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放疗联合脂质体伊立替康、卡瑞利珠单抗及抗血管生成治疗对晚期骨与软组织肉瘤的疗效与安全性:CAP研究的亚组分析

Efficacy and Safety of Radiotherapy Combined with Liposomal Irinotecan, Camrelizumab, and Anti-angiogenic Therapy in Advanced Bone and Soft Tissue Sarcoma: A Retrospective Subgroup Analysis of CAP Study

  • 摘要:
    目的 评估立体定向放疗(SBRT)联合脂质体伊立替康、卡瑞利珠单抗及抗血管生成药物治疗(CAP)在晚期骨与软组织肉瘤患者中的疗效和安全性。
    方法 本研究为多中心、开放标签、单臂Ⅱ期CAP研究的前瞻性亚组分析。纳入2020年11月—2023年2月期间参加CAP临床研究(NCT04569916)的60例经标准治疗后进展的晚期实体瘤患者,其中晚期骨与软组织肉瘤患者11例。所有患者均接受立体定向放疗(SBRT)后48 h内联合脂质体伊立替康,随后序贯卡瑞利珠单抗及抗血管生成药物维持治疗,直至疾病进展或出现不可耐受的毒性。主要疗效终点为ORR,次要终点包括DCR、PFS、OS及安全性。
    结果 骨与软组织肉瘤亚组(n=11)中,3例达到部分缓解(PR),5例疾病稳定(SD),3例疾病进展(PD)。客观缓解率(ORR)为27.3%,疾病控制率(DCR)为72.7%。中位无进展生存期(mPFS)为5.8个月(95%CI:2.2~10.3),中位总生存期(mOS)未达到。安全性方面,不良反应类型以骨髓抑制、乏力及胃肠道反应为主,提示毒性总体可控。
    结论 作为CAP研究的亚组分析,本研究提示放疗联合脂质体伊立替康、卡瑞利珠单抗及抗血管生成治疗在经多线治疗失败的晚期骨与软组织肉瘤中具有一定疗效,且不良反应总体可控;后续需进一步扩大样本量进行研究。

     

    Abstract:
    Objective To evaluate the efficacy and safety of a combination therapy regimen comprising stereotactic body radiation therapy (SBRT) combined with liposomal irinotecan, camrelizumab, and anti-angiogenic therapy (CAP) in patients with advanced bone and soft tissue sarcomas.
    Methods This study is a prospective subgroup analysis of the multicenter, open-label, single-arm phase Ⅱ CAP trial (NCT04569916), which enrolled 60 patients with advanced solid tumors who had progressed after standard therapy between November 2020 and February 2023, including 11 patients with advanced bone and soft tissue sarcomas. All patients received sequential liposomal irinotecan within 48 hours after stereotactic body radiotherapy (SBRT), followed by maintenance therapy with camrelizumab and an anti-angiogenic agent until disease progression or intolerable toxicity. The primary efficacy endpoint was objective response rate (ORR). Secondary endpoints included disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and safety.
    Results In the bone and soft tissue sarcoma subgroup (n=11), three patients achieved partial response (PR), five had stable disease (SD), and three experienced disease progression (PD). ORR was 27.3%, and DCR was 72.7%. mPFS was 5.8 months (95%CI: 2.2-10.3), and mOS not reached. Regarding safety, adverse reactions primarily included bone marrow suppression, fatigue, and gastrointestinal reactions, indicating overall manageable toxicity.
    Conclusion As a subgroup analysis of the CAP study, this research suggests that radiotherapy combined with liposomal irinotecan, camrelizumab, and anti-angiogenic therapy demonstrates certain efficacy in advanced bone and soft tissue sarcomas that have failed multiple lines of treatment, with overall manageable adverse reactions. Future studies should expand the sample size.

     

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