Sacituzumab Tirumotecan (MK-2870) in Post Platinum and Post Immunotherapy Endometrial Cancer (MK-2870-005)
Endometrial CancerResearchers are looking for new ways to treat people with endometrial cancer (EC) who have previously received treatment with platinum based therapy (a type of chemotherapy) and immunotherapy. Immunotherapy is a treatment that helps the immune system fight cancer. This clinical study will compare MK-2870 sacituzumab tirumotecan to chemotherapy. The goal of the study is to learn if people who receive MK-2870 sacituzumab tirumotecan live longer overall and without the cancer getting worse compared to people who receive chemotherapy.
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Participation Requirements
-
Sex:
FEMALE -
Eligible Ages:
18 and up
Participation Criteria
The main inclusion and exclusion criteria include but are not limited to the following:
Inclusion Criteria:
* Has a histologically-confirmed diagnosis of endometrial carcinoma or carcinosarcoma.
* Has radiographically evaluable disease, either measurable or nonmeasurable per response evaluation criteria in solid tumors (RECIST 1.1), as assessed by blinded independent central review (BICR).
* Has received prior platinum-based chemotherapy and anti-programmed cell death 1 protein (PD-1)/anti- programmed cell death ligand 1 (PD-L1) therapy, either separately or in combination.
Exclusion Criteria:
* Has neuroendocrine tumors or endometrial sarcoma, including stromal sarcoma, leiomyosarcoma, adenosarcoma, or other types of pure sarcomas
* Has a history of documented severe dry eye syndrome, severe Meibomian gland disease and/or blepharitis, or severe corneal disease that prevents/delays corneal healing
* Has active inflammatory bowel disease requiring immunosuppressive medication or previous history of inflammatory bowel disease
* Has had a recurrence of endometrial carcinoma or carcinosarcoma more than \>12 months after completing platinum-based therapy administered in the curative-intent setting without any additional platinum-based therapy received in the recurrent setting. Note: 1) If Immunotherapy-based treatment is administered in the recurrent setting, then platinum rechallenge is not required, regardless of the duration of the platinum-free interval from time of adjuvant therapy 2) For Stage IVb disease, treatment that includes gynecological surgery followed by a platinum-based regimen is NOT considered curative-intent per protocol and does not require platinum rechallenge in the recurrent setting, regardless of the duration of the platinum-free interval
* Has received more than 3 prior lines of therapy for endometrial carcinoma or carcinosarcoma
* Has history of (noninfectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease
* Has received prior treatment with single-agent nonplatinum based chemotherapy in the third-line setting
* Has received prior treatment with a trophoblast cell surface antigen 2 (TROP2)-targeted antibody drug conjugate (ADC) (eg, sacituzumab govitecan)
* Has received prior treatment with a topoisomerase I inhibitor-containing ADC (eg, sacituzumab govitecan or fam-trastuzumab deruxtecan-nxki)
* Has previously received both single-agent paclitaxel and single-agent doxorubicin in any setting for prior treatment of endometrial cancer
Study Location
BC Cancer Vancouver ( Site 1415)
BC Cancer Vancouver ( Site 1415)Vancouver, British Columbia
Canada
Contact Study Team
Study Coordinator
6048776000 x 674634Centre Hospitalier de l'Université de Montréal ( Site 1403)
Centre Hospitalier de l'Université de Montréal ( Site 1403)Montréal, Quebec
Canada
Contact Study Team
Study Coordinator
514-890-8000Cross Cancer Institute ( Site 1414)
Cross Cancer Institute ( Site 1414)Edmonton, Alberta
Canada
Contact Study Team
Study Coordinator
7804328560CIUSSS de l'Est-de-l'Île-de-Montréal ( Site 1405)
CIUSSS de l'Est-de-l'Île-de-Montréal ( Site 1405)Montreal, Quebec
Canada
Contact Study Team
Study Coordinator
5142523400Trillium Health Partners - Credit Valley Hospital ( Site 1410)
Trillium Health Partners - Credit Valley Hospital ( Site 1410)Mississauga, Ontario
Canada
Contact Study Team
Study Coordinator
9058131100x5135McGill University Health Centre ( Site 1404)
McGill University Health Centre ( Site 1404)Montréal, Quebec
Canada
Contact Study Team
Study Coordinator
514-934-1934 ext. 34049Arthur J.E. Child Comprehensive Cancer Centre ( Site 1413)
Arthur J.E. Child Comprehensive Cancer Centre ( Site 1413)Calgary, Alberta
Canada
Contact Study Team
Study Coordinator
403 521-3921CIUSSS- saguenay-Lac-Saint-Jean ( Site 1408)
CIUSSS- saguenay-Lac-Saint-Jean ( Site 1408)Chicoutimi, Quebec
Canada
Contact Study Team
Study Coordinator
41854112342707- Study Sponsored By
- Merck Sharp & Dohme LLC
- Participants Required
- More Information
- Study ID:
NCT06132958