Intensity-modulated radiation therapy, proton therapy, or conformal radiation therapy and morbidity and disease control in localized prostate cancer - PubMed (original) (raw)
Comparative Study
Intensity-modulated radiation therapy, proton therapy, or conformal radiation therapy and morbidity and disease control in localized prostate cancer
Nathan C Sheets et al. JAMA. 2012.
Abstract
Context: There has been rapid adoption of newer radiation treatments such as intensity-modulated radiation therapy (IMRT) and proton therapy despite greater cost and limited demonstrated benefit compared with previous technologies.
Objective: To determine the comparative morbidity and disease control of IMRT, proton therapy, and conformal radiation therapy for primary prostate cancer treatment.
Design, setting, and patients: Population-based study using Surveillance, Epidemiology, and End Results-Medicare-linked data from 2000 through 2009 for patients with nonmetastatic prostate cancer.
Main outcome measures: Rates of gastrointestinal and urinary morbidity, erectile dysfunction, hip fractures, and additional cancer therapy.
Results: Use of IMRT vs conformal radiation therapy increased from 0.15% in 2000 to 95.9% in 2008. In propensity score-adjusted analyses (N = 12,976), men who received IMRT vs conformal radiation therapy were less likely to receive a diagnosis of gastrointestinal morbidities (absolute risk, 13.4 vs 14.7 per 100 person-years; relative risk [RR], 0.91; 95% CI, 0.86-0.96) and hip fractures (absolute risk, 0.8 vs 1.0 per 100 person-years; RR, 0.78; 95% CI, 0.65-0.93) but more likely to receive a diagnosis of erectile dysfunction (absolute risk, 5.9 vs 5.3 per 100 person-years; RR, 1.12; 95% CI, 1.03-1.20). Intensity-modulated radiation therapy patients were less likely to receive additional cancer therapy (absolute risk, 2.5 vs 3.1 per 100 person-years; RR, 0.81; 95% CI, 0.73-0.89). In a propensity score-matched comparison between IMRT and proton therapy (n = 1368), IMRT patients had a lower rate of gastrointestinal morbidity (absolute risk, 12.2 vs 17.8 per 100 person-years; RR, 0.66; 95% CI, 0.55-0.79). There were no significant differences in rates of other morbidities or additional therapies between IMRT and proton therapy.
Conclusions: Among patients with nonmetastatic prostate cancer, the use of IMRT compared with conformal radiation therapy was associated with less gastrointestinal morbidity and fewer hip fractures but more erectile dysfunction; IMRT compared with proton therapy was associated with less gastrointestinal morbidity.
Conflict of interest statement
Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Stürmer reports receiving investigator-initiated research funding and support as principal investigator (RO1 AG023178) and coinvestigator (RO1 AG018833) from the National Institute on Aging at the National Institutes of Health (NIH), funding as principal investigator of the University of North Carolina (UNC) Developing Evidence to Inform Decisions about Effectiveness (DEcIDE) center from the Agency for Healthcare Research and Quality, salary support from the UNC Center of Excellence in Pharmacoepidemiology and Public Health, consultancy on the Genentech CER advisory board, and from unrestricted research grants from Merck and sanofi-aventis to the UNC. Dr Godley reports receiving compensation for participating in the data and safety monitoring committee for Ferring Pharmaceuticals, which manufactures Degarelix, a hormonal treatment for prostate cancer that is not directly related to the subject of this study, and receiving compensation for consultancy with GlaxoSmithKline. No other disclosures were reported.
Figures
Figure 1
Propensity Score–Adjusted Rates of Additional Cancer Treatment for Patients Treated With Intensity-Modulated Radiation Therapy vs Conformal Radiation Therapy
Figure 2
Propensity Score–Matched Rates of Additional Cancer Treatment for Patients Treated With Intensity-Modulated Radiation Therapy vs Proton Therapy
Comment in
- Is it time for medicine-based evidence?
