Dhakal, Giri, Siwakoti, Rayamajhi, and Bhatt: Renal Cancer in Recipients of Kidney Transplant

Renal Cancer in Recipients of Kidney Transplant

Abstract

The aim of our study is to determine characteristics and outcomes of kidney cancer in renal transplant recipients. MEDLINE® database was searched in June 2015 to identify cases of kidney cancer in renal transplant recipients. We include also a new case. Descriptive statistics were used for analysis. Forty-eight (48) recipients reported in 25 papers met the eligibility criteria. The median age was 47 years (range 9-66); 27% were females. Chronic glomerulonephritis, cystic kidney disease and hypertension were common indications for renal transplant. Among donors 24% were females and the median age was 52.5 years (17-73); 62% of kidney cancers were donor-derived. The median interval between transplant and cancer diagnosis was shorter for cancer of recipient versus donor origin (150 vs. 210 days). Clear cell carcinoma was diagnosed in 17%. 25% had metastasis at diagnosis. Kidney explantation or excision was done in 90% and 84% of cases with and without metastasis respectively. The median survival was 72 months. Actuarial 1-year and 5-year survival rates were 73.4% and 55.1% respectively. Among the recipients from 7 donors who subsequently developed malignancy, 57% were dead within a year. Kidney transplant recipients have a small risk of kidney cancer, which affects younger patients and occurs within a year of transplant, likely due to immunosuppression. Whether the use of older donors may increase the likelihood needs further investigation. The presence of metastasis, explantation or excision of affected kidney and development of cancer in donors predict outcomes. The results may guide patient education and informed decision-making.




Competing interest statement

Conflict of interest: the authors declare no potential conflict of interest.

Introduction

Transmission of malignancy from organ donor to recipient, well-recognized complication of transplantation,1 is rare but frequently unavoidable.2 About 17,000 of kidney transplants are performed in the US yearly and malignancy is the second most common cause of death (after cardiovascular events and infection) in these cases.3 In patients with transplants, the incidence of kidney cancer is estimated to be approximately 5%; 10% of these kidney cancers arise in renal grafts.4,5 The rarity of kidney cancers in kidney transplant recipients precludes understanding of the demographics, characteristics, treatment methods and outcomes of this entity. Most of these cancers are treated with explantation or excision of the graft. Chemotherapy and radiotherapy are used mostly as an adjunct. Here we present a case which was treated with explantation, followed by radiation therapy for recurrent disease. We have also reviewed cases of renal malignancy in renal transplant recipients.

Materials and Methods

A systematic search of MEDLINE database (via PubMed) was conducted in July 2015 to identify articles describing a new diagnosis of kidney cancer following kidney transplant. The following terms were utilized for selecting the articles: (Kidney Transplantation OR Renal Transplantation OR Organ Transplantation) AND (malignant OR cancer OR tumor) AND (transmission). The bibliography of each article was hand-searched for additional reports. Only reports published in English language were included. Of a total of 420 searches, 24 articles met the eligibility criteria (Figure 1). Additionally, we also describe an original case report.

During analysis, details of the patient, transplant history, diagnosis of kidney cancer, therapy, complications and outcomes were obtained until the last follow-up of the patient.

Results

A 55-year-old male presented to emergency department complaining of abdominal pain, distention, as well as nausea and vomiting of 2 days’ duration. He had a bilateral kidney transplant one year ago for end stage renal disease secondary to chronic hypertension. His post-transplant course was complicated by ureteral strictures, enterocutaneous fistula and recurrent small bowel obstructions. The patient was on mycophenolate mofetil, prednisone and tacrolimus to avoid graft rejection. He had a history of heavy smoking, alcohol consumption and cocaine use, but had quit one year ago. Physical examination revealed heart rate of 109 beats/min, blood pressure of 134/96 mm Hg, respiratory rate of 20/min and temperature of 36.6°C. On abdominal examination, there was diffuse tenderness and high-pitched bowel sounds. Rest of the examination was normal.

