Evidence map›Paper›PMID 37903992›Full record

ArticleBone marrow transplantation2024

Post-transplantation cyclophosphamide is associated with increased bacterial infections.

Celalettin Ustun, Min Chen, Soyoung Kim, Jeffery J Auletta, Marjorie V Batista, Minoo Battiwalla, Jan Cerny, Lohith Gowda, Joshua A Hill, Hongtao Liu and 9 more

Open access · greenAbstract read
In one paragraph

Article in Bone marrow transplantation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.9field-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.

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, 17 citations in OpenAlex.

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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

19 authors at 15 institutions in 3 countries.

Celalettin UstunDivision of Hematology/Oncology/Cell Therapy, Rush University, Chicago, IL, USA. Celalettin_Ustun@rush.edu.ORCID 0000-0001-6896-6213
Min ChenCIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Soyoung KimCIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.ORCID 0000-0003-1404-0575
Jeffery J AulettaCIBMTR® (Center for International Blood and Marrow Transplant Research), National Marrow Donor Program/Be The Match, Minneapolis, MN, USA.
Marjorie V BatistaA.C. Camargo Cancer Center, Sao Paulo, Brazil.
Minoo BattiwallaSarah Cannon Transplant and Cell Therapy Network, Nashville, TN, USA.
Jan CernyDivision of Hematology/Oncology, Department of Medicine, University of Massachusetts Chan Medical School and Medical Center, Worcester, MA, USA.
Lohith GowdaYale Cancer Center and Yale School of Medicine, New Haven, CT, USA.
Joshua A HillFred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-7665-7100
Hongtao LiuSection of Hematology/Oncology, University of Chicago Medicine, Chicago, IL, USA.ORCID 0000-0002-3190-7807
Pashna N MunshiStem Cell Transplant and Cellular Immunotherapy Program, MedStar Georgetown University Hospital, Washington, DC, USA.ORCID 0000-0002-8079-9443
Sunita NathanDivision of Hematology/Oncology/Cell Therapy, Rush University, Chicago, IL, USA.ORCID 0000-0001-7920-4265
Matthew D SeftelDepartment of Medicine, University of British Columbia, Vancouver, Canada.
John R WingardDivision of Hematology & Oncology, Department of Medicine, University of Florida, Gainesville, FL, USA.
Roy F ChemalyThe University of Texas, M.D. Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-0277-3088
Christopher E DandoyCincinnati Children's Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, OH, USA.ORCID 0000-0002-4001-9203
Miguel-Angel PeralesAdult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0002-5910-4571
Marcie RichesCIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Genovefa A PapanicolaouDepartment of Medicine, Weill Cornell Medical College, New York, NY, USA.ORCID 0000-0002-2891-079X
Medical College of Wisconsin · USMemorial Sloan Kettering Cancer Center · USRush University · USAC Camargo Hospital · BRCincinnati Children's Hospital Medical Center · USGeorgetown University · USNationwide Children's Hospital · USSarah Cannon · USThe University of Texas MD Anderson Cancer Center · USUniversity of British Columbia · CAUniversity of Chicago · USUniversity of Florida · USUniversity of Massachusetts Chan Medical School · USUniversity of Washington · USYale Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
NTP INFORMATION SYSTEMS SUPPORT27305C0011 · NIEHS · Z-TECH CORPORATION · 2007 to 2009
$4.3M
PROVIDE RABBITS, RATS, MICE, HAMSTERS, GERBILS, GUINEA PIGS27307C0011 · NIEHS · PI BOLEN, WAYNE · 2007 to 2007
$500k
NCI NIH HHS P30 CA008748NCI NIH HHS U24 CA076518NIEHS NIH HHS 27305C0011NIEHS NIH HHS 27307C0011NIEHS NIH HHS 27398C0011
6 · The paper itself

Abstract

Post-transplant cyclophosphamide (PTCy) is increasingly used to reduce graft-versus-host disease after hematopoietic cell transplantation (HCT); however, it might be associated with more infections. All patients who were ≥2 years old, receiving haploidentical or matched sibling donor (Sib) HCT for acute leukemias or myelodysplastic syndrome, and either calcineurin inhibitor (CNI)- or PTCy-based GVHD prophylaxis [Haploidentical HCT with PTCy (HaploCy), 757; Sibling with PTCy (SibCy), 403; Sibling with CNI-based (SibCNI), 1605] were included. Most bacterial infections occurred within the first 100 days; 953 patients (34.5%) had at least 1 infection and 352 patients (13%) had ≥2 infections. Patients receiving PTCy had a greater incidence of bacterial infections by day 180 [HaploCy 46%; SibCy 48%; SibCNI 35%; p < 0.001]. Compared with the SibCNI without infection cohort, 1.99-fold, 3.33-fold, 2.78-fold, and 2.53-fold increased TRM was seen for the HaploCy cohort without infection and HaploCy, SibCy, and SibCNI cohorts with infection, respectively. Bacterial infections increased mortality [HaploCy (HR1.84, 99% CI: 1.45-2.33, p < 0.0001), SibCy cohort (HR,1.68, 99% CI: 1.30-2.19, p < 0.0001), and SibCNI cohort (HR,1.76, 99% CI: 1.43-2.16, p < 0.0001). PTCy was associated with increased bacterial infections regardless of donor, and bacterial infections were associated with increased mortality irrespective of GVHD prophylaxis. Patients receiving PTCy should be monitored carefully for bacterial infections following PTCy.

Indexed as

Bacterial InfectionsGraft vs Host DiseaseHematopoietic Stem Cell TransplantationCalcineurin InhibitorsChild, PreschoolCyclophosphamideHumansRetrospective StudiesTissue DonorsCalcineurin InhibitorsCyclophosphamide

Identifiers

PMID37903992
PMCPMC11164622
OpenAlexW4388033236

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.