首页> 外文期刊>Journal of Clinical Oncology >Axitinib in Combination With Toripalimab, a Humanized Immunoglobulin G(4) Monoclonal Antibody Against Programmed Cell Death-1, in Patients With Metastatic Mucosal Melanoma: An Open-Label Phase IB Trial
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Axitinib in Combination With Toripalimab, a Humanized Immunoglobulin G(4) Monoclonal Antibody Against Programmed Cell Death-1, in Patients With Metastatic Mucosal Melanoma: An Open-Label Phase IB Trial

机译:Axitinib与Toripalimab组合,一种用于转移性粘膜黑素瘤的患者的人源化免疫球蛋白G(4)单克隆抗体,用于转移粘膜黑素瘤的患者:开放标签相IB试验

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摘要

PURPOSEMetastatic mucosal melanoma responds poorly to anti?programmed cell death-1 (PD-1) monotherapy. Vascular endothelial growth factor (VEGF) has been shown to play an important immunosuppressive role in the tumor microenvironment. The combination of VEGF inhibition and PD-1 blockade provides therapeutic opportunities for patients refractory to either therapy alone.PATIENTS AND METHODSWe conducted a single-center, phase IB trial evaluating the safety and preliminary efficacy of toripalimab, a humanized immunoglobulin G(4) monoclonal antibody against PD-1 in combination with the VEGF receptor inhibitor axitinib in patients with advanced melanoma, including patients with chemotherapy-na?ve mucosal melanomas (88%). Patients received toripalimab at 1 or 3 mg/kg via intravenous infusion every 2 weeks, in combination with axitinib 5 mg orally twice a day, in a dose-escalation and cohort-expansion study until confirmed disease progression, unacceptable toxicity, or voluntary withdrawal. The primary objective was safety. Secondary objectives included efficacy, pharmacokinetics, pharmacodynamics, immunogenicity, and tumor tissue biomarkers.RESULTSThirty-three patients were enrolled. No dose-limiting toxicities were observed. Ninety-seven percent of patients experienced treatment-related adverse events (TRAEs). The most common TRAEs were mild (grade 1 or 2) and included diarrhea, proteinuria, hand and foot syndrome, fatigue, AST or ALT elevation, hypertension, hypo- or hyperthyroidism, and rash. Grade 3 or greater TRAEs occurred in 39.4% of patients. By the cutoff date, among 29 patients with chemotherapy-na?ve mucosal melanoma, 14 patients (48.3%; 95% CI, 29.4% to 67.5%) achieved objective response, and the median progression-free survival time was 7.5 months (95% CI, 3.7 months to not reached) per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.CONCLUSIONThe combination of toripalimab plus axitinib was tolerable and showed promising antitumor activity in patients with treatment-na?ve metastatic mucosal melanoma. Patients enrolled in this study were all Asian, and this combination therapy must be validated in a randomized phase III trial that includes a non-Asian population before it can become a standard of care.
机译:purposemetaxatic粘膜黑素瘤对抗膜的细胞死亡-1(PD-1)单药治疗差异很差。已经显示血管内皮生长因子(VEGF)在肿瘤微环境中起重要的免疫抑制作用。 VEGF抑制和PD-1阻断的组合为患者单独治疗难以进行难治的患者提供治疗机会。患者和方法进行单中心,相IB试验评估替诺蛋白的安全性和初步效果,人源化免疫球蛋白G(4)单克隆针对PD-1的抗体与VEGF受体抑制剂Axitinib在先进的黑色素瘤中,包括化学疗效-NA'VE粘膜melanomas(88%)。患者每2周通过静脉内输注在1或3mg / kg的患者接受均荷扣,与Axitinib 5mg每日口服两次,在剂量升级和群组 - 膨胀研究中,直至确认疾病进展,毒性不可接受,或自愿戒断。主要目标是安全。次要目的包括疗效,药代动力学,药效学,免疫原性和肿瘤组织生物标志物。注册了3例患者。没有观察到剂量限制的毒性。百分之九十七名患者经历了与治疗有关的不良事件(Traes)。最常见的特性是轻度(1或2级),包括腹泻,蛋白尿,手和足综合征,疲劳,AST或ALT升高,高血压,低聚或甲状腺功能亢进和皮疹。 39.4%的患者发生了3级或更大的TRAES。由截止日期,29例化疗-NA'VE粘膜黑素瘤,14例患者(48.3%; 95%CI,29.4%至67.5%)实现了客观反应,中位进展生存时间为7.5个月(95个月%CI,3.7个月未达到)固体肿瘤的响应评估标准(RECIST)1.1。结论TOLIPIMAB PLUS AXITINIB的组合是可耐受的,并且在治疗 - NA转移性粘膜黑色素瘤患者中显示出有前途的抗肿瘤活性。患有本研究的患者均为亚洲,这种联合治疗必须在随机阶段III试验中验证,其中包括非亚洲人口,才能成为护理标准。

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  • 来源
    《Journal of Clinical Oncology》 |2019年第32期|共13页
  • 作者单位

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

    0RigiMed Shanghai Peoples R China;

    Shanghai Junshi Biosci Shanghai Peoples R China;

    Shanghai Junshi Biosci Shanghai Peoples R China;

    Shanghai Junshi Biosci Shanghai Peoples R China;

    Shanghai Junshi Biosci Shanghai Peoples R China;

    Shanghai Junshi Biosci Shanghai Peoples R China;

    Massachusetts Gen Hosp Canc Ctr Boston MA 02114 USA;

    Peking Univ Canc Hosp &

    Inst Beijing Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
  • 关键词

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