 weeks for 2 cycles; CapeOx-RT consisted of radiotherapy with 45 Gy/25 daily fractions±5.4 Gy/3 fractions, oxaliplatin 50 mg/m weekly for 5 weeks, and capecitabine 825 mg/m twice daily on days 1 to 38. Total mesorectal excision and simultaneous liver metastasectomy were planned within 6 weeks after completion of preoperative treatments. The primary endpoint was R0 resection rate of both the primary tumor and LMs.

RESULTS

Thirty-eight patients were randomly assigned to the present study, 18 to arm A and 20 to arm B. The overall R0 resection rate for both the primary tumor and LMs was 77.8% in arm A and 70.0% in arm B (P=0.72). The median progression-free survival was 14.2 versus 15.1 months (P=0.422) and the 3-year overall survival rate was 75.0% versus 88.8% (P=0.29), respectively.

CONCLUSIONS

Both treatment strategies showed considerable R0 resection rates; however, further study will be warranted to apply these intensified strategies in clinical practice.

摘要

目的

局部晚期直肠癌合并可同步切除肝转移瘤(LMs)患者的治疗存在争议。本研究旨在改善这些患者的全身和局部控制。

方法

局部晚期直肠癌(cT3 - 4N0或cTanyN1 - 2)合并可同步切除的局限于肝脏的转移瘤(cM1a)患者被随机分配接受术前诱导性 CapeOx 治疗,随后进行 CapeOx 同步放化疗(A组)或单纯 CapeOx 同步放化疗(B组)。诱导性 CapeOx 方案为第1天静脉滴注奥沙利铂130mg/m²,第1至14天口服卡培他滨1000mg/m²,每日2次,每3周重复,共2个周期;CapeOx同步放化疗方案为放疗剂量45Gy/25次(每日1次)±5.4Gy/3次,奥沙利铂50mg/m²静脉滴注,每周1次,共5周,卡培他滨825mg/m²口服,每日2次,第1至38天。术前治疗结束后6周内计划行全直肠系膜切除术及同期肝转移瘤切除术。主要终点是原发肿瘤和肝转移瘤的R0切除率。

结果

38例患者被随机分配至本研究,18例入A组,20例入B组。A组原发肿瘤和肝转移瘤的总体R0切除率为77.8%,B组为70.0%(P = 0.72)。中位无进展生存期分别为14.2个月和15.1个月(P = 0.422),3年总生存率分别为75.0%和88.8%(P = 0.29)。

结论

两种治疗策略均显示出相当高的R0切除率;然而,需要进一步研究以将这些强化策略应用于临床实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adc6/5120770/e24c318dea04/coc-39-623-g001.jpg

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