Evidence map›Paper›PMID 40772822›Full record

ArticleCancer2025

Outpatient cytarabine consolidation in acute myeloid leukemia safely reduces hospitalization time and treatment costs.

Hannah Burton, Leora Boussi, David Nemirovsky, Andriy Derkach, Jenna Ciervo, Christopher Famulare, Kuo-Kai Chin, Yannis Valtis, Meira Yisraeli Salman, Kishan Patel and 7 more

Abstract read
In one paragraph

Article in Cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

17 authors.

Hannah BurtonDrexel University College of Medicine, Philadelphia, Pennsylvania, USA.
Leora BoussiDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0000-0001-7018-2071
David NemirovskyDepartment of Biostatistics and Epidemiology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Andriy DerkachDepartment of Biostatistics and Epidemiology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Jenna CiervoDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Christopher FamulareDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Kuo-Kai ChinDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Yannis ValtisDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Meira Yisraeli SalmanDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0000-0002-8504-2773
Kishan PatelDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Gunjan L ShahDepartment of Medicine, Bone Marrow Transplant and Cellular Therapy Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Aaron D GoldbergDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Mark B GeyerDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Meghan C ThompsonDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Martin S TallmanDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Eytan M SteinDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Sheng F CaiDepartment of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
CLINICAL SCHOLARS BIOMEDICAL RESEARCH TRAINING PROGRAMT32CA009512 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Ping Chi · 1985 to 2026
$6.3M
NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA009512
6 · The paper itself

Abstract

backgroundAdministration of intensive induction chemotherapy followed by consolidation with postremission high- or intermediate-dose cytarabine (H/IDAC) remains a standard therapeutic approach in fit patients with nonadverse risk acute myeloid leukemia (AML). Historically, H/IDAC has been administered in the inpatient (IP) rather than outpatient (OP) setting given infection risk, transfusion and supportive care needs, and logistical challenges of OP treatment. However, the financial toxicity associated with IP chemotherapy hospitalization as well as risk of nosocomial infections and improvements in antimicrobial prophylaxis have highlighted the potential role for OP H/IDAC administration.

methodsAccordingly, an OP H/IDAC treatment program was developed at Memorial Sloan Kettering Cancer Center in 2014 using an ambulatory pump system. To investigate the benefits and risks of this approach compared with standard IP H/IDAC administration, a retrospective single-center cohort study was conducted of 198 adult patients with AML who received either IP (59) or OP (139) H/IDAC consolidation.

resultsIn the OP-treated group, this approach safely reduced hospitalization days per cycle (median, 0.8 vs 7.5, p < .001) without leading to increased incidence of hospitalization for febrile neutropenia (incidence rate ratio, 1.07, p = .8) or higher rate of major treatment complications. Total cost per cycle was significantly lower for the OP-treated group (median, $14,244 compared to $36,688, p < .001).

conclusionsIn the largest cohort study of adult AML patients receiving OP H/IDAC, OP treatment administration was feasible, led to decreased hospital days and cost savings, and did not impact relapse free or overall survival compared to IP administration.

Indexed as

Antimetabolites, AntineoplasticConsolidation ChemotherapyCytarabineHospitalizationLeukemia, Myeloid, AcuteAdultAgedAmbulatory CareFemaleHealth Care CostsHumansInduction ChemotherapyMaleMiddle AgedOutpatientsRetrospective StudiesAntimetabolites, AntineoplasticCytarabineacute myeloid leukemiacytarabine consolidationoutpatient chemotherapy

Identifiers

PMID40772822
PMCPMC12330780

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.