PMID- 34110507 OWN - NLM STAT- MEDLINE DCOM- 20220218 LR - 20220218 IS - 1534-6277 (Electronic) IS - 1534-6277 (Linking) VI - 22 IP - 8 DP - 2021 Jun 10 TI - BCL-2 Inhibition as Treatment for Chronic Lymphocytic Leukemia. PG - 66 LID - 10.1007/s11864-021-00862-z [doi] AB - At the end of the 1990s, with the advent of imatinib for chronic myeloid leukemia and rituximab for B cell lymphoproliferative diseases with CD20 expression, there was a great conceptual evolution in the treatment of onco-hematological diseases. Researchers from around the world and the pharmaceutical industry began to focus their efforts on the so-called target therapy used alone or associated with classic chemotherapeutic drugs. In chronic lymphocytic leukemia, the development of second-generation anti-CD20 antibodies, biosimilars, PI3K (phosphatidylinositol 3-kinases) inhibitors, BTK (Bruton's tyrosine kinase) inhibitors, and anti-bcl 2 drugs represented mainly by venetoclax brought new, broader, and more effective opportunities in the treatment of this disease. This breakthrough occurred mainly regarding patients with alteration in 17p or mutation of the p53 gene for whom selecting the new drugs that act on B cell signaling (BTK and PI3K inhibitors) in the first line is mandatory. In fit patients with immunoglobulin heavy chain mutation, it is still acceptable to use the chemotherapy regimen with fludarabine, cyclophosphamide, and rituximab (FCR) and, in those who do not fit or are not IgVH-mutated, bendamustine-rituximab regimen. However, the first-line use of ibrutinib or venetoclax associated with immunotherapy within the concepts of infinite (ibrutinib) or finite (venetoclax) treatment has been increasingly used. In the second line, venetoclax, ibrutinib, and idelalisib have become the preferred treatments. I believe that a process of instruction and decision shared with patients considering the risks-benefits-cost and access to treatments should guide the choices within these concepts. Another fundamental aspect to discuss is the objective of the treatment for chronic lymphocytic leukemia (CLL) for a specific patient: the increase progression-free survival and overall survival and/or the achievement of minimal residual disease. CLL is the most common leukemia in adults with a median age at diagnosis of 72 years. The clinical course is heterogeneous, and outcomes are influenced by individual clinical presentation and disease biology. Molecular and genomic factors, including fluorescence in situ hybridization (FISH) testing, karyotype, and immunoglobulin heavy chain variable region gene (IGHV) mutational status, are important to treatment decisions and to predict the clinical course. However, despite disease biology, the presence of active disease is the most important criteria to initiate treatment. In the past decade, target therapies that inhibit B cell receptor signaling pathways and, more recently, BCL2 antagonists have emerged as a new treatment paradigm: chemo-free with fixed duration therapy. Bruton's tyrosine kinase inhibitors (BTK) are a class of oral medications approved for frontline and relapsed disease, effective for achieving lasting response and disease control with a good safety profile. BTK inhibitors are an attractive option for high-risk patients who are not candidates for an intensive regimen. However, it is a continuous therapy, and drug resistance or severe adverse events could lead to treatment suspension. BCL2 antagonists are an attractive alternative to BTK inhibitors. Anti-apoptotic BCL2 is associated with tumor genesis and chemotherapy resistance. The BCl2, an anti-apoptotic protein located in the mitochondrial membrane, is a major contributor to the pathogenesis of lymphoid malignancies and is overexpressed in CLL cells promoting clonal cell survival. Venetoclax is a potent and selective member of the BH3 mimetic drugs and a physiologic antagonist of BCL2. Venetoclax has demonstrated quick and durable responses in naive and relapsed or refractory CLL (r/r CLL) patients, including high-risk patients. Furthermore, it has shown deeper responses, achieving a higher incidence of negative minimal residual disease (MRD) with a fixed duration therapy. In the past decade, there was a remarkable progress in CLL treatment. However, neither of the new target therapies is considered curative or free of toxicity. This article will focus on the treatment approach of CLL patients with BCl2 antagonists. Treatment strategy (combined versus monotherapy; continuous versus limited duration therapy), toxicity profile, and future directions will be exposed in this review. FAU - Perini, Guilherme Fleury AU - Perini GF AD - Bone Marrow Transplantation Unit, Hospital Israelita Albert Einstein, Av. Albert Einstein (SP), Sao Paulo, 627/520, Brazil. AD - Americas Centro de Oncologia Integrado and Hospital Albert Israelita Albert Einstein, Rio de Janeiro, Brazil. FAU - Feres, Carolina Cristina Pellegrino AU - Feres CCP AD - Bone Marrow Transplantation Unit, Hospital Israelita Albert Einstein, Av. Albert Einstein (SP), Sao Paulo, 627/520, Brazil. FAU - Teixeira, Larissa Lane Cardoso AU - Teixeira LLC AD - Bone Marrow Transplantation Unit, Hospital Israelita Albert Einstein, Av. Albert Einstein (SP), Sao Paulo, 627/520, Brazil. FAU - Hamerschlak, Nelson AU - Hamerschlak N AUID- ORCID: 0000-0002-5140-5310 AD - Bone Marrow Transplantation Unit, Hospital Israelita Albert Einstein, Av. Albert Einstein (SP), Sao Paulo, 627/520, Brazil. hamer@einstein.br. AD - Americas Centro de Oncologia Integrado and Hospital Albert Israelita Albert Einstein, Rio de Janeiro, Brazil. hamer@einstein.br. LA - eng PT - Journal Article PT - Review DEP - 20210610 PL - United States TA - Curr Treat Options Oncol JT - Current treatment options in oncology JID - 100900946 RN - 0 (Antineoplastic Agents) RN - 0 (Bridged Bicyclo Compounds, Heterocyclic) RN - 0 (Proto-Oncogene Proteins c-bcl-2) RN - 0 (Sulfonamides) RN - EC 2.7.10.2 (Agammaglobulinaemia Tyrosine Kinase) RN - N54AIC43PW (venetoclax) SB - IM MH - Agammaglobulinaemia Tyrosine Kinase/antagonists & inhibitors MH - Antineoplastic Agents/pharmacology/*therapeutic use MH - Bridged Bicyclo Compounds, Heterocyclic/adverse effects/pharmacokinetics/therapeutic use MH - Humans MH - Leukemia, Lymphocytic, Chronic, B-Cell/*drug therapy/mortality MH - Proto-Oncogene Proteins c-bcl-2/*antagonists & inhibitors MH - Sulfonamides/adverse effects/pharmacokinetics/therapeutic use OTO - NOTNLM OT - BCL2 inhibitors OT - Chronic lymphocytic leukemia OT - Targeted therapy OT - Venetoclax EDAT- 2021/06/11 06:00 MHDA- 2022/02/19 06:00 CRDT- 2021/06/10 12:30 PHST- 2021/04/30 00:00 [accepted] PHST- 2021/06/10 12:30 [entrez] PHST- 2021/06/11 06:00 [pubmed] PHST- 2022/02/19 06:00 [medline] AID - 10.1007/s11864-021-00862-z [pii] AID - 10.1007/s11864-021-00862-z [doi] PST - epublish SO - Curr Treat Options Oncol. 2021 Jun 10;22(8):66. doi: 10.1007/s11864-021-00862-z.