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T3-4/N0+ 直肠癌新辅助中程与长程放化疗:伊斯坦布尔 R-02 期随机研究。

Neoadjuvant intermediate-course versus long-course chemoradiotherapy in T3-4/N0+ rectal cancer: Istanbul R-02 phase II randomized study.

机构信息

Department of Radiation Oncology, Koc University School of Medicine, Istanbul, 34450, Türkiye.

Department of Medical Oncology, Demiroglu Bilim University Faculty of Medicine, Istanbul, 34394, Türkiye.

出版信息

Oncol Res. 2023 Jul 21;31(5):689-696. doi: 10.32604/or.2023.030351. eCollection 2023.

Abstract

Radiation therapy (RT) is typically applied using one of two standard approaches for preoperative treatment of resectable locally advanced rectal cancer (LARC): short-course RT (SC-RT) alone or long-course RT (LC-RT) with concurrent fluorouracil (5-FU) chemotherapy. The Phase II single-arm KROG 11-02 study using intermediate-course (IC) (33 Gy (Gray)/10 fr (fraction) with concurrent capecitabine) preoperative chemoradiotherapy (CRT) demonstrated a pathologically complete response rate and a sphincter-sparing rate that were close to those of LC-CRT. The current trial aim to compare the pathological/oncological outcomes, toxicity, and quality of life results of LC-CRT and IC-CRT in cases of LARC. The prescribed dose was 33 Gy/10 fr for the IC-CRT group and 50.4 Gy/28 fr for the LC-CRT group. Concurrent chronomodulated capecitabine (Brunch regimen) 1650 mg/m/daily chemotherapy treatment was applied in both groups. The European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Colorectal Cancer Module (EORTC QLQ-CR29) was administered at baseline and at three and six months after CRT. A total of 60 patients with LARC randomized to receive IC-CRT (n = 30) or LC-CRT (n = 30) were included in this phase II randomized trial. No significant difference was noted between groups in terms of pathological outcomes, including pathological response rates (ypT0N0-complete response: 23.3% 16.7%, respectively, and ypT0-2N0-downstaging: 50% for each; = 0.809) and Dworak score-based pathological tumor regression grade (Grade 4-complete response: 23.3 16.7%, = 0.839). The 5-year overall survival (73.3 86.7%, = 0.173) rate was also similar. The acute radiation dermatitis ( < 0.001) and any hematological toxicity = 0.004) rates were significantly higher in the LC-CRT group, while no significant difference was noted between treatment groups in terms of baseline, third month, and sixth month EORTC QLQ-CR29 scores.

摘要

放射治疗(RT)通常采用两种标准方法之一用于术前治疗局部进展期可切除直肠癌(LARC):短程放疗(SC-RT)单独或长程放疗(LC-RT)联合氟尿嘧啶(5-FU)化疗。使用中间疗程(IC)(33 Gy(格雷)/10 fr(分数)联合卡培他滨)术前放化疗(CRT)的 KROG 11-02 期单臂研究表明,病理完全缓解率和保留括约肌率接近 LC-CRT。目前的试验旨在比较 LC-CRT 和 IC-CRT 在 LARC 病例中的病理/肿瘤学结果、毒性和生活质量结果。规定的剂量为 IC-CRT 组 33 Gy/10 fr,LC-CRT 组 50.4 Gy/28 fr。两组均应用同步时相卡培他滨(Brunch 方案)1650 mg/m/d 化疗治疗。在 CRT 前后三个月和六个月时使用欧洲癌症研究和治疗组织生活质量问卷-结直肠癌模块(EORTC QLQ-CR29)进行评估。共有 60 例 LARC 患者随机分为 IC-CRT(n = 30)或 LC-CRT(n = 30)组。两组在病理结果方面无显著差异,包括病理缓解率(ypT0N0-完全缓解:分别为 23.3%和 16.7%,ypT0-2N0-降级:各为 50%;=0.809)和 Dworak 评分基于肿瘤消退分级(完全缓解 4 级:23.3%和 16.7%,=0.839)。5 年总生存率(73.3%和 86.7%,=0.173)也相似。LC-CRT 组急性放射性皮炎(<0.001)和任何血液学毒性(=0.004)发生率显著较高,而两组在 EORTC QLQ-CR29 基线、第三个月和第六个月评分方面无显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/547a/10398395/e01a74637c6e/OncolRes-31-30351-f001.jpg

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