Declining incidence of keratinocyte carcinoma in organ transplant recipients.


Journal

The British journal of dermatology
ISSN: 1365-2133
Titre abrégé: Br J Dermatol
Pays: England
ID NLM: 0004041

Informations de publication

Date de publication:
11 2019
Historique:
accepted: 30 04 2019
pubmed: 3 5 2019
medline: 12 1 2021
entrez: 4 5 2019
Statut: ppublish

Résumé

All organ transplant populations are predisposed to increased rates of keratinocyte carcinoma (KC). Since this increased risk was first appreciated, immunosuppressive regimens have changed and organ transplant recipients (OTRs) have been aggressively screened for KC. There is a perception that these measures have impacted on KC incidence but there is a paucity of population-based studies on post-transplant rates of basal cell carcinoma (BCC). To identify trends in incidence rates for KC following solid organ transplantation over the past two decades. This nationwide, population-based study included all solid OTRs transplanted between 1994 and 2014. Patient data were matched to national cancer registry data to determine the standardized incidence ratio (SIR) of KC in solid OTRs compared with the general population. In total 3580 solid OTRs were included. The total follow-up time was 28 407 person-years (median follow-up 7·11 years). The overall SIRs for squamous cell carcinoma (SCC) and BCC were 19·7 and 7·0, respectively. Our study documents a progressive fall in the SIRs for SCC and BCC from peak SIRs (95% confidence intervals) in 1994-1996 of 26·4 (21·5-32·4) and 9·1 (7·4-11·3) to 6·3 (2·3-16·7) and 3·2 (1·4-7·1) in 2012-2014, respectively. The ratio of SCC to BCC has remained at 3 to 1 over the last two decades. Our study is the first to demonstrate a significant reduction over the past two decades in the incidences of both SCC and BCC following solid organ transplantation. The SCC-to-BCC ratio was maintained, demonstrating that both are reducing equally. This trend coincided with temporal changes in immunosuppressive protocols and the introduction of skin cancer prevention programmes. What's already known about this topic? Prior studies have shown that the risk of cutaneous squamous cell carcinoma (SCC) has declined over recent decades following solid organ transplantation. It is not known whether the risk of basal cell carcinoma (BCC) has reduced in line with this. What does this study add? Our study documents a progressive fall in the risk of SCC and BCC following solid organ transplantation over the last two decades. The SCC-to-BCC ratio was maintained, demonstrating that both are reducing equally. The trends observed in our study coincided with temporal changes in immunosuppressive protocols and the introduction of cancer prevention programmes, suggesting that these factors have positively impacted on the risk of keratinocyte carcinoma in this cohort.

Sections du résumé

BACKGROUND
All organ transplant populations are predisposed to increased rates of keratinocyte carcinoma (KC). Since this increased risk was first appreciated, immunosuppressive regimens have changed and organ transplant recipients (OTRs) have been aggressively screened for KC. There is a perception that these measures have impacted on KC incidence but there is a paucity of population-based studies on post-transplant rates of basal cell carcinoma (BCC).
OBJECTIVES
To identify trends in incidence rates for KC following solid organ transplantation over the past two decades.
METHODS
This nationwide, population-based study included all solid OTRs transplanted between 1994 and 2014. Patient data were matched to national cancer registry data to determine the standardized incidence ratio (SIR) of KC in solid OTRs compared with the general population.
RESULTS
In total 3580 solid OTRs were included. The total follow-up time was 28 407 person-years (median follow-up 7·11 years). The overall SIRs for squamous cell carcinoma (SCC) and BCC were 19·7 and 7·0, respectively. Our study documents a progressive fall in the SIRs for SCC and BCC from peak SIRs (95% confidence intervals) in 1994-1996 of 26·4 (21·5-32·4) and 9·1 (7·4-11·3) to 6·3 (2·3-16·7) and 3·2 (1·4-7·1) in 2012-2014, respectively. The ratio of SCC to BCC has remained at 3 to 1 over the last two decades.
CONCLUSIONS
Our study is the first to demonstrate a significant reduction over the past two decades in the incidences of both SCC and BCC following solid organ transplantation. The SCC-to-BCC ratio was maintained, demonstrating that both are reducing equally. This trend coincided with temporal changes in immunosuppressive protocols and the introduction of skin cancer prevention programmes. What's already known about this topic? Prior studies have shown that the risk of cutaneous squamous cell carcinoma (SCC) has declined over recent decades following solid organ transplantation. It is not known whether the risk of basal cell carcinoma (BCC) has reduced in line with this. What does this study add? Our study documents a progressive fall in the risk of SCC and BCC following solid organ transplantation over the last two decades. The SCC-to-BCC ratio was maintained, demonstrating that both are reducing equally. The trends observed in our study coincided with temporal changes in immunosuppressive protocols and the introduction of cancer prevention programmes, suggesting that these factors have positively impacted on the risk of keratinocyte carcinoma in this cohort.

Identifiants

pubmed: 31049932
doi: 10.1111/bjd.18094
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

983-991

Subventions

Organisme : The City of Dublin Skin and Cancer Hospital Charity
Pays : International

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 British Association of Dermatologists.

Références

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Auteurs

S Menzies (S)

Department of Dermatology, Mater Misericordiae University Hospital, Dublin, Ireland.

E O'Leary (E)

National Cancer Registry Ireland, Cork, Ireland.

G Callaghan (G)

Department of Dermatology, Mater Misericordiae University Hospital, Dublin, Ireland.

M Galligan (M)

School of Medicine, University College Dublin, Dublin, Ireland.

S Deady (S)

National Cancer Registry Ireland, Cork, Ireland.

B Gadallah (B)

National Lung Transplantation Centre, Mater Misericordiae University Hospital, Dublin, Ireland.

P Lenane (P)

Department of Dermatology, Mater Misericordiae University Hospital, Dublin, Ireland.

A Lally (A)

Department of Dermatology, St Vincent's University Hospital, Dublin, Ireland.

D D Houlihan (DD)

Department of Hepatology, St Vincent's University Hospital, Dublin, Ireland.

P G Morris (PG)

Department of Oncology, Beaumont Hospital, Dublin, Ireland.

D J Sexton (DJ)

Department of Nephrology & Transplantation, Beaumont Hospital, Dublin, Ireland.
Department of Medicine, Royal College of Surgeons in Ireland, Dublin, Ireland.

P A McCormick (PA)

Department of Hepatology, St Vincent's University Hospital, Dublin, Ireland.

J J Egan (JJ)

National Lung Transplantation Centre, Mater Misericordiae University Hospital, Dublin, Ireland.

J P O'Neill (JP)

Department of Otolaryngology, Head and Neck Surgery, Beaumont Hospital, Dublin, Ireland.

P J Conlon (PJ)

Department of Nephrology & Transplantation, Beaumont Hospital, Dublin, Ireland.

F J Moloney (FJ)

Department of Dermatology, Mater Misericordiae University Hospital, Dublin, Ireland.
School of Medicine, University College Dublin, Dublin, Ireland.

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