Treatment Exposure-Adjusted Event Rates (EAERs) for Grade 3/4 AEs Associated with Emerging and Existing Systemic Therapies for mCRC with at Least 2 Prior Lines of Therapy: Informing Payer and Pathway Formulary Decision Making
Speaker(s)
Howe A1, Hernandez LG1, Paly V1, Eng C2, Dasari A3, Samuel L4, Kasper S5, Tougeron D6
1Takeda Pharmaceuticals America, Inc., Lexington, MA, USA, 2Division Hematology and Oncology, Vanderbilt-Ingram Cancer Center, Nashville, TN, USA, 3Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA, 4Aberdeen Royal Infirmary, Aberdeen, UK, 5West German Cancer Center, Department of Medical Oncology, University Hospital Essen, Essen, Germany, 6Department of Hepato-Gastroenterology, Poitiers University Hospital and University of Poitiers, Poitiers, France
Presentation Documents
OBJECTIVES: To characterize grade 3/4 adverse event (AE) rates associated with fruquintinib, regorafenib, trifluridine/tipiracil (T/T), and trifluridine/tipiracil+bevacizumab (T/T+bev) for previously treated – with at least two prior lines – metastatic colorectal cancer (mCRC) using drug exposure-adjusted event rates (EAERs) to inform payer formulary and pathway decisions.
METHODS: Grade 3/4 AEs occurring in at least 5% of patients for any treatment in an individual trial were identified from Phase III randomized clinical trial publications FRESCO and FRESCO-2 for fruquintinib (N=734), RECOURSE and SUNLIGHT for T/T (N=779), CORRECT for regorafenib (N=500), and SUNLIGHT for T/T+bev (N=246). Treatment durations reported in the same clinical trials were converted to total treatment days (1 month = 30.325 days). AE incidence rates were then calculated to reflect an occurrence per 100 and per 1,000 treatment-days for each treatment.
RESULTS: Grade 3/4 AE occurring in at least 5% of patients for any treatment included: anemia, asthenia, diarrhea, fatigue, hand foot syndrome, hypertension, leukopenia, neutropenia, rash, thrombocytopenia, and laboratory abnormalities (increased alanine aminotransferase, alkaline phosphatase level, aspartate aminotransferase, and total bilirubin). EAERs per 1,000 patient-days of treatment exposure were estimated to be 3.87 for fruquintinib, 17.33 for T/T, 16.70 for regorafenib and 4.19 for T/T+bev treatment arms. EAERs per 100 patient-days treatment exposure were estimated to be 0.387 for fruquintinib, 1.733 for T/T, 1.670 for regorafenib and 0.419 for T/T+bev treatment arms.
CONCLUSIONS: Patients with mCRC previously treated with at least two prior lines of therapy experienced lower treatment EAERs associated with grade 3/4 AEs when treated with fruquintinib vs. other treatment options. Population health and healthcare plans decision makers may consider the use of EAERS of as an additional quantification measure when reviewing formulary and pathway choices of emerging and existing systemic therapies for patients with mCRC.
Code
CO170
Topic
Clinical Outcomes, Health Policy & Regulatory
Topic Subcategory
Clinical Outcomes Assessment, Insurance Systems & National Health Care
Disease
No Additional Disease & Conditions/Specialized Treatment Areas, Oncology