Evidence map›Paper›PMID 41671437›Full record

SynthesisBlood advances2026

Conventional therapy vs HMA or LDAC with or without venetoclax in older adults with AML: systematic review and meta-analysis.

Sara Ibrahim, Barbara Burgos-Mansilla, Yetiani Roldan, Maria Jose Oliveros, Gurleen Bhogal, Gonzalo Bravo-Soto, Mobina Bagherianlemraski, Hamed Movahed, Ruvistay Gutierrez-Arias, Francesca Mulazzani and 11 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Blood advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Sara IbrahimDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.ORCID 0000-0002-7713-6171
Barbara Burgos-MansillaDepartamento de Ciencias de la Rehabilitación, Facultad de Medicina, Universidad de La Frontera, Temuco, Chile.ORCID 0000-0002-3100-5491
Yetiani RoldanDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.ORCID 0009-0009-4564-5973
Maria Jose OliverosDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.ORCID 0000-0002-9327-6844
Gurleen BhogalFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.ORCID 0009-0006-6399-936X
Gonzalo Bravo-SotoDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.ORCID 0000-0003-3111-3975
Mobina BagherianlemraskiDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.ORCID 0000-0002-3369-4948
Hamed MovahedDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.
Ruvistay Gutierrez-AriasDepartamento de Apoyo en Rehabilitación Cardiopulmonar Integral, Instituto Nacional del Tórax, Santiago, Chile.
Francesca MulazzaniDepartment of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy.ORCID 0009-0003-8425-6117
Tanin Khorrami TajSchool of Interdisciplinary Science, McMaster University, Hamilton, ON, Canada.
Seyed Kaveh HadeiyEmergency Department, Bahari Hospital, Hamedan University of Medical Sciences, Hamedan, Iran.ORCID 0000-0002-9104-971X
Manahil QureshiSchool of Earth, Environment & Society, Faculty of Science, McMaster University, Hamilton, ON, Canada.ORCID 0009-0009-1302-7927
Saifur R ChowdhuryDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.
Rachel CoubanFaculty of Health Sciences, McMaster University, Hamilton, ON, Canada.ORCID 0000-0001-8672-2845
Andrew ArtzCity of Hope, Duarte, CA.ORCID 0000-0003-0803-9607
Luke FletcherWillamette Valley Cancer Institute, Eugene, OR.
Linda GilbertoJacksonville, FL.
Ryan MattisonDivision of Hematology, Medical Oncology and Palliative Care, University of Wisconsin-Madison, Madison, WI.
Mikkael A SekeresSylvester Comprehensive Cancer Center, University of Miami, Miami, FL.ORCID 0000-0003-2009-6524
Romina Brignardello-PetersenDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.ORCID 0000-0002-6010-9900

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractThis systematic review summarizes the evidence informing 2 recommendations from the updated American Society of Hematology guidelines for the treatment of newly diagnosed acute myeloid leukemia in older adults, comparing conventional induction and postremission therapy vs hypomethylating agents (HMA)- or low-dose cytarabine (LDAC)-based strategies, with or without venetoclax. We searched Ovid MEDLINE and Embase, and Cochrane CENTRAL through February 2024, and monitored these databases for new studies throughout November 2024. We included randomized controlled trials (RCTs) and nonrandomized studies (NRS). Reviewers screened studies, extracted data, assessed risk of bias, conducted random-effects meta-analyses, and rated certainty of evidence using GRADE (grading of recommendations, assessment, development, and evaluation). We included 21 studies (3 RCTs, 18 NRS). Compared with HMA- or LDAC-based monotherapy, conventional 7+3-type remission induction therapy may reduce mortality at longest follow-up (risk ratio [RR], 0.94; 95% confidence interval [CI], 0.85-1.04; low certainty), increase complete remission rates (odds ratio, 1.75; 95% CI, 1.25-2.38; high certainty), and may reduce recurrence at longest follow-up (RR, 0.81; 95% CI, 0.64-1.04; low certainty). Conventional therapies probably increase most severe toxicities (moderate certainty). Compared with HMA or LDAC combined with venetoclax, very low certainty evidence suggests that conventional therapy may reduce 1-year mortality (RR, 0.72; 95% CI, 0.60-0.87), increase allogeneic transplant rates (RR, 2.28; 95% CI, 1.70-3.06), result in no important differences in complete remission or recurrence, and have variable effects on severe toxicities. Conventional therapy may have benefits over HMA or LDAC alone; however, compared with HMA or LDAC plus venetoclax, the evidence remains of very low certainty.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBridged Bicyclo Compounds, HeterocyclicCytarabineLeukemia, Myeloid, AcuteSulfonamidesAgedHumansRemission InductionBridged Bicyclo Compounds, HeterocyclicCytarabineSulfonamidesvenetoclax

Identifiers

PMID41671437
PMCPMC13261932

What OpenQuestion holds

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Registered trials

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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.