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Twenty-Five-Year Experience With Radical Chemoradiation for Anal Cancer

Abstract

Purpose: To evaluate the prognostic factors, patterns of failure, and late toxicity in patients treated with chemoradiation (CRT) for anal cancer. Methods and Materials: Consecutive patients with nonmetastatic squamous cell carcinoma of the anus treated by CRT with curative intent between February 1983 and March 2008 were identified through the institutional database. Chart review and telephone follow-up were undertaken to collect demographic data and outcome. Results: Two hundred eighty-four patients (34% male; median age 62 years) were identified. The stages at diagnosis were 23% Stage I, 48% Stage II, 10% Stage IIIA, and 18% Stage IIIB. The median radiotherapy dose to the primary site was 54 Gy. A complete clinical response to CRT was achieved in 89% of patients. With a median follow-up time of 5.3 years, the 5-year rates of locoregional control, distant control, colostomy-free survival, and overall survival were 83% (95% confidence interval [CI] 78-88), 92% (95% CI, 89-96), 73% (95% CI, 68-79), and 82% (95% CI, 77-87), respectively. Higher T stage and male sex predicted for locoregional failure, and higher N stage predicted for distant metastases. Locoregional failure occurred most commonly at the primary site. Omission of elective inguinal irradiation resulted in inguinal failure rates of 1.9%  More>>
Authors:
Tomaszewski, Jonathan M., E-mail: jonathan.tomaszewski@petermac.org; [1]  Link, Emma; [2]  Leong, Trevor; [1]  University of Melbourne, Parkville, Victoria (Australia)]; Heriot, Alexander; [3]  Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)]; Vazquez, Melisa; [4]  Chander, Sarat; Chu, Julie; Foo, Marcus; Lee, Mark T; [1]  Lynch, Craig A; [5]  Mackay, John; [3]  Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)]; Michael, Michael; [3]  Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)]; Tran, Phillip; [1]  Ngan, Samuel Y; [1]  University of Melbourne, Parkville, Victoria (Australia)]
  1. Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)
  2. Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)
  3. University of Melbourne, Parkville, Victoria (Australia)
  4. Research Division, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)
  5. Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)
Publication Date:
Jun 01, 2012
Product Type:
Journal Article
Resource Relation:
Journal Name: International Journal of Radiation Oncology, Biology and Physics; Journal Volume: 83; Journal Issue: 2; Other Information: Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Subject:
62 RADIOLOGY AND NUCLEAR MEDICINE; CARCINOMAS; DIAGNOSIS; FRACTURES; IRRADIATION; MALES; METASTASES; PATIENTS; PELVIS; RADIATION DOSES; RADIOTHERAPY; SEX; SKELETON; TOXICITY
OSTI ID:
22056384
Country of Origin:
United States
Language:
English
Other Identifying Numbers:
Journal ID: ISSN 0360-3016; CODEN: IOBPD3; Other: PII: S0360-3016(11)03012-4; TRN: US12R2712016765
Availability:
Available from http://dx.doi.org/10.1016/j.ijrobp.2011.07.007
Submitting Site:
USN
Size:
page(s) 552-558
Announcement Date:
Feb 21, 2013

