Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Haematologica. 2022 Jun 1;107(6):1243-1263. doi: 10.3324/haematol.2021.279512.
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.
化疗引起的血小板减少症(CIT)是治疗非血液系统恶性肿瘤的常见并发症。许多与患者相关的变量(例如年龄、肿瘤类型、先前化疗周期的数量、骨髓肿瘤受累的程度)决定了 CIT 的严重程度。CIT 与化疗类型和剂量有关,含有吉西他滨、铂类或替莫唑胺的方案最常引起 CIT。CIT 中出血和血小板输注的需求相当罕见,除非血小板计数低于 25x109/L,在这种情况下出血率显著增加,血小板输注是唯一的治疗方法。尽管如此,血小板计数低于 70x109/L 仍然是一个挑战。对于血小板计数如此低的患者,重要的是要排除其他引起血小板减少症的原因(药物、感染、血栓性微血管病、输血后紫癜、凝血功能障碍和免疫性血小板减少症)。如果不存在这些原因,常见的方法是减少化疗剂量强度或改用其他药物。不幸的是,相对剂量强度的降低与肿瘤反应率和缓解率的降低有关。血小板生成素生长因子(重组人血小板生成素、聚乙二醇化人巨核细胞生长和发育因子、罗米司亭、艾曲波帕、avatrombopag 和 hetrombopag)可改善预处理和最低点血小板计数,减少血小板输注的需求,并使化疗剂量强度得以维持。国家综合癌症网络指南允许使用这些药物,但需要充分的 III 期随机、安慰剂对照研究来证明维持相对剂量强度、减少血小板输注和出血、并可能改善生存,才能广泛采用。它们的潜在适当应用还取决于肿瘤学界就适当的预处理血小板计数达成共识,以及确定可能预测出血的患者相关和治疗变量。