Laboratory studies included white blood cell count of 10,200/μL with 78% granulocytes, hemoglobin of 16.6 g/dL and platelet count of 155,000/μL. He had a creatinine of 1.04 mg/dL, blood urea nitrogen of 13 mg/dL, sodium of 138 mmol/L, potassium of 3.3 mmol/L, and chloride of 100 mmol/L. Ultrasonography (USG) of right kidney demonstrated a transplanted kidney with a heterogeneous hyperechoic mass measuring 5.5*4.9X5.6 cm. Computed tomography (CT) scan of abdomen revealed right lower quadrant transplanted kidney with a new complex enhancing mass involving the lower pole measuring 5.4×73×6.5 cm, which was highly concerning for malignancy. CT scan also demonstrated new gastric distention, dilated loops of small bowel, fecal material in distal small bowel loops, and air and stool throughout colon, which was concerning for small bowel obstruction. Whole body positron emission tomography (PET) scan depicted a 73×6.4×6.2 cm inferior pole mass within right lower quadrant kidney transplant with a maximum SUV of 9.6, suspicious for primary renal cell carcinoma versus lymphoma. Biopsy of the mass showed sarcomatoid carcinoma with squamous differentiation, possibly of the uroepithelial origin.

The patient underwent nephrectomy of the right transplanted kidney. Pathology revealed high-grade carcinoma with squamous differentiation and sarcomatoid areas (sarcomatoid carcinoma/carcinosarcoma) with a tumor size of 6.7 cm in the greatest dimension. Tumor appeared to be arising in the setting of keratinizing squamous metaplasia involving the right renal pelvis and calyceal system with invasion into renal parenchyma and peripelvic adipose tissue (pT3). Margins were positive in areas where capsule was stripped but there was no lymphovascular invasion. Periureteral tissue was also involved with invasive carcinoma with squamous differentiation. Cytogenetics report showed: 68-77, XXY,+1, add (1)(p11),i(1)(p10)x2,-3,+6, add(7)(p15),add(7)(p21),add(7)(q32),add(8 )(p22),-9, i(9)(q10)x2,add(11)(q14),-13,-13,add(16)(q24), add(17)(p13),+add (19)(q133),+21,add(21)(p11.1)x2,-22,+7-12 mar,0-3dmin[cp 17]/129,slx2[1]//46,XX[2].

A repeat PET/CT scan in a month revealed 2.1×53 cm soft tissue fullness in the right pelvis at the site of prior mass resection/nephrectomy. This lesion was markedly hypermetabolic with maximum standardized uptake value (SUV) of 13.0 compatible with recurrent local malignancy. Retroperitoneal and inguinal lymph nodes were not enlarged or PET-avid. The patient refused chemotherapy and therefore, was treated with a course of radiotherapy to 4230 cGy in 16 fractions. A follow-up PET scan showed a 1.9×1.7 cm minimally hyper metabolic focus of activity in the right pelvis with a SUV of 3.6. At 18 months’ follow-up, the patient is alive without any recurrence of cancer.

Review of reported cases

A total of 48 patients reported in 25 articles (along with our case report) met the eligibility criteria (Table 1). The median age of recipients was 47 years (range 9-66), and 27% were females. The cause for renal transplant were: chronic glomerulonephritis (22%, n=6),6-10 polycystic kidney disease (11%, n=3),8,11,12 hypertension (11%, n=3),13,14 IgA nephropathy (8%, n=2),10 renal pelvis carcinoma with left nephrectomy (4%, n=1),15 nephronopthisis (4%, n=1),16 congenital nephrotic syndrome (4%, n=1),10 amyloid disease (4%, n=1),17 diabetes mellitus (4%, n=1),6 interstitial nephritis (4%, n=1),18 Henoch-Schonlen purpura (4%, n=1),19 Alport syndrome (4%, n=1),18 neurogenic bladder (4%, n=1), obstructive uropathy (4%, n=1) and ESRD of unknown origin (8%, n=2).20,21

The median age of donors was 52.5 years (range 17-73) with 24% of them being females. Where data was available, 60% (n=22) of the donors were cadaver,6-8,12-15,17,18,21-28 while the rest (n=15, 40%) were living.2,11,16,19,20,28,29 Six of the living donors were related to the recipients.16,19,20,28,29

