Evidence map›Paper›PMID 40227639›Full record

ArticleCancers2025

Impact of Venetoclax Treatment Schedule on Hematologic Recovery and Treatment Response in AML Patients Unfit for Intensive Chemotherapy.

Anja Schüpbach, Dilara Akhoundova, Ulrike Bacher, Henning Nilius, Michèle Hoffmann, Carlo R Largiadèr, Yolanda Aebi, Michael Hayoz, Marie-Noëlle Kronig, Thomas Pabst

Abstract read
In one paragraph

Article in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
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

10 authors.

Anja SchüpbachDepartment of Medical Oncology, Inselspital, University of Bern, CH-3010 Bern, Switzerland.
Dilara AkhoundovaDepartment of Medical Oncology, Inselspital, University of Bern, CH-3010 Bern, Switzerland.ORCID 0000-0003-1639-3059
Ulrike BacherDepartment of Hematology, Inselspital, University of Bern, CH-3010 Bern, Switzerland.ORCID 0000-0001-8771-947X
Henning NiliusDepartment of Clinical Chemistry, Inselspital, University of Bern, CH-3010 Bern, Switzerland.ORCID 0000-0002-1323-3116
Michèle HoffmannDepartment of Medical Oncology, Inselspital, University of Bern, CH-3010 Bern, Switzerland.
Carlo R LargiadèrDepartment of Clinical Chemistry, Inselspital, University of Bern, CH-3010 Bern, Switzerland.ORCID 0000-0002-0889-8922
Yolanda AebiDepartment of Clinical Chemistry, Inselspital, University of Bern, CH-3010 Bern, Switzerland.
Michael HayozDepartment of Clinical Chemistry, Inselspital, University of Bern, CH-3010 Bern, Switzerland.
Marie-Noëlle KronigDepartment of Medical Oncology, Inselspital, University of Bern, CH-3010 Bern, Switzerland.
Thomas PabstDepartment of Medical Oncology, Inselspital, University of Bern, CH-3010 Bern, Switzerland.ORCID 0000-0002-6055-5257

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Background: The combination of venetoclax and hypomethylating agents (HMAs) is a standard first-line regimen for acute myeloid leukemia (AML) patients unfit for intensive chemotherapy. Since venetoclax-HMAs are usually administered until progression and delayed hematologic recovery is one of the limiting toxicities, cyclic administration including 7-14-day breaks is recommended. However, whether longer venetoclax schedules lead to higher response rates and how venetoclax pharmacokinetics correlate with toxicity and efficacy remains unclarified. In this single-center retrospective study, we analyzed how venetoclax plasma levels and treatment duration impact hematologic toxicity and treatment responses. (2) Methods: We analyzed the safety and efficacy of venetoclax-HMA combination regimens in a cohort of AML patients unfit for intensive chemotherapy treated at our institution between June 2020 and September 2023. The primary endpoint was the correlation between venetoclax plasma levels or administration schedule with hematologic recovery after the first cycle. Secondary endpoints included the following clinical outcomes: correlation with complete response (CR) status, progression-free survival, and overall survival. (3) Results: Within our cohort of 75 AML patients, we found no correlation between venetoclax plasma peak and trough levels, or venetoclax treatment duration (≤ or >14 days), and hematologic toxicity. Patients receiving shorter venetoclax schedules (≤14 days) had similar CR rates compared to patients treated with longer schedules. (4) Conclusions: Our results suggest that shorter (≤14 days) venetoclax schedules may have no negative impact on tumor responses in AML patients receiving venetoclax and HMA combinations. However, prospective validation studies would be required to confirm these findings.

Indexed as

acute myeloid leukemia (AML)complete response rateefficacyhematologic toxicitypharmacokineticstreatment durationvenetoclax

Identifiers

PMID40227639
PMCPMC11987944

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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.