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Long-term survival of stage I multiple myeloma given chemotherapy just after diagnosis or at progression of the disease: a multicentre randomized study

机译:诊断后或疾病进展后进行化疗的I期多发性骨髓瘤的长期生存:一项多中心随机研究

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摘要

We conducted a randomized trial to evaluate whether melphalan-prednisone (MPH-P) treatment administered just after diagnosis improves survival of stage I multiple myeloma (MM). Between January 1987 and March 1993, 145 consecutive previously untreated patients with stage I MM were randomized between treatment with MPH-P (administered for 4 days every 6 weeks) just after diagnosis and treatment only at disease progression. Survival was not influenced by MPH-P treatment either administered just after diagnosis or at disease progression (64 vs 71 months respectively). Comparing the first with the second group the odds ratio of death is 1.17 (95% confidence interval 0.57–2.42;P = 0.64). Disease progression occurred within a year in about 50% of patients who were initially untreated. Response rate was similar in both groups, but duration of response was shorter in patients who were treated at disease progression (48 vs 79 months, P = 0.044). Patients actually treated at disease progression (34/70) survived shorter than those who had neither disease progression nor treatment (56 vs > 92 months;P = 0.005). Starting MPH-P just after diagnosis does not improve survival and response rate in stage I MM, with respect to deferring therapy until disease progression. However, patients with stage I MM randomized to have treatment delayed and who actually progressed and were treated had shorter survival than those with stable disease and no treatment. Biologic or other disease features could identify these subgroups of patients. © 2000 Cancer Research Campaign
机译:我们进行了一项随机试验,以评估诊断后立即进行的美法仑-泼尼松(MPH-P)治疗是否能改善I期多发性骨髓瘤(MM)的存活率。在1987年1月至1993年3月之间,仅在疾病诊断和治疗后,就对145例先前未经治疗的I期MM连续患者进行了MPH-P治疗(每6周给药4天)之间的随机分配。诊断后或疾病进展时均未受MPH-P治疗影响生存(分别为64个月和71个月)。将第一组与第二组进行比较,死亡的几率是1.17(95%置信区间0.57–2.42; P = 0.64)。最初未经治疗的患者中,约有50%在一年之内发生了疾病进展。两组的缓解率相似,但在疾病进展期接受治疗的患者的缓解时间较短(48 vs 79个月,P = 0.044)。实际处于疾病进展状态的患者(34/70)比没有疾病进展也没有治疗的患者生存时间短(56 vs> 92个月; P = 0.005)。就将治疗推迟到疾病进展而言,仅在诊断后开始MPH-P并不能改善I MM期的生存率和缓解率。但是,I期MM患者被随机分配以延迟治疗,并且实际进展并接受治疗的患者的生存期要短于那些疾病稳定且未进行治疗的患者。生物学或其他疾病特征可以确定这些患者亚组。 ©2000癌症研究运动

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