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辅助性重组人血管内皮抑素联合特瑞普利单抗(anti-PD-1)治疗局部晚期黑色素瘤:一项纳入单细胞 RNA/TCR/BCR 测序的探索性 2 期临床试验

英文原题:Adjuvant recombinant human endostatin combined with toripalimab (anti-PD-1) in locally advanced melanoma: an exploratory phase 2 clinical trial incorporating single-cell RNA/TCR/BCR sequencing.

PubMed 2026/04/27(内容时间) Mol Cancer Q1 · IF 42.2(JCR 2025)

研究概要

辅助重组人血管内皮抑制素联合特瑞普利单抗在中国已切除的局部晚期黑色素瘤患者中显示出令人鼓舞的临床活性,并可能与潜在的生存获益相关。不良反应可控。外周T细胞、NK细胞、B细胞和单核细胞亚群数量增加及功能变化,为免疫治疗的优化提供了机制性见解。

研究思路结论见上方概要

在东亚,黑色素瘤主要以肢端雀斑样亚型出现,其次为皮肤亚型。东亚地区完全切除的III期或IV期黑色素瘤患者疾病复发风险高。PD-1抑制剂单药辅助治疗在该患者群体中的疗效仍然有限,凸显了联合治疗策略的必要性。

这项前瞻性、单臂、II期试验(NCT05907512)旨在探讨辅助重组人内皮抑素(rh-endostatin,一种血管生成抑制剂)联合特瑞普利单抗(一种PD-1抑制剂)用于中国可切除III期至寡转移IV期黑色素瘤患者。主要终点为1年无复发生存期(RFS)。收集联合辅助治疗前后的配对外周血样本,用于单细胞RNA测序、TCR/BCR测序及生物标志物鉴定。评估两个独立的局部晚期黑色素瘤患者真实世界队列以验证这些生物标志物。

43例符合条件的可切除III期黑色素瘤患者被前瞻性纳入。未纳入可切除寡转移IV期疾病患者。患者的1年RFS为74.4%,中位RFS为27个月(95%置信区间:19,未达到)。贫血(12/43,27.9%)、肝酶升高(11/43,25.6%)和甲状腺功能障碍(9/43,20.9%)是三种最常见的治疗相关不良事件。联合辅助治疗扩大了患者外周总T细胞和NK细胞,增加了循环CD8+ Tem和Teff细胞及其TCR克隆多样性,改善了B细胞的抗原呈递能力,提高了BCR克隆多样性,并增加了非经典单核细胞数量及其抗原呈递能力。中性粒细胞与淋巴细胞比值和循环CD8+ Tem细胞在独立的真实世界队列中被支持为与结局相关的候选生物标志物。

展开英文摘要原文

PURPOSE: In East Asia, melanoma mainly presents as the acral lentiginous subtype, followed by the cutaneous subtype. Patients with completely resected stage III or IV melanoma in East Asia are at a high risk of disease recurrence. The adjuvant efficacy of PD-1 inhibitors as monotherapy remains limited in this patient population, underscoring the need for combination strategies. PATIENTS AND METHODS: This prospective, single-arm, phase II trial (NCT05907512) aimed to investigate adjuvant recombinant human endostatin (rh-endostatin, an angiogenesis inhibitor) combined with toripalimab (a PD-1 inhibitor) in Chinese patients with resectable stage III to oligometastatic stage IV melanoma. The primary endpoint was 1-year relapse-free survival (RFS). Paired peripheral blood samples before and after the combined adjuvant therapy were collected for single-cell RNA sequencing, TCR/BCR sequencing, and biomarker identification. Two independent real-world cohorts of patients with locally advanced melanoma were assessed to validate the biomarkers. RESULTS: Forty-three eligible patients with resected stage III melanoma were prospectively enrolled. No patients with resected oligometastatic stage IV disease were enrolled. The 1-year RFS of the patients was 74.4%, with a median RFS of 27 months (95% confidence interval: 19, not reached). Anemia (12/43, 27.9%), elevated liver enzymes (11/43, 25.6%), and thyroid dysfunction (9/43, 20.9%) were the three most common treatment-related adverse events. The combined adjuvant therapy expanded the patients’ peripheral total T and NK cells, increased circulating CD8+ Tem and Teff cells and their TCR clonal diversities, improved the antigen-presenting capacity of B cells, elevated BCR clonal diversity, and raised the number of non-classical monocytes and their antigen-presenting capacity. The neutrophil-to-lymphocyte ratio and circulating CD8+ Tem cells were supported as candidate biomarkers associated with outcomes in the independent real-world cohorts. CONCLUSIONS: Adjuvant rh-endostatin combined with toripalimab shows encouraging clinical activity and may be associated with a potential survival benefit in Chinese patients with resected locally advanced melanoma. Adverse reactions were manageable. The increased quantities and functional changes of peripheral T cells, NK cells, B cells, and monocyte subsets provide mechanistic insights for the optimization of immunotherapy.

论文信息

作者
Hu X、Xu Y、Wang Z、Yang L、Zheng B、Sun F、Liu D、Shi B
第一作者单位
Department of Musculoskeletal Oncology, Fudan University Shanghai Cancer Center, 270 Dong'an Road, Shanghai, 200032, China.China
通讯作者单位
Department of Musculoskeletal Oncology, Fudan University Shanghai Cancer Center, 270 Dong'an Road, Shanghai, 200032, China. cmwang_gr@fudan.edu.cn.China
文献类型
II 期临床试验
期刊
Molecular cancer2026 Apr 27
原文标识
PubMed 42046135 · DOI 10.1186/s12943-026-02675-w