Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
A Phase 1 Study of INCMGA00012 in Patients With Advanced Solid Tumors
Excerpt:...Patients enrolled to Cohort H (endometrial cancer 500 mg Q4W) must have MSI-H or dMMR endometrial cancer, as determined by a local laboratory using IHC or PCR methods and must also have tissue (fresh or archival) available for central confirmation of diagnosis...
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
Safety and Efficacy of Retifanlimab (INCMGA00012) Alone or in Combination With Other Therapies in Participants With Advanced or Metastatic Endometrial Cancer Who Have Progressed on or After Platinum-based Chemotherapy.
Excerpt:...Tumor tissue tested as MSI-High...
More C2 evidence
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
An Umbrella Study of INCMGA00012 Alone and in Combination With Other Therapies in Participants With Advanced or Metastatic Endometrial Cancer Who Have Progressed on or After Platinum-Based Chemotherapy (POD1UM-204)
Excerpt:...Group A only: Tumor tissue centrally tested as MSI-H.6. ...
Less C2 evidence
Evidence Level:Sensitive: C3 – Early Trials
Title:
755P - Retifanlimab in patients with recurrent microsatellite instability-high (MSI-H) or deficient mismatch repair (dMMR) endometrial cancer: Final results from the POD1UM-101 study (Cohort H)
Excerpt:The overall response rate by ICR was 43% (95% CI: 32–55)….Retifanlimab has shown notable clinical activity in previously treated MSI-H or dMMR endometrial cancer, which is consistent with other checkpoint immunotherapies.
Evidence Level:Sensitive: C3 – Early Trials
Title:
268 A phase 1 study of retifanlimab (INCMGA00012), a PD-1 inhibitor, in patients with advanced solid tumors: preliminary results in recurrent MSI-high or dMMR endometrial cancer (POD1UM-101)
Excerpt:Retifanlimab was generally well tolerated with preliminary evidence of encouraging antitumor activity in MSI-H pretreated advanced endometrial cancer.
DOI:10.1136/jitc-2020-SITC2020.0268