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[多发性骨髓瘤的一线治疗]

[First-line treatment of multiple myeloma].

作者信息

Breitkreutz I, Raab M, Goldschmidt H

机构信息

Medizinische Klinik V, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Deutschland.

出版信息

Internist (Berl). 2019 Jan;60(1):23-33. doi: 10.1007/s00108-018-0527-x.

Abstract

Within the last two decades the therapeutic options for newly diagnosed multiple myeloma have changed dramatically. The implementation of high-dose chemotherapy with melphalan and subsequent autologous blood stem cell transplantation initially led to prolonged survival in younger, fit patients. Furthermore, recent data suggest that patients with high-risk disease seem to benefit most from tandem transplantation approaches. Therefore, risk stratification at initiation of first-line treatment is of great importance. With the advent and integration of the so-called novel agents, such as thalidomide, lenalidomide and bortezomib into first-line treatment, both transplant eligible and ineligble patients gained new therapeutic perspectives. In Germany, the combination of bortezomib with cyclophosphamide and dexamethasone is currently considered the standard of care as induction regimen before high-dose treatment and transplantation; however, the combination of lenalidomide, bortezomib and dexamethasone is increasingly being used, but is still not yet approved in Germany. For patients where high-dose therapy and stem cell transplantation are not feasible, bortezomib and lenalidomide are available as backbone agents of various combination regimens. Recently, the anti-CD38 antibody daratumumab has been approved in combination with bortezomib, melphalan and prednisone as primary treatment for newly diagnosed patients. An allogeneic stem cell transplantation can be considered for younger patients without relevant comorbidities and with high-risk disease or early relapse after autologous blood stem cell transplantation but should only be performed within controlled clinical trials and in specialized centers.

摘要

在过去二十年中,新诊断的多发性骨髓瘤的治疗选择发生了巨大变化。美法仑高剂量化疗及随后的自体造血干细胞移植的实施最初使年轻、健康的患者生存期延长。此外,近期数据表明,高危疾病患者似乎从串联移植方法中获益最大。因此,一线治疗开始时的风险分层非常重要。随着沙利度胺、来那度胺和硼替佐米等所谓新型药物的出现并纳入一线治疗,适合和不适合移植的患者都获得了新的治疗前景。在德国,硼替佐米与环磷酰胺和地塞米松联合目前被视为高剂量治疗和移植前诱导方案的标准治疗;然而,来那度胺、硼替佐米和地塞米松的联合使用越来越多,但在德国仍未获批。对于高剂量治疗和干细胞移植不可行的患者,硼替佐米和来那度胺可作为各种联合方案的基础药物。最近,抗CD38抗体达雷妥尤单抗已获批与硼替佐米、美法仑和泼尼松联合用于新诊断患者的一线治疗。对于无相关合并症、患有高危疾病或自体造血干细胞移植后早期复发的年轻患者,可考虑进行异基因干细胞移植,但应仅在对照临床试验和专业中心内进行。

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