J Korean Soc Transplant.  2010 Sep;24(3):182-186. 10.4285/jkstn.2010.24.3.182.

Crude Incidence Rate of Malignancy after Kidney Transplantation

Affiliations
  • 1Division of Transplant and Vascular Surgery, Department of Surgery, Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea. htkim@dsmc.or.kr
  • 2Division of Nephrology, Department of Internal Medicine, Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea.
  • 3Department of Urology, Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea.
  • 4Transplant Coordinator, Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea.

Abstract

BACKGROUND
The incidence pattern of malignancy after kidney transplantation is different from that of the general population. Because increased exposure to immunosuppressants results in an increased incidence of malignancy, institutional reports that do not consider duration of immunosuppression have limited value for providing future kidney recipients with the actual risk for malignancy or for developing a kidney allograft recipient surveillance program. Thus, we retrospectively analyzed our institutional data with regard to the duration of exposure to immunosuppressants.
METHODS
A total of 757 patients who had kidney transplantation and were followed-up for at least 6 months at our hospital were reviewed retrospectively. The crude incidence rate (CI) was calculated by counting the days of exposure to immunosuppressants.
RESULTS
Most malignancies after kidney transplantation were solid tumors (85.3%). The CI of malignancies was 641.1 in allograft recipients and 329.6 in the general population per 100,000 persons per year. Solid tumor cancers of the stomach, liver, lung, breast, cervix, and pancreas showed an increased CI in the allograft recipient group than the general population but cancers of the thyroid and colon did not. Based on the type of immunosuppressive agent, the CI was highest in the cyclosporine group (866/12 months/100,000 persons) than the other groups.
CONCLUSIONS
We have provided the CIs of cancers after kidney transplantation at our institute. The pattern of post-transplant malignancy is different from that of western countries. Nationwide registration is needed to provide a more rational approach to post-transplant cancer surveillance in Korea.

Keyword

Post-transplant malignancy; Crude incidence rate; Postoperative complications

MeSH Terms

Breast
Cervix Uteri
Colon
Cyclosporine
Female
Humans
Immunosuppression
Immunosuppressive Agents
Incidence
Kidney
Kidney Transplantation
Korea
Liver
Lung
Pancreas
Postoperative Complications
Retrospective Studies
Stomach
Thyroid Gland
Transplantation, Homologous
Cyclosporine
Immunosuppressive Agents

Figure

  • Fig. 1. Crude incidence rate of overall malignancy (number/12 months/100,000 population).

  • Fig. 2. Crude incidence rate according to immunosuppressive agents (number/12 months/100,000 population).


Cited by  2 articles

Successful Sirolimus Treatment of Kaposi's Sarcoma in Multiple Pulmonary Nodules after Kidney Transplantation
Si Yeon Kim, Hyo Jung Lee, Yun Jung Chung, Seungsoo Sheen, Jong Hoon Lee, Chang-Kwon Oh
J Korean Soc Transplant. 2012;26(4):299-304.    doi: 10.4285/jkstn.2012.26.4.299.

Incidence of Post-transplant Malignancy after Renal Transplantation: Single Center Analysis
Seung Jo Choi, Dongho Choi, Oh Jung Kwon
J Korean Soc Transplant. 2014;28(4):204-210.    doi: 10.4285/jkstn.2014.28.4.204.


