Sporadic renal cell carcinoma in young and elderly patients: are there different clinicopathological features and disease specific survival rates?
© Denzinger et al; licensee BioMed Central Ltd. 2007
Received: 05 December 2006
Accepted: 05 February 2007
Published: 05 February 2007
Sporadic renal cell carcinoma (RCC) is rare in young adults. In the present retrospective study we reviewed clinicopathological features and disease specific survival rates in young patients (≤45 years) with RCC and compared them to old patients (≥75 years) with RCC.
Between 1992 and 2005 a total of 1042 patients were treated for RCC at our institution. We found 70 patients 45 years or younger (YP) and 150 patients 75 years or older (OP) at time of diagnosis. There were no differences in therapeutical approaches between both groups. Clinical and biologic parameters at diagnosis were compared and subjected to uni- and multivariate analysis to study cancer specific survival and progression rate. Mean postoperative follow-up in both groups was 50.1 months.
Mean age was 39 years in YP and 80 years in OP, respectively. YP demonstrated significantly lower stage (pT1-pT2 N0 M0, p = 0.03), lower tumor grade (p = 0.01) and higher male-to-female ratio (p < 0.001). The rate of lymph node metastases or distant metastatic disease at presentation did not differ significantly between both groups. In multivariate analysis young age was independently associated with a higher 5-year cancer specific survival (95.2% vs. 72.3%, p = 0.009) and a lower 5-year progression rate (11.3% vs. 42.5%, p = 0.002).
Sporadic RCC in young patients have lower tumor stages and grades and a better outcome compared to elderly. Age≤45 years was an independent prognostic factor for survival and progression.
Renal cell carcinoma (RCC) is the most common renal parenchymal malignancy and represents 3% – 6% of all adult malignancies . Patients are generally older than 40 years at diagnosis and the disease occurs predominantly in the seventh decade of life . Only 3 to 7% of all sporadic RCC patients have been reported to be below 40 years [3–7].
Previous RCC studies and cancer specific survival rates of young and old RCC patients.
5-year cancer specific survival rate
Boykin et al. 
Abou El Fettouh et al. 
Eggener et al. 
Schiff et al. 
486 (≥41 y)
p < 0.01
Rainwater et al. 
34 (≥80 y)
Yusim et al. 
107 (≥50 y)
p < 0.05
Gillett et al. 
958 (60–70 y)
Goetzl et al. 
99 (≥41 y)
Sanchez-Ortiz et al. 
145 (58–61 y)
p < 0.01
Siemer et al. 
2164 (≥41 y)
Between 1992 and 2005 a total of 1042 patients underwent partial or radical nephrectomy for renal masses at the Department of Urology of the University of Regensburg. The medical and histopathological data of 70 YP (range: 26 to 45 years, mean: 39 years) and 150 OP (range: 75 to 91 years, mean: 80 years) suffering from RCC were reviewed We did not include middle-aged patients (>45 years and < 75 years) to avoid masking any potential differences in tumor biology between young and old patients. All familial RCC syndromes including von Hippel-Lindau disease were excluded. Pathological evaluation was reviewed and tumor stage was adapted according to the 2002 TNM classification. Patients were evaluated preoperatively by physical examination, laboratory studies, ultrasonography and radiographic staging including chest x-ray and computerized tomography. Staging lymph nodes dissection was performed for all patients. The postoperative outcomes and duration of follow-up were compiled by chart review and patient interview. Complete follow-up information was available for all patients through a department registry. Statistical analysis were completed using SPSS version 12.0 (SPSS, Chicago, IL). Contingency table analysis and two-sided Fisher's exact tests were used to study the statistical association between the two groups. Significant differences concerning tumor progression and cancer specific survival were calculated using the Kaplan-Meier method and log rank test. For cancer related death, patients were surveyed at the time of their last clinical follow-up appointment or at their date of death not related to the tumor. Deaths from causes other than RCC were censored. Uni- and multivariate Cox proportional hazards models were performed to evaluate the relationship between cancer specific survival, tumor progression, TNM pathologic stage, histologic subtypes, tumor grade, incidental or symptomatic disease and, in addition to other variables, age (separated into YP and OP). P values < 0.05 were considered significant.
Comparison of histopathological and clinical parameters according to age
Comparison of clinical and pathological features of young (YP) and elderly (OP) RCC patients.
YP (70 patients) No. (%)
OP (150 patients) No. (%)
Sex ratio (male/female)
p = 0.19
WHO 2002 stage of primary tumor
p = 0.03
pT1- pT2, N0, M0
pT3, N0, M0
pT4 and/or N+, and/or M+
p = 0.01
p = 0.32
Other histological types
YP were more likely to smoke tobacco (>10 cigarettes per day, 46.3% vs. 9.7%, p < 0.001) but did not differ concerning obesity (BMI >30; 20.9% vs. 22.1%, p = 0.93). There were no significant differences in the rate of secondary malignancies (p = 0.07).
RCC was an incidental finding in 71.6% YP and 65.5% OP (p = 0.19). In both groups dominant symptoms were flank pain (17.9% vs. 12.4%, p = 0.23) and macroscopic hematuria (13.1% vs. 10.4%, p = 0.43). While there was a tendency for OP to present more often with fever, night sweat or loss of weight (11.7% vs. 4.5%), this failed to reach the level of significance (p = 0.09). The rate of lymph node metastases (YP: 3.2%, OP: 8.7%, p = 0.24) or distant metastatic disease (YP: 1.8%, OP: 5.6%, p = 0.71) at presentation did not differ significantly between both groups.
