Abstract 223P
Background
Given the multiple treatment choices for advanced renal cell carcinoma (RCC), it is important to understand the treatment preferences of patients and physicians for the treatment of advanced RCC. This study aimed to understand patients’ and physicians’ preferences that influence their treatment choices for advanced RCC.
Methods
Qualitative interviews were conducted for 16 physicians and 10 advanced RCC patients in South Korea, Australia, Hong Kong and Taiwan. Physicians and patients each ranked 36 attributes related to treatment efficacy, side effects and mode of administration (score, 1-10) in terms of their preference for the treatment of advanced RCC. The scores of the top 10 attributes were aggregated among physicians and among patients to derive the overall score.
Results
For attributes related to treatment efficacy, physicians ranked years of survival (score =78), progression-free survival (score =78) and overall survival at 1 year (score =71) as most important, while patients ranked progression-free survival (score =54), years of survival (score =45), and duration of response (score =39) as most important. For attributes related to treatment side effects, physicians ranked grade 3 or 4 pneumonitis (score =40), chance of admission due to treatment side effects (score =37) and grade 3 or 4 gastrointestinal perforation (score = 33) as most important, while patients ranked grade 3 or 4 chronic kidney disease (score = 20), grade 3 or 4 myelosuppression (score =19) and chance of admission due to treatment side effects (score =17) as most important. The attributes prioritized by physicians did not differ by favourable vs intermediate/poor risk patient groups. Physicians and patients did not rank attributes related to mode of administration within the top 10.
Conclusions
Physicians and patients have slightly different preferences while making treatment choices. This study demonstrates that physicians and patients prioritized attributes related to treatment efficacy compared to side effects. A more effective dialogue between HCP and patient is needed to help decision-making in selecting the most appropriate treatment for advanced RCC.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
IQVIA Solutions Asia Pte. Ltd.
Funding
MSD International GmbH, Singapore Branch.
Disclosure
N. Oliveira, B.C.W. Li, M. Kim, I. Park, Y. Su, C.K. Yang, A. Zhang, K.C.W. Wong: Financial Interests, Personal, Advisory Board: MSD. A. Dsouza: Financial Interests, Personal, Full or part-time Employment: MSD Singapore. S. Chua, E.M. Tan: Financial Interests, Personal, Full or part-time Employment, Commissioned to carry out this study (IQVIA): IQVIA Asia Pacific, Singapore. C. Spiteri: Financial Interests, Personal, Full or part-time Employment: MSD Australia.
Resources from the same session
561P - Mechanisms of osimertinib resistance using circulating tumor DNA analyses for EGFR-mutated non-small cell lung cancer, results from ELUCIDATOR: A prospective observational multicenter study
Presenter: Daijiro Harada
Session: Poster Display
Resources:
Abstract
562P - First-line (1L) osimertinib (osi) ± platinum-pemetrexed in patients (pts) with EGFRm advanced NSCLC: FLAURA2 China cohort
Presenter: Yan Yu
Session: Poster Display
Resources:
Abstract
563P - Real-world effectiveness and safety of first-line osimertinib for EGFR-mutated advanced NSCLC in China (FLOURISH study)
Presenter: Jianya Zhou
Session: Poster Display
Resources:
Abstract
564P - Co-occurring EGFR p.E709X mutation affects the treatment response to the third-generation EGFR-TKIs in EGFR p.G719X-mutant patients with advanced NSCLC
Presenter: Wen Feng Fang
Session: Poster Display
Resources:
Abstract
565P - Genome-guided targeted therapy combination improves survival in patients with advanced EGFR mutation positive NSCLC failing osimertinib
Presenter: Molly Li
Session: Poster Display
Resources:
Abstract
566P - Safety of tepotinib + osimertinib in EGFR-mutant NSCLC with MET amplification after first-line osimertinib
Presenter: Chong Kin Liam
Session: Poster Display
Resources:
Abstract
567P - Furmonertinib in combination with bevacizumab and intrathecal chemotherapy as later-line re-challenge treatment in EGFR –mutated NSCLC patients with leptomeningeal metastasis after third-generation EGFR-TKIs treatment failure
Presenter: Fang Cun
Session: Poster Display
Resources:
Abstract
568P - First-line (1L) osimertinib + platinum-pemetrexed in EGFR-mutated (EGFRm) advanced NSCLC: Updated FLAURA2 safety run-in (SRI) results
Presenter: David Planchard
Session: Poster Display
Resources:
Abstract
569P - Whole-transcriptome sequencing of transformed small-cell lung cancer from EGFR-mutated lung adenocarcinoma reveals LUAD–like and SCLC–like subsets
Presenter: Chan-Yuan Zhang
Session: Poster Display
Resources:
Abstract
570P - First-line osimertinib for patients with advanced NSCLC harboring EGFR mutations: A real-world study
Presenter: Wenxiang Ji
Session: Poster Display
Resources:
Abstract