Seven donors were subsequently found to have malignancy including clear cell carcinoma,20 hypernephroma,11 anaplastic tumor on nephrostomy scar,29 metastatic adenocarcinoma with unknown primary,13 primary hepatocellular carcinoma,9 metastatic giant and spindle cell carcinoma of thyroid,15 and a lung tumor.30 Out of seven, 2 donors were diagnosed with malignancy after 8 months and 10 months of transplantation.28,29 One donor had a renal cyst which was excised during the transplantation, and subsequently found to be a renal cell carcinoma.20 Three donors had history of malignancy in other organs with no identified metastasis to kidney at the time of donation.9,13,15 Tunner et al. described a case in which a kidney with resected renal cell carcinoma was transplanted to a man in desperate need of functioning kidney.11

The median time interval from transplantation to presentation or diagnosis of the malignancy in recipients was 210 days. The latency period between transplant and cancer diagnosis was 272 days in cancer of recipient origin in comparison to 210 days in those with cancer of donor origin.

Biopsy was done for the diagnosis of cancer in 100% (n=48) of recipients, and 69% (n=33) of the cancers had RCC. The most common type of RCC was clear cell carcinoma (27%, n=9)7,10,12-14,20,21,31 while the other types were: sarcomatoid (15%, n=5),2,8 angiosarcoma (6%, n=2),18 renal papillary tumor (6%, n=2),28,31 anaplastic (6%, n=2),25,29 chromophobe (3%, n=1),16 cystic adenocarcinoma (3%, n=1),31 anaplastic adenocarcinoma (3%, n=1),29 giant and spindle cell carcinoma (3%, n=1),15 and undifferentiated (6%, n=2).17,22 The type of renal cell carcinoma was not mentioned in the rest (22%, n=7),2,6,19,31 Other tumors (31%, n=15) comprised 31% of the cases which included: undifferentiated cancer (20%, n=3),6 invasive urothelial carcinoma (7%, n=1),24 papillary transitional cell carcinoma of bladder (7%, n=1).31 Thirty-three percent of the tumors were subsequently found to be benign and the type of cancer was not mentioned in the rest (33%, n=5).

Fifty-five percent (n=31) of the tumors were donor in origin, while 39% (n=22) originated from the recipient. The rest (6%, n=3) were determined to be derived from both donor and recipient. For example, one of the tumors in Pedotti et al.31 had 60% recipient and 40% donor DNA material indicative origin from both donor and recipient cell.

Explantation of the graft or excision of the tumor or a part of the graft, and discontinuation of immunosuppressants along with supportive treatment were used for management in most cases. Explantation or excision was done in 90% of the nonmetastatic malignancies, while 84% of metastatic malignancies underwent explantation or excision. Chemotherapy,6,7,12,24,28 radiotherapy,13,18,29 or both18 were also used in 9 cases. While 64% (n=7) of the 9 cases had metastasis,7,12,13,17,18,24,32 18% (n=2),29 had no metastasis, and the status of metastasis was not mentioned in the rest, (18%, n=2).6 In one case treated with local irradiation, distant metastasis was diagnosed at autopsy.29 Local irradiation was administered to treat recurrent local malignancy in our case after initial explantation.

The median survival was estimated to be approximately 72 months. Actuarial 1-year and 5-year survival rates were 73.4% and 55.1% respectively. Out of eleven recipients, who died after transplant, 9 were due to malignancy-related causes,6,8,11,15,17,18,24,26,29 while 2 were due to other causes.2 The recipient in Llamas et al.8 died 9 months post-transplant due to peritonitis secondary to sarcomatoid neoplasm of renal graft. Metastasis of the cancer was the cause of death in four recipients,15,17,18,29 while two recipients died due to intracerebral hemorrhage.6,24 Death due to invasion of renal cell carcinoma (RCC) aggressively into adjacent tissue accounted for the death in the patient reported by Tunner et al.11 Among the recipients from 7 donors who subsequently developed malignancy, 57% (n=4),9,11,15,29 were dead within a year. The cause of death in all these recipients was malignancy-related.

