Updates in the Use of BCL-2-Family Small Molecule Inhibitors for the Treatment of Relapsed/Refractory Multiple Myeloma

被引:7
|
作者
Parrondo, Ricardo D. [1 ]
Paulus, Aneel [2 ]
Ailawadhi, Sikander [1 ,2 ]
机构
[1] Mayo Clin, Div Hematol Oncol, Jacksonville, FL 32224 USA
[2] Mayo Clin, Dept Canc Biol, Jacksonville, FL 32224 USA
关键词
multiple myeloma; Bcl-2; inhibitors; apoptosis; small molecule inhibitors; TARGETED THERAPY; BCL-2; ANTISENSE; MCL1; INHIBITOR; VENETOCLAX; DEXAMETHASONE; LENALIDOMIDE; SENSITIVITY; COMBINATION; BORTEZOMIB; APOPTOSIS;
D O I
10.3390/cancers14143330
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Monumental therapeutic advances have been made over the past two decades for the treatment of multiple myeloma. Anti-apoptotic proteins, such as Bcl-2, Bcl-xL, and Mcl-1, have been found to be upregulated in multiple myeloma cell lines, and small molecule inhibitors that target these proteins are in clinical development with the goal of enhancing apoptosis, reversing drug resistance, and improving the survival outcomes of patients with relapsed/refractory multiple myeloma. In this paper, we review the available clinical data for the Bcl-2-family protein inhibitors currently in clinical development for relapsed/refractory multiple myeloma. Despite considerable advances in the treatment of multiple myeloma over the past decade, progression of disease is inevitable, and patients ultimately succumb to relapsed and refractory disease. Efficacious therapeutic regimens that target the key biological pathways that are essential for malignant plasma cell survival are necessary in the efforts to improve patient survival outcomes. The Bcl-2 family of proteins comprise oncogenes that promote myeloma cell survival by conferring resistance to apoptosis. These proteins are frequently upregulated in myeloma cells, thus making them attractive therapeutic targets. Several small molecule inhibitors of Bcl-2-family proteins are currently in clinical development for the treatment of relapsed/refractory multiple myeloma. Venetoclax, a Bcl-2-specific inhibitor, has generated the most clinical data and has shown promising results in patients with multiple myeloma harboring the t (11;14) translocation. Venetoclax has shown efficacy when combined with anti-CD38 monoclonal antibodies, immunomodulatory drugs, and proteasome inhibitors. Several other Bcl-2 inhibitors are in clinical development, as are inhibitors of Mcl-1, a Bcl-2-family oncoprotein that is perhaps more critical for myeloma cell survival than Bcl-2. This review will summarize the latest clinical data regarding the clinical development of Bcl-2-family protein inhibitors in the treatment of relapsed/refractory multiple myeloma.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] BCL2 Family Inhibitors in the Biology and Treatment of Multiple Myeloma
    Gupta, Vikas A.
    Ackley, James
    Kaufman, Jonathan L.
    Boise, Lawrence H.
    BLOOD AND LYMPHATIC CANCER-TARGETS AND THERAPY, 2021, 11 : 11 - 24
  • [2] Multiple myeloma: Updates for pharmacists in the treatment of relapsed and refractory disease
    Ashjian, Emily
    Redic, Kimberly
    JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2016, 22 (02) : 289 - 302
  • [3] Updates in the management of relapsed/refractory multiple myeloma
    Hanna, Kirollos S.
    Larson, Samantha
    Nguyen, Jenny
    Tu, Sarah
    Boudreau, Jenna
    Rose, Sarah
    JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2021, 27 (06) : 1477 - 1490
  • [4] Role of Venetoclax in the Treatment of Relapsed and Refractory Multiple Myeloma
    Ehsan, Hamid
    Wahab, Ahsan
    Shah, Zunairah
    Sana, Muhammad Khawar
    Masood, Adeel
    Rafae, Abdul
    Hashmi, Hamza
    JOURNAL OF HEMATOLOGY, 2021, 10 (03) : 89 - 97
  • [5] Updates on Therapeutic Strategies in the Treatment of Relapsed/Refractory Multiple Myeloma
    Parekh, Deevyashali S.
    Tiger, Yun Kyoung Ryu
    Jamouss, Kevin Tony
    Hassani, Justin
    Bou Zerdan, Maroun
    Raza, Shahzad
    CANCERS, 2024, 16 (17)
  • [6] Bortezomib mitigates adverse prognosis conferred by Bcl-2 overexpression in patients with relapsed/refractory multiple myeloma
    Ailawadhi, Sikander
    Miecznikowski, Jeff
    Gaile, Dan P.
    Wang, Dongliang
    Sher, Taimur
    Mulligan, George
    Bryant, Barb
    Wilding, Gregory E.
    Mashtare, Terry
    Stein, Leighton
    Masood, Aisha
    Neuwirth, Rachel
    Lee, Kelvin P.
    Chanan-Khan, Asher
    LEUKEMIA & LYMPHOMA, 2012, 53 (06) : 1174 - 1182
  • [7] Molecular dynamics study of small molecule inhibitors of the Bcl-2 family
    Acoca, Stephane
    Cui, Qizhi
    Shore, Gordon C.
    Purisima, Enrico O.
    PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2011, 79 (09) : 2624 - 2636
  • [8] The use of novel agents in the treatment of relapsed and refractory multiple myeloma
    Laubach, J. P.
    Mahindra, A.
    Mitsiades, C. S.
    Schlossman, R. L.
    Munshi, N. C.
    Ghobrial, I. M.
    Carreau, N.
    Hideshima, T.
    Anderson, K. C.
    Richardson, P. G.
    LEUKEMIA, 2009, 23 (12) : 2222 - 2232
  • [9] Daratumumab and its use in the treatment of relapsed and/or refractory multiple myeloma
    Chehab, Sarah
    Panjic, Elyse Hall
    Gleason, Charise
    Lonial, Sagar
    Nooka, Ajay K.
    FUTURE ONCOLOGY, 2018, 14 (30) : 3111 - 3121
  • [10] The use of novel agents in the treatment of relapsed and refractory multiple myeloma
    J P Laubach
    A Mahindra
    C S Mitsiades
    R L Schlossman
    N C Munshi
    I M Ghobrial
    N Carreau
    T Hideshima
    K C Anderson
    P G Richardson
    Leukemia, 2009, 23 : 2222 - 2232