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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >A randomized phase 3 trial of thalidomide and prednisone as maintenance therapy after ASCT in patients with MM with a quality-of-life assessment: the National Cancer Institute of Canada Clinicals Trials Group Myeloma 10 Trial.
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A randomized phase 3 trial of thalidomide and prednisone as maintenance therapy after ASCT in patients with MM with a quality-of-life assessment: the National Cancer Institute of Canada Clinicals Trials Group Myeloma 10 Trial.

机译:沙利度胺和强的松作为ASCT治疗维持性MM患者的一项3期随机试验,进行了生活质量评估:加拿大国家癌症研究所临床试验组骨髓瘤10试验。

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We conducted a randomized, controlled trial comparing thalidomide-prednisone as maintenance therapy with observation in 332 patients who had undergone autologous stem cell transplantation with melphalan 200 mg/m2. The primary end point was overall survival (OS); secondary end points were myeloma-specific progression-free survival,progression-free survival, incidence of venous thromboembolism, and health-related quality of life (HRQoL). With a median follow-up of 4.1 years, no differences in OS between thalidomide-prednisone and observation were detected (respective 4-year estimates of 68% vs 60%, respectively; hazard ratio = 0.77; P = .18); thalidomide-prednisone was associated with superior myeloma-specific progression-free survival and progression-free survival (for both outcomes, the 4-year estimates were 32% vs 14%; hazard ratio = 0.56; P < .0001) and more frequent venous thromboembolism (7.3% vs none; P = .0004). Median survival after first disease recurrence was 27.7 months with thalidomide-prednisone and 34.1 months in the observation group. Nine second malignancies were observed with thalidomide-prednisone versus 6 in the observation group. Those allocated to thalidomide-prednisone reported worse HRQoL with respect to cognitive function, dyspnea, constipation, thirst, leg swelling, numbness, dry mouth, and balance problems. We conclude that maintenance therapy with thalidomide-prednisone after autologous stem cell transplantation improves the duration of disease control, but is associated with worsening of patient-reported HRQoL and no detectable OS benefit.
机译:我们进行了一项随机对照试验,比较了沙利度胺-泼尼松作为维持治疗与332例接受美法仑200 mg / m2自体干细胞移植的患者的观察结果。主要终点是总体生存期(OS)。次要终点是骨髓瘤特异性无进展生存期,无进展生存期,静脉血栓栓塞的发生率以及与健康相关的生活质量(HRQoL)。中位随访时间为4.1年,沙利度胺-泼尼松和观察到的OS无差异(4年估计分别为68%和60%;危险比= 0.77; P = .18);沙利度胺-泼尼松与较高的骨髓瘤特异性无进展生存期和无进展生存期相关(两种结果的4年估计分别为32%vs 14%;危险比= 0.56; P <.0001)和更频繁的静脉血栓栓塞(7.3%vs.无; P = .0004)。沙利度胺-泼尼松组首次疾病复发后的中位生存期为27.7个月,观察组为34.1个月。沙利度胺-泼尼松组观察到9例第二恶性肿瘤,而观察组则为6例。那些分配给沙利度胺-泼尼松的患者在认知功能,呼吸困难,便秘,口渴,腿部肿胀,麻木,口干和平衡问题方面报告了较差的HRQoL。我们得出的结论是,自体干细胞移植后使用沙利度胺-泼尼松维持治疗可改善疾病控制的持续时间,但与患者报告的HRQoL恶化相关,且无可检测的OS获益。

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