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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.
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页码:437 / 448
页数:12
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