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拓扑替康、阿糖胞苷、顺铂和泼尼松龙(TOPOSHAP)用于难治性和复发性淋巴瘤患者:一项I期试验的结果

Topotecan, Ara-C, cisplatin and prednisolone (TOPOSHAP) for patients with refractory and relapsing lymphomas: results of a phase I trial.

作者信息

Coutinho Fernando, Manhani Ana Rita, Velasquez William S, Del Giglio Auro

机构信息

Hematology-Oncology Division, ABC Foundation School of Medicine, São Paulo, Brazil.

出版信息

Acta Haematol. 2004;112(3):121-5. doi: 10.1159/000079721.

Abstract

We designed a phase I trial to assess the feasibility of the combination of topotecan, Ara-C, cisplatin and solumedrol (TOPOSHAP) in patients with relapsed or primary refractory lymphomas. We included 9 patients with measurable non-Hodgkin's (n = 8) and Hodgkin's (n = 1) lymphomas. Level 1 consisted of topotecan 1.0 mg/m(2)/day, i.v., given on days 1-3, cisplatin 25 mg/m(2)/day, i.v., on days 1-3, Ara-C 500 mg/m(2), i.v., on day 4, methylprednisolone 250 mg, i.v., on days 1-4. The regimen was repeated every 3-4 weeks. The maximum tolerated dose was already reached at level 1. G-CSF was added systematically after the 5th patient was included. The most significant toxicity in this trial was hematologic (all had neutropenia WHO grade 4 and 7 had grade 4 thrombocytopenia). Three patients had neutropenic fever. We observed two instances of WHO grade 3 and one of grade 4 diarrhea. Two patients achieved a complete response and 6 a partial response. We conclude that TOPOSHAP with G-CSF support is feasible and should be further studied in phase II studies.

摘要

我们设计了一项I期试验,以评估拓扑替康、阿糖胞苷、顺铂和甲泼尼龙联合方案(TOPOSHAP)用于复发或原发性难治性淋巴瘤患者的可行性。我们纳入了9例可测量的非霍奇金淋巴瘤患者(n = 8)和霍奇金淋巴瘤患者(n = 1)。第1剂量水平为拓扑替康1.0mg/m²/天,静脉注射,第1 - 3天给药;顺铂25mg/m²/天,静脉注射,第1 - 3天给药;阿糖胞苷500mg/m²,静脉注射,第4天给药;甲泼尼龙250mg,静脉注射,第1 - 4天给药。该方案每3 - 4周重复一次。在第1剂量水平就已达到最大耐受剂量。纳入第5例患者后系统性地添加了粒细胞集落刺激因子(G - CSF)。该试验中最显著的毒性是血液学毒性(所有患者均有4级中性粒细胞减少,7例有4级血小板减少)。3例患者发生中性粒细胞减少性发热。我们观察到2例3级和1例4级腹泻。2例患者达到完全缓解,6例达到部分缓解。我们得出结论,在G - CSF支持下的TOPOSHAP方案是可行的,应在II期研究中进一步研究。

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