The Evaluation of Renal Tumor Diagnostics in Global Pathology Practice

Background The 2022 World Health Organization (WHO) fifth Edition introduced major revisions to renal neoplasm classification, incorporating novel and molecularly defined entities. However, the extent to which these advances are adopted in routine pathology practice remains unclear. This international survey evaluated the global diagnostic work-up of kidney tumors, including access to ancillary tests (immunohistochemistry [IHC], fluorescence in situ hybridization [FISH], next-generation sequencing [NGS]) and familiarity with the current classification. Methods A 30-question online survey was distributed via SurveyMonkey to pathologists involved in renal tumor diagnostics between January and July 2024. The survey assessed demographics, practice setting, training background, WHO classification familiarity, and availability of IHC and molecular testing. Responses were analyzed using descriptive and inferential statistics. Results Of 427 respondents, 399 (94.8%) reported encountering kidney tumors and were included, representing 45 countries. The most represented were the United States (18.8%), Egypt (15.8%), Turkey (12.6%), the United Kingdom (8.8%), and India (7.3%). Nearly half (49.4%) had >10 years of practice, 41.1% lacked formal genitourinary pathology training, and 70.7% worked in academic settings. IHC was widely available (96.0%), whereas access to FISH (50.1%) and NGS (43.8%) was limited. High-resource academic centers had significantly greater access to molecular diagnostics than community settings (all p < .001). Kidney-specific molecular panels were available in only 18.1% of institutions. Emerging biomarkers (SDHB, FH, cathepsin K, TFE3, TRIM63) were substantially less available than conventional markers. Although 66.3% reported familiarity with the WHO classification, 33.6% cited barriers such as rapid updates, financial constraints, and workload. Conclusions Marked global disparities persist in renal tumor diagnostics. While IHC is widely accessible, advanced molecular tools and novel biomarkers remain unevenly distributed, underscoring the need for targeted educational and resource-sharing strategies.

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Journal
International Journal of Surgical Pathology
Published
2026-06-29
DOI
https://doi.org/10.1177/10668969261458406
Primary Topic
Renal cell carcinoma treatment
Type
article
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article

The Evaluation of Renal Tumor Diagnostics in Global Pathology Practice

Burcu Biltekin, Dilek Ertoy Baydar, Mahmut Akgül, Anandi Lobo et al.
International Journal of Surgical Pathology
Renal cell carcinoma treatment
article

The Evaluation of Renal Tumor Diagnostics in Global Pathology Practice

Burcu Biltekin, Dilek Ertoy Baydar, Mahmut Akgül, Anandi Lobo, Laurence A. Galea, Onur Ertunç, Maria Sarah L. Lenon, Büşra Yaprak Bayrak, Levente Kuthi, Ankur R. Sangoi, Manana Jikurashvili, Maryna Slisarenko, Dilara Akbulut, Yazgı Köy, Nazif Alperen Yıldırım, Laila Farid, Sean R Williamson, Ahmed Montasser, Sana Malik, Elza Tjio, Liang Cheng, Dimitrios Korentzelos
article en

Abstract

Background The 2022 World Health Organization (WHO) fifth Edition introduced major revisions to renal neoplasm classification, incorporating novel and molecularly defined entities. However, the extent to which these advances are adopted in routine pathology practice remains unclear. This international survey evaluated the global diagnostic work-up of kidney tumors, including access to ancillary tests (immunohistochemistry [IHC], fluorescence in situ hybridization [FISH], next-generation sequencing [NGS]) and familiarity with the current classification. Methods A 30-question online survey was distributed via SurveyMonkey to pathologists involved in renal tumor diagnostics between January and July 2024. The survey assessed demographics, practice setting, training background, WHO classification familiarity, and availability of IHC and molecular testing. Responses were analyzed using descriptive and inferential statistics. Results Of 427 respondents, 399 (94.8%) reported encountering kidney tumors and were included, representing 45 countries. The most represented were the United States (18.8%), Egypt (15.8%), Turkey (12.6%), the United Kingdom (8.8%), and India (7.3%). Nearly half (49.4%) had >10 years of practice, 41.1% lacked formal genitourinary pathology training, and 70.7% worked in academic settings. IHC was widely available (96.0%), whereas access to FISH (50.1%) and NGS (43.8%) was limited. High-resource academic centers had significantly greater access to molecular diagnostics than community settings (all p < .001). Kidney-specific molecular panels were available in only 18.1% of institutions. Emerging biomarkers (SDHB, FH, cathepsin K, TFE3, TRIM63) were substantially less available than conventional markers. Although 66.3% reported familiarity with the WHO classification, 33.6% cited barriers such as rapid updates, financial constraints, and workload. Conclusions Marked global disparities persist in renal tumor diagnostics. While IHC is widely accessible, advanced molecular tools and novel biomarkers remain unevenly distributed, underscoring the need for targeted educational and resource-sharing strategies.

International Journal of Surgical Pathology
Semmelweis University (HU), University of Santo Tomas Hospital (PH), Brigham and Women's Hospital (US), All India Institute of Medical Sciences Raipur (IN), National Institutes of Health (US), Cleveland Clinic (US), Koç University (TR), Brown University (US), Kyiv Medical University (UA), Gülhane Askerî Tıp Akademisi (TR), Atlas Scientific (United States) (US), Ain Shams University Hospital (EG), National Institute of Oncology (HU), Sağlık Bilimleri Üniversitesi (TR), Sonic Healthcare (Germany) (DE), University of Pittsburgh Medical Center (US), National Kidney and Transplant Institute (PH), Kocaeli Üniversitesi (TR), Istanbul University (TR), Albany Medical Center Hospital (US), Tbilisi State Medical University (GE), Theodor Bilharz Research Institute (EG), Gazi University (TR), Stanford University (US)
Partnerships for the goals
Openalex Percentile: Top 8%
Renal cell carcinoma treatment
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