Discussion

Our review revealed post renal transplant malignancy in a total of 48 recipients. RCC, the most common type of kidney cancer in adults, was diagnosed in the majority of our cases. Twenty-seven percent of the renal cell carcinoma were clear cell carcinoma which is the most common RCC type. RCC is also known to be the most frequently reported non-central nervous system (CNS) tumor transmitted by transplantation, followed by melanoma and choriocarcinoma.33 Twelve percent of the cases in our review, including our case, had a sarcomatoid differentiation. The incidence of tumors with sarcomatoid differentiation in general population is estimated as 1-8%, although as high as 32% has been reported.34-37

In our review, the median age of recipients at diagnosis was 49 years while the median age of donors was 52.5 years. The median age at diagnosis for RCC is 64 in normal population, and is unusual in patients under 40 years of age and rare in children.38-40 Immunosuppression in recipients may be one of the factors behind the development of malignancy at an early age. In addition, RCC may also occur in children receiving renal allografts from adults.16

Chronic glomerulonephritis, hypertension and cystic diseases of kidney were the common factors leading to end stage renal disease in our review. Our case also had a history of chronic hypertension and heavy smoking. In fact, hypertension, smoking, obesity and polycystic kidney disease have been well-recognized risk factors for the development of RCC in normal adults.41-45

The malignancy in post-transplant cases might be due to de novo occurrence, recurrence of malignancy or donor-related malignancy. Compared to 3% in general population, RCC occurs de novo in 4.6% of cancers in organ allograft recipients.46 Transmission of malignancy in an immunosuppressed recipient usually occurs when the tumor is undetected before the organ donation or it may be misdiagnosed as a benign condition such as cyst.24 This incidence of tumor transmission may also have risen in recent years with the increased donor age.8 In our review, more than half of the tumors were donor in origin-including both donor-derived and donor-transmitted malignancies. Thirty-nine percent of the tumors in our review were recipient in origin. Nineteen out of the twenty cases were recipient in origin in Pedotti et al.,31 thus, suggesting that donor transmission of solid cancer was an unlikely event in their study. Microchimerism, a phenomenon of harboring small numbers of cells that originated in a genetically different individual, has been described in previous post-transplant cases. Three cases in our review demonstrated microchimerism.10,31 In a case review by Mengel et al., two metanephric adenomas demonstrated microchimerism comprising both donor-and recipient-derived tumor cells, however, four other tumors were all of donor origin without chimerism.10 Thus, they concluded that tumors arising in renal transplants originate completely from graft cells except for metanephric adenomas. One of the cases in Pedotti et al.31 was also analyzed to be 60% recipient and 40% donor in origin. However, the cancer was considered to be a recipient origin because of greater percentage of recipient DNA.

Different factors such as type, level and extent of immunosuppression, the use of drugs such as cyclosporine and azathioprine, carcinogenic factors such as sun exposure, genetic predisposition to cancer, pretransplantation dialysis, and the presence of particular viral infections are associated with development of de novo neoplasia in transplant recipients.47,48 The overall level and extent of immunosuppression, as illustrated by more malignancies after cardiac transplant in comparison to renal transplant, appears to be the principal factor that increases the risk of post-transplant malignancy.49 This is probably related to decreased immunosurveillance of neoplastic cells and depressed antiviral immune activity. A total of 7 donors in our review had a history of or were diagnosed after transplant with malignancy. Previous studies have shown that about 45% of recipients of kidney transplant from donors with known or incidentally discovered malignancy develop the malignancy.24 The risk of cancer transmission from donor to recipient is largely similar for all solid organ recipients.50 The median time interval from transplantation to presentation or diagnosis of the malignancy in recipients was 270 days in our review. In a study published by Buell et al., the mean time was approximately 2 months.50 The short latency period may indicate a possibility of undetected cancer at the time of transplantation or rapidity of tumorigenesis in immunosuppressant transplant recipients. Almost two-thirds of the cases underwent explantation of the graft. Eleven percent underwent excision of the tumor of a part of the graft. In our case, explantation was done initially and then local irradiation was performed later to treat local recurrent malignancy. The patient refused chemotherapy but was doing well till last follow-up at 18 months. In one case treated with local irradiation, distant metastasis was diagnosed at autopsy.29 Radiation therapy was used after explantation in 2 prior cases out of which one died,18 while the other remained in good clinical condition waiting for another kidney.13 Although guidelines are lacking, most cases with transplant related renal malignancy are treated primarily with explantation of the graft with chemotherapy and radiation therapy as adjunct in selected cases. Ribal et al.46 have reported successful conservative surgery of renal tumors (nephron sparing) with preservation of graft function, but this is only recommended for single carcinoma less than 4 cm in size.

