Changing pattern and safety of pretransplant malignancy in kidney transplant recipients

Tae Hyun Ban; Woo Yeong Park; Kyubok Jin; Seungyeup Han; Byung Ha Chung; Sun Cheol Park; Bum Soon Choi; Cheol Whee Park; Sang-Seob Yun; Yong-Soo Kim; Chul Woo Yang

doi:10.23876/j.krcp.19.047

Kidney Res Clin Pract > Volume 38(4); 2019 > Article

Ban, Park, Jin, Han, Chung, Park, Choi, Park, Yun, Kim, and Yang: Changing pattern and safety of pretransplant malignancy in kidney transplant recipients

Original Article

Kidney Research and Clinical Practice 2019;38(4):509-516.

Published online: December 31, 2019

DOI: https://doi.org/10.23876/j.krcp.19.047

Changing pattern and safety of pretransplant malignancy in kidney transplant recipients

Tae Hyun Ban^1,^2,^*, Woo Yeong Park^3,^*, Kyubok Jin³, Seungyeup Han³, Byung Ha Chung^1,², Sun Cheol Park^1,⁴, Bum Soon Choi^1,², Cheol Whee Park^1,², Sang-Seob Yun^1,⁴, Yong-Soo Kim^1,², Chul Woo Yang^1,²

¹Transplant Research Center, The Catholic University of Korea, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Rebublic of Korea

²Division of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Rebublic of Korea

³Division of Nephrology, Department of Internal Medicine, Keimyung University School of Medicine, Keimyung University Kidney Institute, Daegu, Rebublic of Korea

⁴Department of General Surgery, The Catholic University of Korea, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Rebublic of Korea

Correspondence: Chul Woo Yang, Department of Internal Medicine, The Catholic University of Korea, Seoul St. Mary’s Hospital, 222 Banpo-daero, Seocho-gu, Seoul 06591, Republic of Korea. E-mail: yangch@catholic.ac.kr

^* Tae Hyun Ban and Woo Yeong Park contributed equally to this work.

Edited by Sangho Lee, Kyung Hee University, Seoul, Republic of Korea

This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Cancer rates are increasing not only in the general population but also in patients with end-stage renal disease. We investigated the changing pattern of pretransplant malignancy in kidney transplant recipients over 5 decades.

Methods

We reviewed 3,748 kidney transplant recipients between 1969 and 2016. We divided patients into three groups (1969–1998, 1999–2006, 2007–2016) based on the era of the cancer screening system used throughout the nation. We analyzed the incidence and pattern of pretransplant malignancy among the three groups. We also evaluated recurrent and de novo malignancy in these patients compared to patients without pretransplant malignancy.

Results

A total of 72 patients exhibited pretransplant malignancy (1.9%). There were no cases of pretransplant cancer until 1998, but the rate of pretransplant malignancy gradually increased to 1.1% during 1999–2006 and further increased to 4.3% thereafter. The most frequent types of pretransplant malignancy changed from the bladder, liver, and stomach cancers to thyroid cancer and renal cell carcinoma. There were no de novo cases, but there were three cases of recurrent cancer in patients with pretransplant malignancy; the recurrence rate among kidney transplant recipients with pretransplant malignancy was not significantly different from the incidence rate of de novo malignancy among kidney transplant recipients without pretransplant malignancy (4.2% vs. 6.9%, P = 0.48).

Conclusion

The incidence of pretransplant malignancy in kidney transplantation candidates is gradually increasing, and recent increases were accompanied by changes in cancer types. Pretransplant malignancy may not be a hindrance to kidney transplantation because of the low incidence of posttransplant recurrence and de novo malignancy.

Keywords: Cancer, Kidney transplant recipients, Kidney transplantation, Malignancy, Pretransplant

Introduction

Since the first kidney transplantation (KT) was successfully performed between identical twins in a Western country in 1954, advances in immunosuppressive (IS) agents have improved short-term outcomes of allografts, reducing acute rejection [1]. Unfortunately, IS agents also cause many unwanted complications, including increased tumors, new-onset diabetes after transplantation, opportunistic infections, hair loss, neuropathy, and paradoxically, nephrotoxicity [2,3]. Malignancy in kidney transplant recipients (KTRs) is an important issue because it is the third most common cause of death and is also related to graft and patient survival during the late period after KT [1]. Previous reports have revealed a higher incidence of cancer in KTRs than in the general population worldwide [4–10]. Therefore, present guidelines recommend regular surveillance to screen for cancer in KTRs [11–14].