Concato J. Concato J. JAMA. 2012 Apr 18;307(15):1641-3. doi: 10.1001/jama.2012.482. JAMA. 2012. PMID: 22511693 No abstract available. - Radiation therapy modalities for prostate cancer.
Jacobs BL, Zhang Y, Hollenbeck BK. Jacobs BL, et al. JAMA. 2012 Aug 1;308(5):450; author reply 451-2. doi: 10.1001/jama.2012.8108. JAMA. 2012. PMID: 22851099 No abstract available. - Radiation therapy modalities for prostate cancer.
Mendenhall NP, Schild S, Slater J. Mendenhall NP, et al. JAMA. 2012 Aug 1;308(5):450-1; author reply 451-2. doi: 10.1001/jama.2012.8112. JAMA. 2012. PMID: 22851100 No abstract available. - Radiation therapy modalities for prostate cancer.
Deville C, Ben-Josef E, Vapiwala N. Deville C, et al. JAMA. 2012 Aug 1;308(5):451; author reply 451-2. doi: 10.1001/jama.2012.8110. JAMA. 2012. PMID: 22851101 No abstract available. - Re: Intensity-modulated radiation therapy, proton therapy, or conformal radiation therapy and morbidity and disease control in localized prostate cancer.
Penson DF. Penson DF. J Urol. 2012 Dec;188(6):2230-1. doi: 10.1016/j.juro.2012.08.075. Epub 2012 Oct 22. J Urol. 2012. PMID: 23141230 No abstract available.
Similar articles
- Outcomes after intensity-modulated versus conformal radiotherapy in older men with nonmetastatic prostate cancer.
Bekelman JE, Mitra N, Efstathiou J, Liao K, Sunderland R, Yeboa DN, Armstrong K. Bekelman JE, et al. Int J Radiat Oncol Biol Phys. 2011 Nov 15;81(4):e325-34. doi: 10.1016/j.ijrobp.2011.02.006. Epub 2011 Apr 16. Int J Radiat Oncol Biol Phys. 2011. PMID: 21498008 Free PMC article. - Comparative effectiveness of intensity-modulated radiotherapy and conventional conformal radiotherapy in the treatment of prostate cancer after radical prostatectomy.
Goldin GH, Sheets NC, Meyer AM, Kuo TM, Wu Y, Stürmer T, Godley PA, Carpenter WR, Chen RC. Goldin GH, et al. JAMA Intern Med. 2013 Jun 24;173(12):1136-43. doi: 10.1001/jamainternmed.2013.1020. JAMA Intern Med. 2013. PMID: 23689844 - Comparing Risk for Second Primary Cancers After Intensity-Modulated vs 3-Dimensional Conformal Radiation Therapy for Prostate Cancer, 2002-2015.
Pithadia KJ, Advani PG, Citrin DE, Bekelman JE, Withrow DR, Berrington de Gonzalez A, Morton LM, Schonfeld SJ. Pithadia KJ, et al. JAMA Oncol. 2023 Aug 1;9(8):1119-1123. doi: 10.1001/jamaoncol.2023.1638. JAMA Oncol. 2023. PMID: 37289449 Free PMC article. - Comparing dosimetric, morbidity, quality of life, and cancer control outcomes after 3D conformal, intensity-modulated, and proton radiation therapy for prostate cancer.
Pearlstein KA, Chen RC. Pearlstein KA, et al. Semin Radiat Oncol. 2013 Jul;23(3):182-90. doi: 10.1016/j.semradonc.2013.01.004. Semin Radiat Oncol. 2013. PMID: 23763884 Review. - Proton versus photon-based radiation therapy for prostate cancer: emerging evidence and considerations in the era of value-based cancer care.
Kamran SC, Light JO, Efstathiou JA. Kamran SC, et al. Prostate Cancer Prostatic Dis. 2019 Dec;22(4):509-521. doi: 10.1038/s41391-019-0140-7. Epub 2019 Apr 9. Prostate Cancer Prostatic Dis. 2019. PMID: 30967625 Review.
