Evidence map›Paper›PMID 39886926›Full record

ArticleJournal of the National Cancer Institute2025

Human papillomavirus-related squamous cell carcinomas after blood or marrow transplantation-a Blood or Marrow Transplant Survivor Study report.

Anna Sällfors Holmqvist, Qingrui Meng, Wendy Landier, Lindsey Hageman, Liton F Francisco, Elizabeth Schlichting Ross, Nora Balas, Alysia Bosworth, Hok Sreng Te, Ravi Bhatia and 4 more

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Nanocarrier drug delivery systems for gynecological cancer therapeutics.Journal of controlled release : official journal of the Controlled Release Society · 2025
    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

14 authors.

Anna Sällfors HolmqvistDepartment of Clinical Sciences, Lund University, Childhood Cancer Center, Skåne University Hospital, Lund, Sweden.ORCID 0000-0002-3756-8148
Qingrui MengInstitute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35233, United States.
Wendy LandierInstitute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35233, United States.ORCID 0000-0003-3319-5652
Lindsey HagemanInstitute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35233, United States.
Liton F FranciscoInstitute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35233, United States.ORCID 0000-0001-8138-9932
Elizabeth Schlichting RossInstitute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35233, United States.
Nora BalasInstitute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35233, United States.ORCID 0000-0002-8371-8821
Alysia BosworthPopulation Sciences, City of Hope, Duarte, CA 91919, United States.ORCID 0000-0002-0662-5699
Hok Sreng TeDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN 55455, United States.
Ravi BhatiaDivision of Hematology, Oncology and Bone Marrow Transplantation, University of Alabama at Birmingham, Birmingham, AL 35233, United States.
F Lennie WongPopulation Sciences, City of Hope, Duarte, CA 91919, United States.ORCID 0000-0002-4333-5017
Daniel WeisdorfDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN 55455, United States.ORCID 0000-0001-8078-8579
Saro H ArmenianPopulation Sciences, City of Hope, Duarte, CA 91919, United States.ORCID 0000-0003-2604-8603
Smita BhatiaInstitute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35233, United States.ORCID 0000-0002-7755-5683

Funding

BMT Survivor Study-2 (BMTSS-2)U01CA213140 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BHATIA, SMITA · 2019 to 2023
$6.8M
BONE MARROW TRANSPLANT (BMT) SURVIVORS STUDYR01CA078938 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI BHATIA, SMITA · 2000 to 2003
$1.6M
Leukemia Lymphoma SocietyNCI NIH HHS R01 CA078938NCI NIH HHS R01CA078938NCI NIH HHS U01 CA213140NCI NIH HHS U01CA213140Swedish Childhood Cancer Fund
6 · The paper itself

Abstract

backgroundHuman papillomavirus (HPV) is associated with an increased risk for a variety of squamous cell carcinomas in the general population. The risk for subsequent squamous cell carcinomas in blood or marrow transplantation survivors that are potentially related to HPV (cervical, oropharyngeal, vulvar, vaginal, anal, and penile cancer; HPV-related squamous cell carcinomas) remains unknown.

methodsWe determined the risk of HPV-related squamous cell carcinomas in 7936 2-year survivors of autologous or allogeneic blood or marrow transplantation performed between 1974 and 2014 and identified the role of demographic and clinical factors associated with HPV-related squamous cell carcinomas using proportional subdistribution hazards model for competing risks. Standardized incidence ratio was used to compare the risk of HPV-related squamous cell carcinoma with age-, sex-, and calendar-specific incidence in the general population.

resultsThe median age at transplantation was 46 years (range = 0-78 years); 58.5% (n = 4642) were male, and 72.2% (n = 5727) were non-Hispanic White. Half (50.3%, n = 3991) of the patients had received an allogeneic blood or marrow transplantation. The standardized incidence ratio for oropharyngeal squamous cell carcinomas (n = 53) was 1.8 (95% confidence interval [CI] = 1.3 to 2.3) and for cervical squamous cell carcinoma among female blood or marrow transplantation recipients (n = 26) was 9.4 (95% CI = 6.3 to 13.6) compared with the general US population. The hazard of an HPV-related squamous cell carcinoma was higher among allogeneic blood or marrow transplantation recipients with chronic graft vs host disease (any HPV-related squamous cell carcinoma: HR = 6.24, 95% CI = 3.11 to 12.50; oropharyngeal: HR = 4.85, 95% CI = 2.11 to 11.15; cervical: HR = 4.98, 95% CI = 1.65 to 15.00; reference: autologous blood or marrow transplantation). Pre-blood or marrow transplantation radiation increased the risk of oropharyngeal squamous cell carcinoma (HR = 2.98, 95% CI = 1.57 to 5.65).

conclusionThese findings underscore the importance of risk-based HPV vaccination and surveillance after blood or marrow transplantation.

Indexed as

Bone Marrow TransplantationCarcinoma, Squamous CellNeoplasms, Second PrimaryPapillomavirus InfectionsAdolescentAdultAgedChildChild, PreschoolFemaleHuman Papillomavirus VirusesHumansIncidenceInfantMaleMiddle Aged

Identifiers

PMID39886926
PMCPMC12145910

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.