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PRIMMO Study Protocol: A Phase II Study Combining PD-1 Blockade, Radiation and Immunomodulation to Tackle Cervical and Uterine Cancer

PRIMMO Study Protocol: A Phase II Study Combining PD-1 Blockade, Radiation and Immunomodulation to Tackle Cervical and Uterine Cancer

Immunotherapeutic approaches have revolutionised oncological practice but in gynaecological malignancies PD-1/PD-L1 blockade monotherapy shows low objective responses (13-17% of patients).

Gynaecological tumours contain an immunosuppressive microenvironment and an altered tumour vasculature. In this study, named PRIMMO, a combination of PD-1 blockade, radiation and immune/environmental-modulating compounds (vitamin D, lansoprazole, aspirin, cyclophosphamide and curcumin) is tested, aiming to tackle the tumour microenvironment and induce anti-tumour immunity. Translational research is performed to discover biomarkers related to the mode of action of the combination.

The publication describes the protocol of this multi-center, open-label, non-randomised, 3-cohort phase 2 study with safety run-in in patients with recurrent/refractory cervical carcinoma, endometrial carcinoma or uterine sarcoma.

Read more about the PRIMMO trial here.

tuyaerts_2019_primmo_study_protocol_-_a_phase_ii_study_combining_pd-1_blockade_radiation_and_immunomodulation.pdf