YP showed significantly lower T stage (p = 0.03) and tumor grade (p = 0.01). While chromophobe RCC was more frequent in OP, this failed to reach the level of significance (10.7% vs. 7.1%, p = 0.32). There were no statistically significant differences in tumor location and focality, mean tumor diameter (YP: 6.5 cm, OP: 7.3 cm, p = 0.39), WHO 2002 N and M stages or UICC stage (table 2).
Nephron sparing approach was chosen more often in YP (19.4% vs. 9.0%, p = 0.031). A similar proportion of patients in the two groups with nodal or distant metastasis received additional therapy (immunotherapy, tumor vaccines or conventional chemotherapy). There were no differences in mean tumor size, tumor location, performance status, ethnicity, family history of cancer, body mass index or type of treatment between YP and OP cohort.
Predictive parameters for cancer specific survival
Univariate Cox regression analysis of factors possibly influencing cancer specific survival in patients with RCC.
YP (≤45 years)
0.15 – 0.72
OP (≥75 years)
1.72 – 12.49
1.98 – 15.64
9.88 – 131.02
0.73 – 21.94
< 7 cm
0.40 – 10.38
0.46 – 4.97
0.23 – 4.78
Other histological types
0.15 – 8.96
0.24 – 1.56
1.71 – 11.37
Multivariate Cox regression analysis of factors possibly influencing cancer specific survival in patients with RCC.
stepwise reverse selection
YP (≤45 years)
0.11 – 0.89
OP (≥75 years)
0.74 – 10.49
0.95 – 5.69
3.32 – 127.78
0.18 – 15.08
< 7 cm
0.46 – 11.18
0.14 – 3.48
0.21 – 5.75
Other histological types
0.06 – 6.56
0.38 – 2.01
0.09 – 2.33
Just 3.4% to 7.5% of all RCC patients have been reported to be young adults . This is reflected in our series, as 7.2% of 968 RCC patients were aged ≤45 years. It has been suspected that young RCC is characterized by different clinicopathological and biologic character. However previous studies are somewhat contradictory and feature various methodologies. Some previous studies lack a pronounced span of age between young patients and the comparison group. While 20 years were chosen by Gillett , Sanchez-Ortiz chose 18 years , but even less has been employed [5, 15, 17, 19]. To compare YP and OP we have determined a minimum of 30 years separating both groups. We thus hoped to increase the discrimination between young and old patients, as some overlap might occur blurring the picture. This approach seems to be backed up by epidemiological data suggesting a significantly lower incidence in patients aged up to 45 years .
OP were a mean 8 years above the major age of regular onset, which has been reported to be roughly 70 . Thus while it has to be taken into consideration, that OP might somewhat differ from regular onset patients, the present series offers a clear separation between OP and YP. Analysis of our population confirmed the usual prognostic factors for RCC: pTNM tumor stage, tumor grade, tumor diameter, N and M stage and circumstances of renal cell carcinoma discovery. Contrary to expectations, symptoms that may be considered as substitutes for performances status were not retained as independent prognostic factors in our multivariate analysis. Moreover, recent studies considering this parameter did not show any difference according to the age at diagnosis [16, 18]. Controversial data exist on the histopathological character of younger patients. In the present series YP clearly demonstrated lower T stages and lower tumor grade (table 2), while other studies only showed lower T stages in YP [6, 16, 18, 19]. Schiff et al. compared patients younger than 40 years old to patients older than 40 years. Their data differed with the most contemporary series in that more patients in the older group presented with T1 tumors .
In contrast to our series a former study of wide span comparison of RCC patients < 40 years and >80 years could not figure out any differences in tumor grade . A variation of distribution of histological subtypes has been reported by Gillett et al. In their to date largest series of 107 younger cases chromophobe RCC were found in 13.1% vs. 3.6% . Also Rodriguez et al. found out differences in histological subtypes, OP significantly more often showed clear cell RCC than YP (91.0% vs. 69.0%, p < 0.001) . In accordance with previous reports [16–19] in our series however there was an even distribution of subtypes among YP and OP. Previous authors have suggested that younger adults may have more aggressive renal tumors with a poorer prognosis than older patients [3, 6]. YP tended to improved cancer specific survival in the present series. 5-year survival rate was 95.2% in YP and 72.3% in OP (p = 0.009). This finding supports previous reports [5, 15], also in non comparative studies young patients showed similar survival rates [3, 12, 13], and is in analogy to favourable histopathology in YP. The less advanced forms of RCC found in YP may explain the better 5- year cancer specific survival. Several earlier studies [5, 6] had reported comparable survival rates, despite their higher percentages of localised forms in young patients, suggesting that early-onset RCC forms might be more aggressive. However, those studies had short follow-up  or had small population size , hereby rendering interpretation of their results more difficult. In the present series, young age was an independent predictor of improved cancer specific survival. Siemer et al. found young patients to present with symptoms more often. While in their series young RCC was still related to favourable outcome, symptoms caused by malign renal masses were associated with poor prognosis [19, 21]. In our series YP did not complain of symptoms more often. In synopsis the factors that determine the improved survival outcome in YP with RCC have yet to be clearly defined.
We do not believe in profoundly different tumor characters per se. This notion is supported by a significant number of young patients presenting with advanced disease and tumor related death in this group. However we suspect a reduced momentum of tumor biology in young patients. We hypothesize a better tumor control, which might be due to a superior immunology in this age group slowing the tumors in growth.
To conclude RCC in younger and elder patients, as defined by a minimum of 30 years as discriminatory span, young patients present with favourable clinicopathology and an improved cancer specific 5-year survival rate after adjusting for clinical and pathological variables on multivariate analysis. These obvious differences contribute to the trend toward improve outcome in younger patients for which their young age was an independent prognostic factor. Our data refute past reports of poorer cancer specific survival in younger patients with RCC.
The authors thank Cornelia Mohaupt and Ingrid Gebhard for excellent assistance.
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