Intensity-modulated radiotherapy improves survival and reduces treatment time in squamous cell carcinoma of the anus: A National Cancer Data Base study

被引:43
作者
Elson, Joshua K. [1 ,2 ]
Kachnic, Lisa A. [3 ]
Kharofa, Jordan R. [1 ,2 ]
机构
[1] Univ Cincinnati, Dept Radiat Oncol, Cincinnati, OH USA
[2] Univ Cincinnati, Barrett Canc Ctr, Cincinnati, OH USA
[3] Vanderbilt Univ, Dept Radiat Oncol, 221 Kirkland Hall, Nashville, TN 37235 USA
关键词
3-dimensional conformal radiation therapy (3DCRT); anal cancer; chemoradiation; intensity-modulated radiotherapy (IMRT); National Cancer Data Base (NCDB); radiation; RADIATION-THERAPY; CONCURRENT CHEMOTHERAPY; ANAL CANCER; COLOSTOMY FAILURE; CISPLATIN; MITOMYCIN; IMPACT; CHEMORADIATION; 5-FLUOROURACIL; TOXICITY;
D O I
10.1002/cncr.31721
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Chemoradiation with 5-fluorouracil and mitomycin remains the standard of care for squamous cell carcinoma (SCC) of the anal canal. A prolonged treatment time is associated with inferior disease-specific outcomes. Radiation Therapy Oncology Group trial 0529 demonstrated decreased toxicity and fewer treatment breaks with intensity-modulated radiotherapy (IMRT), but this has not been assessed in a randomized trial. Using data from the National Cancer Data Base (NCDB), this study evaluated the impact of IMRT on treatment time and survival in anal SCC. Methods The NCDB was used to identify patients with anal cancer from 2004 to 2013. The included patients were those with stage I to III squamous cell cancer of the anal canal who had received definitive chemoradiation by IMRT or 3-dimensional conformal radiation therapy (3DCRT). Statistical analyses were performed with logistic regression, Kaplan-Meier analysis, Cox proportional hazards analysis, and propensity score-matched analysis. Results Of 6814 patients, 57.4% were treated with 3DCRT, whereas 42.6% received IMRT. Patients receiving IMRT had a reduced risk of a long treatment time in a multivariate analysis (P < .001). The 5-year overall survival (OS) rates with IMRT and 3DCRT were 80.8% and 78.9%, respectively (P = .0036). According to a propensity analysis, patients receiving IMRT had improved OS (P = .039) and a reduced risk of a long treatment time (P < .0001) in a multivariate analysis. Conclusions IMRT use was associated with significantly reduced overall treatment time and improved survival in comparison with 3DCRT. It is important to note that NCDB data are not as robust as randomized data. However, these results further support the use of IMRT as part of sphincter-preserving therapy for the anal canal. (c) 2018 American Cancer Society.
引用
收藏
页码:4383 / 4392
页数:10
相关论文
共 21 条
[1]   Fluorouracil, mitomycin, and radiotherapy vs fluorouracil, cisplatin, and radiotherapy for carcinoma of the anal canal - A randomized controlled trial [J].
Ajani, Jaffer A. ;
Winter, Kathryn A. ;
Gunderson, Leonard L. ;
Pedersen, John ;
Benson, Al B., III ;
Thomas, Charles R., Jr. ;
Mayer, Robert J. ;
Haddock, Michael G. ;
Rich, Tyvin A. ;
Willett, Christopher .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2008, 299 (16) :1914-1921
[2]   Impact of Facility Volume on Outcomes in Patients With Squamous Cell Carcinoma of the Anal Canal: Analysis of the National Cancer Data Base [J].
Amini, Arya ;
Jones, Bernard L. ;
Ghosh, Debashis ;
Schefter, Tracey E. ;
Goodman, Karyn A. .
CANCER, 2017, 123 (02) :228-236
[3]   Impact of Overall Treatment Time on Survival and Local Control in Patients With Anal Cancer: A Pooled Data Analysis of Radiation Therapy Oncology Group Trials 87-04 and 98-11 [J].
