Evidence map›Paper›PMID 40287589›Full record

ArticleBone marrow transplantation2025

Subsequent cancers following non-myeloablative conditioning for allogeneic hematopoietic cell transplantation.

Phuong Vo, Kevin Ng, Gary Schoch, Jason Cooper, Abhishek Vupalanchi, Mary Flowers, Brenda M Sandmaier, Ted Gooley, Rainer Storb

Abstract read
In one paragraph

Article in Bone marrow transplantation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Phuong VoClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. ptvo@fredhutch.org.ORCID 0000-0002-0823-0244
Kevin NgClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Gary SchochClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Jason CooperClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0003-0023-8054
Abhishek VupalanchiSummer Program, University of Washington, Seattle, WA, USA.
Mary FlowersClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Brenda M SandmaierClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-9767-9739
Ted GooleyClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Rainer StorbClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-9343-4099

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Project 3: Stem Cell Allografts for Lymphoid MalignanciesP01CA078902 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SANDMAIER, BRENDA MARIE · 1999 to 2025
$46.1M
NCI NIH HHS P01 CA078902NCI NIH HHS P30 CA015704U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) CA 078902U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P30 CA 015704
6 · The paper itself

Abstract

We examined the risk of subsequent malignant neoplasms (SMNs) in 1720 patients with hematologic cancers given allogeneic hematopoietic grafts from 03/1998 to 08/2023 after nonmyeloablative conditioning regimens. With a median follow-up of 12 years, the cumulative incidence of SMNs was 17% (95% CI, [15%, 19%]). Most SMNs (n = 543) were non-melanoma skin cancers seen in 208 patients; unfortunately, information on these cancers was not available in the Surveillance, Epidemiology, and End Results (SEER) database for comparison with such tumors in the general population. However, developing non-melanoma skin cancers was statistically significantly associated with chronic GVHD and, thus, unlikely to be conditioning regimen related. Eighty-six patients (5%) developed 93 other SMNs. This number (93 SNMs) significantly exceeded the expected 73.4 cases in the comparison group (p = 0.03). This increase was driven exclusively by increases in uterine adenocarcinoma (n = 2), squamous lip cancer (n = 5), and squamous penile cancer (n = 2); the latter two cancers were, again, associated with chronic GVHD. Apart from these three tumor types, there were no observed increases in the risk of other tumors compared to those in the general population.

Indexed as

Hematologic NeoplasmsHematopoietic Stem Cell TransplantationNeoplasms, Second PrimaryTransplantation ConditioningAdolescentAdultAgedAllograftsChildFemaleFollow-Up StudiesGraft vs Host DiseaseHumansMaleMiddle AgedSEER Program

Identifiers

PMID40287589
PMCPMC13374389

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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.