The outcome for transplant recipients with neoplastic complications is unclear. We calculated the median survival to be 72 months. Actuarial 1-year and 5-year survival rates were 73.4% and 55.1% respectively. In our review, 25% of deaths were related to malignancy. In a review of data from different sources by Briggs et al.,51 malignancy was thought to account for 9-16% of all deaths in renal transplant recipients. Various factors affect the prognosis of RCC in general. The survival difference is largely due to differences in stage in particular and grade, although cytogenetics also play a role.52-54 Cytogenetic abnormalities such as del(8p)/-8, +12, and +20, p53, and gain of 5q31 have prognostic implications.52,55,56 The prognostic value of cytogenetic changes in RCC in transplant recipients has not been studied. The patient reported here had complex cytogenetic changes and was alive at 18-month follow-up.

Conclusions

Kidney transplant recipients have a small but definite risk of kidney cancer. It affects younger patients and usually occurs within a year of transplant, likely due to immunosuppression. Whether the use of older donors may increase the likelihood needs further investigation. Explantation or excision of the graft is the most important treatment for localized disease, while radiotherapy and chemotherapy may be used as adjunct in select cases. The presence of metastasis, explantation or excision of affected kidney and development of cancer in donors may predict outcomes. The results may guide patient education and informed decision-making.

Acknowledgement

Vijaya Bhatt is supported by the 2015-2016 Physician-Scientist Training Program Grant from the College of Medicine, University of Nebraska Medical Center.

References

1. 

J Murray, R Gleason, A. Bartholomay Fourth report of the human kidney transplant registry: 16 September 1964 to 15 March 19651. Transplantation 1965;3:684.

2. 

R Desai, D Collett, CJ Watson. Cancer transmission from organ donors-unavoidable but low risk. Transplantation 2012;94:1200-7.

3. 

J Xu, SL Murphy, KD Kochanek, E. Arias Mortality in the United States, 2015. NCHS data brief 2016:1-8.

4. 

I Penn. Primary kidney tumors before and after renal transplantation. Transplantation 1995;59:480-5.

5. 

I Penn. Occurrence of cancers in immunosuppressed organ transplant recipients. Clin Transpl 1998:147-58.

6. 

OH Bentdal, IB Brekke, B Lien. Rapid development of cancer in both kidney grafts after transplantation from a donor with undiagnosed malignant disease. Transplantation Proc 1994;26:1763.

7. 

M Kunisch-Hoppe, M Hoppe, RM Bohle. Metastatic RCC arising in a transplant kidney. Eur Radiol 1998;8: 1441-3.

8. 

F Llamas, E Gallego, A Salinas. Sarcomatoid renal cell carcinoma in a renal transplant recipient. Transplant Proc 2009;41:4422-4.

9. 

CF Zukoski, DA Killen, E Ginn. Transplanted carcinoma in an immunosuppressed patient. Transplantation 1970;9:71-4.

10. 

M Mengel, D Jonigk, L Wilkens. Chimerism of metanephric adenoma but not of carcinoma in kidney transplants. Am J Pathol 2004;165:2079-85.

11. 

WS Tunner, EI Goldsmith, JC Whitsell 2nd. Human homotransplantation of normal and neoplastic tissue from the same organ. J Urol 1971;105:18-20.

12. 

S Yaich, N El’Aoud, S Zaghdane. Primary adenocarcinoma in a kidney allograft: a case report and review of the literature. Transplant Proc 2011;43:660-2.

13. 

A Homburg, J Kindler, F Hofstadter. Regression of an adenocarcinoma transmitted by a cadaver kidney graft. Transplantation 1988;46:777-9.

14. 

TC McCanty, J Jonsson, N Khawand. Transferral of a malignancy with a transplanted kidney. Transplantation 1989;48:877-9.

15. 

HW Muiznieks, JW Berg, W Lawrence Jr., HT Randall. Suitability of donor kidneys from patients with cancer. Surgery 1968;64:871-7.

16. 

