Sacituzumab govitecan in heavily pretreated, platinum-resistant high grade serous ovarian cancer

•Treatment of recurrent platinum-resistant high grade serous ovarian cancer remains a challenge.•A patient with recurrent HGSOC that failed several lines of chemotherapy had a durable response to sacituzumab govitecan.•Sacituzumab govitecan may represent an effective treatment for recurrent platinum...

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Veröffentlicht in:Gynecologic oncology reports 2024-08, Vol.54, p.101459, Article 101459
Hauptverfasser: Greenman, Michelle, Bellone, Stefania, Demirkiran, Cem, Max Philipp Hartwich, Tobias, Santin, Alessandro D.
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Sprache:eng
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Zusammenfassung:•Treatment of recurrent platinum-resistant high grade serous ovarian cancer remains a challenge.•A patient with recurrent HGSOC that failed several lines of chemotherapy had a durable response to sacituzumab govitecan.•Sacituzumab govitecan may represent an effective treatment for recurrent platinum-sensitive HGSOC. Treatment of recurrent platinum-resistant high grade serous ovarian cancer (HGSOC) remains a challenge. Novel treatment options for recurrent disease are an unmet need. A 69-year-old with recurrent, metastatic, platinum-resistant HGSOC overexpressing TROP2 experienced a significant response to the antibody-drug conjugate (ADC) sacituzumab govitecan after multiple failed lines of chemotherapy and targeted treatment. Following sacituzumab govitecan treatment she experienced a confirmed partial response as well as a return of CA-125 to baseline. Having now completed 8 cycles (ie, over 6 months of treatment), her disease continues to demonstrate a response to sacituzumab govitecan treatment. The ADC has been well tolerated at a dose of 10 mg/kg with no dose-limiting toxicity or need for dose reductions. Sacituzumab govitecan may represent a treatment option for platinum-resistant/recurrent HGSOC that have previously failed prior lines of chemotherapy. Clinical trials with sacituzumab govitecan in platinum-resistant ovarian cancer patients are currently ongoing (https://classic.clinicaltrials.gov/ct2/show/NCT06028932).
ISSN:2352-5789
2352-5789
DOI:10.1016/j.gore.2024.101459