4.7 Article

Venetoclax-Based Regimens for Relapsed/Refractory Acute Myeloid Leukemia in a Real-Life Setting: A Retrospective Single-Center Experience

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 10, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/jcm10081684

Keywords

leukemia; venetoclax; chemoresistant

Funding

  1. AIRC 5x1000 call Metastatic disease: the key unmet need in oncology [21267]

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For patients with relapsed/refractory acute myeloid leukemia, venetoclax-based regimens show promise in achieving composite complete response rates, with particular benefit seen in patients with NPM1 mutations. The possibility of undergoing transplant in intention-to-treat patients was 54%.
Relapsed/refractory (R/R) acute myeloid leukemia (AML) is a largely unmet medical need, owing to the lack of standardized, effective treatment approaches, resulting in an overall dismal outcome. The only curative option for R/R AML patients is allogeneic hematopoietic stem cell transplantation (HSCT) which is only applicable in a fraction of patients due to the scarce efficacy and high toxicity of salvage regimens. Recently, a number of targeted agents with relatively favorable toxicity profiles have been explored in clinical trials for R/R AML patients. The Bcl-2 inhibitor venetoclax, in combination with hypomethylating agents or low dose cytarabine, has produced impressive results for newly diagnosed AML, while its role in R/R disease is not well defined yet. We retrospectively analyzed the clinical outcomes of 47 R/R AML patients treated with venetoclax-based regimens between March 2018 and December 2020 at our institution. Overall, we report a composite complete response rate of 55% with an overall acceptable toxicity profile. Outcomes were particularly favorable for NPM1 mutated patients, unlike for FLT3-ITD positive patients irrespective of NPM1 status. For patients treated with intention to transplant, the procedure could be finally performed in 54%. These findings suggest a role for venetoclax-based regimens in R/R AML patients and support the design of prospective studies.

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