Hari Parameswaran
Division of Hematology/Oncology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Hematol Oncol Stem Cell Ther. 2017 Dec;10(4):267-271. doi: 10.1016/j.hemonc.2017.05.005. Epub 2017 Jun 13.
There have been major recent advancements in the understanding and management of multiple myeloma which in turn has led to unprecedented survival outcomes for patients. Diagnostic and response criteria have been recently revised. Our understanding of clonal progression, evolution, and clonal tides will inform therapeutic choices and appropriate treatment for patients. Response rates to initial induction with modern triplet therapies containing proteasome inhibitors and immunomodulators have made this approach the global standard for initial treatment. Although the relevance of autologous transplantation has been questioned in the setting of modern induction therapy, we have new data suggesting its continued relevance. Recent studies performed in the context of novel agent induction suggest that autologous transplantation continues to improve response rates and progression-free survival, thus underscoring its role in transplant-eligible patients. Emerging paradigms in the treatment of multiple myeloma include immune approaches, such as adoptive cellular therapies, vaccines, or antibody-based immune manipulations, all of which seem to synergize with a transplant platform. Allogeneic transplantation is limited in scope by the concern of prohibitive toxicity and is applicable mainly to younger patients with high-risk disease. However, the allogeneic approach offers even more options of immunotherapy at relapse, including donor lymphocyte infusions, immunomodulatory drug maintenance, and withdrawal of immune suppression.
近年来,在多发性骨髓瘤的认识和管理方面取得了重大进展,这反过来又为患者带来了前所未有的生存结果。诊断和反应标准最近已修订。我们对克隆进展、演变和克隆潮的理解将为患者的治疗选择和适当治疗提供依据。使用包含蛋白酶体抑制剂和免疫调节剂的现代三联疗法进行初始诱导的反应率,使其成为全球初始治疗的标准方法。尽管在现代诱导治疗背景下自体移植的相关性受到质疑,但我们有新数据表明其仍具有相关性。在新型药物诱导背景下进行的最新研究表明,自体移植继续提高反应率和无进展生存期,从而突出了其在适合移植患者中的作用。多发性骨髓瘤治疗中出现的新范式包括免疫方法,如过继性细胞疗法、疫苗或基于抗体的免疫操纵,所有这些似乎都与移植平台协同作用。异基因移植因毒性过高的担忧而范围有限,主要适用于患有高危疾病的年轻患者。然而,异基因方法在复发时提供了更多免疫治疗选择,包括供体淋巴细胞输注、免疫调节药物维持和免疫抑制的撤除。