Malhotra Pankaj, Yanamandra Uday, Khadwal Alka, Prakash Gaurav, Lad Deepesh, Law Arjun D, Khurana Harshit, Sachdeva M U S, Bose Praveen, Das Reena, Varma Neelam, Varma Subhash
1Clinical Haematology Division, Department of Internal Medicine, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, 160012 India.
2Department of Haematology and Stem Cell Transplant, Army Hospital (Research and Referral), Delhi, 110010 India.
Indian J Hematol Blood Transfus. 2018 Apr;34(2):261-267. doi: 10.1007/s12288-017-0876-y. Epub 2017 Sep 19.
Autologous stem cell transplantation (ASCT) is considered as standard of care in patients with multiple myeloma (MM) patients aged 65 years or younger. We analyzed data of 94 patients of plasma cell dyscrasias who underwent 95 autologous transplants at our institute from October 2003 to Aug 2016. Other than 76 patients of newly diagnosed multiple myeloma, we also transplanted two patients of POEMS syndrome, two patients of plasma cell leukemia, three patients of concurrent light chain deposition disease, three patients of multifocal plasmacytomas, and eight patients of isolated light chain myeloma. One patient underwent transplant twice. The median age of patients was 53 years (range 21-65). The average interval between diagnosis and transplant was 10.51 ± 5.42 months. The predominant stage in the study cohort was ISS-III. IgG kappa was the commonest subtype of plasma cell dyscrasia (27.9%) followed by IgG lambda (16.27%). Renal involvement was seen in 25% patients at the time of transplantation. Following chemotherapy, 42% patients were in CR, 39% in VGPR, 5% had PR and 14% had progressive disease at the time of transplantation. All patients were conditioned with melphalan (dose 120-200 mg/m) except for one who received an additional bortezomib for his second transplant. The mean time to neutrophil and platelet engraftment was 11.09 ± 1.82 and 12.69 ± 4.55 days respectively. Mucositis was noted in all patients (grade 3 in 37.5% patients). The median PFS (biochemical) was 55.8% and PFS (clinical) was 76.7% at 6.5 years. Thirteen percent of the transplanted patients succumbed to their illness of which three patients died within 30 days of transplant. Median OS was 76.7% at 6.5 years. ASCT is a feasible option for MM in India and the results are comparable.
自体干细胞移植(ASCT)被视为65岁及以下多发性骨髓瘤(MM)患者的标准治疗方法。我们分析了2003年10月至2016年8月在我院接受95次自体移植的94例浆细胞异常增生患者的数据。除76例新诊断的多发性骨髓瘤患者外,我们还为2例POEMS综合征患者、2例浆细胞白血病患者、3例合并轻链沉积病患者、3例多灶性浆细胞瘤患者和8例孤立性轻链骨髓瘤患者进行了移植。1例患者接受了两次移植。患者的中位年龄为53岁(范围21 - 65岁)。诊断与移植之间的平均间隔为10.51±5.42个月。研究队列中主要分期为国际分期系统(ISS)-III期。IgG κ是浆细胞异常增生最常见的亚型(27.9%),其次是IgG λ(16.27%)。25%的患者在移植时出现肾脏受累。化疗后,42%的患者在移植时处于完全缓解(CR),39%处于非常好的部分缓解(VGPR),5%达到部分缓解(PR),14%病情进展。除1例第二次移植时额外接受硼替佐米治疗的患者外,所有患者均接受马法兰预处理(剂量120 - 200mg/m)。中性粒细胞和血小板植入的平均时间分别为11.09±1.82天和12.69±4.55天。所有患者均出现黏膜炎(37.5%的患者为3级)。6.5年时无进展生存期(生化)的中位数为55.8%,无进展生存期(临床)为76.7%。13%的移植患者因病死亡,其中3例在移植后30天内死亡。6.5年时总生存期的中位数为76.7%。自体干细胞移植在印度对于多发性骨髓瘤是一种可行的选择,结果具有可比性。