Induction therapy prior to autologous stem cell transplantation (ASCT) in newly diagnosed multiple myeloma: an update

被引:0
作者
Abdul Hamid Bazarbachi
Rama Al Hamed
Florent Malard
Ali Bazarbachi
Jean-Luc Harousseau
Mohamad Mohty
机构
[1] Albert Einstein College of Medicine,Department of Internal Medicine, Jacobi Medical Center
[2] Hôpital Saint Antoine,Sorbonne University, Service d’Hematologie Clinique et Therapice Cellulaire
[3] and INSERM UMR 938,Department of Internal Medicine
[4] American University of Beirut,Institut de Cancerologie de l’Ouest
[5] Centre René Gauducheau,undefined
来源
Blood Cancer Journal | / 12卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
The current standard of care model for newly diagnosed fit multiple myeloma (NDMM) patients is the sequential treatment of induction, high dose melphalan, autologous stem cell transplantation (ASCT), and maintenance. Adequate induction is required to achieve good disease control and induce deep response rates while minimizing toxicity as a bridge to transplant. Doublet induction regimens have greatly fallen out of favor, with current international guidelines favoring triplet or quadruplet induction regimens built around the backbone of the proteasome inhibitor bortezomib and dexamethasone (Vd). In fact, the updated 2021 European Haematology Association (EHA) and European Society for Medical Oncology (ESMO) clinical practice guidelines recommend the use of either lenalidomide-Vd (VRd), or daratumumab-thalidomide-Vd (Dara-VTd) as first-line options for transplant-eligible NDMM patients, and when not available, thalidomide-Vd (VTd) or cyclophosphamide-Vd (VCd) as acceptable alternatives. Quadruplet regimens featuring anti-CD38 monoclonal antibodies are extremely promising and remain heavily investigated, as is the incorporation of more recent proteasome inhibitors such as carfilzomib. This review will focus on induction therapies prior to ASCT examining the latest data and guidelines on triplet and quadruplet regimens.
引用
收藏
相关论文
共 240 条
  • [1] McElwain TJ(1983)High-dose intravenous melphalan for plasma-cell leukaemia and myeloma Lancet 2 822-4
  • [2] Powles RL(1986)High-dose melphalan with autologous bone marrow transplantation for multiple myeloma Blood. 67 1298-301.
  • [3] Barlogie B(1987)High-dose chemoradiotherapy and autologous bone marrow transplantation for resistant multiple myeloma Blood. 70 869-72.
  • [4] Hall R(2017)Multiple myeloma: ESMO clinical practice guidelines for diagnosis, treatment and follow-up Ann Oncol. 28 iv52-iv61
  • [5] Zander A(2021)Multiple myeloma: EHA-ESMO clinical practice guidelines for diagnosis Treat Follow- Hemasphere 5 e528-20.
  • [6] Dicke K(2017)Lenalidomide, bortezomib, and dexamethasone with transplantation for myeloma N Engl J Med 376 1311-64.
  • [7] Alexanian R(2020)Early versus late autologous stem cell transplant in newly diagnosed multiple myeloma: long-term follow-up analysis of the IFM 2009 trial Blood. 136 39-99.
  • [8] Barlogie B(2018)Minimal residual disease negativity using deep sequencing is a major prognostic factor in multiple myeloma Blood. 132 2456-e68.
  • [9] Alexanian R(2020)A large meta-analysis establishes the role of MRD negativity in long-term survival outcomes in patients with multiple myeloma Blood Adv 4 5988-8
  • [10] Dicke KA(2020)Autologous haematopoietic stem-cell transplantation versus bortezomib-melphalan-prednisone, with or without bortezomib-lenalidomide-dexamethasone consolidation therapy, and lenalidomide maintenance for newly diagnosed multiple myeloma (EMN02/HO95): a multicentre, randomised, open-label, phase 3 study Lancet Haematol 7 e456-20