Přehled o publikaci
2025
Genomic complexity and evolution of high-grade serous ovarian cancer treated with platinum-based chemotherapy: advancing precision oncology beyond BRCA1/BRCA2
POKORNÁ, Petra; Jana ORLÍČKOVÁ; Táňa MACHÁČKOVÁ; Jitka HAUSNEROVÁ; Lucie EHRLICHOVÁ et al.Basic information
Original name
Genomic complexity and evolution of high-grade serous ovarian cancer treated with platinum-based chemotherapy: advancing precision oncology beyond BRCA1/BRCA2
Authors
POKORNÁ, Petra; Jana ORLÍČKOVÁ; Táňa MACHÁČKOVÁ; Jitka HAUSNEROVÁ; Lucie EHRLICHOVÁ; Robin JUGAS; Eliška HLOUŠKOVÁ; Alena HOMOLOVÁ; Sára VILMANOVÁ; Júlia BOHOŠOVÁ; Kamila SOUČKOVÁ; Marek SVOBODA; Vít WEINBERGER; Ondřej SLABÝ and Markéta BEDNAŘÍKOVÁ
Edition
JOURNAL OF OVARIAN RESEARCH, LONDON, BMC, 2025, 1757-2215
Other information
Language
English
Type of outcome
Article in a journal
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
is not subject to a state or trade secret
References:
Marked to be transferred to RIV
No
Organization
Lékařská fakulta – Repository – Repository
UT WoS
EID Scopus
Keywords in English
Ovarian cancer; High-grade serous ovarian carcinoma; Comprehensive genomic profiling; Targeted treatment
Links
LX22NPO5102, research and development project. NU21-03-00306, research and development project.
Changed: 17/1/2026 00:51, RNDr. Daniel Jakubík
Abstract
In the original language
Background High-grade serous ovarian carcinoma (HGSOC) remains one of the most lethal gynecologic malignancies due to its aggressive nature, frequent late-stage diagnosis, and the development of treatment resistance. Although platinum-based chemotherapy remains the cornerstone of therapy, the underlying genomic heterogeneity complicates the prediction of treatment response and the development of effective therapies. Results We performed comprehensive genomic profiling of 523 cancer-associated genes using the TruSight Oncology 500 HT panel in a retrospective cohort of 42 HGSOC patients, including 22 platinum-sensitive (Pt-S) and 20 primary platinum-resistant (Pt-R) cases. In 14 cases, paired tumor samples collected before and after recurrence or neoadjuvant chemotherapy were analyzed to assess the changes in clinically relevant and actionable alterations. Genomic profiling revealed significant heterogeneity in molecular alterations between Pt-S and Pt-R tumors, with CCNE1 amplification confirmed as more frequent in Pt-R cases. Actionable findings ranked in ESCAT tiers I-III were identified in 54.5% and 55% of Pt-S and Pt-R patients, respectively. A total of 18% and 20% of patients harbored tier III hypothetical targets, highlighting opportunities for future targeted therapies in HGSOC. Analysis of paired samples demonstrated dynamic genomic changes, with 60% of Pt-S and 44% of Pt-R patients exhibiting shifts that could affect therapeutic actionability. Conclusions Our findings highlight the importance of comprehensive genomic profiling in HGSOC management. While platinum-based chemotherapy remains central to treating newly diagnosed and recurrent disease, its molecular complexity might require more personalized strategies. Beyond established markers such as BRCA1/2, additional genomic changes present opportunities to expand therapeutic options. The evolving tumor genomic landscape further underscores the need for repeated biopsies or alternative methods to assess tumor evolution, enabling more adaptive and individualized treatment approaches.