Evidence map›Paper›PMID 39626307›Full record

ArticleJournal of the National Cancer Institute2025

Increased occurrence of malignancy before and after chemoradiation for anal squamous cell carcinoma: a multi-institutional analysis.

Ritesh Kumar, Chris L Hallemeier, Daniel T Chang, Shou-En Lu, Lara Hathout, Vasilis C Hristidis, Krishnan R Jethwa, J Richelcyn M Baclay, Veeraswamy Manne, Zakaria Chakrani and 7 more

Abstract readMulticenter Study
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. 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

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.

Ritesh KumarDepartment of Radiation Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08901, United States.ORCID 0000-0002-0982-6277
Chris L HallemeierDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN 55905, United States.
Daniel T ChangDepartment of Radiation Oncology, University of Michigan, Ann Arbor, MI 48109, United States.
Shou-En LuDepartment of Biostatistics and Epidemiology, Rutgers University School of Public Health, Piscataway, NJ 08854, United States.
Lara HathoutDepartment of Radiation Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08901, United States.
Vasilis C HristidisDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.
Krishnan R JethwaDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN 55905, United States.ORCID 0000-0002-7590-558X
J Richelcyn M BaclayDepartment of Radiation Oncology, Stanford University, Stanford, CA 94305, United States.ORCID 0000-0002-8081-6928
Veeraswamy ManneDepartment of Radiation Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08901, United States.ORCID 0000-0002-1179-5529
Zakaria ChakraniDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.ORCID 0009-0003-2932-6960
Michael G HaddockDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN 55905, United States.
Diego Augusto Santos ToescaDepartment of Radiation Oncology, Mayo Clinic, Phoenix, AZ 85054, United States.
Erqi Liu PollomDepartment of Radiation Oncology, Stanford University, Stanford, CA 94305, United States.ORCID 0000-0003-2908-6293
Abraham J WuDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.ORCID 0000-0002-2597-7091
Harigopal SandhyavenuDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN 55905, United States.ORCID 0000-0002-2567-6651
Paul B RomesserDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.ORCID 0000-0001-8268-2903
Salma K JabbourDepartment of Radiation Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08901, United States.ORCID 0000-0001-8200-5371

Funding

Investigating the contribution of cellular senescence to the efficacy of radiation therapy.K08CA255574 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI ROMESSER, PAUL BERNARD · 2021 to 2025
$1.2M
Dr. Salma Jabbour’s NCI Research Specialist (Clinician Scientist) Award (R50)R50CA275877 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Salma Jabbour · 2023 to 2026
$785k
NCI NIH HHS K08 CA255574NCI NIH HHS R50 CA275877
6 · The paper itself

Abstract

backgroundAnal squamous cell carcinoma is a rare cancer with increased occurrence of multiple cancers before and after the anal squamous cell carcinoma diagnosis. However, there are limited data on this aspect. This multi-institutional analysis aimed to define the occurrence of malignancies before and after anal squamous cell carcinoma, time trends, and impact on survival and to identify prognostic factors.

methodsInitial primary malignancy was defined as a malignancy occurring before the anal squamous cell carcinoma. Second primary malignancy was defined as a distinct primary cancer that developed after anal squamous cell carcinoma diagnosis. Retrospective multi-institutional chart review was done. Progression-free survival (PFS), overall survival, and prognostic factors were evaluated.

resultsA total of 647 patients with anal squamous cell carcinoma treated with curative intent were analyzed. Median age was 61.2 years with 72% as females. Of these, 150 (23.3%) patients had multiple malignancies with initial primary malignancy in 16% and second primary malignancy in 8%. Patients without prior cancer had better 5-year PFS (81.2% vs 67.2%, P = .011) and overall survival (81% vs 69%, P = .008) compared with those with prior cancer. Second primary malignancies had a statistically significant adverse impact on PFS (hazard ratio [HR] = 4.22) and overall survival (HR = 3.56). Females had better 5-year PFS (82% vs 70%, P = .016) as compared with males. The median time interval for developing anal squamous cell carcinoma (as second primary malignancy) after initial primary malignancy was 9.32 years.

conclusionsAnal squamous cell carcinoma patients have an increased risk of multiple malignancies. These patients who have prior cancers have inferior outcomes. Second primary malignancy is a poor prognostic factor in patients with anal cancer. Second primary malignancy can develop years after treatment of primary anal squamous cell carcinoma.

Indexed as

Anus NeoplasmsCarcinoma, Squamous CellChemoradiotherapyNeoplasms, Multiple PrimaryNeoplasms, Second PrimaryAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisRetrospective Studies

Identifiers

PMID39626307
PMCPMC13338817

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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.