Department of Precision Medicine, Università Degli Studi Della Campania "Luigi Vanvitelli," Napoli, Italy.
Medical Oncology, Fondazione IRCCS Casa Sollievo Della Sofferenza, San Giovanni Rotondo, Italy.
JAMA Oncol. 2023 Jul 1;9(7):966-970. doi: 10.1001/jamaoncol.2023.0655.
Current third-line therapies for patients with metastatic colorectal cancer (MCRC) have limited efficacy. Rechallenge with epidermal growth factor receptor (EGFR) inhibitors for RAS wild-type (WT) MCRC may be valuable for these patients.
To compare the anti-EGFR monoclonal antibody panitumumab plus standard-of-care trifluridine-tipiracil with trifluridine-tipiracil alone as third-line therapy for RAS WT MCRC.
DESIGN, SETTING, AND PARTICIPANTS: This phase 2 randomized clinical trial (RCT) was conducted in 7 Italian centers from June 2019 to April 2022. Patients with refractory RAS WT MCRC who had a partial or complete response to first-line chemotherapy plus an anti-EGFR monoclonal antibody and an anti-EGFR drug-free interval of 4 or more months during second-line therapy were included.
Patients were randomized 1:1 to receive panitumumab plus trifluridine-tipiracil or trifluridine-tipiracil alone.
The primary end point was progression-free survival (PFS). Circulating tumor DNA (ctDNA) extended sequence variation analysis was performed in a subgroup of patients.
Of 62 included patients, 31 received panitumumab plus trifluridine-tipiracil (19 [61.3%] male; median age, 65 years [range, 39-81 years]) and 31 received trifluridine-tipiracil alone (17 [54.8%] male; median age, 66 years [range, 32-82 years]). The primary end point was met. Median PFS was 4.0 months (95% CI, 2.8-5.3 months) in the panitumumab plus trifluridine-tipiracil arm vs 2.5 months (95% CI, 1.4-3.6 months) in the trifluridine-tipiracil only (hazard ratio [HR], 0.48; 95% CI, 0.28-0.82; P = .007). Pretreatment plasma RAS/BRAF WT ctDNA identified patients obtaining prolonged clinical benefit with panitumumab plus trifluridine-tipiracil compared with trifluridine-tipiracil, with PFS rates at 6 months of 38.5% vs 13.0% and at 12 months of 15.4% vs 0%. A ctDNA liquid-biopsy extended mutation analysis by FoundationOne Liquid CDx (profiling 324 genes) was performed in a subgroup of patients with baseline plasma RAS/BRAF WT ctDNA; in 15 of 23 patients (65.2%) whose tumors were WT for KRAS, NRAS, BRAFV600E, EGFR, ERBB2, MAP2K1, and PIK3CA, median PFS was 6.4 months (95% CI, 3.7-9.2 months). Within this group of 15 patients, 2 (13.3%) had partial response, 11 (73.3%) had stable disease, and 2 (13.3%) had disease progression as best response.
In this RCT, third-line treatment with the anti-EGFR monoclonal antibody panitumumab plus the standard-of-care trifluridine-tipiracil resulted in improved PFS compared with treatment with trifluridine-tipiracil alone among patients with refractory RAS WT MCRC. The findings support the clinical utility of liquid biopsy-guided anti-EGFR rechallenge therapy for refractory RAS WT MCRC.
ClinicalTrials.gov Identifier: NCT05468892.
重要性:目前转移性结直肠癌(MCRC)的三线治疗方法疗效有限。对于 RAS 野生型(WT)MCRC 患者,重新使用表皮生长因子受体(EGFR)抑制剂进行挑战可能具有价值。
目的:比较抗 EGFR 单克隆抗体帕尼单抗联合标准护理三氟尿苷-替匹嘧啶与三氟尿苷-替匹嘧啶单药作为 RAS WT MCRC 的三线治疗。
设计、地点和参与者:这是一项在 2019 年 6 月至 2022 年 4 月期间在意大利 7 个中心进行的 2 期随机临床试验(RCT)。纳入的患者为在一线化疗联合抗 EGFR 单克隆抗体治疗后获得部分或完全缓解,且二线治疗中抗 EGFR 药物无间隔 4 个月或更长时间的 RAS WT MCRC 难治性患者。
干预措施:患者以 1:1 的比例随机接受帕尼单抗联合三氟尿苷-替匹嘧啶或三氟尿苷-替匹嘧啶单药治疗。
主要结局和测量指标:主要终点是无进展生存期(PFS)。对部分患者进行了循环肿瘤 DNA(ctDNA)扩展序列变异分析。
结果:在纳入的 62 名患者中,31 名接受了帕尼单抗联合三氟尿苷-替匹嘧啶治疗(19 名男性;中位年龄 65 岁[范围,39-81 岁]),31 名接受了三氟尿苷-替匹嘧啶单药治疗(17 名男性;中位年龄 66 岁[范围,32-82 岁])。主要终点得到满足。在帕尼单抗联合三氟尿苷-替匹嘧啶组,中位 PFS 为 4.0 个月(95%CI,2.8-5.3 个月),而三氟尿苷-替匹嘧啶组为 2.5 个月(95%CI,1.4-3.6 个月)(HR,0.48;95%CI,0.28-0.82;P=0.007)。预处理血浆 RAS/BRAF WT ctDNA 鉴定出与三氟尿苷-替匹嘧啶相比,接受帕尼单抗联合三氟尿苷-替匹嘧啶治疗的患者获得了更长的临床获益,6 个月时的 PFS 率分别为 38.5%和 13.0%,12 个月时的 PFS 率分别为 15.4%和 0%。在基线血浆 RAS/BRAF WT ctDNA 存在的患者亚组中,进行了 FoundationOne Liquid CDx(对 324 个基因进行了分析)的 ctDNA 液体活检扩展突变分析。在 23 名肿瘤 KRAS、NRAS、BRAFV600E、EGFR、ERBB2、MAP2K1 和 PIK3CA 均为 WT 的患者中,15 名患者的中位 PFS 为 6.4 个月(95%CI,3.7-9.2 个月)。在这 15 名患者中,2 名(13.3%)患者有部分缓解,11 名(73.3%)患者病情稳定,2 名(13.3%)患者疾病进展为最佳缓解。
结论和相关性:在这项 RCT 中,与三氟尿苷-替匹嘧啶单药治疗相比,抗 EGFR 单克隆抗体帕尼单抗联合标准护理三氟尿苷-替匹嘧啶的三线治疗可改善 RAS WT MCRC 难治性患者的 PFS。这些发现支持基于液体活检指导的抗 EGFR 再挑战治疗对 RAS WT MCRC 的临床应用。
试验注册:ClinicalTrials.gov 标识符:NCT05468892。