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帕尼单抗联合替氟尿苷替匹嘧啶作为抗表皮生长因子受体再挑战治疗用于难治性 RAS 野生型转移性结直肠癌:一项 2 期随机临床试验。

Panitumumab Plus Trifluridine-Tipiracil as Anti-Epidermal Growth Factor Receptor Rechallenge Therapy for Refractory RAS Wild-Type Metastatic Colorectal Cancer: A Phase 2 Randomized Clinical Trial.

机构信息

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.

出版信息

JAMA Oncol. 2023 Jul 1;9(7):966-970. doi: 10.1001/jamaoncol.2023.0655.

Abstract

IMPORTANCE

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.

OBJECTIVE

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.

INTERVENTIONS

Patients were randomized 1:1 to receive panitumumab plus trifluridine-tipiracil or trifluridine-tipiracil alone.

MAIN OUTCOMES AND MEASURES

The primary end point was progression-free survival (PFS). Circulating tumor DNA (ctDNA) extended sequence variation analysis was performed in a subgroup of patients.

RESULTS

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.

CONCLUSIONS AND RELEVANCE

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.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT05468892.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ab9/10196928/07cfd8573560/jamaoncol-e230655-g001.jpg

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