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Clinical Trials and Observations: Seven-year median time to progression with thalidomide for smoldering myeloma: partial response identifies subset requiring earlier salvage therapy for symptomatic disease

机译:临床试验和观察:沙利度胺治疗阴燃性骨髓瘤的中位进展时间为7年:部分反应可识别需要对症治疗的早期治疗

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摘要

Smoldering multiple myeloma (SMM) is usually followed expectantly without therapy. We conducted a phase 2 trial in 76 eligible patients with SMM, combining thalidomide (THAL, 200 mg/d) with monthly pamidronate. In the first 2 years, THAL dose reduction was required in 86% and drug was discontinued in 50%. Within 4 years, 63% improved, including 25% qualifying for partial response (PR); by then, 34 patients had progressed and 17 required salvage therapy. Unexpectedly, attaining PR status was associated with a shorter time to salvage therapy for disease progression (P < .001), perhaps reflecting greater drug sensitivity of more aggressive disease. Low beta-2-microglobulin levels less than 2 mg/L were independently associated with superior overall and event-free survival. Four-year survival and event-free survival estimates of 91% and 60%, respectively, together with a median postsalvage therapy survival of more than 5 years justify the conduct of a prospective randomized clinical trial to determine the clinical value of preemptive therapy in SMM. Trial registered at under identifier .
机译:闷热多发性骨髓瘤(SMM)通常无需治疗即可接受。我们对76名合格的SMM患者进行了一项2期试验,将沙利度胺(THAL,200 mg / d)与每月的帕米膦酸盐联合使用。在最初的2年中,需要减少86%的THAL剂量,而停止使用50%的药物。在4年内,改善了63%,其中包括25%的人获得了部分缓解(PR);到那时,已有34例患者进展,其中17例需要抢救治疗。出乎意料的是,获得PR状态与挽救疾病进展的治疗时间较短有关(P <.001),这可能反映了对更具侵略性的疾病具有更高的药物敏感性。低于2 mg / L的低β-2-微球蛋白水平独立地具有较高的总体生存率和无事件生存率。四年生存率和无事件生存率估计分别为91%和60%,加上中位治疗后生存期超过5年证明进行前瞻性随机临床试验以确定SMM抢先治疗的临床价值是合理的。试用版已在标识符下注册。

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