Due to advances in medical therapy, an extension of life span has been achieved in populations worldwide, including patients with end-stage renal disease (ESRD) [15–17]. In addition to an increasingly aging population, advances in medical equipment and an accumulation of experience have led to an increase in the number of patients with cancer diagnosis and treatment, in parallel with the increase in tumor incidence associated with aging [18]. The incidence of cancer has also increased over time in Korea [19]. As a result, the number of KT candidates receiving cancer treatment before transplantation is increasing.

Guidelines for KT candidates emphasize more frequent cancer screening among older patients [20]. Patients with pretransplant malignancies were not considered KT candidates in the past. However, an increase in cancer-free survival has increased the demand for transplant among ESRD patients with a previous malignancy to achieve freedom from lifelong dialysis. Therefore, the consensus KT guidelines were changed to permit transplantation on a case-by-case basis [2,14,21,22].

Despite an emphasis on tumor screening related to KT in the guidelines [20], the presence of cancer during the posttransplant period has rarely been investigated in KTRs with pretransplant malignancies. In this study, we sought to measure cancer recurrence and incidence rates in KTRs treated for pretransplant malignancies before KT.

Methods

Patient classification and clinical outcomes

We retrospectively reviewed data from 3,748 KTRs from The Catholic University of Korea, Seoul St. Mary’s Hospital after March 1969 and from Keimyung University Kidney Institute after November 1982, when the first KT was conducted in each institute, until December 2016. In each center, both pre- and posttransplant data of KT included donor and recipient information registered in a computerized system. KTRs with pretransplant malignancies were divided into three eras based on the progression of the nationwide regular surveillance system in Korea.

In the Republic of Korea, a cancer surveillance plan that covers the entire nation and targets medical aid beneficiaries was initiated in 1999. The national surveillance system gradually extended the diseases and cancer types monitored over time. Finally, the national policy recommended surveillance of specific cancer types in the entire adult population aged 40 and 66 years in a program called “The Life Transition Period Health Examination at the Korea Association of Health Promotion” in 2007. Therefore, we defined the first era as before and including 1998, the second era as between 1999 and 2006, and the third era as 2007 and beyond.

We investigated the proportion of KTRs with pretransplant malignancies, cancer type of pretransplant malignancies, cancer-free intervals until KT in KTRs with pretransplant malignancies, and posttransplant outcomes. All patients with pretransplant malignancies were monitored in the two transplant centers, including eight KTRs among these patients who experienced allograft failure. All tumors were confirmed by histopathological and radiological findings. Patients were diagnosed with only one cancer type. Patients with pretransplant malignancies in our institutes underwent KT based on previous guidelines [14,21,22]. This study was retrospective and exempted from written informed consent. This study was approved by the institutional review boards of The Catholic University of Korea, Seoul St. Mary’s Hospital and Keimyung University Dongsan Hospital (KC17REDI0665; 2017-10-007).

Changes in immunosuppressive regimen

Maintenance IS agents in the two centers consisted of azathioprine and corticosteroids until 1984. After that time, IS agents consisted of cyclosporine, as a calcineurin inhibitor, combined with corticosteroids, with or without azathioprine. Tacrolimus was introduced in 1998. Mycophenolate mofetil was introduced in 1999 for treatment of patients. However, since 2001, mycophenolate mofetil has been administered as an initial maintenance strategy. The target trough levels of tacrolimus and cyclosporine were 8 to 12 ng/mL and 150 to 300 ng/mL during the first 3 months and 3 to 8 ng/mL and 50 to 100 ng/mL thereafter, respectively. In May 2002, basiliximab was introduced as an induction therapy for most patients. Antithymocyte globulin was used as an induction therapy in highly immunized patients. At both centers, in 2009, a tailored desensitization strategy was initiated with combination therapy consisting of rituximab, plasmapheresis, and intravenous immunoglobulin for ABO-incompatible KT and for transplantation in highly sensitized patients.

Statistical analysis

Statistical analyses were performed using IBM SPSS Statistics ver. 24.0 (IBM Corp., Armonk, NY, USA). Continuous variables are expressed as the means and standard deviation and categorical variables are presented as frequencies (%). For normally distributed variables, between-group differences were evaluated using a Student’s t test. All tests were 2-tailed, and the results were considered significant when P < 0.05.