Reference

References

1). Adami J, Gäbel H, Lindelöf B, Ekström K, Rydh B, Glimelius B, et al. Cancer risk following organ transplantation: a nationwide cohort study in Sweden. Br J Cancer. 2003; 89:1221–7.
Article
2). Kasiske BL, Snyder JJ, Gilbertson DT, Wang C. Cancer after kidney transplantation in the United States. Am J Transplant. 2004; 4:905–13.
Article
3). Vajdic CM, McDonald SP, McCredie MR, van Leeuwen MT, Stewart JH, Law M, et al. Cancer incidence before and after kidney transplantation. JAMA. 2006; 296:2823–31.
Article
4). Kong JM. Malignancy in renal transplant recipients. J Korean Soc Transplant. 2009; 23:130–4. (공진민. 신장이식 환자의 악성종양. 대한이식학회지 2009;23: 130–4.).
Article
5). Kim SS, Min SK, Huh S, Jung IM, Ha JW, Ahn CR, et al. Malignancy in renal transplant recipient. J Korean Soc Transplant. 1999; 13:133–9. (김성수, 민승기, 허승, 정인목, 하종원, 안규리, 등. 신이식 후 발생한 악성종양. 대한이식학회지 1999;13: 133–9.).
6). Kim GH, Choi JH, Jeong JH. Malignancy in renal transplant recipients. J Korean Soc Transplant. 2002; 16:215–8. (김근환, 최재호, 정준헌. 신이식 후 발생한 악성종양. 대한이식학회지 2002;16: 215–8.).
Article
7). Kim MJ, Kim HJ. Prevalence of cancers in korean recipients of renal transplant. Korean J Nephrol. 2002; 21:367–74. (김명재, 김희진. 한국인의 신 이식 후 암 발생빈도. 대한신장학회지 2002;21: 367–74.).
8). Kim JY, Kim SH, Kim YS, Choi BS, Kim JC, Park SC, et al. Report of 1,500 kidney transplants at the Catholic University Of Korea. J Korean Soc Transplant. 2006; 20:172–80. (김진영, 김수현, 김영수, 최범순, 김준철, 박순철, 등. 톨릭대학교 의과대학에서 시행한 신장이식 1,500예의 성적보고. 대한이식학회지 2006;20: 172–80.).
9). Ro H, Kim SM, Kim KW, Hwang YH, Yang JS, Oh KH, et al. Malignancy after kidney transplantation. J Korean Soc Transplant. 2006; 20:187–92. (노한, 김선문, 김기원, 황영환, 양재석, 오국환, 등. 신이식 후 발생한 악성종양: 단일기관에서의 37년 발생양상 분석. 대한이식학회지 2006;20: 187–92.).
10). Buell JF, Gross TG, Woodle ES. Malignancy after transplantation. Transplantation. 2005; 80(2 Suppl):S254–64.
Article
11). Mazuecos A, Muñoz Terol JM, García Alvárez T, Sola E, Rodríguez Benot A, Dsuna A, et al. Increase in malignancies as cause of death in renal transplant patients. Transplant Proc. 2009; 41:2159–62.
Article
12). Park SH, Cho JH, Jang MH, Shin YB, Cho YJ, Kim JC, et al. Malignancy following renal transplantation. J Korean Soc Transplant. 2000; 14:81–6. (박선희, 조지형, 장민화, 신용봉, 조영준, 김준철, 등. 신이식 후에 발생한 악성종양. 대한이식학회지 2000;14: 81–6.).
13). van Leeuwen MT, Webster AC, McCredie MR, Stewart JH, McDonald SP, Amin J, et al. Effect of reduced immunosuppression after kidney transplant failure on risk of cancer: population based retrospective cohort study. BMJ. 2010; 340:c570.
Article
14). Webster AC, Woodroffe RC, Taylor RS, Chapman JR, Craig JC. Tacrolimus versus ciclosporin as primary immunosuppression for kidney transplant recipients: meta-analysis and meta-regression of randomised trial data. BMJ. 2005; 331:810.
Article
15). Kauffman HM, Cherikh WS, Cheng Y, Hanto DW, Kahan BD. Maintenance immunosuppression with tar-get-of-rapamycin inhibitors is associated with a reduced incidence of de novo malignancies. Transplantation. 2005; 80:883–9.
Article
16). Bang BK. Malignancy in renal transplant recipients. Korean J Nephrol. 2006; 25:S497–503. (방병기. 신장이식 환자에서 암의 발생. 대한신장학회지 2006;25: s497-s503.).
17). Campistol JM. Minimizing the risk of posttransplant malignancy. Transplantation. 2009; 87(8 Suppl):S19–22.
Article
18). Webster AC, Craig JC, Simpson JM, Jones MP, Chapman JR. Identifying high risk groups and quantifying absolute risk of cancer after kidney transplantation: a cohort study of 15,183 recipients. Am J Transplant. 2007; 7:2140–51.
Full Text Links
  • JKSTN
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr