Evidence map›Paper›PMID 34507002›Full record

ArticleTransplantation and cellular therapy2021

Planned Granulocyte Colony-Stimulating Factor Adversely Impacts Survival after Allogeneic Hematopoietic Cell Transplantation Performed with Thymoglobulin for Myeloid Malignancy.

Nina Orfali, Mei-Jie Zhang, Mariam Allbee-Johnson, Jaap Jan Boelens, Andrew S Artz, Claudio G Brunstein, Ian K McNiece, Filippo Milano, Muhammad Bilal Abid, Lynette Chee and 17 more

Open access · hybridAbstract read
In one paragraph

Article in Transplantation and cellular therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
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

27 authors at 20 institutions in 8 countries.

Nina OrfaliHaematology Department, St. James's Hospital, Dublin, Ireland; Department of Medicine, Weill Cornell Medicine, New York, New York. Electronic address: orfalin@tcd.ie.
Mei-Jie ZhangDivision of Biostatistics, Institute for Heath and Equity, Medical College of Wisconsin, Milwaukee, Wisconsin.
Mariam Allbee-JohnsonCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Jaap Jan BoelensPediatric Transplantation and Cellular Therapy Division, Memorial Sloan Kettering Cancer Center, New York, New York.
Andrew S ArtzDepartment of Hematology & Hematopoietic Cell Transplantation, City of Hope, Duarte, California.
Claudio G BrunsteinDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota.
Ian K McNieceStem Cell Transplantation and Cellular Therapy Clinical Laboratory, MD Anderson Cancer Center, Houston, Texas.
Filippo MilanoClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Muhammad Bilal AbidDivision of Infectious Diseases, Medical College of Wisconsin, Milwaukee, Wisconsin.
Lynette CheeHaematology Department, Peter MacCallum Cancer Centre, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.
Miguel A DiazPediatric Haematology Division, Hospital Infantil Universitario "Niño Jesus" Madrid, Spain.
Michael R GrunwaldDepartment of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health, Charlotte, North Carolina.
Peiman HemattiDivision of Hematology, Medical Oncology and Palliative Care, University of Wisconsin, Madison, Wisconsin.
Jingmei HsuDepartment of Medicine, Weill Cornell Medicine, New York, New York.
Hillard M LazarusDepartment of Hematologic Oncology, Case Western Reserve University, Cleveland, Ohio.
Pashna N MunshiStem Cell Transplant and Cellular Immunotherapy division, MedStar Georgetown University Hospital, Washington, DC.
Timothy PrestidgeBlood and Cancer Centre, Starship Hospital, University of Auckland, Auckland, New Zealand.
Olle RingdenDepartment of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
David RizzieriDepartment of Medicine, Duke University Medical Center, Durham, North Carolina.
Marcie L RichesDepartment of Medicine, University of North Carolina, Chapel Hill, North Carolina.
Sachiko SeoDepartment of Hematology and Oncology, Dokkyo Medical University, Tochigi, Japan.
Melhem SolhBlood and Marrow Transplant Program, Northside Hospital, Atlanta, Georgia.
Scott SolomonBlood and Marrow Transplant Program, Northside Hospital, Atlanta, Georgia.
David SzwajcerDepartment of Hematology and Oncology, Cancer Care Manitoba, Winnipeg, Manitoba, Canada.
Jean YaredDepartment of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Koen van BesienDepartment of Medicine, Weill Cornell Medicine, New York, New York.
Mary EapenCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Medical College of Wisconsin · USCornell University · USNorthside Hospital · USCancerCare Manitoba · CACase Western Reserve University · USCity of Hope · USDokkyo Medical University · JPDuke Medical Center · USFred Hutch Cancer Center · USGeorgetown University · USHospital Infantil Universitario Niño Jesús · ESKarolinska Institutet · SELevine Cancer Institute · USMemorial Sloan Kettering Cancer Center · USThe Royal Melbourne Hospital · AUThe University of Texas MD Anderson Cancer Center · USUniversity of Auckland · NZUniversity of Maryland, Baltimore · USUniversity of Minnesota · USUniversity of North Carolina at Chapel Hill · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 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
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
NCI NIH HHS P30 CA008748NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294
6 · The paper itself

Abstract

The in vivo depletion of recipient and donor T lymphocytes using antithymocyte globulin (ATG; Thymoglobulin) is widely adopted in allogeneic hematopoietic stem cell transplantation (HCT) to reduce the incidence of both graft failure and graft-versus-host disease (GVHD). However, excess toxicity to donor lymphocytes may hamper immune reconstitution, compromising antitumor effects and increasing infection. Granulocyte-colony stimulating factor (G-CSF) administered early after HCT may increase ATG-mediated lymphotoxicity. This study aimed to investigate the effect of an interaction between ATG and post-transplantation granulocyte colony-stimulating factor (G-CSF) on allogeneic HCT outcomes, using the Center for International Blood and Marrow Transplant Research (CIBMTR) registry. We studied patients age ≥18 years with acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS) who received Thymoglobulin-containing preparative regimens for HLA-matched sibling/unrelated or mismatched unrelated donor HCT between 2010 and 2018. The effect of planned G-CSF that was started between pretransplantation day 3 and post-transplantation day 12 was studied in comparison with transplantations that did not include G-CSF. Cox regression models were built to identify risk factors associated with outcomes at 1 year after transplantation. A total of 874 patients met the study eligibility criteria, of whom 459 (53%) received planned G-CSF. HCT with planned G-CSF was associated with a significantly increased risk for nonrelapse mortality (NRM) (hazard ratio [HR] 2.03; P <.0001; 21% versus 12%) compared to HCT without G-CSF. The 6-month incidence of viral infection was higher with G-CSF (56% versus 47%; P = .007), with a particular increase in Epstein-Barr virus infections (19% versus 11%; P = .002). The observed higher NRM with planned G-CSF led to lower overall survival (HR, 1.52; P = .0005; 61% versus 72%). There was no difference in GVHD risk between the treatment groups. We performed 2 subgroup analyses showing that our findings held true in patients age ≥50 years and in centers where G-CSF was used in some, but not all, patients. In allogeneic peripheral blood HCT performed with Thymoglobulin for AML and MDS, G-CSF administered early post-transplantation resulted in a 2-fold increase in NRM and a 10% absolute decrement in survival. The use of planned G-CSF in the early post-transplantation period should be carefully considered on an individual patient basis, weighing any perceived benefits against these risks.

Indexed as

Epstein-Barr Virus InfectionsHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteAdolescentAntilymphocyte SerumGranulocyte Colony-Stimulating FactorHerpesvirus 4, HumanHumansMiddle AgedTransplantation, HomologousAntilymphocyte SerumGranulocyte Colony-Stimulating FactorthymoglobulinAntithymocyte globulinFilgrastimGranulocyte colony-stimulating factorHematopoietic stem cell transplantationThymoglobulin

Identifiers

PMID34507002
PMCPMC8671234
OpenAlexW3196719306

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.