AJ Greco, JH Baluarte, KE Meyers. Chromophobe renal cell carcinoma in a pediatric living-related kidney transplant recipient. Am J Kidney Dis 2005;45:e105-8.

17. 

IJ Beckingham, JS O’Rourke, MC Bishop. The use of DNA typing to clarify the origin of metastatic carcinoma after renal transplantation. A clinical and medico-legal problem. Transpl Int 1994;7:379-81.

18. 

J Thoning, Y Liu, C Bistrup. Transmission of angiosarcomas from a common multiorgan donor to four transplant recipients. Am J Transplant 2013;13:167-73.

19. 

GW Lamb, GM Baxter, RS Rodger, M. Aitchison Partial nephrectomy used to treat renal cell carcinoma arising in a live donor transplant kidney. Urol Res 2004;32:89-92.

20. 

M Neipp, A Schwarz, S Pertschy. Accidental transplantation of a kidney with a cystic renal cell carcinoma following living donation: management and 1 yr follow-up. Clin Transplant 2006;20:147-50.

21. 

G Heinz-Peer, T Helbich, B Nottling. Renal cell carcinoma in an allograft kidney transplant. Transplantation 1994;57:475-8.

22. 

B Barrou, MO Bitker, A Delcourt. Fate of a renal tubulopapillary adenoma transmitted by an organ donor. Transplantation 2001;72:540-1.

23. 

O Detry, A De Roover, L de Leval. Transmission of an undiagnosed sarcoma to recipients of kidney and liver grafts procured in a non-heart beating donor. Liver Transpl 2005;11: 696-9.

24. 

GF Ferreira, RA de Oliveira, LB Jorge. Urothelial carcinoma transmission via kidney transplantation. Nephrol Dial Transplant 2010;25:641-3.

25. 

D Lotan, J. Laufer Metastatic renal carcinoma in a pediatric recipient of an adult cadaveric donor kidney. Am J Kidney Dis 1995;26:960-2.

26. 

B Matter, CF Zukoski, DA Killen, E. Ginn Transplanted carcinoma in an immunosuppressed patient. Transplantation 1970;9:71-4.

27. 

B Detroz, O Detry, M D’Silva. Organ transplantation with undetected donor neoplasm. Transplant Proc 1991;23:2657.

28. 

Kauffman H Myron, MA McBride, WS Cherikh. Transplant tumor registry: donor related malignancies. Transplantation 2002;74:358-62.

29. 

AJ Mocelin. Letter: inadvertent transplant of a malignancy. Transplantation 1975;19:430.

30. 

HM Kauffman. Malignancies in organ transplant recipients. J Surg Oncol 2006;94:431-3.

31. 

P Pedotti, F Poli, E Longhi. Epidemiologic study on the origin of cancer after kidney transplantation. Transplantation 2004;77:426-8.

32. 

Kauffman H Myron, MA McBride, WS Cherikh. Transplant tumor registry: donor related malignancies. Transplantation 2002;74:358-62.

33. 

I Penn. Transmission of cancer from organ donors. Ann Transplant 1997;2:7-12.

34. 

M de Peralta-Venturina, H Moch, M Amin. Sarcomatoid differentiation in renal cell carcinoma: a study of 101 cases. Am J Surg Pathol 2001;25:275-84.

35. 

B Shuch, J Said, JC La Rochelle. Cytoreductive nephrectomy for kidney cancer with sarcomatoid histology: is up-front resection indicated and, if not, is it avoidable? J Urol 2009;182:2164-71.

36. 

JC Cheville, CM Lohse, H Zincke. Sarcomatoid renal cell carcinoma: an examination of underlying histologic subtype and an analysis of associations with patient outcome. Am J Surg Pathol 2004;28:435-41.

37. 

KM Tomera, GM Farrow, MM Lieber. Sarcomatoid renal carcinoma. J Urol 1983;130:657-9.

38. 

S Siemer, M Hack, J Lehmann. Outcome of renal tumors in young adults. J Urol 2006;175:1240-4.

39. 

RH Thompson, MA Ordonez, A Iasonos. Renal cell carcinoma in young and old patients: is there a difference? J Urol 2008;180:1262-6.

40. 

