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Risk of second primary colorectal cancer among colorectal cancer cases: A population-based analysis

BACKGROUND: Patients with history of colorectal cancer (CRC) are at increased risk for developing a second primary colorectal cancer (SPCRC) as compared to the general population. However, the degree of risk is uncertain. Here, we attempt to quantify the risk, using data from the large population-ba...

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Autores principales: Raj, Kavitha P., Taylor, Thomas H., Wray, Charlie, Stamos, Michael J., Zell, Jason A.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072650/
https://www.ncbi.nlm.nih.gov/pubmed/21483654
http://dx.doi.org/10.4103/1477-3163.78114
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author Raj, Kavitha P.
Taylor, Thomas H.
Wray, Charlie
Stamos, Michael J.
Zell, Jason A.
author_facet Raj, Kavitha P.
Taylor, Thomas H.
Wray, Charlie
Stamos, Michael J.
Zell, Jason A.
author_sort Raj, Kavitha P.
collection PubMed
description BACKGROUND: Patients with history of colorectal cancer (CRC) are at increased risk for developing a second primary colorectal cancer (SPCRC) as compared to the general population. However, the degree of risk is uncertain. Here, we attempt to quantify the risk, using data from the large population-based California Cancer Registry (CCR). MATERIALS AND METHODS: We analyzed the CCR data for cases with surgically-treated colon and rectal cancer diagnosed during the period 1990-2005 and followed through up to January 2008. We excluded those patients diagnosed with metastatic disease and those in whom SPCRC was diagnosed within 6 months of the diagnosis of the primary CRC. Standardized incidence ratios (SIR) with 95% confidence intervals (CI) were calculated to evaluate risk as compared to the underlying population after taking into account age, sex, ethnicity, and time at risk. RESULTS: The study cohort consisted of 69809 cases with colon cancer and 34448 with rectal cancer. Among these patients there were 1443 cases of SPCRCs. The SIR for developing SPCRC was higher in colon cancer survivors (SIR=1.4; 95% CI: 1.3 to 1.5) as compared to the underlying population. The incidence of SPCRC was also higher in females (SIR=1.5; 95% CI: 1.3 to 1.6) and Hispanics (SIR=2.0; 95% CI: 1.7 to 2.4) with primary colon cancer. The SIR for developing an SPCRC was higher only among those whose initial tumor was located in the descending colon (SIR=1.6; 95% CI: 1.3 to 2.0) and proximal colon (SIR=1.4; 95% CI: 1.3 to 1.6). CONCLUSIONS: Our results confirm that CRC patients, especially females and Hispanics, are at a higher risk of developing SPCRC than the general population. Differential SPCRC risk by colorectal tumor subsite is dependent on gender and ethnicity, underscoring the heterogeneous nature of CRC.
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spelling pubmed-30726502011-04-11 Risk of second primary colorectal cancer among colorectal cancer cases: A population-based analysis Raj, Kavitha P. Taylor, Thomas H. Wray, Charlie Stamos, Michael J. Zell, Jason A. J Carcinog Original Article BACKGROUND: Patients with history of colorectal cancer (CRC) are at increased risk for developing a second primary colorectal cancer (SPCRC) as compared to the general population. However, the degree of risk is uncertain. Here, we attempt to quantify the risk, using data from the large population-based California Cancer Registry (CCR). MATERIALS AND METHODS: We analyzed the CCR data for cases with surgically-treated colon and rectal cancer diagnosed during the period 1990-2005 and followed through up to January 2008. We excluded those patients diagnosed with metastatic disease and those in whom SPCRC was diagnosed within 6 months of the diagnosis of the primary CRC. Standardized incidence ratios (SIR) with 95% confidence intervals (CI) were calculated to evaluate risk as compared to the underlying population after taking into account age, sex, ethnicity, and time at risk. RESULTS: The study cohort consisted of 69809 cases with colon cancer and 34448 with rectal cancer. Among these patients there were 1443 cases of SPCRCs. The SIR for developing SPCRC was higher in colon cancer survivors (SIR=1.4; 95% CI: 1.3 to 1.5) as compared to the underlying population. The incidence of SPCRC was also higher in females (SIR=1.5; 95% CI: 1.3 to 1.6) and Hispanics (SIR=2.0; 95% CI: 1.7 to 2.4) with primary colon cancer. The SIR for developing an SPCRC was higher only among those whose initial tumor was located in the descending colon (SIR=1.6; 95% CI: 1.3 to 2.0) and proximal colon (SIR=1.4; 95% CI: 1.3 to 1.6). CONCLUSIONS: Our results confirm that CRC patients, especially females and Hispanics, are at a higher risk of developing SPCRC than the general population. Differential SPCRC risk by colorectal tumor subsite is dependent on gender and ethnicity, underscoring the heterogeneous nature of CRC. Medknow Publications 2011-03-17 /pmc/articles/PMC3072650/ /pubmed/21483654 http://dx.doi.org/10.4103/1477-3163.78114 Text en © 2011 Raj http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Raj, Kavitha P.
Taylor, Thomas H.
Wray, Charlie
Stamos, Michael J.
Zell, Jason A.
Risk of second primary colorectal cancer among colorectal cancer cases: A population-based analysis
title Risk of second primary colorectal cancer among colorectal cancer cases: A population-based analysis
title_full Risk of second primary colorectal cancer among colorectal cancer cases: A population-based analysis
title_fullStr Risk of second primary colorectal cancer among colorectal cancer cases: A population-based analysis
title_full_unstemmed Risk of second primary colorectal cancer among colorectal cancer cases: A population-based analysis
title_short Risk of second primary colorectal cancer among colorectal cancer cases: A population-based analysis
title_sort risk of second primary colorectal cancer among colorectal cancer cases: a population-based analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072650/
https://www.ncbi.nlm.nih.gov/pubmed/21483654
http://dx.doi.org/10.4103/1477-3163.78114
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