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Allo-SCT for multiple myeloma in the era of novel agents: A retrospective study on behalf of Swiss Blood SCT

机译:新药时代下的Allo-SCT治疗多发性骨髓瘤:代表Swiss Blood SCT的回顾性研究

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Despite the introduction of novel drugs, cure of multiple myeloma remains rare. Allo-SCT can induce long-term remission, but randomized studies in advanced disease are lacking and the influence of novel drugs remains unclear. In our retrospective analysis of all patients with myeloma allografted in Switzerland, 95 patients were transplanted between 1988 and 2011. Most patients were heavily pre-treated, and 53% received novel drugs before transplant. In all, 51% were allografted after relapse or progression. Transplant trends changed over time with an increase in reduced intensity conditioning and unrelated donors. At the time of analysis 47 patients remained alive, with a median follow-up of survivors of 53 months. Acute GVHD II-IV and chronic GVHD (cGVHD) occurred in 49% and 53%, respectively; TRM at 5 years was 18%. Five-year OS and PFS were 51% and 29%, respectively. Patients who received transplant upfront vs after relapse had a significantly better outcome, as well as those who had a related donor and achieved CR post transplant. We found no impact of pre-treatment with novel drugs or cGVHD. Although long-term remission following allo-SCT can be achieved, GVHD and TRM remain major limitations. Our series suggests that benefit is highest when allo-SCT is used early in the disease. ? 2013 Macmillan Publishers Limited. All rights reserved.
机译:尽管引入了新药,但多发性骨髓瘤的治愈仍然很少。 Allo-SCT可以诱导长期缓解,但是缺乏对晚期疾病的随机研究,并且新药的影响尚不清楚。在我们对瑞士所有同种异体骨髓瘤患者的回顾性分析中,1988年至2011年间有95例患者被移植。大多数患者接受了严格的预处理,其中53%的患者在移植前接受了新药治疗。共有51%的患者在复发或进展后接受了同种异体移植。随着强度调节的减少和不相关供体的增加,移植的趋势随着时间而改变。在分析时,有47名患者还活着,幸存者的中位随访时间为53个月。急性GVHD II-IV和慢性GVHD(cGVHD)的发生率分别为49%和53%。 5年的TRM为18%。五年OS和PFS分别为51%和29%。预先接受移植而复发后接受移植的患者,以及有相关供体并在移植后获得CR的患者,其转归明显更好。我们发现用新药或cGVHD进行预处理没有影响。尽管可以实现allo-SCT后的长期缓解,但GVHD和TRM仍然是主要限制。我们的系列表明,在疾病早期使用allo-SCT时,获益最大。 ? 2013 Macmillan Publishers Limited。版权所有。

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