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Treatment of Chemotherapy-induced Thrombocytopenia in Patients with Non-hematologic Malignancies

Overview
Journal Haematologica
Specialty Hematology
Date 2022 Jun 1
PMID 35642485
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Abstract

Chemotherapy-induced thrombocytopenia (CIT) is a common complication of the treatment of non-hematologic malignancies. Many patient-related variables (e.g., age, tumor type, number of prior chemotherapy cycles, amount of bone marrow tumor involvement) determine the extent of CIT. CIT is related to the type and dose of chemotherapy, with regimens containing gemcitabine, platinum, or temozolomide producing it most commonly. Bleeding and the need for platelet transfusions in CIT are rather uncommon except in patients with platelet counts below 25x109/L in whom bleeding rates increase significantly and platelet transfusions are the only treatment. Nonetheless, platelet counts below 70x109/L present a challenge. In patients with such counts, it is important to exclude other causes of thrombocytopenia (medications, infection, thrombotic microangiopathy, post-transfusion purpura, coagulopathy and immune thrombocytopenia). If these are not present, the common approach is to reduce chemotherapy dose intensity or switch to other agents. Unfortunately decreasing relative dose intensity is associated with reduced tumor response and remission rates. Thrombopoietic growth factors (recombinant human thrombopoietin, pegylated human megakaryocyte growth and development factor, romiplostim, eltrombopag, avatrombopag and hetrombopag) improve pretreatment and nadir platelet counts, reduce the need for platelet transfusions, and enable chemotherapy dose intensity to be maintained. National Comprehensive Cancer Network guidelines permit their use but their widespread adoption awaits adequate phase III randomized, placebo-controlled studies demonstrating maintenance of relative dose intensity, reduction of platelet transfusions and bleeding, and possibly improved survival. Their potential appropriate use also depends on consensus by the oncology community as to what constitutes an appropriate pretreatment platelet count as well as identification of patient-related and treatment variables that might predict bleeding.

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References
1.
Reese J, Li X, Hauben M, Aster R, Bougie D, Curtis B . Identifying drugs that cause acute thrombocytopenia: an analysis using 3 distinct methods. Blood. 2010; 116(12):2127-33. PMC: 2951857. DOI: 10.1182/blood-2010-03-276691. View

2.
Krop I, LoRusso P, Miller K, Modi S, Yardley D, Rodriguez G . A phase II study of trastuzumab emtansine in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer who were previously treated with trastuzumab, lapatinib, an anthracycline, a taxane, and capecitabine. J Clin Oncol. 2012; 30(26):3234-41. DOI: 10.1200/JCO.2011.40.5902. View

3.
Wiseman G, Gordon L, Multani P, Witzig T, Spies S, Bartlett N . Ibritumomab tiuxetan radioimmunotherapy for patients with relapsed or refractory non-Hodgkin lymphoma and mild thrombocytopenia: a phase II multicenter trial. Blood. 2002; 99(12):4336-42. DOI: 10.1182/blood.v99.12.4336. View

4.
Zent C, Ding W, Reinalda M, Schwager S, Hoyer J, Bowen D . Autoimmune cytopenia in chronic lymphocytic leukemia/small lymphocytic lymphoma: changes in clinical presentation and prognosis. Leuk Lymphoma. 2009; 50(8):1261-8. PMC: 3917557. DOI: 10.1080/10428190903026492. View

5.
Gronberg B, Bremnes R, Flotten O, Amundsen T, Brunsvig P, Hjelde H . Phase III study by the Norwegian lung cancer study group: pemetrexed plus carboplatin compared with gemcitabine plus carboplatin as first-line chemotherapy in advanced non-small-cell lung cancer. J Clin Oncol. 2009; 27(19):3217-24. DOI: 10.1200/JCO.2008.20.9114. View