GOG-3119 (MK2870-033): Randomized, Open-Label Study to Compare the Efficacy and Safety of Sacituzumab Tirumotecan in Combination with Pembrolizumab Versus Pembrolizumab Alone as First-Line Maintenance Treatment in Pts with pMMR Endometrial Cancer
Disease: Endometrial Cancer
Eligibility Criteria: None
NCT: 06952504
Inclusion:
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Advanced (Stage III/IV) or recurrent endometrial cancer
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pMMR
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Measurable Stage III; Measurable or Non-Measurable Stage IV or recurrent (ALL STAGES MUST HAVE EVALUABLE DISEASE ON SCANS)
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May have 1 prior line of systemic platinum-based adjuvant and/or neoadjuvant chemo in the setting of curative intent. This may have been given as treatment involving chemo alone, concurrent chemoradiation or as part of a sequential approach such as in a regimen involving concurrent chemoradiation followed by chemo
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May have received prior radiation with or without radiosensitizing chemo if ˃2 weeks before the start of induction chemo
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Unlimited number of prior hormone tx lines
Exclusion:
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Carcinosarcoma, neuroendocrine or sarcoma
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Known POLE mutation
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dMMR
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Is a candidate for curative-intent surgery or radiotherapy
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Prior anti-PD-1/L1/L2 or agent directed to another stimulatory or coinhibitory T-cell receptor (ie CTLA-4); Prior Trop2 ADC
Requirements:
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Pts must be advised to avoid tobacco and alcohol
Have questions about participation?
Our clinical research team is happy to answer questions about eligibility, the study process, or next steps.
Contact the Research Team