Evidence map›Paper›PMID 34146734›Full record

ArticleTransplantation and cellular therapy2021

Female Sex Is Associated with Improved Long-Term Survival Following Allogeneic Hematopoietic Stem Cell Transplantation.

Prioty Islam, Helen Tang, Haesu Jin, Felicia Cao, Lauren M Bohannon, Yi Ren, Nelson J Chao, Taewoong Choi, Cristina Gasparetto, Mitchell E Horwitz and 5 more

Open access · greenAbstract 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
1.2field-weighted citation impact, top 21% 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, 12 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Turkish Hematologists’ Preferences for Related Donor Selection: Results of a Multicenter SurveyTurkish journal of haematology : official journal of Turkish Society of Haematology · 2024
    Article
  5. Article
  6. Review
  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

15 authors at 2 institutions in 1 country.

Prioty IslamDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Helen TangDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Haesu JinDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Felicia CaoDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Lauren M BohannonDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Yi RenDuke Cancer Institute, Biostatistics Shared Resources, Duke University, Durham, North Carolina.
Nelson J ChaoDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Taewoong ChoiDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Cristina GasparettoDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Mitchell E HorwitzDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Gwynn D LongDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Richard D LopezDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
David A RizzieriDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Stefanie SarantopoulosDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Anthony D SungDivision of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina. Electronic address: anthony.sung@duke.edu.
Duke Medical Center · USDuke University · US

Funding

Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Virginia B Kraus · 2006 to 2026
$24.6M
NIA NIH HHS P30 AG028716
6 · The paper itself

Abstract

Life expectancy for long-term survivors of allogeneic hematopoietic stem cell transplantation (alloHSCT), defined as those living ≥5 years post-transplantation, is significantly lower compared with that of the age-matched general population despite a relatively low primary disease relapse rate at >2 years post-transplantation. Among several factors, patient sex is increasingly recognized as a prognostic indicator of long-term survival. We examined the influence of patient sex and donor-recipient sex matching on overall survival (OS) in a landmark analysis of long-term survivors. Using our institutional database supplemented with individual patient record review, we retrospectively investigated the relative influence of recipient sex and donor-recipient sex matching on outcomes of long-term survivors of alloHSCT between 1994 and 2014. Over this 20-year period, 247 met inclusion criteria for analysis; males and females had similar demographic and treatment characteristics. However, significantly more deaths after the 5-year landmark occurred in male recipients. Interestingly, donor sex did not have a significant impact on OS in multivariate analysis, and differences in OS of donor-recipient sex pairs was driven by recipient sex. In addition to recipient sex, only chronic graft-versus-host disease (cGVHD) retained significance as a covariate with an impact on OS in multivariate analysis. Men experienced slightly higher, but statistically nonsignificant, rates and increased severity of cGVHD, and had higher cGVHD-related mortality compared with females. In this long-term survival analysis of adult alloHSCT recipients, one of the only to include follow-up to 15 years, our results show that women survive significantly longer than men irrespective of their age at transplantation. This outcome is independent of other common pretransplantation prognostic indicators, such as donor sex or performance status at transplantation. The inferior survival in males is consistent with survival outcomes described in the transplantation literature. Increasing evidence suggests a biological basis for long-term sex-determined outcomes, possibly owing to differing rates or severity of cGVHD or sustained alloimmune tolerance in females. Larger studies are warranted to validate these retrospective clinical results.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationChild, PreschoolFemaleHumansMaleRetrospective StudiesTissue DonorsTransplantation, HomologousAllogeneic bone marrow transplantLate complicationsLong-term survivalSex and survival

Identifiers

PMID34146734
PMCPMC8403653
OpenAlexW3172025044

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.