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Importance of predosing of recombinant human thrombopoietin to reduce chemotherapy-induced early thrombocytopenia.

机译:预先配制重组人血小板生成素以减少化疗诱导的早期血小板减少症的重要性。

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PURPOSE: Recombinant human thrombopoietin (rhTPO) increases platelets, and the peak response of rhTPO is delayed and is, therefore, not uniformly effective when administered after chemotherapy. The purpose of this study was to identify an effective schedule of rhTPO to best attenuate early thrombocytopenia. PATIENTS AND METHODS: Cohorts of six patients with sarcoma (66 assessable patients) were treated sequentially with doxorubicin and ifosfamide (AI), with rhTPO by a fixed dose and varying schedules being administered before and/or after chemotherapy in cycle 2 and subsequent cycles. Cycle 1 without rhTPO served as an internal control. RESULTS: AI causes cumulative thrombocytopenia. The platelet nadir in cycle 2 was higher than in cycle 1 (mean nadir +/- SEM, 119 +/- 12 x 10(3)/microL v 80 +/- 7 x 10(3)/microL, respectively; P <.001) in 24 (80%) of the 30 patients (P <.001) in whom rhTPO (1.2 microg/kg) was administered starting from 5 days before chemotherapy (pre/postdoses, three/one or one/one) compared with only four (17%) of 24 patients given rhTPO by other schedules (pre/postdoses, two/two, one/three, zero/four, or four/zero) and none of 15 historical control patients. The need for platelet transfusions in four cycles was significantly lower (13 [11%] of 114 cycles, P <.001) in patients who received rhTPO from day -5 (pre/post doses, three/one or one/one) compared with patients who received rhTPO at later time points (28 [47%] of 60 cycles). Bone marrow megakaryocytes increased markedly (four-fold) before chemotherapy with predosing rhTPO and remained elevated (two-fold) after chemotherapy, which may explain the possible mechanism for response. One patient developed subclavian vein thrombosis, and no patients developed neutralizing antibodies to rhTPO. CONCLUSION: These results demonstrate the importance of timing of rhTPO in relation to chemotherapy and indicate that, by optimizing the timing, only two doses of rhTPO (one before and one after chemotherapy) were required to significantly reduce the severity of chemotherapy-related early thrombocytopenia.
机译:目的:重组人血小板生成素(rhTPO)增加血小板,并且rhTPO的峰值反应被延迟,因此在化疗后给药时效果不一致。这项研究的目的是确定有效减少rhTPO的时间表,以最好地减轻早期血小板减少症。病人和方法:对6例肉瘤患者(66例可评估患者)的队列依次接受阿霉素和异环磷酰胺(AI),rhTPO的固定剂量治疗,并在第2周期及以后的周期中化疗前后进行不同的治疗。没有rhTPO的第1个周期用作内部对照。结果:AI导致累积性血小板减少。第2周期的血小板最低点高于第1周期(平均最低+/- SEM,119 +/- 12 x 10(3)/ microL v 80 +/- 7 x 10(3)/ microL; P <比较30例患者中有24例(0.001)(80%)(P <.001)(p <.001),其中从化疗前5天开始服用rhTPO(1.2 microg / kg)(给药前/给药后,三/一或一/一) 24例患者中只有4例(17%)按其他时间表(给药前/给药后,二/二,一/三,零/四或四/零)接受了rhTPO治疗,而15例历史对照患者中没有一例。与第-5天(给药前/给药后,三/一或一/一)相比,接受rhTPO的患者在四个循环中输注血小板的需求显着降低(114个循环中的13个[11%],P <.001)在较晚的时间点接受rhTPO的患者(60个周期中的28个[47%])。预先用rhTPO进行化疗之前,骨髓巨核细胞显着增加(四倍),而在化疗后仍保持升高(两倍),这可能解释了可能的应答机制。一名患者发生了锁骨下静脉血栓形成,没有患者发生针对rhTPO的中和抗体。结论:这些结果证明了rhTPO时机对化疗的重要性,并表明通过优化时机,仅需要两剂rhTPO(一次化疗前和一次在化疗后)即可显着降低化疗相关的早期血小板减少症的严重程度。

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