Cited by
- Preliminary patient-reported outcomes analysis of 3-dimensional radiation therapy versus intensity-modulated radiation therapy on the high-dose arm of the Radiation Therapy Oncology Group (RTOG) 0126 prostate cancer trial.
Bruner DW, Hunt D, Michalski JM, Bosch WR, Galvin JM, Amin M, Xiao C, Bahary JP, Patel M, Chafe S, Rodrigues G, Lau H, Duclos M, Baikadi M, Deshmukh S, Sandler HM. Bruner DW, et al. Cancer. 2015 Jul 15;121(14):2422-30. doi: 10.1002/cncr.29362. Epub 2015 Apr 2. Cancer. 2015. PMID: 25847819 Free PMC article. Clinical Trial. - Variation in the Cost of Radiation Therapy Among Medicare Patients With Cancer.
Paravati AJ, Boero IJ, Triplett DP, Hwang L, Matsuno RK, Xu B, Mell LK, Murphy JD. Paravati AJ, et al. J Oncol Pract. 2015 Sep;11(5):403-9. doi: 10.1200/JOP.2015.005694. Epub 2015 Aug 11. J Oncol Pract. 2015. PMID: 26265172 Free PMC article. - Uptake and outcomes of intensity-modulated radiation therapy for uterine cancer.
Wright JD, Deutsch I, Wilde ET, Ananth CV, Neugut AI, Lewin SN, Siddiq Z, Herzog TJ, Hershman DL. Wright JD, et al. Gynecol Oncol. 2013 Jul;130(1):43-8. doi: 10.1016/j.ygyno.2013.03.006. Epub 2013 Mar 13. Gynecol Oncol. 2013. PMID: 23500087 Free PMC article. - Moderately hypofractionated radiotherapy for localized prostate cancer: long-term outcome using IMRT and volumetric IGRT.
Guckenberger M, Lawrenz I, Flentje M. Guckenberger M, et al. Strahlenther Onkol. 2014 Jan;190(1):48-53. doi: 10.1007/s00066-013-0443-x. Epub 2013 Nov 8. Strahlenther Onkol. 2014. PMID: 24196279 Clinical Trial. - Radiation-induced acid ceramidase confers prostate cancer resistance and tumor relapse.
Cheng JC, Bai A, Beckham TH, Marrison ST, Yount CL, Young K, Lu P, Bartlett AM, Wu BX, Keane BJ, Armeson KE, Marshall DT, Keane TE, Smith MT, Jones EE, Drake RR Jr, Bielawska A, Norris JS, Liu X. Cheng JC, et al. J Clin Invest. 2013 Oct;123(10):4344-58. doi: 10.1172/JCI64791. Epub 2013 Sep 16. J Clin Invest. 2013. PMID: 24091326 Free PMC article.
References
- Siegel R, Ward E, Brawley O, Jemal A. Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on premature cancer deaths. CA Cancer J Clin. 2011;61(4):212–236. - PubMed
- Institute of Medicine. Initial National Priorities for Comparative Effectiveness Research. Washington, DC: National Academies Press; 2009.
- Institute for Clinical and Economic Review. Management Options for Low-Risk Prostate Cancer: A Report on Comparative Effectiveness and Value. Boston, MA: Institute for Clinical & Economic Review; 2009.
- Wilt TJ, MacDonald R, Rutks I, Shamliyan TA, Taylor BC, Kane RL. Systematic review: comparative effectiveness and harms of treatments for clinically localized prostate cancer. Ann Intern Med. 2008;148(6):435–448. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- T32 NR008856/NR/NINR NIH HHS/United States
- P30 CA016086/CA/NCI NIH HHS/United States
- R01 AG023178/AG/NIA NIH HHS/United States
- HHSA290-2005-0040-I-TO6/PHS HHS/United States
- 2T32NR008856/NR/NINR NIH HHS/United States
- U54 CA153602/CA/NCI NIH HHS/United States
- R01 AG018833/AG/NIA NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical