Methods
This study used deidentified data from electronic medical records and claims from the ConcertAI RWD360 oncology dataset. Patients diagnosed with CCA and with evidence of initial treatment with pemigatinib or futibatinib in 2023 or later were included, with the first FGFR inhibitor as the index treatment. Patient characteristics and treatment patterns pre- and post-index were examined. Adverse medical events of interest (MEI) were identified with ICD codes. Kaplan-Meier analyses were used to describe the real-world time to discontinuation (rwTTD) and time to next treatment or death (rwTTNTD) from the index date.
Results
This study included 50 futibatinib and 55 pemigatinib patients. Overall, patient characteristics were similar across the two treatment groups (Table 1). The most common treatment regimen before index was cisplatin + gemcitabine + durvalumab (pemigatinib patients 38%, futibatinib patients 28%). Approximately 15% of patients in both groups received a subsequent line of therapy after the index treatment. Occurrence of any adverse MEI during the index treatment was similar in pemigatinib (33%) and futibatinib (28%) patients (p = 0.60); the most common MEI for pemigatinib and futibatinib patients were fatigue (18% and 12%, respectively) and diarrhea (5% and 12%, respectively). Other MEIs, including retinal pigment epithelial detachment, nail disorders, Palmar-Plantar erythrodysesthesia, dry eye, etc., were less common. Patients treated with futibatinib and pemigatinib had similar median rwTTD (2.9 vs 3.1 months, respectively) and rwTTNTD (5.7 vs 5.4 months, respectively).
Conclusions
Overall, patient demographics, prior treatment regimens, and adverse MEI were similar across the two treatment groups. Patients treated with futibatinib and pemigatinib demonstrated comparable real-world treatment pattern characteristics. Additional comprehensive analysis on survival outcomes and safety profile will be performed when a larger sample size is available.