SMARCA4-deficient dedifferentiated ovarian carcinoma with rapid progression during adjuvant platinum-based chemotherapy: a case report and implications for molecular-driven treatment strategies

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Publikace nespadá pod Pedagogickou fakultu, ale pod Lékařskou fakultu. Oficiální stránka publikace je na webu muni.cz.
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BEDNAŘÍKOVÁ Markéta HAUSNEROVÁ Jitka POKORNÁ Petra FELSINGER Michal RICHTER Svatopluk EHRLICHOVÁ Lucie ORLÍČKOVÁ Jana MINÁŘ Luboš SLABÝ Ondřej WEINBERGER Vít

Rok publikování 2025
Druh Článek v odborném periodiku
Časopis / Zdroj THERAPEUTIC ADVANCES IN MEDICAL ONCOLOGY
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://journals.sagepub.com/doi/10.1177/17588359251376858
Doi https://doi.org/10.1177/17588359251376858
Klíčová slova case report; dedifferentiated ovarian carcinoma; personalized treatment; SLFN11; SMARCA4; SWI/SNF chromatin remodeling complex
Přiložené soubory
Popis Dedifferentiated ovarian carcinomas (DDOC) are rare and aggressive malignancies characterized by a mixture of differentiated and undifferentiated tumor components, often associated with poor prognosis. This case report describes a 55-year-old woman initially diagnosed with early-stage high-grade endometrioid ovarian carcinoma who experienced rapid disease progression during adjuvant platinum-based chemotherapy, culminating in death within 4 months. Retrospective molecular analyses revealed pathogenic variants in the SMARCA4 gene, leading to a revised diagnosis of DDOC. The tumor exhibited resistance to conventional chemotherapy, highlighting the challenges associated with managing this aggressive tumor subtype. In our case, molecular profiling identified two potentially targetable alterations: biallelic SMARCA4 loss and a pathogenic PIK3CA mutation, both of which may inform future therapeutic strategies. This case underscores the importance of integrating molecular diagnostics into routine practice for accurate classification and highlights the urgent need for personalized treatment strategies, including targeted and immunotherapy options, for this formidable tumor subtype.
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