Suppr超能文献

泊马度胺、环磷酰胺和利妥昔单抗后继以阿仑单抗治疗复发或难治性慢性淋巴细胞白血病:ECOG-ACRIN 癌症研究组(E2903)的 2 期试验。

Pentostatin, Cyclophosphamide, and Rituximab Followed by Alemtuzumab for Relapsed or Refractory Chronic Lymphocytic Leukemia: A Phase 2 Trial of the ECOG-Acrin Cancer Research Group (E2903).

机构信息

Beth Israel Comprehensive Cancer Center, New York, New York, USA,

Dana Farber Cancer Institute-ECOG-ACRIN Biostatistics Center, Boston, Massachusetts, USA.

出版信息

Acta Haematol. 2019;142(4):224-232. doi: 10.1159/000500164. Epub 2019 Jul 23.

Abstract

Patients with relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL) may benefit from salvage chemoimmunotherapy (CIT). To explore further the use of CIT in the pre-novel agent era, ECOG-ACRIN undertook a phase 2 trial (E2903) for R/R CLL utilizing pentostatin, cyclophosphamide, and rituximab (PCR) followed by a consolidation course of alemtuzumab. This trial enrolled 102 patients with a median age of 64 years. Treatment consisted of 6 cycles of PCR followed by alemtuzumab for either 4 or 18 weeks depending on the initial response to PCR. The overall response after PCR (complete remission, CR, nodular partial remission, nPR, and partial remission, PR) was 55%. Major responses (CR or nPR) were achieved in 6%. The median overall survival (OS) and the median progression-free survival were 28 and 12 months, respectively. The most serious nonlethal adverse events were myelosuppression, febrile neutropenia, fatigue, nausea, and hyponatremia. PCR is an effective and well-tolerated nucleoside-based regimen for heavily pretreated CLL patients with R/R disease. The addition of alemtuzumab to CLL patients with a minor response (PR) or stable disease did not result in a significant number of higher responses (CR or nPR) nor an improvement in OS.

摘要

复发/难治性 (R/R) 慢性淋巴细胞白血病 (CLL) 患者可能从挽救性化疗免疫治疗 (CIT) 中获益。为了在新型药物出现之前进一步探索 CIT 的应用,ECOG-ACRIN 开展了一项针对 R/R CLL 的 2 期试验 (E2903),采用了苯达莫司汀、环磷酰胺和利妥昔单抗 (PCR),随后进行了阿仑单抗巩固治疗。该试验纳入了 102 例中位年龄为 64 岁的患者。治疗包括 6 个周期的 PCR,随后根据对 PCR 的初始反应,给予阿仑单抗 4 或 18 周的治疗。PCR 后的总体缓解率(完全缓解 (CR)、结节部分缓解 (nPR) 和部分缓解 (PR))为 55%。主要缓解(CR 或 nPR)的发生率为 6%。中位总生存期 (OS) 和中位无进展生存期分别为 28 个月和 12 个月。最严重的非致命性不良事件为骨髓抑制、发热性中性粒细胞减少、疲劳、恶心和低钠血症。PCR 是一种有效的、耐受性良好的核苷类方案,适用于 R/R 疾病的大量预处理过的 CLL 患者。在对 PCR 有轻微缓解 (PR) 或疾病稳定的 CLL 患者中添加阿仑单抗,并未导致更高比例的缓解(CR 或 nPR),也未改善 OS。

相似文献

8
Cumulative experience and long term follow-up of pentostatin-based chemoimmunotherapy trials for patients with chronic lymphocytic leukemia.
Expert Rev Hematol. 2018 Apr;11(4):337-349. doi: 10.1080/17474086.2018.1442716. Epub 2018 Feb 26.

引用本文的文献

1
Phytotherapeutics in Cancer: From Potential Drug Candidates to Clinical Translation.
Curr Top Med Chem. 2024;24(12):1050-1074. doi: 10.2174/0115680266282518231231075311.
2
Revolutionizing cancer treatment: comprehensive insights into immunotherapeutic strategies.
Med Oncol. 2024 Jan 9;41(2):51. doi: 10.1007/s12032-023-02280-7.
3
Maintenance therapy for chronic lymphocytic leukaemia.
Cochrane Database Syst Rev. 2024 Jan 4;1(1):CD013474. doi: 10.1002/14651858.CD013474.pub2.
4
Dipyridamole and adenosinergic pathway in Covid-19: a juice or holy grail.
Egypt J Med Hum Genet. 2022;23(1):140. doi: 10.1186/s43042-022-00354-1. Epub 2022 Sep 23.

本文引用的文献

1
Ibrutinib Regimens versus Chemoimmunotherapy in Older Patients with Untreated CLL.
N Engl J Med. 2018 Dec 27;379(26):2517-2528. doi: 10.1056/NEJMoa1812836. Epub 2018 Dec 1.
2
Venetoclax-Rituximab in Relapsed or Refractory Chronic Lymphocytic Leukemia.
N Engl J Med. 2018 Mar 22;378(12):1107-1120. doi: 10.1056/NEJMoa1713976.
3
Cumulative experience and long term follow-up of pentostatin-based chemoimmunotherapy trials for patients with chronic lymphocytic leukemia.
Expert Rev Hematol. 2018 Apr;11(4):337-349. doi: 10.1080/17474086.2018.1442716. Epub 2018 Feb 26.
4
Single-agent ibrutinib in treatment-naïve and relapsed/refractory chronic lymphocytic leukemia: a 5-year experience.
Blood. 2018 Apr 26;131(17):1910-1919. doi: 10.1182/blood-2017-10-810044. Epub 2018 Feb 2.
5
Early-onset invasive aspergillosis and other fungal infections in patients treated with ibrutinib.
Blood. 2018 Apr 26;131(17):1955-1959. doi: 10.1182/blood-2017-11-818286. Epub 2018 Feb 1.
6
Current understanding of bleeding with ibrutinib use: a systematic review and meta-analysis.
Blood Adv. 2017 May 9;1(12):772-778. doi: 10.1182/bloodadvances.2016001883.
7
FCR achieves long-term durable remissions in patients with -mutated CLL.
Blood. 2017 Nov 23;130(21):2278-2282. doi: 10.1182/blood-2017-07-731588. Epub 2017 Oct 12.
8
Chemoimmunotherapy Is Not Dead Yet in Chronic Lymphocytic Leukemia.
J Clin Oncol. 2017 Sep 10;35(26):2989-2992. doi: 10.1200/JCO.2017.72.6810. Epub 2017 Jul 25.
10
Ibrutinib-associated bleeding: pathogenesis, management and risk reduction strategies.
J Thromb Haemost. 2017 May;15(5):835-847. doi: 10.1111/jth.13651. Epub 2017 Mar 27.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验