Riccardi A, Mora O, Tinelli C, Valentini D, Brugnatelli S, Spanedda R, De Paoli A, Barbarano L, Di Stasi M, Giordano M, Delfini C, Nicoletti G, Bergonzi C, Rinaldi E, Piccinini L, Ascari E
Medicina Interna e Oncologia Medica, Università and Istituto di Ricovero e Cura a Carattere Scientifico Policlinico S Matteo, Pavia, Italy.
Br J Cancer. 2000 Apr;82(7):1254-60. doi: 10.1054/bjoc.1999.1087.
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.
我们进行了一项随机试验,以评估在诊断后立即给予美法仑-泼尼松(MPH-P)治疗是否能提高Ⅰ期多发性骨髓瘤(MM)患者的生存率。在1987年1月至1993年3月期间,145例连续的未经治疗的Ⅰ期MM患者被随机分为两组,一组在诊断后立即接受MPH-P治疗(每6周给药4天),另一组仅在疾病进展时进行治疗。无论是在诊断后立即给予MPH-P治疗还是在疾病进展时给予治疗,生存率均未受到影响(分别为64个月和71个月)。将第一组与第二组进行比较,死亡比值比为1.17(95%置信区间0.57 - 2.42;P = 0.64)。约50%最初未经治疗的患者在1年内出现疾病进展。两组的缓解率相似,但在疾病进展时接受治疗的患者缓解持续时间较短(48个月对79个月,P = 0.044)。在疾病进展时实际接受治疗的患者(34/70)的生存期比既无疾病进展也未接受治疗的患者短(5并个月对>92个月;P = 0.005)。与将治疗推迟至疾病进展相比,在诊断后立即开始MPH-P治疗并不能提高Ⅰ期MM患者的生存率和缓解率。然而,随机分配接受延迟治疗且实际出现疾病进展并接受治疗的Ⅰ期MM患者的生存期比疾病稳定且未接受治疗的患者短。生物学或其他疾病特征可能会识别出这些患者亚组。