4.3 Article

The propriety of upgrading responses to venetoclax plus azacitidine in newly diagnosed patients with acute myeloid leukemia

Journal

LEUKEMIA & LYMPHOMA
Volume 62, Issue 6, Pages 1466-1473

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/10428194.2020.1864358

Keywords

AML; venetoclax; upgrade; ELN; response

Funding

  1. University of Colorado Department of Medicine Outstanding Early Career Scholars Program
  2. Leukemia and Lymphoma Society's Scholar in Clinical Research award

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Response criteria developed for AML in the context of intensive chemotherapy may underestimate responses in continuously-administered venetoclax-based therapies. Interrupting venetoclax-based therapies after an end-of-cycle bone marrow biopsy showing morphologic remission with cytopenias is recommended. Results suggest consideration of new response criteria for venetoclax-based regimens, as outcomes differ from traditional intensive chemotherapy.
Widely-used response criteria, conditional upon count recovery, were developed for acute myeloid leukemia (AML) in the context of intensive chemotherapy (IC). Extending these definitions to continuously-administered venetoclax-based therapies might underestimate responses. Best practices for venetoclax-based therapies mandate interruption after an end-of-cycle 1 bone marrow biopsy shows morphologic remission with cytopenias. We analyzed 435 patients with newly-diagnosed AML and follow-up response assessments. Of the 101 who responded to venetoclax + azacitidine, overall survival for patients whose response was upgraded due to count recovery during a 14-day post-disease assessment period, from complete remission (CR) with incomplete recovery of blood counts to CR, was not different compared to patients who did not need the 14-day period for count recovery. These results were distinct from 138 IC patients. Although sample sizes for the comparison groups were small, and conclusions are exploratory and must be verified, these findings support consideration of new response criteria for venetoclax-based regimens.

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