Abstract 1750P
Background
Hepatitis B and C virus (HBV, HCV) reactivations are an emerging problem. Several societies have composed screening guidelines, but HBV reactivation still occurs in daily practice. This survey aims to assess knowledge and awareness of HBV/HCV reactivation in oncologists.
Methods
A questionnaire was designed to assess descriptive variables (i.e., subdiscipline, years of experience, working in an academic center, and having witnessed an HBV reactivation in clinical practice) and nine content questions (four background and five clinically oriented). The survey was disseminated in spring 2022 in 11 hospitals in Belgium (3 university, 8 non-university).
Results
Table: 1750P
Characteristics of responding oncologists
N=64 | % | ||
Subdiscipline | Solid tumours | 33 | 52.4 |
Haematological malignancies | 21 | 33.3 | |
Gastrointestinal tumours | 9 | 14.3 | |
Years of experience | <5 years | 20 | 31.2 |
>5 years | 44 | 68.8 | |
Working in an academic center | Yes | 26 | 40.6 |
No | 38 | 59.4 | |
Already witnessed a HBV reactivation in clinical practice | Yes | 24 | 37.5 |
No | 40 | 62.5 |
The table provides an overview of characteristics of responding oncologists. Mean overall scores were 33.7%, and mean scores for background and clinical questions were 20.3% and 44.4%, respectively. Less than half of participating oncologists was aware of universal HBV screening prior to initiation of chemotherapy (48.4%) and immunosuppression (37.5%). Only 7.8% of them was aware of the high reactivation risk that comes with administration of anthracyclines. Moreover, oncologists that have already witnessed a hepatitis B reactivation in clinical practice, are better aware of hepatitis B screening guidelines prior to administration of chemotherapy (p=0.005) and immunosuppression (p=0.033).
Conclusions
Knowledge of HBV/HCV reactivation is insufficient in oncologists. In addition, HBV screening guidelines prior to initiation of chemotherapy and immunosuppression are poorly implemented, given that over one third of responding oncologists already witnessed an HBV reactivation in clinical practice. Encouragingly, these respondents are also better aware of HBV screening guidelines. Oncology organisations play an important role in raising awareness and providing clear guidance.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Gilead Sciences.
Disclosure
M. Coessens: Financial Interests, Personal, Other, Travel Grant: Gilead Sciences. W. Verlinden: Financial Interests, Personal and Institutional, Research Grant: Gilead Sciences; Financial Interests, Personal, Invited Speaker: Gilead Sciences. J. Schouten: Financial Interests, Personal and Institutional, Research Grant: Gilead Sciences. All other authors have declared no conflicts of interest.
Resources from the same session
1757P - A real-world evaluation of the effectiveness of thermogram along with clinical breast examination in community-based breast cancer screening program
Presenter: Rahul Ravind
Session: Poster session 23
1758P - Body composition meets precision medicine: The prognostic value of sarcopenia in patients (pt) treated with Molecularly Targeted Agents (MTA)
Presenter: Cinta Hierro
Session: Poster session 23
1760P - Systematic review of quality of life (QoL) inclusion among endpoints, reporting and impact of QoL results in phase III non-inferiority trials of systemic treatments in oncology
Presenter: Jessica Paparo
Session: Poster session 23
1761P - Incidence of herpes zoster in cancer patients in Europe: A systematic review
Presenter: Inga Posiuniene
Session: Poster session 23
1762P - Are published data up-to-date? Analysis of time to publication in major oncological journals
Presenter: Pawel Sobczuk
Session: Poster session 23
1763P - The challenge for Cancer Trials Ireland (CTI) to sponsor NCI and non-EU sponsored trials in the EU
Presenter: Eibhlin Mulroe
Session: Poster session 23
1886P - Pembrolizumab and denosumab in clear cell renal cell carcinoma (ccRCC): A phase II trial (KeyPAD, ANZUP1601)
Presenter: Craig Gedye
Session: Poster session 23
1887P - Adjuvant everolimus (EVE) in patients (pts) with completely resected very high-risk renal cell cancer (RCC) and clear cell histology: Results from the phase III SWOG S0931 (EVEREST) trial
Presenter: Primo Lara
Session: Poster session 23
1888P - 24-month follow up of durvalumab and savolitinib combination in MET-driven clear cell and non-clear cell renal cancer
Presenter: Francesca Jackson-Spence
Session: Poster session 23