Clinical challenges and promising therapies for chemotherapy-induced thrombocytopenia

被引:51
作者
Al-Samkari, Hanny [1 ,2 ]
Soff, Gerald A. [3 ]
机构
[1] Massachusetts Gen Hosp, Div Hematol Oncol, Zero Emerson Pl Suite 118 Off 112, Boston, MA 02114 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Mem Sloan Kettering Canc Ctr, Hematol Serv, 1275 York Ave, New York, NY 10021 USA
关键词
Chemotherapy; chemotherapy-induced thrombocytopenia; thrombocytopenia; supportive care; romiplostim; eltrombopag; thrombopoietin; thrombopoietin receptor agonist; bleeding; HUMAN MEGAKARYOCYTE GROWTH; RECOMBINANT HUMAN THROMBOPOIETIN; RELATIVE DOSE INTENSITY; GEMCITABINE-BASED CHEMOTHERAPY; PLACEBO-CONTROLLED TRIAL; ADVANCED SOLID TUMORS; DOUBLE-BLIND; PHASE-III; IMMUNE THROMBOCYTOPENIA; HUMAN INTERLEUKIN-11;
D O I
10.1080/17474086.2021.1924053
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Chemotherapy-induced thrombocytop enia (CIT) is a common complication of cancer treatment causing chemotherapy delays, dose reductions, and treatment discontinuation, negatively impacting treatment outcomes and putting patients at risk for bleeding complications. There is no FDA-approved agent available to manage CIT. Areas covered: This article covers the diagnosis, definitions, and clinical challenges of CIT, and then focuses on the therapeutics developed to manage CIT. The first-generation thrombopoietic agents (oprelvekin and recombinant human thrombopoietins) are reviewed for critical background and context, followed by a detailed discussion of the data for the thrombopoietin receptor agonists (TPO-RAs) to manage CIT. Efficacy of TPO-RAs in treatment and prevention of CIT, as well as safety concerns such as the risk of thromboembolic complications, are reviewed in detail. For this review, a PubMed/MEDLINE literature search was undertaken for relevant articles published from 1995-2021. Expert opinion: After over two decades of drug development for CIT, multiple clinical trials and observational studies have found TPO-RAs, in particular romiplostim, to be safe and effective agents to manage patients with CIT, although no agent is yet FDA-approved for this indication. Active management of CIT with TPO-RAs is likely to improve oncologic outcomes, although additional data are needed. Phase 3 trials are ongoing.
引用
收藏
页码:437 / 448
页数:12
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