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单独使用及联合使用2-氯脱氧腺苷治疗初治的华氏巨球蛋白血症。

2-Chlorodeoxyadenosine alone and in combination for previously untreated Waldenstrom's macroglobulinemia.

作者信息

Weber Donna M, Dimopoulos Meletios A, Delasalle Kay, Rankin Kim, Gavino Maria, Alexanian Raymond

机构信息

Department of Lymphoma-Myeloma, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Semin Oncol. 2003 Apr;30(2):243-7. doi: 10.1053/sonc.2003.50070.

Abstract

Treatment for Waldenstrom's macroglobulinemia (WM) has usually been reserved for symptomatic patients and has included alkylating agent-steroid combinations and, more recently, nucleoside analogues. We now describe our experience with 2-chlorodeoxyadenosine (2-CdA) alone and in combination at our center. We treated 90 consecutive, previously untreated patients with symptomatic WM using either 2-CdA alone or in combination with other agents including prednisone (pred), cyclophosphamide (Cy), and rituximab (Rit) as follows: January 1991 to December 1992- 2-CdA 0.1 mg/kg by continuous infusion (CI) over 24 hours for days (16 patients); December 1992 to December 1995-2-CdA 0.1 mg/kg CI over 24 hours for 7 days plus pred 60 mg/m(2) orally daily for 7 days (20 patients); July 1996 to March 1998-2-CdA 1.5 mg/m(2) by subcutaneous injection (SC) every 8 hours for 7 days plus Cy 40 mg/m(2) orally twice daily for 7 days (37 patients); August 1999 to December 2001-2-CdA 1.5 mg/m(2) SC every 8 hours for 7 days plus Cy 40 mg/m(2) orally twice daily for 7 days plus Rit 375 mg/m(2) by intravenous infusion (IV) weekly for 4 weeks (17 patients). For nearly all patients, a second course was repeated after at least 6 weeks. Responding patients were monitored without further treatment until relapse. Overall response (complete [CR] + partial response [PR]) was 94% for 2-CdA alone, 60% for 2-CdA/pred, 84% for 2-CdA/Cy, and 94% for 2-CdA/Cy/Rit. Median overall survival is 73 months for 2-CdA, 41 months for 2-CdA/pred, and has not been reached for 2-CdA/Cy or 2-CdA/Cy/Rit. Cause-specific survival for 2-CdA/pred is 78 months and has not been reached for all other programs. The only poor prognostic factor for cause-specific survival was hemoglobin < 9 g/dL. 2-CdA regimens provide excellent response rates and improve cause-specific survival, with minimal treatment and little toxicity. These observations support the potential role of 2-CdA regimens as the treatment of choice for previously untreated WM.

摘要

华氏巨球蛋白血症(WM)的治疗通常针对有症状的患者,治疗方法包括烷化剂与类固醇联合使用,以及最近使用的核苷类似物。我们现在介绍我们中心单独使用和联合使用2-氯脱氧腺苷(2-CdA)的经验。我们连续治疗了90例之前未接受过治疗的有症状WM患者,单独使用2-CdA或与其他药物联合使用,这些药物包括泼尼松(Pred)、环磷酰胺(Cy)和利妥昔单抗(Rit),具体如下:1991年1月至1992年12月——2-CdA 0.1mg/kg,24小时持续静脉输注(CI),共5天(16例患者);1992年12月至1995年12月——2-CdA 0.1mg/kg,24小时CI,共7天,加Pred 60mg/m²,口服,每日1次,共7天(20例患者);1996年7月至1998年3月——2-CdA 1.5mg/m²,皮下注射(SC),每8小时1次,共7天,加Cy 40mg/m²,口服,每日2次,共7天(37例患者);1999年8月至2001年12月——2-CdA 1.5mg/m²,SC,每8小时1次,共7天,加Cy 40mg/m²,口服,每日2次,共7天,加利妥昔单抗375mg/m²,静脉输注(IV),每周1次,共4周(17例患者)。几乎所有患者在至少6周后重复第二个疗程。对有反应的患者进行监测,不再进一步治疗,直至复发。单独使用2-CdA的总体缓解率(完全缓解[CR]+部分缓解[PR])为94%,2-CdA/Pred为60%,2-CdA/Cy为84%,2-CdA/Cy/Rit为94%。2-CdA治疗的中位总生存期为73个月,2-CdA/Pred为41个月,2-CdA/Cy或2-CdA/Cy/Rit尚未达到。2-CdA/Pred治疗的病因特异性生存期为78个月,其他所有治疗方案均未达到。病因特异性生存的唯一不良预后因素是血红蛋白<9g/dL。2-CdA治疗方案具有出色的缓解率,可提高病因特异性生存率,治疗最少且毒性小。这些观察结果支持2-CdA治疗方案作为初治WM的首选治疗方法的潜在作用。

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