Evidence map›Paper›PMID 24735965›Full record

ArticleBlood2014

Lower risk for serious adverse events and no increased risk for cancer after PBSC vs BM donation.

Michael A Pulsipher, Pintip Chitphakdithai, Brent R Logan, Willis H Navarro, John E Levine, John P Miller, Bronwen E Shaw, Paul V O'Donnell, Navneet S Majhail, Dennis L Confer

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

57 citing papers in PubMed, 123 citations in OpenAlex.

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  3. Pharmacodynamics, safety, and immunogenicity of PelmegPharmacology research & perspectives · 2019
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  4. The Concentration of Total Nucleated Cells in Harvested Bone Marrow for Transplantation Has Decreased over Time.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Michael A PulsipherUniversity of Utah School of Medicine, Primary Children's Hospital, Salt Lake City, UT;
Pintip ChitphakdithaiCenter for International Blood and Marrow Transplant Research, Minneapolis, MN;
Brent R LoganCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI;
Willis H NavarroCenter for International Blood and Marrow Transplant Research, Minneapolis, MN; National Marrow Donor Program, Minneapolis, MN;
John E LevineThe University of Michigan, Ann Arbor, MI;
John P MillerNational Marrow Donor Program, Minneapolis, MN;
Bronwen E ShawAnthony Nolan Research Institute, London, United Kingdom;
Paul V O'DonnellFred Hutchinson Cancer Research Center, Seattle, WA; and.
Navneet S MajhailCenter for International Blood and Marrow Transplant Research, Minneapolis, MN; Cleveland Clinic, Cleveland, OH.
Dennis L ConferCenter for International Blood and Marrow Transplant Research, Minneapolis, MN; National Marrow Donor Program, Minneapolis, MN;
National Marrow Donor Program · USAnthony Nolan · GBFred Hutch Cancer Center · USMedical College of Wisconsin · USPrimary Children's Hospital · USUniversity of Michigan–Ann Arbor · US

Funding

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
RDSafe: A Multi-Institutional Study of HSC Donor Safety and Quality LifeR01HL085707 · NHLBI · UNIVERSITY OF UTAH · PI PULSIPHER, MICHAEL A, SWITZER, GALEN E. · 2009 to 2013
$3.1M
NCI NIH HHS U24 CA076518NCI NIH HHS U24-CA076518NHLBI NIH HHS 5U10HL069294NHLBI NIH HHS R01 HL085707NHLBI NIH HHS U10 HL069294PHS HHS HHSH234200637020CPHS HHS HHSH250201200016CPHS HHS HHSH250201200024C
6 · The paper itself

Abstract

We compared serious early and late events experienced by 2726 bone marrow (BM) and 6768 peripheral blood stem cell (PBSC) donors who underwent collection of PBSC or BM between 2004 and 2009 as part of a prospective study through the National Marrow Donor Program. Standardized FDA definitions for serious adverse events (SAEs) were used, and all events were reviewed by an independent physician panel. BM donors had an increased risk for SAEs (2.38% for BM vs 0.56% for PBSC; odds ratio [OR], 4.13; P < .001), and women were twice as likely to experience an SAE (OR for men, 0.50; P = .005). Restricting the analysis to life-threatening, unexpected, or chronic/disabling events, BM donors maintained an increased risk for SAEs (0.99% for BM vs 0.31% for PBSC; OR, 3.20; P < .001). Notably, the incidence of cancer, autoimmune illness, and thrombosis after donation was similar in BM vs PBSC donors. In addition, cancer incidence in PBSC donors was less than that reported in the general population (Surveillance, Epidemiology, and End Results Program database). In conclusion, SAEs after donation are rare but more often occurred in BM donors and women. In addition, there was no evidence of increased risk for cancer, autoimmune illness, and stroke in donors receiving granulocyte colony-stimulating factor during this period of observation.

Indexed as

Bone MarrowHematopoietic Stem CellsTissue DonorsAdolescentAdultBone Marrow TransplantationFemaleGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHumansMaleMiddle AgedNeoplasmsPeripheral Blood Stem Cell TransplantationPostoperative ComplicationsRisk FactorsGranulocyte Colony-Stimulating Factor

Identifiers

PMID24735965
PMCPMC4047500
OpenAlexW2071411325

What OpenQuestion holds

Textmetadata
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.