RecruitingPhase 1NCT05819892

Phase I Trial Testing the Safety and Tolerability of Chemoradiation Followed by Chemotherapy + Dostarlimab for Stage IIIC, Node Positive, Endometrial Cancer


Sponsor

M.D. Anderson Cancer Center

Enrollment

21 participants

Start Date

Jul 17, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

To learn if chemotherapy given in combination with radiation therapy, followed by maintenance therapy, can help to control endometrial cancer. The safety and effects of this study treatment will also be studied


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This phase I trial tests a new treatment approach for women with advanced endometrial cancer (cancer of the uterine lining) that has spread to lymph nodes. The study combines chemoradiation (chemotherapy given alongside radiation) with additional chemotherapy afterward, to find the safest doses and assess tolerability of this combined regimen. **You may be eligible if...** - You have been diagnosed with stage IIIC endometrial cancer confirmed by surgical staging - You have had a complete hysterectomy and lymph node removal - You are eligible to receive chemoradiation followed by chemotherapy - You are in good enough health to undergo treatment (ECOG 0–2) **You may NOT be eligible if...** - Your cancer has spread beyond lymph nodes (e.g., to organs like liver or lungs) - You have serious heart, liver, or kidney problems - You have had prior radiation to the abdomen or pelvis - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPaclitaxel

Given by IV (vein)

DRUGCarboplatin

Given by IV (vein)

DRUGDostarlimab

Given by IV (vein)

DRUGCisplatin

Given by IV (vein)


Locations(1)

M D Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT05819892


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