Results

Proportion of kidney transplant recipients with pretransplant malignancies

The mean age of the total patients was 40.6 years, and the proportion of males was approximately 60%. Table 1 summarizes the clinical characteristics of the patients. The incidence of KTRs with pretransplant malignancies based on regular surveillance is shown in Fig. 1. A total of 1.9% (72 patients) of KTRs among the total patients were cured of pretransplant malignancies. No patients with cancer underwent transplantation prior to 1998. A total of 1.1% (7 patients) of KT patients with pretransplant malignancies underwent transplantation between 1999 and 2006. The percentage of those patients increased to 4.3% (65 patients) during the third era. The proportion of KTRs with pretransplant malignancies significantly increased over time (P < 0.001).

Changing patterns in cancer type

Types of cancer in KTRs with pretransplant malignancies are summarized in Fig. 2. The major types of cancer in the second era were stomach (n = 2), liver (n = 2), and bladder (n = 2) cancer. Thyroid cancer (n = 20), renal cell carcinoma (RCC) (n = 13), stomach cancer (n = 6), and breast cancer (n = 6) were common in the third era. Therefore, the most common type of pretransplant malignancy for the entire period was thyroid cancer (n = 21), followed by RCC (n = 13), stomach cancer (n = 8), and breast cancer (n = 6). The cancer types in the remaining patients included cervical, colorectal, acute myeloid leukemia, carcinoid, endometrial, lymphoma, melanoma, pituitary, and anal cancer. During the third era, the majority of cancers were thyroid cancer and RCC. All thyroid cancers were classified as the papillary type, and all RCCs were classified as the clear cell type.

Cancer-free interval and incidence of posttransplant malignancy in patients with pretransplant malignancies

The mean cancer-free duration of each tumor type is displayed in Table 2. The mean cancer-free duration of all patients with pretransplant malignancies was 70.0 ± 66.6 months. In the KTRs with pretransplant malignancies, cancer was found in 3 patients (4.2%) during the posttransplant period. However, 259 (6.9%) KTRs without pretransplant malignancies were treated for cancer during the same period. The incidence of cancer in KTRs with pretransplant malignancies was not significantly different from the incidence in those without pretransplant malignancies (P = 0.48).

The types of cancer in all patients after transplantation are summarized in Table 3. Recurrent cancer occurred only in KTRs with pretransplant malignancy. After transplantation, the interval between de novo malignancy and recurrent cancer was 122.6 months and 59.8 months, respectively. These were not significantly different.

Discussion

The results of our study demonstrated that the number of KTRs treated for pretransplant malignancy has increased over time, and the common cancer types before KT have changed. The most common cancer types in KTRs with pretransplant malignancies were thyroid cancer and RCC. However, the recurrence rate of cancer was not increased in KTRs with pretransplant malignancies.

The most important finding of this study was that the proportion of KTRs with pretransplant malignancies increased over time. No cancer patients were reported for approximately 30 years prior to 1998. However, the proportion of cancer patients was 1.1% during the next 10 years and markedly increased to 4.3% during the final 10 years. The reason for this trend may be inferred from previous reports based on the regional population. The National Cancer Screening Program (NCSP) was initiated in 1999. Thereafter, the cancer types monitored by the NCSP gradually expanded, and the number of beneficiaries also increased over time. In addition, the number of participants who were also potential beneficiaries continuously increased during this time [23,24]. The national surveillance strategy includes the entire adult population aged 40 to 66 years for cancer screenings according to the policy of “The Life Transition Period Health Examination at the Korea Association of Health Promotion” instituted in 2007 [25]. Additionally, life span extension has occurred in all populations, including ESRD patients [15–17]. Both an increment of the aging population and advances in medical techniques have contributed to cancer diagnoses and cures [18]. The outcome of these factors has been an increase in the detection of cancer in the regional population over time [19]. In particular, early cancer detection has gradually increased, while the mortality from each type of cancer has decreased [26]. These findings suggest that we may encounter an increased number of KTRs with pretransplant malignancies in the near future. Thus, it is important to address the issue of safety associated with posttransplant cancer development in KTRs with pretransplant malignancies.

Pretransplant malignancies were barriers to KT in the past. These factors included an unestablished guideline for KT candidates cured of pretransplant cancer, inappropriate living donors, a limited number of deceased donors, and the introduction of the desensitization protocol. However, several guidelines were helpful for conducting KT in these subjects [14,21,22]. Some patients waited a long time for their children to reach adulthood in order to be a donor or to find another suitable deceased donor. Recently, other patients have been allowed to undergo KT after desensitization, resulting in the development of an acceptable strategy to treat KTRs with pretransplant malignancy over time.

