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重组人血小板生成素预给药对减少化疗引起的早期血小板减少症的重要性。

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

作者信息

Vadhan-Raj Saroj, Patel Shreyaskumar, Bueso-Ramos Carlos, Folloder Jody, Papadopolous Nicholas, Burgess Andrew, Broemeling Lyle D, Broxmeyer Hal E, Benjamin Robert S

机构信息

Department of Bioimmunotherapy, Box 422, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030, USA.

出版信息

J Clin Oncol. 2003 Aug 15;21(16):3158-67. doi: 10.1200/JCO.2003.08.003.

Abstract

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.

摘要

目的

重组人血小板生成素(rhTPO)可增加血小板数量,但其峰值反应延迟,因此在化疗后给药时效果并不一致。本研究旨在确定一种有效的rhTPO给药方案,以最佳程度减轻早期血小板减少症。

患者与方法

将6例肉瘤患者(共66例可评估患者)分为不同队列,依次接受阿霉素和异环磷酰胺(AI)治疗,在第2周期及后续周期化疗前和/或化疗后,按照固定剂量和不同给药方案给予rhTPO。第1周期未使用rhTPO作为内部对照。

结果

AI会导致累积性血小板减少症。在30例患者中,24例(80%)从化疗前5天开始给予rhTPO(1.2μg/kg)(给药前/给药后剂量,分别为三/一或一/一),其第2周期的血小板最低点高于第1周期(平均最低点±标准误,分别为119±12×10³/μL和80±7×10³/μL;P<.001),而在24例按其他给药方案给予rhTPO的患者中(给药前/给药后剂量,分别为二/二、一/三、零/四或四/零)仅有4例(17%)出现这种情况,15例历史对照患者均未出现。与在较晚时间点接受rhTPO的患者相比,从第-5天开始接受rhTPO(给药前/给药后剂量,分别为三/一或一/一)的患者在四个周期中对血小板输注的需求显著降低(114个周期中有13个周期[11%],P<.001)(60个周期中有28个周期[47%])。化疗前给予rhTPO可使骨髓巨核细胞显著增加(四倍),化疗后仍保持升高(两倍),这可能解释了反应的可能机制。1例患者发生锁骨下静脉血栓形成,无患者产生针对rhTPO的中和抗体。

结论

这些结果证明了rhTPO给药时间相对于化疗的重要性,并表明通过优化给药时间,仅需两剂rhTPO(化疗前一剂和化疗后一剂)就能显著降低化疗相关早期血小板减少症的严重程度。

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