A Cook, AJ Lorenzo, JL Salle. Pediatric renal cell carcinoma: single institution 25-year case series and initial experience with partial nephrectomy. J Urol 2006;175:1456-60.

41. 

MG Cumberbatch, M Rota, JW Catto, C. La Vecchia The role of tobacco smoke in bladder and kidney carcinogenesis: a comparison of exposures and meta-analysis of incidence and mortality risks. Eur Urol 2016;70:458-66.

42. 

KF Adams, MF Leitzmann, D Albanes. Body size and renal cell cancer incidence in a large US cohort study. Am J Epidemiol 2008;168:268-77.

43. 

B Ljungberg, SC Campbell, HY Choi. The epidemiology of renal cell carcinoma. Eur Urol 2011;60:615-21.

44. 

JF Brennan, MM Stilmant, RK Babayan, MB Siroky. Acquired renal cystic disease: implications for the urologist. Br J Urol 1991;67:342-8.

45. 

JB Wetmore, JP Calvet, ASL Yu. Polycystic kidney disease and cancer after renal transplantation. J Am Soc Nephrol 2014;25:2335-41.

46. 

MJ Ribal, F Rodriguez, M Musquera. Nephron-sparing surgery for renal tumor: a choice of treatment in an allograft kidney. Transplant Proc 2006;38:1359-62.

47. 

Y Miao, JJ Everly, TG Gross. De novo cancers arising in organ transplant recipients are associated with adverse outcomes compared with the general population. Transplantation 2009;87:1347-59.

48. 

C Morath, M Mueller, H Goldschmidt. Malignancy in renal transplantation. J of Am Soc Nephrol 2004;15:1582-8.

49. 

JF Buell, TG Gross, ES Woodle. Malignancy after transplantation. Transplantation 2005;80:S254-64.

50. 

JF Buell, TM Beebe, J Trofe. Donor transmitted malignancies. Ann Transplant 2004;9:53-6.

51. 

JD Briggs. Causes of death after renal transplantation. Nephrol Dialysis Transplant 2001;16:1545-9.

52. 

T Gudbjartsson, S Hardarson, V Petursdottir. Histological subtyping and nuclear grading of renal cell carcinoma and their implications for survival: a retrospective nation-wide study of 629 patients. Eur Urol 2005;48:593-600.

53. 

KH Tsui, O Shvarts, RB Smith. Prognostic indicators for renal cell carcinoma: a multivariate analysis of 643 patients using the revised 1997 TNM staging criteria. J Urol 2000;163: 1090-5.

54. 

P Elfving, N Mandahl, R Lundgren. Prognostic implications of cytogenetic findings in kidney cancer. Br J Urol 1997;80:698-706.

55. 

B Gunawan, W Huber, M Holtrup. Prognostic impacts of cytogenetic findings in clear cell renal cell carcinoma: gain of 5q31-qter predicts a distinct clinical phenotype with favorable prognosis. Cancer Res 2001; 61:7731-8.

56. 

B Ljungberg, B Bozoky, G Kovacs. p53 expression in correlation to clinical outcome in patients with renal cell carcinoma. Scand J Urol Nephrol 2001;35:15-20.

Figure 1.

Flow diagram for selection of the articles.

rt-2017-1-6550-g001.jpg
Table 1.

Kidney cancer in recipients of kidney transplant.

Variables Non-metastatic kidney cancer Metastatic kidney cancer
Age in years, median (range) 47 (12-64) 48 (27-66)
Female 40% 29%
Donor type Living 55%; Cadaver 45% Living 0%; Cadaver 100%
Donor age in years 54 (22-73) 52 (17-68)
Concomitant cancer in the donor 13% 20%
Latency period since kidney transplant (days) Median 120 (0-6780) Median- 210 (90-2190)
Histology (%RCC) 66 80
Explantation or excision 90% 84%
Abstract views:
448

Views:
PDF
208
HTML
122

Article Metrics

Metrics Loading ...

Metrics powered by PLOS ALM


Copyright (c) 2017 Prajwal Dhakal, Smith Giri, Krishmita Siwakoti, Supratik Rayamajhi, Vijaya Raj Bhatt

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
 
© PAGEPress 2008-2017     -     PAGEPress is a registered trademark property of PAGEPress srl, Italy.     -     VAT: IT02125780185