The cancer types observed have also changed. In this study, the most common pretransplant malignancy found was thyroid cancer, followed by RCC. These two cancers have recently shown an increasing incidence. Indeed, not only was the cancer incidence distinct compared to those of other countries [27–29], but the pattern was different from that in the general population in Korea [19,24]. In domestic studies of CKD patients before dialysis and ESRD patients on dialysis, there were high incidences of colorectal, stomach, kidney, lung, thyroid, breast, prostate, and liver cancers [30–32]. The difference in prevalence of common cancer incidence and pretransplant malignancy in renal transplant recipients may be related to the age-related distribution of carcinoma patients, the cancer-free interval, and the increase in patient condition or mortality between the waiting periods during treatment. The major burden of these cancers affects the NCSP. The local population showed the highest incidence of gastric cancer, followed by thyroid, colorectal, and lung malignancies over the past 15 years [19]. In particular, the number of patients with small thyroid cancers rapidly increased, and these patients underwent thyroidectomy in considerable numbers, according to recent regional data [19,33]. Therefore, marked increases in thyroid cancer were observed in this study. Most subjects in the current study underwent dialysis for more than 5 years prior to KT. The presence of ESRD and its duration are independent risk factors for RCC. Therefore, RCC is the second leading cause of pretransplant malignancy in this study [34]. Interestingly, all thyroid cancer and RCC patients had the same type of cancer, papillary cell type and clear cell type, respectively. The types of cancer observed were comparatively less dangerous than other types of cancer [35,36]. These two relatively curable cancer types are different from the cancer types reported in previous studies [37]. Therefore, these findings suggest regular screening for thyroid cancer and RCC before KT.

The mean cancer-free interval before KT in the total patient group was 70.2 months, which was a substantial cancer-free interval despite the wide range of cancer types. Considering previous guidelines [14,21,22], this interval also complied with the criteria. Therefore, the favorable results of the current study were possibly due to achieving a cure for each cancer and a sufficient cancer-free interval. The other interesting finding in the present study was the lack of a significant difference in the cancer incidence of KTRs with pretransplant malignancies compared to that of KTRs without pretransplant malignancies. Only 3 patients in this study developed recurrent cancers; however, no patient developed de novo cancer. The low incidence of posttransplant malignancies among KTRs with pretransplant malignancies was inconsistent with the results found in other studies [37,38]. This discrepancy may be due to the slightly younger mean age of our patients [37]. Several studies have described a considerable incidence of cancer during the early period after KT [5,37,39]. However, this observational study followed patients for approximately 5 years (the longest follow-up duration was 17 years) and was able to significantly demonstrate the trend toward increasing safety in terms of posttransplant malignancy in KTRs with pretransplant malignancies.

This study has some limitations. First, cancer staging was not performed in this study. Second, the follow-up duration may not have been sufficient to analyze the incidence of all tumors. However, the mean follow-up time in the pretransplant malignancy group was approximately 5 years. Therefore, this duration may provide evidence that contradicts the high incidence of malignancy reported during the early period after KT in previous studies [5,37,39]. Third, despite cancer work-up before KT and regular posttransplant cancer screening, the issue of patient adherence may have affected cancer incidence. Although additional investigations of malignancies before transplantation are needed, we aimed to assess whether transplantation is safe after cancer treatment in KTRs with pretransplant malignancies compared to those without pretransplant malignancies. Nevertheless, the results of the current study showed that pretransplant cancer screening requires different strategies based on regional data, which may allow safer transplantation in KT candidates with pretransplant malignancies.

In conclusion, the number of KTRs with pretransplant malignancies is gradually increasing, and changes in the type of cancer presented have been observed. This observational study suggests that KT in patients who have been cured of pretransplant malignancies and have achieved a sufficient cancer-free interval may be safe with regard to recurrent and de novo cancer during the posttransplant period. Regular surveillance based on the present guideline is equally helpful for detecting cancer in KTRs with and without pretransplant malignancies.

Acknowledgments

This work was supported by the Korean Health Technology R&D Project, Ministry for Health and Welfare, Republic of Korea (HI14C3417).

Notes

Conflicts of interest

All authors have no conflicts of interest to declare.

