Purpose: Dedifferentiated melanoma (DedM) poses significant diagnostic chal-lenges. We aimed to investigate the clinical, histopathological and molecular features of DedM. Methylation signature (MS) and copy number profiling (CNP) were carried out in a subgroup of cases.Patients and methods: A retrospective series of 78 DedM tissue samples from 61 patients retrieved from EORTC (European Organisation for Research and Treatment of Cancer) Melanoma Group centres were centrally reviewed. Clinical and histopathological features were retrieved. In a subgroup of patients, genotyping through Infinium Methylation micro -array and CNP analysis was carried out.Results: Most patients (60/61) had a metastatic DedM showing most frequently an un-classified pleomorphic, spindle cell, or small round cell morphology akin to undifferentiated soft tissue sarcoma, rarely associated with heterologous elements. Overall, among 20 suc-cessfully analysed tissue samples from 16 patients, we found retained melanoma-like MS in only 7 tissue samples while a non-melanoma-like MS was observed in 13 tissue samples. In two patients from whom multiple specimens were analysed, some of the samples had a pre-served cutaneous melanoma MS while other specimens exhibited an epigenetic shift towards a mesenchymal/sarcoma-like profile, matching the histological features. In these two patients, CNP was largely identical across all analysed specimens, in line with their common clonal origin, despite significant modification of their epigenome.Conclusions: Our study further highlights that DedM represents a real diagnostic challenge. While MS and genomic CNP may help pathologists to diagnose DedM, we provide proof-of -concept that dedifferentiation in melanoma is frequently associated with epigenetic mod-ifications.(c) 2023 Elsevier Ltd. All rights reserved.

Clinical, histopathological and molecular features of dedifferentiated melanomas: An EORTC Melanoma Group Retrospective Analysis / Hench, Juergen; Mihic-Probst, Daniela; Agaimy, Abbas; Frank, Stephan; Meyer, Peter; Hultschig, Claus; Simi, Sara; Alos, Lucia; Balamurugan, Thiagarajah; Blokx, Willeke; Bosisio, Francesca; Cappellesso, Rocco; Griewank, Klaus; Hadaschik, Eva; van Kempen, Leon C; Kempf, Werner; Lentini, Maria; Mazzucchelli, Luca; Rinaldi, Gaetana; Rutkowski, Piotr; Schadendorf, Dirk; Schilling, Bastian; Szumera-Cieckiewicz, Anna; van den Oord, Joost; Mandalà, Mario; Massi, Daniela. - In: EUROPEAN JOURNAL OF CANCER. - ISSN 1879-0852. - ELETTRONICO. - 187:(2023), pp. 7-14. [10.1016/j.ejca.2023.03.032]

Clinical, histopathological and molecular features of dedifferentiated melanomas: An EORTC Melanoma Group Retrospective Analysis

Simi, Sara;Massi, Daniela
2023

Abstract

Purpose: Dedifferentiated melanoma (DedM) poses significant diagnostic chal-lenges. We aimed to investigate the clinical, histopathological and molecular features of DedM. Methylation signature (MS) and copy number profiling (CNP) were carried out in a subgroup of cases.Patients and methods: A retrospective series of 78 DedM tissue samples from 61 patients retrieved from EORTC (European Organisation for Research and Treatment of Cancer) Melanoma Group centres were centrally reviewed. Clinical and histopathological features were retrieved. In a subgroup of patients, genotyping through Infinium Methylation micro -array and CNP analysis was carried out.Results: Most patients (60/61) had a metastatic DedM showing most frequently an un-classified pleomorphic, spindle cell, or small round cell morphology akin to undifferentiated soft tissue sarcoma, rarely associated with heterologous elements. Overall, among 20 suc-cessfully analysed tissue samples from 16 patients, we found retained melanoma-like MS in only 7 tissue samples while a non-melanoma-like MS was observed in 13 tissue samples. In two patients from whom multiple specimens were analysed, some of the samples had a pre-served cutaneous melanoma MS while other specimens exhibited an epigenetic shift towards a mesenchymal/sarcoma-like profile, matching the histological features. In these two patients, CNP was largely identical across all analysed specimens, in line with their common clonal origin, despite significant modification of their epigenome.Conclusions: Our study further highlights that DedM represents a real diagnostic challenge. While MS and genomic CNP may help pathologists to diagnose DedM, we provide proof-of -concept that dedifferentiation in melanoma is frequently associated with epigenetic mod-ifications.(c) 2023 Elsevier Ltd. All rights reserved.
2023
187
7
14
Hench, Juergen; Mihic-Probst, Daniela; Agaimy, Abbas; Frank, Stephan; Meyer, Peter; Hultschig, Claus; Simi, Sara; Alos, Lucia; Balamurugan, Thiagarajah; Blokx, Willeke; Bosisio, Francesca; Cappellesso, Rocco; Griewank, Klaus; Hadaschik, Eva; van Kempen, Leon C; Kempf, Werner; Lentini, Maria; Mazzucchelli, Luca; Rinaldi, Gaetana; Rutkowski, Piotr; Schadendorf, Dirk; Schilling, Bastian; Szumera-Cieckiewicz, Anna; van den Oord, Joost; Mandalà, Mario; Massi, Daniela
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1331933
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