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沙利度胺-地塞米松与美法仑-泼尼松在老年多发性骨髓瘤患者中的比较。

Thalidomide-dexamethasone compared with melphalan-prednisolone in elderly patients with multiple myeloma.

作者信息

Ludwig Heinz, Hajek Roman, Tóthová Elena, Drach Johannes, Adam Zdenek, Labar Boris, Egyed Miklós, Spicka Ivan, Gisslinger Heinz, Greil Richard, Kuhn Ingrid, Zojer Niklas, Hinke Axel

机构信息

Department of Medicine I, Wilhelminenspital Vienna, Vienna, Austria.

出版信息

Blood. 2009 Apr 9;113(15):3435-42. doi: 10.1182/blood-2008-07-169565. Epub 2008 Oct 27.

Abstract

We compared thalidomide-dexamethasone (TD) with melphalan-prednisolone (MP) in 289 elderly patients with multiple myeloma (MM). Patients received either thalidomide 200 mg plus dexamethasone 40 mg, days 1 to 4 and 15 to 18 on even cycles and days 1 to 4 on odd cycles, during a 28-day cycle or to melphalan 0.25 mg/kg and prednisolone 2 mg/kg orally on days 1 to 4 during a 28- to 42-day cycle. Patients achieving stable disease or better were randomly assigned to maintenance therapy with either thalidomide 100 mg daily and 3 MU interferon alpha-2b thrice weekly or to 3 MU interferon alpha-2b thrice weekly only. TD resulted in a higher proportion of complete and very good remissions (26% vs 13%; P= .006) and overall responses (68% vs 50%; P= .002) compared with MP. Time to progression (21.2 vs 29.1 months; P= .2), and progression-free survival was similar (16.7 vs 20.7 months; P= .1), but overall survival was significantly shorter in the TD group (41.5 vs 49.4 months; P= .024). Toxicity was higher with TD, particularly in patients older than 75 years with poor performance status. The study was registered at ClinicalTrials.gov as NCT00205751.

摘要

我们在289例老年多发性骨髓瘤(MM)患者中比较了沙利度胺-地塞米松(TD)与美法仑-泼尼松(MP)的疗效。患者在28天周期内,偶数周期的第1至4天和第15至18天以及奇数周期的第1至4天接受沙利度胺200 mg加地塞米松40 mg治疗,或者在28至42天周期的第1至4天口服美法仑0.25 mg/kg和泼尼松2 mg/kg。疾病达到稳定或更好状态的患者被随机分配至维持治疗组,一组为每日口服沙利度胺100 mg并每周三次皮下注射300万单位α-2b干扰素,另一组仅每周三次皮下注射300万单位α-2b干扰素。与MP相比,TD组获得完全缓解和非常好的缓解的比例更高(26%对13%;P = 0.006),总体缓解率也更高(68%对50%;P = 0.002)。进展时间(21.2对29.1个月;P = 0.2)和无进展生存期相似(16.7对20.7个月;P = 0.1),但TD组的总生存期显著更短(41.5对49.4个月;P = 0.024)。TD的毒性更高,尤其是在75岁以上且体能状态较差的患者中。该研究已在ClinicalTrials.gov注册,注册号为NCT00205751。

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