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Daratumumab, Lenalidomide, and Dexamethasone for Multiple Myeloma.达雷妥尤单抗、来那度胺和地塞米松治疗多发性骨髓瘤。
N Engl J Med. 2016 Oct 6;375(14):1319-1331. doi: 10.1056/NEJMoa1607751.
2
Association of Minimal Residual Disease With Superior Survival Outcomes in Patients With Multiple Myeloma: A Meta-analysis.微小残留病与多发性骨髓瘤患者更好的生存结果的关联:一项荟萃分析。
JAMA Oncol. 2017 Jan 1;3(1):28-35. doi: 10.1001/jamaoncol.2016.3160.
3
Role of MRD status in relation to clinical outcomes in newly diagnosed multiple myeloma patients: a meta-analysis.微小残留病状态在新诊断的多发性骨髓瘤患者临床结局中的作用:一项荟萃分析。
Bone Marrow Transplant. 2016 Dec;51(12):1565-1568. doi: 10.1038/bmt.2016.222. Epub 2016 Sep 5.
4
Treatment of acquired drug resistance in multiple myeloma by combination therapy with XPO1 and topoisomerase II inhibitors.采用XPO1与拓扑异构酶II抑制剂联合疗法治疗多发性骨髓瘤获得性耐药
J Hematol Oncol. 2016 Aug 24;9(1):73. doi: 10.1186/s13045-016-0304-z.
5
Daratumumab, Bortezomib, and Dexamethasone for Multiple Myeloma.达雷妥尤单抗、硼替佐米和地塞米松治疗多发性骨髓瘤。
N Engl J Med. 2016 Aug 25;375(8):754-66. doi: 10.1056/NEJMoa1606038.
6
International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma.国际骨髓瘤工作组多发性骨髓瘤反应和微小残留病评估的共识标准。
Lancet Oncol. 2016 Aug;17(8):e328-e346. doi: 10.1016/S1470-2045(16)30206-6.
7
T cells expressing an anti-B-cell maturation antigen chimeric antigen receptor cause remissions of multiple myeloma.表达抗B细胞成熟抗原嵌合抗原受体的T细胞可使多发性骨髓瘤缓解。
Blood. 2016 Sep 29;128(13):1688-700. doi: 10.1182/blood-2016-04-711903. Epub 2016 Jul 13.
8
Benefit-Risk Summary of Crizotinib for the Treatment of Patients With ROS1 Alteration-Positive, Metastatic Non-Small Cell Lung Cancer.克唑替尼用于治疗ROS1改变阳性转移性非小细胞肺癌患者的获益-风险总结
Oncologist. 2016 Aug;21(8):974-80. doi: 10.1634/theoncologist.2016-0101. Epub 2016 Jun 21.
9
APRIL and BCMA promote human multiple myeloma growth and immunosuppression in the bone marrow microenvironment.APRIL和BCMA促进人多发性骨髓瘤在骨髓微环境中的生长及免疫抑制。
Blood. 2016 Jun 23;127(25):3225-36. doi: 10.1182/blood-2016-01-691162. Epub 2016 Apr 28.
10
Oral Ixazomib, Lenalidomide, and Dexamethasone for Multiple Myeloma.来那度胺、伊沙佐米和地塞米松联合治疗多发性骨髓瘤。
N Engl J Med. 2016 Apr 28;374(17):1621-34. doi: 10.1056/NEJMoa1516282.

多发性骨髓瘤监管与治疗史的回顾与展望:新型药物的获批、新药研发及患者生存期延长

A look backward and forward in the regulatory and treatment history of multiple myeloma: Approval of novel-novel agents, new drug development, and longer patient survival.

作者信息

Kazandjian Dickran, Landgren Ola

机构信息

Myeloma program, Lymphoid Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health and the Office of Hematology and Oncology Products, Food and Drug Administration, Bethesda, MD.

Myeloma Service, Memorial Sloan-Kettering Cancer Center, New York, NY.

出版信息

Semin Oncol. 2016 Dec;43(6):682-689. doi: 10.1053/j.seminoncol.2016.10.008. Epub 2016 Nov 16.

DOI:10.1053/j.seminoncol.2016.10.008
PMID:28061986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5282737/
Abstract

The past decade has seen significant advances in our understanding and treatment of multiple myeloma (MM) and its precursor diseases. These advances include gains in knowledge of the underlying pathobiology including molecular and cellular prognostic factors for disease progression. In parallel we have witnessed the availability of novel therapeutics. Together these advances have translated into improvements in long-term clinical benefit and survival in MM. Indeed, it has been shown that patients diagnosed in the last decade have experienced almost doubling of median survival time. We aim to review and give further insight into drug development and novel drug approvals that have revolutionized the treatment of MM.

摘要

在过去十年中,我们对多发性骨髓瘤(MM)及其前驱疾病的理解和治疗取得了重大进展。这些进展包括对潜在病理生物学的认识有所增加,包括疾病进展的分子和细胞预后因素。与此同时,我们见证了新型疗法的出现。这些进展共同转化为MM长期临床获益和生存率的提高。事实上,已经表明,在过去十年中诊断出的患者中位生存时间几乎翻了一番。我们旨在回顾并进一步深入了解彻底改变MM治疗的药物研发和新型药物批准情况。