Purpose: We determined the prognostic significance of incidentally discover
ed renal cell carcinoma in the era of increased incidental detection.
Materials and Methods: We reviewed the records of 633 consecutive patients
who underwent radical or partial nephrectomy for renal cell carcinoma at ou
r institution between 1987 and 1998. Patients were divided into those who w
ere asymptomatic and tumor was diagnosed incidentally and those diagnosed a
fter presenting with any of the classic symptoms of renal cell carcinoma or
subsequent metastasis. All renal cell carcinoma lesions were assigned a st
age and grade according to 1997 TNM criteria. All patients were followed po
stoperatively to assess survival rates, and monitor recurrence and metastas
is.
Results: Of the 633 patients 95 (15%) were treated fur incidentally discove
red renal cell carcinoma and 538 (85%) presented with symptoms secondary to
renal cell carcinoma at diagnosis. Patient age and sex distribution were s
imilar in the 2 groups. Stage I lesions were observed in 62.1% of patients
with incidental renal cell carcinoma and in 23% with symptomatic renal cell
carcinoma. In contrast, stage TV lesions were present in 27.4% of patients
with incidental versus 54% with symptomatic renal cell carcinoma. Thus, in
cidental lesions were of significantly lower stage than those causing sympt
oms (p < 0.001). Similarly 15.8% of incidental but 42.4% of symptomatic les
ions were grade 3 or 4 (p = 0.006). Patients were followed postoperatively
for a mean of 47 months plus or minus 40 months. The 5-year cancer specific
survival rate was significantly higher for incidental than for symptomatic
tumors (85.3% versus 62.5%). Likewise, the local and distal recurrence rat
es were higher for symptomatic lesions. When adjusted for stage, no differe
nce in survival was noted in the 2 groups for stages I to III disease and a
minimally significant difference was noted for stage TV cancer. Multivaria
te analysis of stage and grade attributed the survival difference in stage
TV disease to the significantly higher grade of symptomatic lesions.
Conclusions: At presentation incidental tumors are of significantly lower s
tage and grade than tumors producing symptoms. Subsequently these clinicall
y and histologically less aggressive lesions lead to better patient surviva
l and decreased recurrence. Thus, the detection of renal cell carcinoma bef
ore symptom onset enables treatment of less aggressive tumors and provides
a better prognosis for patients. Given these data efforts should be directe
d toward the development of a screening protocol to detect these lesions ea
rly, so that they may be prevented from progressing to the point when sympt
oms are apparent and prognosis becomes worse. In addition, the significant
correlation of tumor grade with survival in our study further demonstrates
the prognostic value of tumor grade and molecular markers for the future ev
aluation and treatment of renal cell carcinoma.