Impact of Young Age at Diagnosis on Survival in Patients with Surgically Treated Renal Cell Carcinoma: a Multicenter Study
The prognostic significance of age in renal cell carcinoma (RCC) is a subject of debate. The aim of the present multi-institutional study was to evaluate the impact of age on clinicopathological features and survival in a large cohort of patients with RCC. A total of 5,178 patients who underwent sur...
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| Published in | Journal of Korean medical science Vol. 31; no. 12; pp. 1976 - 1982 |
|---|---|
| Main Authors | , , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Korea (South)
The Korean Academy of Medical Sciences
01.12.2016
대한의학회 |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1011-8934 1598-6357 1598-6357 |
| DOI | 10.3346/jkms.2016.31.12.1976 |
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| Abstract | The prognostic significance of age in renal cell carcinoma (RCC) is a subject of debate. The aim of the present multi-institutional study was to evaluate the impact of age on clinicopathological features and survival in a large cohort of patients with RCC. A total of 5,178 patients who underwent surgery for RCC at eight institutions in Korea between 1999 and 2011 were categorized into three groups according to age at diagnosis as follows: young age (< 40 years, n = 541), middle-age (≥ 40 and < 60 years, n = 2,551), and old age (≥ 60 years, n = 2,096) groups. Clinicopathological variables and survival rates were compared between the three groups. Young patients had lower stage tumors with a low Fuhrman grade, a lower rate of lymphovascular invasion than patients in the other age groups. Regarding histologic type, the young age group had a lower percentage of clear cell histology and a greater incidence of Xp11.2 translocation RCC. Kaplan-Meier estimates showed that cancer-specific survival was significantly better in the young age group than in the other groups (log rank test, P = 0.008). However, age at diagnosis was not an independent predictor of survival in multivariate analysis. In conclusion, young age at diagnosis was associated with favorable pathologic features, although it was not an independent prognostic factor for survival in patients with surgically-treated RCC. Age itself should not be regarded as a crucial determinant for the treatment of RCC. |
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| AbstractList | The prognostic significance of age in renal cell carcinoma (RCC) is a subject of debate. The aim of the present multi-institutional study was to evaluate the impact of age on clinicopathological features and survival in a large cohort of patients with RCC. A total of 5,178 patients who underwent surgery for RCC at eight institutions in Korea between 1999 and 2011 were categorized into three groups according to age at diagnosis as follows: young age (< 40 years, n = 541), middle-age (≥ 40 and < 60 years, n = 2,551), and old age (≥ 60 years, n = 2,096) groups. Clinicopathological variables and survival rates were compared between the three groups. Young patients had lower stage tumors with a low Fuhrman grade, a lower rate of lymphovascular invasion than patients in the other age groups. Regarding histologic type, the young age group had a lower percentage of clear cell histology and a greater incidence of Xp11.2 translocation RCC. Kaplan-Meier estimates showed that cancer-specific survival was significantly better in the young age group than in the other groups (log rank test, P = 0.008). However, age at diagnosis was not an independent predictor of survival in multivariate analysis. In conclusion, young age at diagnosis was associated with favorable pathologic features, although it was not an independent prognostic factor for survival in patients with surgically-treated RCC. Age itself should not be regarded as a crucial determinant for the treatment of RCC. The prognostic significance of age in renal cell carcinoma (RCC) is a subject of debate. The aim of the present multi-institutional study was to evaluate the impact of age on clinicopathological features and survival in a large cohort of patients with RCC. A total of 5,178 patients who underwent surgery for RCC at eight institutions in Korea between 1999 and 2011 were categorized into three groups according to age at diagnosis as follows: young age (< 40 years, n = 541), middle-age (≥ 40 and < 60 years, n = 2,551), and old age (≥ 60 years, n = 2,096) groups. Clinicopathological variables and survival rates were compared between the three groups. Young patients had lower stage tumors with a low Fuhrman grade, a lower rate of lymphovascular invasion than patients in the other age groups. Regarding histologic type, the young age group had a lower percentage of clear cell histology and a greater incidence of Xp11.2 translocation RCC. Kaplan-Meier estimates showed that cancer-specific survival was significantly better in the young age group than in the other groups (log rank test, P = 0.008). However, age at diagnosis was not an independent predictor of survival in multivariate analysis. In conclusion, young age at diagnosis was associated with favorable pathologic features, although it was not an independent prognostic factor for survival in patients with surgically-treated RCC. Age itself should not be regarded as a crucial determinant for the treatment of RCC.The prognostic significance of age in renal cell carcinoma (RCC) is a subject of debate. The aim of the present multi-institutional study was to evaluate the impact of age on clinicopathological features and survival in a large cohort of patients with RCC. A total of 5,178 patients who underwent surgery for RCC at eight institutions in Korea between 1999 and 2011 were categorized into three groups according to age at diagnosis as follows: young age (< 40 years, n = 541), middle-age (≥ 40 and < 60 years, n = 2,551), and old age (≥ 60 years, n = 2,096) groups. Clinicopathological variables and survival rates were compared between the three groups. Young patients had lower stage tumors with a low Fuhrman grade, a lower rate of lymphovascular invasion than patients in the other age groups. Regarding histologic type, the young age group had a lower percentage of clear cell histology and a greater incidence of Xp11.2 translocation RCC. Kaplan-Meier estimates showed that cancer-specific survival was significantly better in the young age group than in the other groups (log rank test, P = 0.008). However, age at diagnosis was not an independent predictor of survival in multivariate analysis. In conclusion, young age at diagnosis was associated with favorable pathologic features, although it was not an independent prognostic factor for survival in patients with surgically-treated RCC. Age itself should not be regarded as a crucial determinant for the treatment of RCC. The prognostic significance of age in renal cell carcinoma (RCC) is a subject of debate. The aim of the present multi-institutional study was to evaluate the impact of age on clinicopathological features and survival in a large cohort of patients with RCC. A total of 5,178 patients who underwent surgery for RCC at eight institutions in Korea between 1999 and 2011 were categorized into three groups according to age at diagnosis as follows: young age (< 40 years, n = 541), middle-age (≥ 40 and < 60 years, n = 2,551), and old age (≥ 60 years, n = 2,096) groups. Clinicopathological variables and survival rates were compared between the three groups. Young patients had lower stage tumors with a low Fuhrman grade, a lower rate of lymphovascular invasion than patients in the other age groups. Regarding histologic type, the young age group had a lower percentage of clear cell histology and a greater incidence of Xp11.2 translocation RCC. Kaplan-Meier estimates showed that cancer-specific survival was significantly better in the young age group than in the other groups (log rank test, P = 0.008). However, age at diagnosis was not an independent predictor of survival in multivariate analysis. In conclusion, young age at diagnosis was associated with favorable pathologic features, although it was not an independent prognostic factor for survival in patients with surgically-treated RCC. Age itself should not be regarded as a crucial determinant for the treatment of RCC. KCI Citation Count: 0 |
| Author | Kim, Wun-Jae Byun, Seok-Soo Hwang, Eu Chang Kim, Won Tae Yun, Seok Joong Kwon, Tae Gyun Seo, Sung Pil Kim, Hyeon Hoe Hong, Sung-Hoo Kang, Ho Won Kang, Seok Ho Chung, Jinsoo Kwak, Cheol Kim, Yong-June Lee, Sang-Cheol |
