Abstract 613P
Background
Physicians have frequent interactions with the pharmaceutical industry (pharma), however, there is concern for possible corporate influence on physicians’ prescribing behaviours. We sought to understand perceptions and interactions between pharma and medical oncologists (MO), in comparison with infectious diseases (ID) physicians.
Methods
We conducted an anonymous online cross-sectional survey of Australian MO and ID physicians comparing self-reported interactions and attitudes with pharma. An additional survey was undertaken at Tan Tock Seng Hospital, Singapore.
Results
A total of 204 Australian and Singaporean physicians were surveyed including 102 oncologists and 102 ID physicians. Demographics including age, gender and years of practice between the two Australian specialties were similar, with an exception that most ID physicians had mainly public work (95% vs. 78% for oncologists, p<0.001). Oncologists had more frequent contact with pharma, the majority (69%) negotiating compassionate access for patients on a monthly/annual basis, compared with ID physicians who had never done so (45%), p<0.001. More ID physicians had never attended a sponsored meeting (15% ID vs. 27% MO respectively, p=0.01) or received travel/accommodation grants from pharma (42% ID vs. 85% MO respectively, p<0.001). However, most physicians (92%) had never received gifts from pharma, with no difference between groups (p=0.17). Most Australian oncologists believed that interacting with pharma was overall beneficial for patient care (78%) compared to ID physicians (34%, p<0.001). This statement was shared by 71% of Singaporean oncologists. Similar rates of Australian oncologists and ID physicians (83% vs. 88%, respectively) felt comfortable for patients to know the details of their interactions with pharma, however, only 57% of Singaporean oncologists agreed with this statement. Most Australian respondents (77%) agreed that there was strong public skepticism of these interactions (p=0.35).
Conclusions
Medical oncologists had more interactions with pharma than ID physicians and were more likely to believe that this was overall beneficial to patient care despite the negative public perception associated with this.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
P.L. Chia: Financial Interests, Personal, Advisory Board: Merck, Roche, Pfizer, Amgen; Financial Interests, Institutional, Research Funding: Merck, Roche, Pfizer, Amgen. T. John: Financial Interests, Personal, Invited Speaker, Speaker tour Vietnam: AstraZeneca; Financial Interests, Personal, Invited Speaker, CTIO: Merck Sharp Dohme; Financial Interests, Personal, Advisory Board: BMS, AstraZeneca, Bayer, Specialised Therapeutics; Financial Interests, Institutional, Advisory Board: Roche, Novartis, Pfizer, Amgen, Takeda, PharmaMar; Financial Interests, Personal, Other, Speaker/Chair: ACE Oncology. All other authors have declared no conflicts of interest.
Resources from the same session
280P - Radium-223 for patients with metastatic castration-resistant prostate cancer with symptomatic bone metastases progressing after first-line abiraterone or enzalutamide: One institutional experience
Presenter: Keng Man Chiang
Session: Poster Display
Resources:
Abstract
281P - 10-year treatment outcome of prostate cancer patients with 3D conformal radiation: Experience of a single cancer institution in Iran
Presenter: Reyhane Bayani
Session: Poster Display
Resources:
Abstract
282P - Predictors of outcomes in patients with clinically lymph node-positive prostate cancer after definitive radiotherapy
Presenter: Jae-Sung Kim
Session: Poster Display
Resources:
Abstract
283P - Radiotherapy utilization rate and treatment patern of protate cancer at Cipto Mangunkusumo Central General Hospital (RSCM): What we learn from pre-pandemic era
Presenter: Riyan Apriantoni
Session: Poster Display
Resources:
Abstract
284TiP - CYCLONE 3: A phase III, randomized, double-blind, placebo-controlled study of abemaciclib in combination with abiraterone plus prednisone in men with high-risk metastatic hormone-sensitive prostate cancer
Presenter: Nobuaki Matsubara
Session: Poster Display
Resources:
Abstract
292P - Comparative characteristics of early cervical cancer diagnosis methods for Tashkent women
Presenter: Gulnoza Goyibova
Session: Poster Display
Resources:
Abstract
293P - Carboplatin in locally advanced cervical cancer treated with chemoradiation: An alternative to cisplatin
Presenter: Natalia Isabel Valdiviezo Lama
Session: Poster Display
Resources:
Abstract
294P - Concurrent chemoradiation with cisplatin every 3 weeks in locally advanced cervical cancer: A single arm phase II clinical trial
Presenter: Long Nguyen
Session: Poster Display
Resources:
Abstract
295P - A prospective study of dose escalated simultaneous integrated boost in node-positive cervical cancer
Presenter: Ritusha Mishra
Session: Poster Display
Resources:
Abstract
296P - Safety, efficacy, and immunogenicity of therapeutic vaccines for patients with high-grade cervical intraepithelial neoplasia (CIN 2/3) associated with human papillomavirus: A systematic review
Presenter: Caroline Amélia Gonçalves
Session: Poster Display
Resources:
Abstract