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early diagnosis. Cancer-specific and overall survival rates

were similar between dialysed and transplanted patients

( Table 5

).

The conclusion of this systematic review highlights the

requirement for regular annual monitoring of the native

kidney in CKD patients and particularly those with a history

of RCC. The reference treatment for a cancer of the native

kidneys is radical nephrectomy.

4.3.2.

Prostate cancer

In this systematic review, the main prognostic factors for

recurrence were: stage, prostate-specific antigen, and

Gleason score. Radical prostatectomy is the preferred

treatment both for staging and curative purposes. Lymph

node resection may be best limited to one side of the pelvis

to preserve the iliac vessels for the transplantation on the

other side

[25] .

Transperineal prostatectomy could also be

an option to preserve the iliac vessels

[26]

.

The studies reported low recurrence rates consistent

with prognostic nomograms. In the Tillou et al

[27]

study,

the risk of biochemical recurrence at 10 yr, calculated using

the Memorial Sloan Kettering Cancer Center nomogram did

not exceed 3% in the worst case and was 1

2% in all other

cases. This nomogram has proven its reliability in other

studies on large cohorts. The nomogram allowed registra-

tion of patients on the transplantation waiting list at an

earlier stage, whilst radical prostatectomy made the

decision to put the patient on the transplant list easier.

The authors reported no recurrence with a mean follow-up

of 3.2 yr, suggesting that there could be no waiting period

for transplantation in cases of cured low-risk PC

[25]

.

In their study, Woodle et al

[9]

(which was an update of the

PC series published by Penn in 1995 and 1997

[4]

) included a

significant number of high-risk extraprostatic tumours.

Despite its shortcomings, this study is still unequalled for

the study of high-risk PC before transplantation

[11] .

4.3.3.

Urothelial carcinoma (bladder and upper urinary tract

urothelial carcinoma)

The included studies showed that UUTUC has a high risk of

recurrence. The risk of synchronous bilateral involvement is

10

16% and the risk of contralateral recurrence is 31

39%

( Table 7 )

. For candidates for transplantation with a history

of UUTUC, two strategies are justified:

1. Systematic treatment of the contralateral upper urinary

tract and/or the bladder by nephroureterectomy and/or

even cystectomy;

2. Close monitoring of the bladder and the contralateral

upper urinary tract.

4.3.4.

Testicular cancer

The level of evidence reported in this study did not allow us

to conclude on the risk of testicular tumour recurrence after

renal transplantation. The two case reports highlighted the

risk of retroperitoneal recurrence after transplantation,

even with a long waiting period

( Table 8

). A case-by-case

discussion is needed to decide on a period of exclusion

before transplantation.

4.4.

Implications for research

Although the findings of this systematic review enabled us

to identify the prognostic factors of recurrence and to

conclude that immunosuppression did not modify the

natural history of urological cancer for selected patients,

the literature in this particular area differed according to the

type of cancer. With the exception of Tillou et al

[25]

(19 patients), we found no comparative study for PC. There

were few studies on bladder cancer, with no data

concerning the stage (tumour invading the vesical muscle

or not) and the use of adjuvant intravesical therapy.

In practice, it appears to be difficult to evaluate the

excess risk of recurrence represented by the initiation of

immunosuppressive therapy and thus the possible delete-

rious impact of transplantation on recurrence and cancer-

specific survival. Randomised controlled trials will ethically

and logistically be difficult to conduct. However, well-

designed prospective cohort studies with homogenous

type/stage of cancer and clear predefined oncological

outcomes at different time points are needed to strongly

support a reduction of the waiting period for low-risk RCC

and PC, which was a tendency suggested in this systematic

review.

4.5.

Limitations of this study

This report is the first systematic review assessing and

appraising all available evidence of the risk of cancer

recurrence for CKD patients on dialysis or who have

undergone transplantation. Limitations mainly consist in

the low level of the references:

The included studies are all retrospective and most of

them are not comparative. As such, the RoB and/or

confounding is high in most studies.

Long-term follow-up is lacking. Several data were not

systematically reported: prognostic score or monograms,

duration, and type of immunosuppressive treatment,

type of recurrence (local or systemic). For PC, the

oncological results of nontransplanted patients were

based on only six patients in two studies.

For urothelial tumours, the majority of studies included

UUTUC occurring in the particular field of aristolochic

acid nephropathy.

4.6.

Conclusions

Although this systematic review summarised all the

available evidence on renal transplantation and history of

cancer, it was limited by the level of evidence of the

included studies, which mainly consisted of noncompara-

tive retrospective cohort studies of preselected patients.

Acknowledging that the comparison is not free from bias,

this systematic review indicates that immunosuppression

does not seem to alter the natural history of recurrence and

mortality for low-risk renal and PC, and could lead to a

shortening of the waiting period in this specific situation.

For high-risk renal and PC, the historical Cincinnati registry

E U R O P E A N U R O L O GY 7 3 ( 2 0 18 ) 9 4

10 8

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