| AuthorAffiliation | 1 Department of Urology, Chungbuk National University College of Medicine, Cheongju, Korea 3 Department of Urology, Korea University School of Medicine, Seoul, Korea 5 Department of Urology, National Cancer Center, Goyang, Korea 8 Department of Urology, Seoul National University Bundang Hospital, Seongnam, Korea 6 Department of Urology, Kyungpook National University College of Medicine, Daegu, Korea 4 Department of Urology, College of Medicine, The Catholic University of Korea, Seoul, Korea 7 Department of Urology, Seoul National University College of Medicine, Seoul, Korea 2 Department of Urology, Chonnam National University Hwasun Hospital, Hwasun, Korea |
| AuthorAffiliation_xml | – name: 2 Department of Urology, Chonnam National University Hwasun Hospital, Hwasun, Korea – name: 4 Department of Urology, College of Medicine, The Catholic University of Korea, Seoul, Korea – name: 7 Department of Urology, Seoul National University College of Medicine, Seoul, Korea – name: 8 Department of Urology, Seoul National University Bundang Hospital, Seongnam, Korea – name: 1 Department of Urology, Chungbuk National University College of Medicine, Cheongju, Korea – name: 3 Department of Urology, Korea University School of Medicine, Seoul, Korea – name: 5 Department of Urology, National Cancer Center, Goyang, Korea – name: 6 Department of Urology, Kyungpook National University College of Medicine, Daegu, Korea |
| Author_xml | – sequence: 1 givenname: Ho Won orcidid: 0000-0002-8164-4427 surname: Kang fullname: Kang, Ho Won organization: Department of Urology, Chungbuk National University College of Medicine, Cheongju, Korea – sequence: 2 givenname: Sung Pil orcidid: 0000-0001-6179-7031 surname: Seo fullname: Seo, Sung Pil organization: Department of Urology, Chungbuk National University College of Medicine, Cheongju, Korea – sequence: 3 givenname: Won Tae orcidid: 0000-0002-7482-4550 surname: Kim fullname: Kim, Won Tae organization: Department of Urology, Chungbuk National University College of Medicine, Cheongju, Korea – sequence: 4 givenname: Seok Joong orcidid: 0000-0001-7737-4746 surname: Yun fullname: Yun, Seok Joong organization: Department of Urology, Chungbuk National University College of Medicine, Cheongju, Korea – sequence: 5 givenname: Sang-Cheol orcidid: 0000-0002-4163-2210 surname: Lee fullname: Lee, Sang-Cheol organization: Department of Urology, Chungbuk National University College of Medicine, Cheongju, Korea – sequence: 6 givenname: Wun-Jae orcidid: 0000-0002-8060-8926 surname: Kim fullname: Kim, Wun-Jae organization: Department of Urology, Chungbuk National University College of Medicine, Cheongju, Korea – sequence: 7 givenname: Eu Chang orcidid: 0000-0002-2031-124X surname: Hwang fullname: Hwang, Eu Chang organization: Department of Urology, Chonnam National University Hwasun Hospital, Hwasun, Korea – sequence: 8 givenname: Seok Ho orcidid: 0000-0002-1524-5233 surname: Kang fullname: Kang, Seok Ho organization: Department of Urology, Korea University School of Medicine, Seoul, Korea – sequence: 9 givenname: Sung-Hoo orcidid: 0000-0002-1952-4010 surname: Hong fullname: Hong, Sung-Hoo organization: Department of Urology, College of Medicine, The Catholic University of Korea, Seoul, Korea – sequence: 10 givenname: Jinsoo orcidid: 0000-0003-2251-5331 surname: Chung fullname: Chung, Jinsoo organization: Department of Urology, National Cancer Center, Goyang, Korea – sequence: 11 givenname: Tae Gyun orcidid: 0000-0002-4390-0952 surname: Kwon fullname: Kwon, Tae Gyun organization: Department of Urology, Kyungpook National University College of Medicine, Daegu, Korea – sequence: 12 givenname: Hyeon Hoe orcidid: 0000-0001-6600-4539 surname: Kim fullname: Kim, Hyeon Hoe organization: Department of Urology, Seoul National University College of Medicine, Seoul, Korea – sequence: 13 givenname: Cheol orcidid: 0000-0002-1987-2111 surname: Kwak fullname: Kwak, Cheol organization: Department of Urology, Seoul National University College of Medicine, Seoul, Korea – sequence: 14 givenname: Seok-Soo orcidid: 0000-0001-9356-9500 surname: Byun fullname: Byun, Seok-Soo organization: Department of Urology, Seoul National University Bundang Hospital, Seongnam, Korea – sequence: 15 givenname: Yong-June orcidid: 0000-0001-7638-7174 surname: Kim fullname: Kim, Yong-June organization: Department of Urology, Chungbuk National University College of Medicine, Cheongju, Korea |
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| Keywords | Recurrence Nephrectomy Renal Cell Carcinoma Survival Age |
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