Evidence map›Paper›PMID 40454395›Full record

ArticleBlood neoplasia2024

Venetoclax and hypomethylating agents in octogenarians and nonagenarians with acute myeloid leukemia.

Ellen Madarang, Jillian Lykon, Wei Zhao, Mikkael A Sekeres, Terrence Bradley, Namrata S Chandhok, Justin Taylor, Sangeetha Venugopal, Tulay Koru-Sengul, Sunil Girish Iyer and 14 more

Abstract read
In one paragraph

Article in Blood neoplasia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Ellen MadarangDepartment of Pharmacy, University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.
Jillian LykonDepartment of Pharmacy, University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.
Wei ZhaoSylvester Comprehensive Cancer Center, Miller School of Medicine at University of Miami, Miami, FL.
Mikkael A SekeresDivision of Hematology, University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.
Terrence BradleyDivision of Hematology, University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.
Namrata S ChandhokDivision of Hematology, University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.
Justin TaylorDivision of Hematology, University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.
Sangeetha VenugopalDivision of Hematology, University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.
Tulay Koru-SengulSylvester Comprehensive Cancer Center, Miller School of Medicine at University of Miami, Miami, FL.
Sunil Girish IyerDivision of Hematology and Oncology, Columbia University Irving Medical Center, New York, NY.
Jason S GilbertDepartment of Internal Medicine, University of Colorado, Anschutz Medical Campus, Aurora CO.
Ryan M MillerDepartment of Oncology Pharmacy, Vanderbilt University Medical Center, Nashville, TN.
Jacopo NanniDipartimento di Scienze Mediche e Chirurgiche, Istituto di Ematologia "Seràgnoli," Università degli Studi di Bologna, Bologna, Italy.
Irene ZacheoIRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori," Meldola, Italy.
Agnese MatteiIRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori," Meldola, Italy.
Najla Al AliMalignant Hematology Department, Moffitt Cancer Center, Tampa, FL.
Ashwin KishtagariDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Giovanni MarconiIRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori," Meldola, Italy.
David A SallmanMalignant Hematology Department, Moffitt Cancer Center, Tampa, FL.
Daniel A PollyeaDepartment of Internal Medicine, University of Colorado, Anschutz Medical Campus, Aurora CO.
Michael R SavonaDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Cristina PapayannidisIRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli," Bologna, Italy.
Rami KomrokjiMalignant Hematology Department, Moffitt Cancer Center, Tampa, FL.
Justin WattsDivision of Hematology, University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Venetoclax (VEN) plus a hypomethylating agent (HMA) regimen is the standard of care for older adults with acute myeloid leukemia (AML); however, it is associated with significant myelosuppression and complications, potentially limiting its use in those who are very old. We performed a multicenter retrospective analysis of VEN-HMA treatment in octogenarians and nonagenarians to further understand the tolerability, feasibility, dosing considerations, and clinical efficacy in this unique group. Patients with AML aged ≥80 years who received VEN-HMA between March 2015 and April 2022 were reviewed. VEN-HMA dosing was determined by treating physician, accounting for CYP3A4 drug interaction dose adjustments. In total, 154 patients were included, with a median age of 82 years (range, 80-92), who received treatment with VEN-HMA (83% with azacitidine and 17% with decitabine). Most patients (53%) had European LeukemiaNet 2017 adverse risk AML, 33% had intermediate, 8% had favorable, and 6% were unknown. With a median follow-up of 7.7 months, 36 patients (23%) remained in remission, with 31 (20%) still on VEN-HMA. The 30-day and 60-day mortality rates were 8.5% and 17%, respectively. The composite complete remission (CRc) rate for patients with newly diagnosed AML without prior myelodysplastic syndrome was 73% (48 of 66). Median overall survival (OS) was 8.1 months, and in patients who achieved a response (CRc), median OS was 13.2 months. Landmark analysis from the time CRc was first achieved showed that patients receiving VEN for ≤14 days had improved OS; median, 24.0 months. Patients who are very old can be treated safely with combination VEN-HMA with expectations of dose reductions and cycle extensions to ensure tolerability over the long term.

Identifiers

PMID40454395
PMCPMC12082125

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.