Evidence map›Paper›PMID 36428678›Full record

ArticleCancers2022

Longitudinal Survival Outcomes in Allogeneic Stem Cell Transplantation: An Institutional Experience.

Justin Jiang, Audrey M Sigmund, Qiuhong Zhao, Patrick Elder, Don M Benson, Sumithira Vasu, Samantha Jaglowski, Alice Mims, Hannah Choe, Karilyn Larkin and 7 more

Abstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Relationship Between anJournal of clinical medicine · 2025
    Article
  3. Article
  4. Article
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

17 authors.

Justin JiangCollege of Medicine, The Ohio State University, Columbus, OH 43210, USA.
Audrey M SigmundDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Qiuhong ZhaoDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Patrick ElderDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Don M BensonDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Sumithira VasuDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Samantha JaglowskiDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Alice MimsDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Hannah ChoeDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Karilyn LarkinDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0002-1898-9836
Jonathan E BrammerDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Sarah WallDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Nicole GrieselhuberDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Ayman SaadDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0003-0003-0130
Sam PenzaDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Yvonne A EfeberaDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.
Nidhi SharmaDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-SCT) is a potentially curative treatment for many hematological disorders, but is often complicated by relapse of the underlying disease, graft-versus-host disease (GVHD), and infectious complications. We conducted a retrospective analysis on patients undergoing allo-SCT from 1984 to 2018 to better understand how survival has changed longitudinally with therapeutic advancements made to mitigate these complications. Method: We analyzed data from 1943 consecutive patients who received allo-SCT. Patients were divided into groups (gps) based on the year (yr) of transplant. Primary endpoints were overall survival (OS), progression free survival (PFS), and GVHD-free relapse-free survival (GRFS). Secondary endpoints were the cumulative incidences of grade II−IV and grade III−IV acute GVHD (aGVHD), chronic GVHD (cGVHD), and non-relapse mortality (NRM). Results: Our study found statistically significant improvements in OS, PFS, and GRFS. Five-year PFS among the groups increased from 24% to 48% over the years. Five-year OS increased from 25% to 53%. Five-year GRFS significantly increased from 6% to 14%, but remained relatively unchanged from 2004 to 2018. Cumulative incidences of grade II−IV aGVHD increased since 2009 (p < 0.001). However, cumulative incidence of NRM decreased since 2004 (p < 0.001). Conclusions: Our data show improved OS, PFS, and GRFS post allo-SCT over decades. This may be attributed to advances in supportive care and treatments focused on mitigation of GVHD and relapse.

Indexed as

allogenic transplantationgraft-versus-host diseaseoverall survivalprogression-free survival

Identifiers

PMID36428678
PMCPMC9688916

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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.