A Phase 2 interventional study of Pembrolizumab in Endometrial Neoplasms, sponsored by Vall d'Hebron Institute of Oncology. Completed at 7 sites in Spain. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-10-05.
Sponsored by Vall d'Hebron Institute of Oncology · Phase 2, Interventional, and Treatment
This is a non-randomized, single arm, multi-center, phase II study of pembrolizumab in combination with doxorubicin in subjects with recurrent/metastatic endometrial cancer.
Eligible subjects must have had only 1 prior line of systemic platinum-based chemotherapy for advanced, recurrent or metastatic endometrial cancer. Patients who have had 2 or more prior chemotherapeutic regimens for advanced, recurrent, or metastatic endometrial cancer are not allowed.
Note: Prior neoadjuvant or adjuvant chemotherapy included in initial treatment may not be considered first- or later-line treatment unless such treatments were completed less than 6 months prior to the current tumor recurrence. Prior treatment may include chemotherapy, chemotherapy/radiation therapy, and/or consolidation/maintenance therapy.
Prior hormonal treatment is not considered a line of therapy in any setting. Prior targeted therapy no directed against PD-1, PD-L1, PD-L2 pathway or any other immunemodulating mAb (including ipilimumab and any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways) are allowed.
Exclusion Criteria:
Doxorubicin 60 mg/kg IV over 30 minutes on day 1 every 3 weeks up to 9 cycles in combination with Pembrolizumab (MK-3475) 200 mg IV Q3W
Drug: Pembrolizumab
pembrolizumab in combination with doxorubicin
PFS rate at 6 months according to RECIST 1.1 criteria
To evaluate the efficacy of anti-PD1 blockade with pembrolizumab in combination with immunogenic chemotherapy with doxorubicin in patients with recurrent endometrial cancer in terms of patients who survived progression free (PFS) at least 6 months.
Time frame: 6 months
To determine PFS rate at 6 months according to RECIST 1.1 criteria in the different groups by the genomic-The Cancer Genome Atlas (TCGA) classification; namely POLE, MSI, and Microsatellite Stable (MSS)
Time frame: 6 months
To determine median PFS and ORR according to RECIST 1.1 criteria.
PFS, defined as the time from allocation to the first documented disease progression according to RECIST 1.1 or death due to any cause, whichever occurs first. ORR will be used as the primary endpoint per RECIST 1.1 criteria, as assessed by investigators.
Time frame: Through study completion, an average of 3 years
To determine median PFS and ORR according to RECIST 1.1 criteria in different genomic-TCGA subgroups
Time frame: Through study completion, an average of 3 years
To determine median OS and OS rate
Time frame: At 1, and 2-years
To evaluate median OS and OS rate at 1, and 2-years according to genomic-TCGA classification.
Time frame: Through study completion, an average of 3 years
To evaluate DoR, defined as the time from first documented evidence of complete response (CR)or partial response (PR) until disease progression or death due to any cause, whichever occurs first
Time frame: Through study completion, an average of 3 years
Number and grade of AEs, ECIs, SAEs, fatal SAEs, and laboratory changes that are Treatment-Related Adverse Events as Assessed by CTCAE v4.0
Time frame: Through study completion, an average of 3 years
Plan to share: Undecided
No publications or documents are linked to this record.
This study is completed, as verified in Oct 2021. You cannot join it, but the record below documents what was studied.
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Vall d'Hebron Institute of Oncology