Evidence map›Paper›PMID 24880021›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2014

Outcomes of human leukocyte antigen-matched sibling donor hematopoietic cell transplantation in chronic lymphocytic leukemia: myeloablative versus reduced-intensity conditioning regimens.

Ronald M Sobecks, Jose F Leis, Robert Peter Gale, Kwang Woo Ahn, Xiaochun Zhu, Mitchell Sabloff, Marcos de Lima, Jennifer R Brown, Yoshihiro Inamoto, Gregory A Hale and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Assessment of Impact of HLA Type on Outcomes of Allogeneic Hematopoietic Stem Cell Transplantation for Chronic Lymphocytic Leukemia.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
    Article
  8. Article
  9. 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

22 authors at 18 institutions in 5 countries.

Ronald M SobecksDepartment of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio. Electronic address: sobeckr@ccf.org.
Jose F LeisDepartment of Hematology/Oncology, Mayo Clinic Arizona, Phoenix, Arizona; Phoenix Children's Hospital, Phoenix, Arizona.
Robert Peter GaleDivision of Experimental Medicine, Department of Medicine, Hematology Research Centre, Imperial College London, London, United Kingdom.
Kwang Woo AhnDepartment of Medicine, Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, Wisconsin.
Xiaochun ZhuDepartment of Medicine, Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Mitchell SabloffDivison of Hematology, Department of Medicine, University of Ottawa and Ottawa Hospital Research Institute, Ottawa, Canada.
Marcos de LimaSeidman Cancer Center, University Hospitals Case Medical Center, Cleveland, Ohio.
Jennifer R BrownDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts.
Yoshihiro InamotoFred Hutchinson Cancer Research Center, Seattle, Washington.
Gregory A HaleDepartment of Hematology/Oncology, All Children's Hospital, St. Petersburg, Florida.
Mahmoud D AljurfDepartment of Oncology, King Faisal Specialist Hospital Center and Research, Riyadh, Saudi Arabia.
Rammurti T KambleDepartment of Hematology/Oncology, Baylor College of Medicine, Center for Cell and Gene Therapy, Houston, Texas.
Jack W HsuDivision of Hematology & Oncology, Department of Medicine, Shands HealthCare and University of Florida, Gainesville, Florida.
Steven Z PavleticNational Institutes of Health-National Cancer Institute Experimental Transplantation and Immunology Branch, Bethesda, Maryland.
Baldeep WirkStony Brook University Medical Center, Stony Brook, New York.
Matthew D SeftelDepartment of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Ian D LewisRoyal Adelaide Hospital, Adelaide, Australia.
Edwin P AlyeaDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts.
Jorge CortesDepartment of Leukemia, Division of Cancer Medicine, MD Anderson Cancer Center, Houston, Texas.
Matt E KalaycioDepartment of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.
Richard T MaziarzCenter for Hematologic Malignancies, Oregon Health and Science University, Portland, Oregon.
Wael SaberDepartment of Medicine, Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Medical College of Wisconsin · USCleveland Clinic · USDana-Farber Cancer Institute · USBaylor College of Medicine · USFred Hutch Cancer Center · USImperial College London · GBJohns Hopkins All Children's Hospital · USKing Faisal Specialist Hospital & Research Centre · SANational Cancer Institute · USOregon Health & Science University · USOttawa Hospital Research InstitutePrincess Margaret Cancer Centre · CARoyal Adelaide Hospital · AUStony Brook University Hospital · USThe University of Texas MD Anderson Cancer Center · USUniversity Hospitals Case Medical Center · USUniversity of Florida Health · USWinnMed · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
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 CA016672NCI NIH HHS U24 CA076518NCI NIH HHS U24-CA076518NHLBI NIH HHS 5U10HL069294NHLBI NIH HHS U10 HL069294
6 · The paper itself

Abstract

Allogeneic hematopoietic cell transplantation (HCT) can cure some chronic lymphocytic leukemia (CLL) subjects. This study compared outcomes of myeloablative (MA) and reduced-intensity conditioning (RIC) transplants from HLA-matched sibling donors (MSD) for CLL. From 1995 to 2007, information regarding 297 CLL subjects was reported to the Center of International Blood and Marrow Transplant Research; of these, 163 underwent MA and 134 underwent RIC MSD HCT. The MA subjects underwent transplantation less often after 2000 and less commonly received antithymocyte globulin (4% versus 13%, P = .004) or prior antibody therapy (14% versus 53%; P < .001). RIC was associated with a greater likelihood of platelet recovery and less grade 2 to 4 acute graft-versus-host disease compared with MA conditioning. One- and 5-year treatment-related mortality (TRM) were 24% (95% confidence intervals [CI], 16% to 33%) versus 37% (95% CI, 30% to 45%; P = .023), and 40% (95% CI, 29% to 51%) versus 54% (95% CI, 46% to 62%; P = .036), respectively, and the relapse/progression rates at 1 and 5 years were 21% (95% CI, 14% to 29%) versus 10% (95% CI, 6% to 15%; P = .020), and 35% (95% CI, 26% to 46%) versus 17% (95% CI, 12% to 24%; P = .003), respectively. MA conditioning was associated with better progression-free (PFS) (relative risk, .60; 95% CI, .37 to .97; P = .038) and 3-year survival in transplantations before 2001, but for subsequent years, RIC was associated with better PFS and survival (relative risk, 1.49 [95% CI, .92 to 2.42]; P = .10; and relative risk, 1.86 [95% CI, 1.11 to 3.13]; P = .019). Pretransplantation disease status was the most important predictor of relapse (P = .003) and PFS (P = .0007) for both forms of transplantation conditioning. MA and RIC MSD transplantations are effective for CLL. Future strategies to decrease TRM and reduce relapses are warranted.

Indexed as

AdultFemaleHematopoietic Stem Cell TransplantationHLA AntigensHumansLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedNeoplasm Recurrence, LocalSiblingsTissue DonorsTransplantation ConditioningTreatment OutcomeHLA AntigensChronic lymphocytic leukemiaMyeloablative allogeneic hematopoietic cell transplantationOutcomesReduced-intensity conditioning

Identifiers

PMID24880021
PMCPMC4174349
OpenAlexW2035688890

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.