Synapse - Clinicopathologic characteristics and clinical outcomes of patients with testicular mesothelioma

Clinicopathologic characteristics and clinical outcomes of patients with testicular mesothelioma Journal Article

Authors:	Agrawal, P.; Baky, F.; Sarungbam, J.; Sheinfeld, J.; Reuter, V. E.; Cercek, A.; Nash, G. M.; Sauter, J. L.; Travis, W. D.; Simone, C. B. 2nd; Bosl, G. J.; Zauderer, M. G.; Matulewicz, R. S.; Offin, M.
Article Title:	Clinicopathologic characteristics and clinical outcomes of patients with testicular mesothelioma
Abstract:	BackgroundMesothelioma of the tunica vaginalis testes (testicular mesothelioma [TM]) is a rare tumor, comprising less than 5% of mesotheliomas. Surgical intervention is the current standard of care, whereas the role of systemic therapies remains undefined.MethodsWe retrospectively reviewed 36 patients with pathologically confirmed TM treated at Memorial Sloan Kettering Cancer Center (MSK) between January 1996 to May 2023. Clinicopathologic data, treatments received, and clinical outcomes were reported. Surgical pathology samples, when available, underwent next-generation sequencing (NGS) using MSK-IMPACT. Overall survival (OS) was calculated by using the Kaplan-Meier method.ResultsMedian age at diagnosis was 64 years (range 24-93). Histologically, 22 (61%) tumors were epithelioid, ten (28%) were biphasic, three (8%) were sarcomatoid, and one (3%) was unable to be further classified. Ten patients (28%) had metastatic disease at initial diagnosis, and 13 more (36%) eventually developed metastatic disease. Orchiectomy was performed in 34 (94%) patients and retroperitoneal lymph node dissection (RPLND) in 12 (33%); 15 (42%) received systemic therapy and five (14%) radiation therapy. Ten samples underwent somatic NGS: five (50%) had CDKN2A/B, four (40%) had NF2, and two (20%) had BAP1 alterations. At a median follow up of 3.5 years, median OS was 4.5 years.ConclusionsThis is the largest single-institution series and genomic dataset for TM. We report unique clinicopathologic and genomic features that distinguish TM from other mesotheliomas, including a lower frequency of BAP1 alterations. Owing to the rarity of this disease, further refinement of the sequence and necessity of surgical and systemic treatment is necessary.
Keywords:	orchiectomy; management; malignant pleural mesothelioma; epithelioid; rare tumor; testicular mesothelioma; non-epithelioid; tunica vaginalis testis
Journal Title:	Annals of Surgical Oncology
ISSN:	1068-9265
Publisher:	Springer
Publication status:	Online ahead of print
Date Published:	2025-07-30
Online Publication Date:	2025-07-30
Language:	English
ACCESSION:	WOS:001539861100001
DOI:	10.1245/s10434-025-17978-3
PROVIDER:	wos
PUBMED:	40739067
Notes:	Article; Early Access -- MSK Cancer Center Support Grant (P30 CA008748) acknowledged in PubMed and PDF -- MSK corresponding author is Michael Offin -- Source: Wos