Abstract 1179P
Background
Recent reports have been shown an increased risk of de-novo malignancies in liver transplant recipients (LTRs) which is reported to be a leading cause of mortality in these patients. The aim of this systematic review and meta-analysis was to assess the prevalence of skin cancer in LTRs.
Methods
We systematically searched in five databases till 20th April 2023 through the search term ("liver transplantation" OR "liver transplant") AND ("skin cancer" OR "melanoma" OR "squamous cell carcinoma" OR "non-melanoma skin cancer" OR "post-transplant cancer" OR "post transplant cancer"). We used random effect model to overcome the significant heterogeneity we observed.
Results
A total of 34 studies, with 147154 LTRs were included. The pooled prevalence of skin cancer (all types) was 4.8% (95%confidence interval (CI): 3.6-6.5). Subgroup analysis based upon the follow up duration of each study, indicated that skin cancer prevalence increased with long duration of follow up: 0-4 years, 2.4% (95%CI: 0.5-9.9), 4-8 years, 4.2% (95%CI 2.9-6.2), and >8 years, 7.6% (95%CI: 4.7-12). Australia followed by South America had the highest prevalence of skin cancer, 20.6% (95%CI: 12.9-31.3), and 9.4% (95%CI: 5.8-14.8), in order; while Asia had the lowest prevalence 0.4% (95%CI: 0-3.8). The most common type of skin cancers was non-melanoma skin cancer reported as a combined type with a prevalence of 2.9% (95%CI: 1.1-6.9), followed by squamous cell carcinoma, basal cell carcinoma and Bowen’s cancer, 2.5% (95%CI: 1.4-4.4), 2.5% (95%CI: 1.5-4.1) and 0.8% (95%CI: 0.2-3.2), in order.
Conclusions
Consistent with what it has been reported for other organ transplants, the results from this study showed that skin cancer following liver transplantation is not rare. LTRs in Australia should receive annual dermatologic examination due to their high prevalence of skin cancers. Moreover, non-melanoma skin cancers may be the prevalent type if skin cancer is suspected in LTRs. Substantial dermatological surveillance programs are recommended in LTRs to improve quality of life as well as the associated mortality; especially with the increased prevalence after long follow up durations.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1119P - Stage IIIA melanoma with isolated tumor cells in lymph nodes: Time for reviewing the AJCC v8 classification
Presenter: Teresa Amaral
Session: Poster session 13
1120P - Development and external validation of a clinical prediction model to predict recurrence-free survival and melanoma-specific survival in patients with melanoma after sentinel lymph node biopsy
Presenter: Robert Stassen
Session: Poster session 13
1121P - Interferon-gamma (IFNy) gene signature as a predictive biomarker for response in lactate dehydrogenase (LDH) low advanced melanoma patients
Presenter: Lotte Hoeijmakers
Session: Poster session 13
1122P - Neutrophil/lymphocyte ratio and systemic inflammatory index as prognostic biomarkers in metastatic melanoma patients under immune checkpoint inhibitors: Could any of them be used?
Presenter: Maria Menezes
Session: Poster session 13
1123P - Baseline tumor-infiltrating lymphocytes and response to immune checkpoint inhibition in advanced melanoma
Presenter: Mark Schuiveling
Session: Poster session 13
1124P - IL-6 as prognostic factor in adjuvant or metastatic skin cancer patients treated with immunotherapy: A deep biomarker analysis
Presenter: Domenico Mallardo
Session: Poster session 13
1125P - Identification of a subset of metastatic melanoma patients demonstrating germline determined insensitivity to immunotherapy
Presenter: Benjamin Fairfax
Session: Poster session 13
1126P - REtrospective Study of definitive therapy for head and neck mUcosal MElanoma: The RESUME study
Presenter: Motoo Nomura
Session: Poster session 13
1127P - Efficacy of immune checkpoint inhibitors (ICIs) in advanced mucosal melanoma (MM): A systematic review and meta-analysis
Presenter: James Pham
Session: Poster session 13
1128P - A phase I dose escalation and expansion study of FHD-286, a novel BRG1/BRM (SMARCA4/SMARCA2) inhibitor, for the treatment of metastatic uveal melanoma
Presenter: Sapna Patel
Session: Poster session 13