Authors’ contributions

Tae Hyun Ban, Woo Yeong Park, Byung Ha Chung, Sun Cheol Park, Kyubok Jin, Bum Soon Choi, Seungyeup Han, Cheol Whee Park, Sang-Seob Yun, Yong-Soo Kim, and Chul Woo Yang participated in the data collection. Tae Hyun Ban, Woo Yeong Park and Chul Woo Yang wrote the manuscript. Byung Ha Chung and Seungyeup Han helped to draft the manuscript. Tae Hyun Ban, Woo Yeong Park, Byung Ha Chung, and Chul Woo Yang participated in the study design. Tae Hyun Ban and Woo Yeong Park performed the statistical analysis. Tae Hyun Ban, Byung Ha Chung, and Chul Woo Yang participated in the conception and analysis. Tae Hyun Ban, Woo Yeong Park, Byung Ha Chung, Sun Cheol Park, Kyubok Jin, Bum Soon Choi, Seungyeup Han, Cheol Whee Park, Sang-Seob Yun, Yong-Soo Kim, and Chul Woo Yang participated in interpretation of data. Tae Hyun Ban, Woo Yeong Park, Byung Ha Chung, and Chul Woo Yang provided intellectual content of critical importance to the work and technical support. All authors read and approved the final manuscript.

Figure 1

The incidence of pretransplant malignancies in kidney transplant recipients over time.

Figure 2

Changes in pretransplant cancer types in kidney transplant recipients over time.

AML, acute myeloid leukemia; RCC, renal cell carcinoma.

Table 1

Clinical characteristics of total patients before KT

Characteristic	Total (1969–2016, n = 3,748)	First era (1969–1998, n = 1,591)	Second era (1999–2006, n = 638)	Third era (2007–2016, n = 1,519)	P value
Male	2,267 (60.5)	1,042 (65.5)	366 (57.4)	859 (56.6)	< 0.001
Age at KT (yr)	40.6 ± 12.3	36.1 ± 11.7	39.4 ± 11.1	45.9 ± 11.5	< 0.001
Dialysis modality (HD/PD/pre-emptive)	2,685/617/443 (71.6/16.5/11.8)	1,227/205/156 (77.1/12.9/9.8)	464/132/42 (72.7/20.7/6.6)	994/280/245 (65.4/18.4/16.1)	< 0.001
Dialysis vintage (months)	30.4 ± 42.9	15.1 ± 18.8	28.0 ± 38.1	48.8 ± 55.5	< 0.001
Primary renal disease
Chronic GN	2,373 (63.3)	1,293 (81.3)	411 (64.4)	669 (44.0)	< 0.001
DM	408 (10.9)	60 (3.8)	54 (8.5)	294 (19.4)
HTN	328 (8.8)	101 (6.3)	42 (6.6)	185 (12.2)
ADPKD	97 (2.6)	12 (0.8)	15 (2.4)	70 (4.6)
SLE	52 (1.4)	7 (0.4)	13 (2.0)	32 (2.1)
Other	85 (2.3)	26 (1.6)	26 (4.1)	33 (2.2)
Unknown	404 (10.8)	91 (5.7)	77 (12.1)	236 (15.5)

Data are presented as number (%), mean ± standard deviation, or number only.

ADPKD, autosomal dominant polycystic kidney disease; DM, diabetes mellitus; GN, glomerulonephritis; HD, hemodialysis; HTN, hypertension; KT, kidney transplantation; PD, peritoneal dialysis; SLE, systemic lupus erythematosus.

Table 2

Cancer-free interval until KT based on cancer type

Cancer type	Pretransplant case (n)	Mean cancer-free interval until KT (mo)
Pituitary gland	1	112.5
Thyroid	21	47.6
Breast cancer	6	113.0
GI tract
Stomach	8	71.2
Colorectal	2	96.6
Liver	5	51.5
Urological
RCC	13	65.0
Bladder	5	30.1
Gynecological
Cervical	3	163.0
Endometrial	1	135.4
Anal	1	89.0
Hematological
AML	2	72.5
Lymphoma	1	294.6
Melanoma	1	30.0
Carcinoid tumor	2	25.1

AML, acute myeloid leukemia; GI, gastrointestinal; KT, kidney transplantation; RCC, renal cell carcinoma.

Table 3

Type and incidence of de novo and recurrent cancers

	De novo cancer	Recurrent cancer
Stomach	44
Lymphoma	34
Thyroid	23
Colorectal	22
Liver	18
Breast	16	1
Cervix	15
Head and neck	15
Lung	11
Bladder	10	2
RCC	10
Urothelial	8
Biliary and pancreas	7
Kaposi sarcoma	7
Other hematologic malignancy	7
Skin	3
Prostate	3
Ovary	2
Adrenal	1
Anus	1
Thymic carcinoma	1
MUO	1
Total	259	3

MUO, metastasis of unknown origin; RCC, renal cell carcinoma.

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