
Of patients enrolled, more than half in each arm are still receiving treatment. Selected clinical characteristics are shown below.
Safety data to date for the Modra 20/20 arm show no incidence of hematologic toxicity, infections, infusion-related reactions, and peripheral neuropathy amongst 14 patients. The 30/20 arm consisting of 20 patients had a 15% incidence of peripheral neuropathy (Grade ½), 15% incidence of thrombocytopenia (Grade ½), 5% incidence of grade 3 neutropenia, 20% incidence of anemia (Grade ½), and no infusion reactions. There was significant GI toxicity with the 30/20 regiment. In contrast, IV docetaxel in 36 patients had had 14% incidence of leukopenia (3% grade 3), 28% incidence of neutropenia (22% Grade 3+), 3% incidence of grade 4 thrombocytopenia and 6% incidence of an infusion reaction. The comparative side effect profiles are illustrated below.
Preliminary efficacy data show that both IV docetaxel and the 20/20 regimen of Modra both have an impact on patient PSA levels, but rPFS data are not yet mature.
The authors of this poster conclude that ModraDoc006 with ritonavir was a convenient drug to take with oral weekly dosing, minimal hematologic and ingestion toxicity relative to IV docetaxel, but clinical efficacy data are not yet mature.
Presented by: Ulka N. Vaishampayan, MBBS, Michigan Medicine, Department of Urology, Oncology Clinic, Rogel Cancer Center.
Written by: Alok Tewari, MD, Ph.D., Medical Oncologist at the Dana-Farber Cancer Institute, at the 2021 American Society of Clinical Oncology Genitourinary Cancers Symposium (#GU21), February 11th-February 13th, 2021