Carfilzomib, lenalidomide, dexamethasone (KRD) in BTKi relapsed or refractory mantle cell lymphoma: A phase II study from Fondazione Italiana Linfomi.

IF 5.1 2区 医学 Q1 HEMATOLOGY British Journal of Haematology Pub Date : 2024-06-28 DOI:10.1111/bjh.19617
Federica Cavallo, Michele Clerico, Elisa Lucchini, Anna Castiglione, Alessandro Re, Vittorio Ruggiero Zilioli, Carlo Visco, Monica Tani, Jacopo Olivieri, Luca Arcaini, Alberto Fabbri, Gianluca Gaidano, Anna Dodero, Francesco Zaja
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Abstract

Mantle cell lymphoma (MCL) is a rare lymphoproliferative neoplasm considered incurable, with a median survival of 3-5 years. In recent years, Bruton's tyrosine kinase inhibitors (BTKi) have been introduced, demonstrating high therapeutic activity. However, the prognosis for MCL patients failing ibrutinib therapy is particularly poor, with a survival expectation of a few months. In this phase II trial, we assessed the efficacy and safety of the carfilzomib-lenalidomide-dexamethasone (KRD) combination in MCL patients who were relapsed/refractory (R/R) or intolerant to BTKi and in need of treatment. The primary objective of the study was to evaluate the antitumor efficacy of the KRD combination in terms of 12-month overall survival (12-month OS). From September 2019 to December 2020, 16 patients were enrolled from 11 Italian centers. After a median follow-up of 2.37 months (95% CI 0.92-6.47), the 12-month OS was 13%. The rate of grade 3-4 adverse events (AEs) was 35%, and the overall response rate (ORR) was 19%. These results led to the premature termination of enrollment, as defined in the protocol stopping rules. The efficacy of the KRD combination in advanced-stage MCL patients who are R/R to BTKi is unsatisfactory and too toxic.

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卡非佐米、来那度胺和地塞米松(KRD)治疗 BTKi 复发或难治套细胞淋巴瘤:意大利林福米基金会的一项II期研究。
套细胞淋巴瘤(MCL)是一种罕见的淋巴增生性肿瘤,被认为是不治之症,中位生存期为 3-5 年。近年来,布鲁顿酪氨酸激酶抑制剂(BTKi)相继问世,显示出很高的治疗活性。然而,伊布替尼治疗失败的MCL患者预后特别差,预期生存期只有几个月。在这项II期试验中,我们评估了卡非佐米-来那度胺-地塞米松(KRD)联合疗法对复发/难治(R/R)或不耐受BTKi且需要治疗的MCL患者的疗效和安全性。研究的主要目的是评估KRD联合疗法在12个月总生存期(12个月OS)方面的抗肿瘤疗效。2019 年 9 月至 2020 年 12 月,来自 11 个意大利中心的 16 名患者入组。中位随访2.37个月(95% CI 0.92-6.47)后,12个月OS为13%。3-4级不良事件(AEs)发生率为35%,总体反应率(ORR)为19%。根据方案终止规则的规定,这些结果导致提前终止入组。KRD联合疗法对BTKi治疗无效的晚期MCL患者的疗效并不令人满意,而且毒性太大。
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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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