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      Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis

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          Abstract

          Venetoclax is efficacious in relapsed/refractory t(11;14) multiple myeloma, thus warranting investigation in light-chain amyloidosis (AL). This retrospective cohort includes 43 patients with previously treated AL, from 14 centers in the US and Europe. Thirty-one patients harbored t(11;14), 11 did not, and one t(11;14) status was unknown. Patients received a venetoclax-containing regimen for at least one 21- or 28-day cycle; the median prior treatments was three. The hematologic response rate for all patients was 68%; 63% achieved VGPR/CR. t(11;14) patients had higher hematologic response (81% vs. 40%) and higher VGPR/CR rate (78% vs. 30%, odds ratio: 0.12, 95% CI 0.02–0.62) than non-t(11;14) patients. For the unsegregated cohort, median progression-free survival (PFS) was 31.0 months and median OS was not reached (NR). For t(11;14), median PFS was NR and for non-t(11;14) median PFS was 6.7 months (HR: 0.14, 95% CI 0.04–0.53). Multivariate analysis incorporating age, sex, prior lines of therapy, and disease stage suggested a risk reduction for progression or death in t(11;14) patients. Median OS was NR for either subgroup. The organ response rate was 38%; most responders harbored t(11;14). Grade 3 or higher adverse events occurred in 19% with 7% due to infections. These promising results require confirmation in a randomized clinical trial.

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          Venetoclax combined with decitabine or azacitidine in treatment-naive, elderly patients with acute myeloid leukemia

          Older patients with acute myeloid leukemia (AML) respond poorly to standard induction therapy. B-cell lymphoma 2 (BCL-2) overexpression is implicated in survival of AML cells and treatment resistance. We report safety and efficacy of venetoclax with decitabine or azacitidine from a large, multicenter, phase 1b dose-escalation and expansion study. Patients (N = 145) were at least 65 years old with treatment-naive AML and were ineligible for intensive chemotherapy. During dose escalation, oral venetoclax was administered at 400, 800, or 1200 mg daily in combination with either decitabine (20 mg/m2, days 1-5, intravenously [IV]) or azacitidine (75 mg/m2, days 1-7, IV or subcutaneously). In the expansion, 400 or 800 mg venetoclax with either hypomethylating agent (HMA) was given. Median age was 74 years, with poor-risk cytogenetics in 49% of patients. Common adverse events (>30%) included nausea, diarrhea, constipation, febrile neutropenia, fatigue, hypokalemia, decreased appetite, and decreased white blood cell count. No tumor lysis syndrome was observed. With a median time on study of 8.9 months, 67% of patients (all doses) achieved complete remission (CR) + CR with incomplete count recovery (CRi), with a CR + CRi rate of 73% in the venetoclax 400 mg + HMA cohort. Patients with poor-risk cytogenetics and those at least 75 years old had CR + CRi rates of 60% and 65%, respectively. The median duration of CR + CRi (all patients) was 11.3 months, and median overall survival (mOS) was 17.5 months; mOS has not been reached for the 400-mg venetoclax cohort. The novel combination of venetoclax with decitabine or azacitidine was effective and well tolerated in elderly patients with AML (This trial was registered at www.clinicaltrials.gov as #NCT02203773).
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            Multiple myeloma.

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              Venetoclax and Obinutuzumab in Patients with CLL and Coexisting Conditions

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                Author and article information

                Contributors
                sl3440@columbia.edu
                Journal
                Blood Cancer J
                Blood Cancer J
                Blood Cancer Journal
                Nature Publishing Group UK (London )
                2044-5385
                11 January 2021
                11 January 2021
                January 2021
                : 11
                : 1
                : 10
                Affiliations
                [1 ]GRID grid.21729.3f, ISNI 0000000419368729, Division of Hematology/Oncology, , Columbia University Irving Medical Center, ; New York, NY USA
                [2 ]GRID grid.414324.4, ISNI 0000 0004 0472 3628, The Patricia Lynch Cancer Center, Holy Name Medical Center, ; Teaneck, NJ USA
                [3 ]GRID grid.21729.3f, ISNI 0000000419368729, Columbia University Irving Medical Center, ; New York, NY USA
                [4 ]GRID grid.416167.3, Division of Hematology and Medical Oncology, , Tisch Cancer Institute, Mount Sinai Medical Center, ; New York, NY USA
                [5 ]GRID grid.168010.e, ISNI 0000000419368956, Stanford Amyloid Center, , Stanford University School of Medicine, ; Stanford, CA USA
                [6 ]GRID grid.411178.a, ISNI 0000 0001 1486 4131, Hematology Department, French Reference Center for AL Amyloidosis (Limoges-Poitiers), CHU Limoges, ; Limoges, France
                [7 ]GRID grid.83440.3b, ISNI 0000000121901201, National Amyloidosis Centre, , University College London, ; London, UK
                [8 ]GRID grid.67033.31, ISNI 0000 0000 8934 4045, John C. Davis Myeloma and Amyloid Program, Tufts Medical Center, ; Boston, MA USA
                [9 ]Amyloidosis Center, Boston University School of Medicine, Boston Medical Center, Boston, MA USA
                [10 ]GRID grid.413328.f, ISNI 0000 0001 2300 6614, Paris 7 University and APHP, Immuno-Hematology Department, Saint-Louis Hospital, ; Paris, France
                [11 ]GRID grid.410425.6, ISNI 0000 0004 0421 8357, Department of Hematology and Hematopoietic Cell Transplantation, , Judy and Bernard Briskin Center for Multiple Myeloma Research, City of Hope, ; Duarte, CA USA
                [12 ]GRID grid.239578.2, ISNI 0000 0001 0675 4725, Department of Hematology and Medical Oncology, , Taussig Cancer Center, Cleveland Clinic, ; Cleveland, OH USA
                [13 ]GRID grid.5253.1, ISNI 0000 0001 0328 4908, Amyloidosis Center, , Heidelberg University Hospital, ; Heidelberg, Germany
                [14 ]GRID grid.417468.8, ISNI 0000 0000 8875 6339, Division of Hematology and Oncology, , Mayo Clinic, ; Phoenix, AZ USA
                [15 ]GRID grid.266102.1, ISNI 0000 0001 2297 6811, Division of Hematology/Oncology, , University of California San Francisco, ; San Francisco, CA USA
                [16 ]GRID grid.66875.3a, ISNI 0000 0004 0459 167X, Division of Hematology, , Mayo Clinic, ; Rochester, MN USA
                Author information
                http://orcid.org/0000-0002-2871-8394
                http://orcid.org/0000-0003-1708-7344
                http://orcid.org/0000-0002-6307-2445
                http://orcid.org/0000-0002-4853-5579
                http://orcid.org/0000-0002-5938-3769
                Article
                397
                10.1038/s41408-020-00397-w
                7801694
                33431806
                fbf6bb30-dcff-46ca-9160-2c05a26ccb06
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 20 July 2020
                : 14 November 2020
                : 24 November 2020
                Funding
                Funded by: Emerson Collective Cancer Research Fund, Cancer Research Institute, the Wade F.B. Thompson/Cancer Research Institute CLIP Grant and the Herbert Irving Comprehensive Cancer Center Support Grant (CCSG) awarded by the National Cancer Institute (NCI P30 CA013696).
                Categories
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                © The Author(s) 2021

                Oncology & Radiotherapy
                myeloma
                Oncology & Radiotherapy
                myeloma

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