Nonmelanoma Skin Cancer Rates Are Not Affected by Chronic HIV(+) or HCV(+) Infection in Organ Transplant Recipients.
K. Nadhan, E. Usedom, S. Shipman, A. Doyle, G. Malat, E. Buchanan, C. Chung.
Dermatology, Drexel, Philadelphia
Meeting: 2017 American Transplant Congress
Abstract number: A303
Keywords: Hepatitis C, High-risk, HIV virus, Malignancy
Session Information
Session Name: Poster Session A: Viral Conundrums
Session Type: Poster Session
Date: Saturday, April 29, 2017
Session Time: 5:30pm-7:30pm
Presentation Time: 5:30pm-7:30pm
Location: Hall D1
Purpose: HIV and HCV are two immune dysregulatory processes that may exacerbate the risk of nonmelanoma skin cancer (NMSC) in organ transplant recipients (OTR), a cohort that exhibits significantly increased risk at baseline due to iatrogenic immunosuppression. Our aim is to elucidate whether OTR with HIV or HCV constitute a unique cohort that demands specialized risk stratification and dermatologic management.
Methods: A retrospective chart review was performed with 427 OTR seen in a 5-year span between 11/1/2011 and 11/1/2016.
Results: Seventy OTR were diagnosed with either HCV or HIV (Table 1). The mean age was 61 years, time of immunosuppression was 7 years, and time from transplant to initial dermatologic visit was 76 days. Two patients were coinfected for both viruses. Nine patients (13%) were diagnosed with NMSC, all of whom were White. Statistical analysis did not reveal significant differences between the HIV/HCV (+) infected White patients vs. non-infected White patients (N=47) for the type or anatomical location of the skin cancer lesions, sun exposure, and time until diagnosis of first lesion. One patient received a heart transplant, 33 received a kidney, 25 received a liver, and 11 received multiorgan transplants.
Demographics of HCV/HIV Sample | |||
Cohort | White | Nonwhite | |
Total Patients | 70 | 25 | 45 |
HCV | 56 | 23 | 33 |
HIV | 16 | 2 | 14 |
Mean Age (Y) | 60.8 | 62.6 | 59.8 |
Gender | |||
Males | 57 | 24 | 33 |
Females | 13 | 1 | 12 |
Organ Transplant Type | |||
Kidney | 33 | 3 | 30 |
Heart, Lung, Heart/Lung | 1 | 1 | |
Liver | 25 | 16 | 9 |
Multi-Organ | 11 | 5 | 6 |
Mean Time of Immunosuppresion (Y) | 7.1 | 7.3 | 7.2 |
Mean Time from Referral (D) | 76 | 90.4 | 67.5 |
Number of lesions | 60 | 60 | |
BCC | 11 | 11 | |
SCC | 16 | 16 | |
SCCIS | 32 | 32 | |
Melanoma | 1 | 1 |
Conclusions: Our data continues to show the White OTR population to be at risk for NMSC while receiving long-term immunosuppression. Our analysis does not indicate HIV or HCV, two pro-inflammatory viruses, to have an effect on the severity, intensity, or incidence of NMSC.
CITATION INFORMATION: Nadhan K, Usedom E, Shipman S, Doyle A, Malat G, Buchanan E, Chung C. Nonmelanoma Skin Cancer Rates Are Not Affected by Chronic HIV(+) or HCV(+) Infection in Organ Transplant Recipients. Am J Transplant. 2017;17 (suppl 3).
To cite this abstract in AMA style:
Nadhan K, Usedom E, Shipman S, Doyle A, Malat G, Buchanan E, Chung C. Nonmelanoma Skin Cancer Rates Are Not Affected by Chronic HIV(+) or HCV(+) Infection in Organ Transplant Recipients. [abstract]. Am J Transplant. 2017; 17 (suppl 3). https://atcmeetingabstracts.com/abstract/nonmelanoma-skin-cancer-rates-are-not-affected-by-chronic-hiv-or-hcv-infection-in-organ-transplant-recipients/. Accessed November 22, 2024.« Back to 2017 American Transplant Congress