Department of Medical Oncology, Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi, India.
Department of Laboratory Oncology, Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi, India.
Indian J Med Res. 2019 Jun;149(6):730-739. doi: 10.4103/ijmr.IJMR_1593_18.
BACKGROUND & OBJECTIVES: Survival of patients with multiple myeloma (MM) has improved in the past two decades following use of novel agents and autologous stem cell transplantation. To determine predictors of long-term outcome, data of MM patients who underwent autologous stem cell transplantation (ASCT) at a tertiary care centre in north India were retrospectively analyzed.
Between 1995 and 2016, 349 MM patients underwent ASCT. Patients' median age was 52 yr, ranging from 29 to 68 yr, 68.2 per cent were males. Thirty three per cent patients had international staging system (ISS) Stage III and 68.5 per cent had received novel agents-based induction. High-dose melphalan (200 mg/m) was used for conditioning; patients with renal insufficiency (estimated glomerular filtration rate <40 ml/min) received melphalan 140-150 mg/m.
Post-transplant, 317 of 349 (90.8%) patients responded; complete [complete response (CR)] -213 (61%)], very good partial response (VGPR) -62 (17.8%) and PR in 42 (12%)]. Induction with novel agents, pre-transplant chemosensitive disease, transplant in first remission and serum albumin (≥3.5 g/dl) were predictors of significant response. At a median follow up of 73 months, median overall survival (OS) was 90 months [95% confidence interval (CI) 70.8-109.2], and progression-free survival (PFS) was 41 months (95% CI 33.0-49.0). On multivariate analysis, achievement of CR post-transplant, transplant in first remission, ISS Stages I and II (vs. III), absence of extramedullary disease and serum albumin ≥3.5 g/dl were predictors of prolonged OS. For PFS, achievement of post-transplant CR and transplant in first remission were predictors of superior outcome.
INTERPRETATION & CONCLUSIONS: Treatment with novel agents, achievement of complete remission post-transplant, ISS Stages I and II, absence of extramedullary disease and transplant in first remission were predictors of long-term survival for patients with MM.
随着新型药物和自体干细胞移植的应用,多发性骨髓瘤(MM)患者的生存状况在过去二十年中得到了改善。为了确定长期预后的预测因素,我们回顾性分析了在印度北部一家三级医疗中心接受自体干细胞移植(ASCT)的 MM 患者的数据。
1995 年至 2016 年,349 例 MM 患者接受了 ASCT。患者的中位年龄为 52 岁,范围为 29 至 68 岁,68.2%为男性。33%的患者为国际分期系统(ISS)III 期,68.5%接受了新型药物诱导治疗。高剂量美法仑(200mg/m2)用于预处理;肾功能不全(估计肾小球滤过率<40ml/min)的患者接受美法仑 140-150mg/m2。
移植后,349 例患者中有 317 例(90.8%)有反应;完全缓解[完全缓解(CR)-213 例(61%)],非常好的部分缓解[62 例(17.8%)]和部分缓解[42 例(12%)]。新型药物诱导、移植前化疗敏感疾病、首次缓解期移植和血清白蛋白(≥3.5g/dl)是显著反应的预测因素。在中位随访 73 个月时,中位总生存期(OS)为 90 个月[95%置信区间(CI)70.8-109.2],无进展生存期(PFS)为 41 个月[95%CI 33.0-49.0]。多变量分析显示,移植后获得 CR、首次缓解期移植、ISS Ⅰ和Ⅱ期(而非Ⅲ期)、无髓外疾病和血清白蛋白≥3.5g/dl 是 OS 延长的预测因素。对于 PFS,移植后获得 CR 和首次缓解期移植是获得更好结果的预测因素。
新型药物治疗、移植后获得完全缓解、ISS Ⅰ和Ⅱ期、无髓外疾病和首次缓解期移植是 MM 患者长期生存的预测因素。