Citation Formats

Tomaszewski, Jonathan M., E-mail: jonathan.tomaszewski@petermac.org, Link, Emma, Leong, Trevor, University of Melbourne, Parkville, Victoria (Australia)], Heriot, Alexander, Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Vazquez, Melisa, Chander, Sarat, Chu, Julie, Foo, Marcus, Lee, Mark T, Lynch, Craig A, Mackay, John, Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Michael, Michael, Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Tran, Phillip, Ngan, Samuel Y, and University of Melbourne, Parkville, Victoria (Australia)]. Twenty-Five-Year Experience With Radical Chemoradiation for Anal Cancer. United States: N. p., 2012. Web. doi:10.1016/J.IJROBP.2011.07.007.
Tomaszewski, Jonathan M., E-mail: jonathan.tomaszewski@petermac.org, Link, Emma, Leong, Trevor, University of Melbourne, Parkville, Victoria (Australia)], Heriot, Alexander, Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Vazquez, Melisa, Chander, Sarat, Chu, Julie, Foo, Marcus, Lee, Mark T, Lynch, Craig A, Mackay, John, Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Michael, Michael, Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Tran, Phillip, Ngan, Samuel Y, & University of Melbourne, Parkville, Victoria (Australia)]. Twenty-Five-Year Experience With Radical Chemoradiation for Anal Cancer. United States. https://doi.org/10.1016/J.IJROBP.2011.07.007
Tomaszewski, Jonathan M., E-mail: jonathan.tomaszewski@petermac.org, Link, Emma, Leong, Trevor, University of Melbourne, Parkville, Victoria (Australia)], Heriot, Alexander, Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Vazquez, Melisa, Chander, Sarat, Chu, Julie, Foo, Marcus, Lee, Mark T, Lynch, Craig A, Mackay, John, Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Michael, Michael, Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Tran, Phillip, Ngan, Samuel Y, and University of Melbourne, Parkville, Victoria (Australia)]. 2012. "Twenty-Five-Year Experience With Radical Chemoradiation for Anal Cancer." United States. https://doi.org/10.1016/J.IJROBP.2011.07.007.
@misc{etde_22056384,
title = {Twenty-Five-Year Experience With Radical Chemoradiation for Anal Cancer}
author = {Tomaszewski, Jonathan M., E-mail: jonathan.tomaszewski@petermac.org, Link, Emma, Leong, Trevor, University of Melbourne, Parkville, Victoria (Australia)], Heriot, Alexander, Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Vazquez, Melisa, Chander, Sarat, Chu, Julie, Foo, Marcus, Lee, Mark T, Lynch, Craig A, Mackay, John, Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Michael, Michael, Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria (Australia)], Tran, Phillip, Ngan, Samuel Y, and University of Melbourne, Parkville, Victoria (Australia)]}
abstractNote = {Purpose: To evaluate the prognostic factors, patterns of failure, and late toxicity in patients treated with chemoradiation (CRT) for anal cancer. Methods and Materials: Consecutive patients with nonmetastatic squamous cell carcinoma of the anus treated by CRT with curative intent between February 1983 and March 2008 were identified through the institutional database. Chart review and telephone follow-up were undertaken to collect demographic data and outcome. Results: Two hundred eighty-four patients (34% male; median age 62 years) were identified. The stages at diagnosis were 23% Stage I, 48% Stage II, 10% Stage IIIA, and 18% Stage IIIB. The median radiotherapy dose to the primary site was 54 Gy. A complete clinical response to CRT was achieved in 89% of patients. With a median follow-up time of 5.3 years, the 5-year rates of locoregional control, distant control, colostomy-free survival, and overall survival were 83% (95% confidence interval [CI] 78-88), 92% (95% CI, 89-96), 73% (95% CI, 68-79), and 82% (95% CI, 77-87), respectively. Higher T stage and male sex predicted for locoregional failure, and higher N stage predicted for distant metastases. Locoregional failure occurred most commonly at the primary site. Omission of elective inguinal irradiation resulted in inguinal failure rates of 1.9% and 12.5% in T1N0 and T2N0 patients, respectively. Pelvic nodal failures were very uncommon. Late vaginal and bone toxicity was observed in addition to gastrointestinal toxicity. Conclusions: CRT is a highly effective approach in anal cancer. However, subgroups of patients fare relatively poorly, and novel approaches are needed. Elective inguinal irradiation can be safely omitted only in patients with Stage I disease. Vaginal toxicity and insufficiency fractures of the hip and pelvis are important late effects that require prospective evaluation.}
doi = {10.1016/J.IJROBP.2011.07.007}
journal = []
issue = {2}
volume = {83}
journal type = {AC}
place = {United States}
year = {2012}
month = {Jun}
}