Ben-Josef, Edgar ;
Moughan, Jennifer ;
Ajani, Jaffer A. ;
Flam, Marshall ;
Gunderson, Leonard ;
Pollock, JonDavid ;
Myerson, Robert ;
Anne, Rani ;
Rosenthal, Seth A. ;
Willett, Christopher .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (34) :5061-5066
[4]   Intensity-modulated Radiation Therapy for Anal Cancer Results From a Multi-Institutional Retrospective Cohort Study [J].
Call, Jason A. ;
Prendergast, Brendan M. ;
Jensen, Lindsay G. ;
Ord, Celine B. ;
Goodman, Karyn A. ;
Jacob, Rojymon ;
Mell, Loren K. ;
Thomas, Charles R. ;
Jabbour, Salma K. ;
Miller, Robert C. .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2016, 39 (01) :8-12
[5]   LONG-TERM FOLLOW-UP OF A PHASE II TRIAL OF HIGH-DOSE RADIATION WITH CONCURRENT 5-FLUOROURACIL AND CISPLATIN IN PATIENTS WITH ANAL CANCER (ECOG E4292) [J].
Chakravarthy, A. Bapsi ;
Catalano, Paul J. ;
Martenson, James. A. ;
Mondschein, Joshua K. ;
Wagner, Henry ;
Mansour, Edward G. ;
Talamonti, Mark S. ;
Benson, Al Bowen .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2011, 81 (04) :E607-E613
[6]  
Chuong Michael D, 2013, Gastrointest Cancer Res, V6, P39
[7]   Concurrent Chemotherapy and Intensity-modulated Radiation Therapy for Anal Carcinoma - Clinical Outcomes in a Large National Cancer Institute-designated Integrated Cancer Centre Network [J].
DeFoe, S. G. ;
Beriwal, S. ;
Jones, H. ;
Rakfal, S. ;
Heron, D. E. ;
Kabolizadeh, P. ;
Smith, R. P. ;
Lalonde, R. .
CLINICAL ONCOLOGY, 2012, 24 (06) :424-431
[8]   Intensity-Modulated Radiation Therapy with Simultaneous Integrated Boost Combined with Concurrent Chemotherapy for the Treatment of Anal Cancer Patients: 4-Year Results of a Consecutive Case Series [J].
Franco, Pierfrancesco ;
Mistrangelo, Massimiliano ;
Arcadipane, Francesca ;
Munoz, Fernando ;
Sciacero, Piera ;
Spadi, Rosella ;
Migliaccio, Fernanda ;
Angelini, Veronica ;
Bombaci, Sebastiano ;
Rondi, Nadia ;
Numico, Gianmauro ;
Ragona, Riccardo ;
Cassoni, Paola ;
Morino, Mario ;
Racca, Patrizia ;
Ricardi, Umberto .
CANCER INVESTIGATION, 2015, 33 (06) :259-266
[9]   Squamous-cell carcinoma of the anus: progress in radiotherapy treatment [J].
Glynne-Jones, Rob ;
Tan, David ;
Hughes, Robert ;
Hoskin, Peter .
NATURE REVIEWS CLINICAL ONCOLOGY, 2016, 13 (07) :447-459
[10]   Anal Carcinoma: Impact of TN Category of Disease on Survival, Disease Relapse, and Colostomy Failure in US Gastrointestinal Intergroup RTOG 98-11 Phase 3 Trial [J].
Gunderson, Leonard L. ;
Moughan, Jennifer ;
Ajani, Jaffer A. ;
Pedersen, John E. ;
Winter, Kathryn A. ;
Benson, Al B., III ;
Thomas, Charles R., Jr. ;
Mayer, Robert J. ;
Haddock, Michael G. ;
Rich, Tyvin A. ;
Willett, Christopher G. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2013, 87 (04) :638-645