首页> 美国卫生研究院文献>Mediterranean Journal of Hematology and Infectious Diseases >Lenalidomide in Combination with Dexamethasone in Elderly Patients with Advanced Relapsed or Refractory Multiple Myeloma and Renal Failure
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Lenalidomide in Combination with Dexamethasone in Elderly Patients with Advanced Relapsed or Refractory Multiple Myeloma and Renal Failure

机译:来那度胺联合地塞米松治疗老年晚期复发或难治性多发性骨髓瘤和肾功能衰竭的老年患者

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摘要

Salvage therapy of elderly patients with advanced, relapsed and refractory multiple myeloma (MM) is often limited by poor marrow reserve and multi-organ impairment. In particular, renal failure occurs in up to 50% of such patients, and this can potentially limit the therapeutic options. Both thalidomide and bortezomib have proven effective in these patients, with an acceptable toxicity, while, in clinical practice, lenalidomide is generally not considered a first-choice drug for MM patients with renal failure as early reports showed an increased hematological toxicity unless appropriate dose reduction is applied. Aim of this study was a retrospective evaluation of the efficacy of the combination Lenalidomide + Dexamethasone in a population of elderly MM patients treated in 5 Italian Centers. The study included 20 consecutive MM patients (9 M, 11 F, median age 76.5 years) with relapsed (N= 6) or refractory (N=13) MM and moderate to severe renal failure, defined as creatinine clearance (Cr Cl) < 50ml/min. Four patients were undergoing hemodyalisis at study entry. 85 % of the patients had been previously treated with bortezomib-containing regimens. Lenalidomide dose was adjusted according to renal function and patients clinical conditions Median treatment duration was 16 months (1–22), therapy was interrupted after 1 21-day cycle in 2 patients. Grade III–IV neutropenia was observed in 7 patients (35%); grade III–IV non hematological toxicity was recorded in 3 cases (28%). A > partial response was observed in 8 patients (40%), 1 of whom obtained a VGPR; 4 additional patients achieved a minor response. Median response duration was 16 months (range 2–19+ months). A complete and partial renal response was obtained in 4 and 3 patients, respectively, all of them were responsive to Lenalidomide-dexamethasone According to our data, LEN+DEX has shown efficacy and acceptable toxicity in this population of elderly patients with advanced MM and renal failure
机译:老年晚期,复发性和难治性多发性骨髓瘤(MM)患者的挽救疗法通常受骨髓储备差和多器官功能障碍的限制。尤其是,多达50%的此类患者会发生肾衰竭,这可能会限制治疗选择。沙利度胺和硼替佐米均已证明对这些患者有效,并且具有可接受的毒性,而在临床实践中,来那度胺通常不被认为是患有肾功能衰竭的MM患者的首选药物,因为早期报道显示除非有适当的剂量减少,血液毒性增加被申请;被应用。这项研究的目的是回顾性评估Lenalidomide +地塞米松联合治疗在5个意大利中心治疗的老年MM患者中的疗效。该研究包括连续20例MM(9 M,11 F,中位年龄76.5岁)复发(N = 6)或难治性(N = 13)MM患者,中度至重度肾衰竭,定义为肌酐清除率(Cr Cl)< 50毫升/分钟四名患者在研究进入时经历了出血性出血。 85%的患者先前曾接受过含硼替佐米的治疗。来那度胺的剂量根据肾功能和患者的临床情况进行调整,中位治疗时间为16个月(1-22),2例患者在1个21天周期后中断治疗。 7例患者(35%)观察到III–IV级中性粒细胞减少; 3例(28%)记录为III–IV级非血液学毒性。在8例患者(40%)中观察到>部分反应,其中1例获得了VGPR。另外4名患者的反应轻微。中位反应持续时间为16个月(范围2-19个月以上)。分别有4例和3例患者获得了完全和部分肾脏反应,他们都对来那度胺-地塞米松有反应。根据我们的数据,LEN + DEX在该年龄段晚期MM和肾病的老年患者中显示出疗效和可接受的毒性失败

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