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培美曲塞联合顺铂一线治疗不可手术切除的恶性胸膜间皮瘤患者

[First-line treatment with pemetrexed in association with cisplatin in patients with non-operable malignant pleural mesothelioma].

作者信息

Burgin M, Gairard-Dory A -C, Mennecier B, Molard A, Beretz L, Quoix A -E

机构信息

Service de pharmacie, stérilisation, pôle pharmacie, pharmacologie, hôpitaux universitaires de Strasbourg, 67000 Strasbourg, France.

出版信息

Rev Pneumol Clin. 2009 Apr;65(2):75-83. doi: 10.1016/j.pneumo.2008.12.002. Epub 2009 Apr 1.

Abstract

Malignant pleural mesothelioma (MPM) is an aggressive disease with a poor prognosis. The optimal treatment of MPM was not clearly defined, until the publication of the multicentre, controlled and randomized phase III trial by Vogelzang et al. in 2003, which made the pemetrexed-cisplatin association the gold standard for the non-operable stages. Eleven patients with histologically proven pleural mesothelioma, not candidates for curative surgery, were assessed for eligibility and treated in our hospital. The response rate was similar to the reference study and the toxicity was acceptable. The median survival time was 12.7 months with an objective response rate of 45.5%. The median time to progression was 7.7 months. Neutropenia (all grades included) was the most common haematological toxicity (42.1%) although only one grade 3/4 was noted. Grade 3/4 anaemia and thrombocytopenia were not reported. Nausea and vomiting were the most commonly reported clinical toxicities with 81.8% reported (all grades included). One cutaneous allergic reaction was reported. The combination of pemetrexed and cisplatin chemotherapy provided the best objectives responses, but new therapeutic regimens are still warranted for these patients with a poor prognosis. The results were similar to those obtained in the Vogelzang et al.'s trial despite a selection bias because they correspond to 36.7% of the total recruitment in the unit.

摘要

恶性胸膜间皮瘤(MPM)是一种侵袭性疾病,预后较差。在2003年Vogelzang等人发表多中心、对照和随机III期试验之前,MPM的最佳治疗方案尚未明确界定,该试验使培美曲塞-顺铂联合方案成为不可手术阶段的金标准。11例经组织学证实为胸膜间皮瘤且不适合进行根治性手术的患者在我院接受了资格评估和治疗。缓解率与参考研究相似,毒性可接受。中位生存时间为12.7个月,客观缓解率为45.5%。中位疾病进展时间为7.7个月。中性粒细胞减少(包括所有级别)是最常见的血液学毒性(42.1%),尽管仅记录到1例3/4级。未报告3/4级贫血和血小板减少。恶心和呕吐是最常报告的临床毒性,报告率为81.8%(包括所有级别)。报告了1例皮肤过敏反应。培美曲塞和顺铂联合化疗提供了最佳的客观缓解,但对于这些预后较差的患者,仍需要新的治疗方案。尽管存在选择偏倚,但结果与Vogelzang等人试验中获得的结果相似,因为它们占该科室总招募人数的36.7%。

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