Evidence map›Paper›PMID 41870848›Full record

ArticleJournal of racial and ethnic health disparities2026

Cancer-Specific and Other-Cause Mortality of Asian Pacific Islanders vs. Caucasians Across Eleven Primary Cancers.

Natali Rodriguez Peñaranda, Francesco Di Bello, Andrea Marmiroli, Fabian Falkenbach, Mattia Longoni, Quynh Chi Le, Calogero Catanzaro, Michele Nicolazzini, Jordan A Goyal, Fred Saad and 14 more

Abstract read
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In one paragraph

Article in Journal of racial and ethnic health disparities, 2026. 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

24 authors.

Natali Rodriguez PeñarandaCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada. natalirodriguez647@gmail.com.ORCID http://orcid.org/0009-0006-3057-3805
Francesco Di BelloCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.
Andrea MarmiroliCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.
Fabian FalkenbachCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.
Mattia LongoniCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.
Quynh Chi LeCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.
Calogero CatanzaroCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.
Michele NicolazziniCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.
Jordan A GoyalCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.
Fred SaadCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.
Shahrokh F ShariatDepartment of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Nicola LongoDepartment of Neurosciences, Science of Reproduction and Odontostomatology, University of Naples Federico II, Naples, Italy.
Gennaro MusiDepartment of Urology, IEO European Institute of Oncology, IRCCS, Via Ripamonti 435, Milan, Italy.
Elisa LodiAOU Di Modena, University of Modena and Reggio Emilia, Modena, Italy.
Markus GraefenMartini-Klinik Prostate Cancer Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Alberto BrigantiDivision of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.
Felix K H ChunDepartment of Urology, Goethe University Frankfurt, University Hospital, Frankfurt Am Main, Germany.
Riccardo SchiavinaDepartment of Urology, University of Bologna, St. Orsola-Malpighi Hospital, Bologna, Italy.
Carlotta PalumboDivision of Urology, Department of Translational Medicine, University of Eastern Piedmont, Maggiore Della Carità Hospital, Novara, Italy.
Filippo OrlandiAOU Di Modena, University of Modena and Reggio Emilia, Modena, Italy.
Stefano RescaAOU Di Modena, University of Modena and Reggio Emilia, Modena, Italy.
Stefano PuliattiAOU Di Modena, University of Modena and Reggio Emilia, Modena, Italy.
Salvatore MicaliAOU Di Modena, University of Modena and Reggio Emilia, Modena, Italy.
Pierre I KarakiewiczCancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, Québec, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSeveral studies reported more favorable cancer-specific mortality (CSM) in Asian Pacific Islanders (APIs) vs. Caucasians. We tested these findings across 11 primary cancers of all stages: cutaneous melanoma, bladder, breast, colorectal, gastric, kidney, liver, lung, nasopharyngeal, prostate, and uterine cancer. MATERIALS AND

methodsWithin the Surveillance, Epidemiology, and End Results database (SEER 2000-2021), we identified APIs and Caucasians with one of the 11 primaries. Multivariable competing risks regression (CRR) models tested the effect of API race/ethnicity on cancer-specific mortality (CSM) and other-cause mortality (OCM).

resultsOverall, 339,576 APIs (8.5%) vs. 3,643,873 (91.5%) Caucasians were identified. The API to Caucasian ratio varied by cancer type, ratio ranged from 1:1.2 for nasopharyngeal cancer (4,007 APIs vs. 4,723 Caucasians) to 1:80.7 for cutaneous melanoma (4,924 vs. 397,549). In general, APIs were younger (median age 64 vs. 67 years) and harbored less frequently localized stage (in ten of 11 primaries), more frequently regional (in nine of 11 primaries) or metastatic (in seven of 11 primaries) stage. In multivariable CRR models, API race/ethnicity predicted lower CSM in eight of 11 primaries (hazard ratios [HRs] ranged 0.80-0.95), except for cutaneous melanoma, kidney, and uterine cancer. Additionally, API race/ethnicity independently predicted lower OCM in ten of 11 primaries (HRs ranged 0.80-0.95), except for cutaneous melanoma. Exploratory analyses separating Asian Americans and Pacific Islanders demonstrated that the observed survival advantage was largely driven by Asian Americans, whereas Pacific Islanders showed distinct demographic, stage distribution, and mortality patterns.

conclusionBy jointly evaluating cancer-specific mortality (CSM) and explicitly reporting other-cause mortality (OCM) across multiple primary cancers using a uniform competing risks framework, this study provides novel and comprehensive evidence that API race/ethnicity, largely driven by Asian Americans, is associated with more favorable survival outcomes in most malignancies, with some exceptions.

Indexed as

APIAsiansCaucasiansCSMOCMSEERSurvival

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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.