Evidence map›Paper›PMID 34351368›Full record

Trial reportBlood2021

Multisite 11-year experience of less-intensive vs intensive therapies in acute myeloid leukemia.

Mohamed L Sorror, Barry E Storer, Amir T Fathi, Andrew Brunner, Aaron T Gerds, Mikkael A Sekeres, Sudipto Mukherjee, Bruno C Medeiros, Eunice S Wang, Pankit Vachhani and 21 more

Registry-linked trialOpen access · bronzeAbstract readClinical TrialComparative StudyMulticenter Study
In one paragraph

Trial report in Blood, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01929408 (Feasibility and Outcomes of Allogeneic Hematopoietic Cell Transplantation), which is not on this map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% of its field
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.

NCT01929408 completednot on this map

Feasibility and Outcomes of Allogeneic Hematopoietic Cell Transplantation (HCT) Compared to Conventional Therapy for Older and Medically Infirm Patients Diagnosed With Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndromes: A Prospective Observational Study

TypeobservationalSponsorFred Hutchinson Cancer CenterRan2013 to 2018Enrolled703ConditionsAcute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS)
3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Observational
  9. Review
  10. Article
  11. Acute Myeloid Leukemia-Use of Measurable Residual Disease to Improve Outcomes.Advances in experimental medicine and biology · 2025
    Review
  12. Article
  13. Experiences of treatment decision-making among older newly diagnosed adults with acute myeloid leukemia: a qualitative descriptive study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2024
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 18 institutions in 2 countries.

Mohamed L SorrorClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0001-5260-1981
Barry E StorerClinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Amir T FathiMassachusetts General Hospital, Harvard Medical School, Boston, MA.ORCID 0000-0003-4907-6447
Andrew BrunnerMassachusetts General Hospital, Harvard Medical School, Boston, MA.
Aaron T GerdsLeukemia & Myeloid Disorders Program, Cleveland Clinic, Cleveland, OH.ORCID 0000-0002-3422-1309
Mikkael A SekeresLeukemia & Myeloid Disorders Program, Cleveland Clinic, Cleveland, OH.
Sudipto MukherjeeLeukemia & Myeloid Disorders Program, Cleveland Clinic, Cleveland, OH.
Bruno C MedeirosDivision of Hematology, Department of Medicine, Stanford University, Stanford, CA.
Eunice S WangRoswell Park Cancer Institute, Buffalo, NY.
Pankit VachhaniRoswell Park Cancer Institute, Buffalo, NY.ORCID 0000-0001-9779-6217
Paul J ShamiDivision of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Esteban PeñaDivision of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Mahmoud ElsawyClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Kehinde AdekolaRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0001-7166-9308
Selina LugerAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
Maria R BaerGreenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD.
David RizzieriDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, NC.ORCID 0000-0001-9886-5771
Tanya M WildesDivision of Oncology, Washington University School of Medicine, St Louis, MO.
Jamie KoprivnikarJohn Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ.
Julie SmithConfluence Health/Wenatchee Valley Hospital and Clinic, Wenatchee, WA.
Mitchell GarrisonConfluence Health/Wenatchee Valley Hospital and Clinic, Wenatchee, WA.
Kiarash KojouriSkagit Valley Hospital, Mount Vernon, WA.
Wendy LeisenringClinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0001-7405-0906
Lynn OnstadClinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Jennifer E NylandPenn State College of Medicine, Hershey, PA.ORCID 0000-0002-4549-3617
Pamela S BeckerClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0001-6235-9463
Jeannine S McCuneClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0002-0795-497X
Stephanie J LeeClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0003-2600-6390
Brenda M SandmaierClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0002-9767-9739
Frederick R AppelbaumClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Elihu H EsteyClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
University of Washington Medical Center · USCleveland Clinic · USFred Hutch Cancer Center · USUniversity of Washington · USHarvard University · USRoswell Park Comprehensive Cancer Center · USUniversity of Utah · USWenatchee Valley Hospital & Clinics · USDalhousie University · CADuke Medical Center · USHackensack University Medical Center · USNorthwestern University · USPenn State Milton S. Hershey Medical Center · USSkagit Valley Hospital · USStanford University · USUniversity of Maryland, Baltimore · USUniversity of Pennsylvania · USWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Less-intensive induction therapies are increasingly used in older patients with acute myeloid leukemia (AML). Using an AML composite model (AML-CM) assigning higher scores to older age, increased comorbidity burdens, and adverse cytogenetic risks, we defined 3 distinct prognostic groups and compared outcomes after less-intensive vs intensive induction therapies in a multicenter retrospective cohort (n = 1292) treated at 6 institutions from 2008 to 2012 and a prospective cohort (n = 695) treated at 13 institutions from 2013 to 2017. Prospective study included impacts of Karnofsky performance status (KPS), quality of life (QOL), and physician perception of cure. In the retrospective cohort, recipients of less-intensive therapies were older and had more comorbidities, more adverse cytogenetics, and worse KPS. Less-intensive therapies were associated with higher risks of mortality in AML-CM scores of 4 to 6, 7 to 9, and ≥10. Results were independent of allogeneic transplantation and similar in those age 70 to 79 years. In the prospective cohort, the 2 groups were similar in baseline QOL, geriatric assessment, and patient outcome preferences. Higher mortality risks were seen after less-intensive therapies. However, in models adjusted for age, physician-assigned KPS, and chance of cure, mortality risks and QOL were similar. Less-intensive therapy recipients had shorter length of hospitalization (LOH). Our study questions the survival and QOL benefits (except LOH) of less-intensive therapies in patients with AML, including those age 70 to 79 years or with high comorbidity burdens. A randomized trial in older/medically infirm patients is required to better assess the value of less-intensive and intensive therapies or their combination. This trial was registered at www.clinicaltrials.gov as #NCT01929408.

Indexed as

Critical CareLeukemia, Myeloid, AcuteQuality of LifeAdolescentAdultAgedAged, 80 and overAge FactorsDisease-Free SurvivalFemaleHumansMaleMiddle AgedProspective StudiesRetrospective StudiesRisk Factors

Identifiers

PMID34351368
PMCPMC8939047
OpenAlexW3157387440

What OpenQuestion holds

Textmetadata
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Registered trials

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.