Department of Radiotherapy and Oncology, University of Frankfurt, Frankfurt, Germany.
Frankfurt Cancer Institute, Frankfurt, Germany.
JAMA Oncol. 2020 Sep 1;6(9):1416-1421. doi: 10.1001/jamaoncol.2020.2394.
Despite numerous published phase 3 trials, the association of treatment adherence with outcomes for patients with rectal cancer remains largely unexplored.
To analyze the association of treatment adherence with disease-free survival (DFS) among patients with rectal cancer in the CAO/ARO/AIO-04 trial.
DESIGN, SETTING, AND PARTICIPANTS: This post hoc analysis of a phase 3 randomized clinical trial was conducted from July 25, 2006, to February 26, 2010, among 1232 patients from 80 centers with T3 to T4 or node-positive rectal adenocarcinoma. Statistical analysis was performed from May 5, 2019, to February 2, 2020.
A total of 625 patients received neoadjuvant fluorouracil-based chemoradiotherapy (nCRT), and a total of 607 patients received fluorouracil-based nCRT with addition of oxaliplatin. Of the 1126 patients who underwent curative surgery, 439 started fluorouracil-based adjuvant chemotherapy and 419 started fluorouracil-based adjuvant chemotherapy with oxaliplatin.
The association of adherence with nCRT and adjuvant chemotherapy with DFS was assessed in both groups in the as-treated population.
Among the 625 patients (442 men; mean age, 63.0 years) who received fluorouracil nCRT and the 607 patients (430 men; mean age, 63.0 years) who received fluorouracil-based nCRT with addition of oxaliplatin, after a median follow-up of 50 months (interquartile range, 38-61 months), 3-year DFS in the as-treated population was 71.1% in the fluorouracil group and 75.8% in the fluorouracil-oxaliplatin group (hazard ratio [HR], 0.803; 95% CI, 0.651-0.990; P = .04). Overall, 419 patients in the fluorouracil nCRT group (67.0%) and 434 patients in the fluorouracil-oxaliplatin nCRT group (71.5%) received full doses of preoperative nCRT. Likewise, 253 of 439 patients in the fluorouracil group (57.6%) and 134 of 419 patients in the fluorouracil-oxaliplatin group (32.0%) received full doses of adjuvant chemotherapy. Adherence to nCRT was associated with 3-year DFS in both the fluorouracil group (complete vs near complete: HR, 1.325; 95% CI, 0.959-1.832; P = .09; complete vs reduced: HR, 1.877; 95% CI, 1.147-3.072; P = .01) and the fluorouracil-oxaliplatin group (complete vs near complete: HR, 1.501; 95% CI, 0.980-2.299; P = .06; complete vs reduced: HR, 1.724; 95% CI, 1.144-2.596; P = .009) in multivariable analyses. In contrast, adjuvant chemotherapy was not associated with DFS in both the fluorouracil group (complete vs near complete: HR, 0.900; 95% CI, 0.559-1.448; P = .66; complete vs incomplete: HR, 1.057; 95% CI, 0.807-1.386; P = .69) and the fluorouracil-oxaliplatin group (complete vs near complete: HR, 1.155; 95% CI, 0.716-1.866; P = .56; complete vs incomplete: HR, 1.073; 95% CI, 0.790-1,457; P = .65).
To our knowledge, this is the first analysis of a phase 3 trial to assess the association of treatment adherence with some clinical outcomes for patients with rectal cancer. The findings emphasize the need for appropriate trial design with optimized nCRT dose and schedule and supportive strategies to facilitate good adherence and precision delivery, especially for intensified nCRT.
ClinicalTrials.gov Identifier: NCT00349076.
尽管有许多已发表的 3 期试验,但治疗依从性与直肠癌患者结局之间的关联在很大程度上仍未得到探索。
分析 CAO/ARO/AIO-04 试验中直肠癌患者的治疗依从性与无病生存(DFS)之间的关系。
设计、地点和参与者:这是一项对 3 期随机临床试验的事后分析,于 2006 年 7 月 25 日至 2010 年 2 月 26 日在 80 个中心进行,共纳入 1232 名 T3 至 T4 或淋巴结阳性直肠腺癌患者。统计分析于 2019 年 5 月 5 日至 2020 年 2 月 2 日进行。
625 例患者接受氟尿嘧啶为基础的新辅助放化疗(nCRT),607 例患者接受氟尿嘧啶为基础的 nCRT 联合奥沙利铂。在 1126 例接受根治性手术的患者中,439 例开始氟尿嘧啶为基础的辅助化疗,419 例开始氟尿嘧啶为基础的辅助化疗联合奥沙利铂。
在治疗人群中评估两组患者 nCRT 和辅助化疗依从性与 DFS 的关系。
在接受氟尿嘧啶 nCRT 的 625 例患者(442 例男性;平均年龄 63.0 岁)和接受氟尿嘧啶联合奥沙利铂 nCRT 的 607 例患者(430 例男性;平均年龄 63.0 岁)中,中位随访 50 个月(四分位距 38-61 个月)后,治疗人群的 3 年 DFS 氟尿嘧啶组为 71.1%,氟尿嘧啶-奥沙利铂组为 75.8%(风险比[HR],0.803;95%CI,0.651-0.990;P=0.04)。总体而言,氟尿嘧啶 nCRT 组有 419 例(67.0%)患者和氟尿嘧啶-奥沙利铂 nCRT 组有 434 例(71.5%)患者接受了全剂量术前 nCRT。同样,氟尿嘧啶组有 253 例(57.6%)患者和氟尿嘧啶-奥沙利铂组有 134 例(32.0%)患者接受了全剂量辅助化疗。在氟尿嘧啶组(完全 vs 接近完全:HR,1.325;95%CI,0.959-1.832;P=0.09;完全 vs 减少:HR,1.877;95%CI,1.147-3.072;P=0.01)和氟尿嘧啶-奥沙利铂组(完全 vs 接近完全:HR,1.501;95%CI,0.980-2.299;P=0.06;完全 vs 减少:HR,1.724;95%CI,1.144-2.596;P=0.009)中,治疗依从性与 3 年 DFS 相关,在多变量分析中。相比之下,氟尿嘧啶组(完全 vs 接近完全:HR,0.900;95%CI,0.559-1.448;P=0.66;完全 vs 不完全:HR,1.057;95%CI,0.807-1.386;P=0.69)和氟尿嘧啶-奥沙利铂组(完全 vs 接近完全:HR,1.155;95%CI,0.716-1.866;P=0.56;完全 vs 不完全:HR,1.073;95%CI,0.790-1.457;P=0.65)中,辅助化疗与 DFS 无关。
据我们所知,这是首次分析 3 期试验,以评估直肠癌患者治疗依从性与某些临床结局之间的关系。研究结果强调需要优化 nCRT 剂量和方案,并制定支持性策略,以促进良好的依从性和精确治疗,特别是对于强化 nCRT。
ClinicalTrials.gov 标识符:NCT00349076。