[异体移植治疗多发性骨髓瘤:2010年2月的结果和建议]。

J A Pérez-Simón
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引用次数: 0

摘要

此时,异体移植应该只在临床试验的背景下提供。采用新药物和自体移植的标准治疗可能会获得长期的完全缓解,这使得异体移植不适合作为大多数患者的一线治疗。在这种情况下,该程序必须仅保留给预后因素非常差或疾病进展的年轻患者,并接受一线治疗。在第一次复发后,应应用于细胞遗传学不良和早期复发(< 18个月)的患者,优化治疗包括新药和自体移植。在任何情况下,患者都应该在病情最小的情况下进行移植。对于剩余的患者,该手术不应被视为最后的治疗手段,因为在这种情况下,成功的可能性非常低。另一方面,实施该程序并不意味着患者不会从其他治疗中获益,如果他们成为必要的话。在解释来自比较研究的现有数据时必须谨慎。我们有义务继续探索和改进这一策略,迄今为止,这是我们可用的最有效的治疗工具。
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[Allogeneic transplantation in multiple myeloma patients: results and recommendations in February 2010].

At this time, allogeneic transplantation should be offered only within the context of clinical trials. The likelihood of achieving prolonged complete remission with standard therapy with new drugs and autografting renders allogeneic transplantation unadvisable as first-line treatment in most patients. In this situation, the procedure must be reserved only for young patients with very poor prognostic factors or with progression of the disease offer receiving first-line treatment. After the first relapse, it should be applied to patients with an adverse cytogenetics and early relapse (< 18 months) after optimized treatment that includes new drugs and autologous transplantation. In any case, the patient should undergo transplantation with minimal disease. For the remaining patients, this procedure should not be considered the last therapeutic resort, since in this context there is a very low probability of success. On the other hand, conducting the procedure does not imply that the patient will not benefit a posteriori from other treatments, should they become necessary. Caution must be used when interpreting the available data from comparative studies. We have an obligation to continue exploring and improving this strategy which, to date, constitutes the most effective therapeutic tool available to us.

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