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Intensity-modulated radiation therapy, proton therapy, or conformal radiation therapy and morbidity and disease control in localized prostate cancer.调强适形放疗、质子治疗或适形放疗与局限性前列腺癌的发病率和疾病控制。
JAMA. 2012 Apr 18;307(15):1611-20. doi: 10.1001/jama.2012.460.
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Emerging technologies in proton therapy.质子治疗中的新兴技术。
Acta Oncol. 2011 Aug;50(6):838-50. doi: 10.3109/0284186X.2011.582513.
3
Late gastrointestinal toxicities following radiation therapy for prostate cancer.前列腺癌放射治疗后的迟发性胃肠道毒性。
Eur Urol. 2011 Nov;60(5):908-16. doi: 10.1016/j.eururo.2011.05.052. Epub 2011 Jun 12.
4
Outcomes after intensity-modulated versus conformal radiotherapy in older men with nonmetastatic prostate cancer.调强放疗与适形放疗治疗非转移性前列腺癌老年男性患者的结果。
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.
5
Cost implications of the rapid adoption of newer technologies for treating prostate cancer.新技术快速应用于前列腺癌治疗的成本影响。
J Clin Oncol. 2011 Apr 20;29(12):1517-24. doi: 10.1200/JCO.2010.31.1217. Epub 2011 Mar 14.
6
Early outcomes from three prospective trials of image-guided proton therapy for prostate cancer.前列腺癌图像引导质子治疗的三项前瞻性研究的早期结果。
Int J Radiat Oncol Biol Phys. 2012 Jan 1;82(1):213-21. doi: 10.1016/j.ijrobp.2010.09.024. Epub 2010 Nov 17.
7
Reimbursement policy and androgen-deprivation therapy for prostate cancer.前列腺癌的报销政策和雄激素剥夺疗法。
N Engl J Med. 2010 Nov 4;363(19):1822-32. doi: 10.1056/NEJMsa0910784.
8
Proton-beam therapy for prostate cancer.质子束疗法治疗前列腺癌。
Cancer J. 2010 Sep-Oct;16(5):405-9. doi: 10.1097/PPO.0b013e3181f8c25d.
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Multi-institutional Phase II study of proton beam therapy for organ-confined prostate cancer focusing on the incidence of late rectal toxicities.多机构质子束治疗局限性前列腺癌的 II 期研究,重点关注晚期直肠毒性的发生率。
Int J Radiat Oncol Biol Phys. 2011 Oct 1;81(2):390-6. doi: 10.1016/j.ijrobp.2010.05.027. Epub 2010 Sep 9.
10
Evaluation of potential proton therapy utilization in a market-based environment.基于市场环境的质子治疗应用潜力评估。
J Am Coll Radiol. 2010 Jul;7(7):522-8. doi: 10.1016/j.jacr.2010.01.024.

质子治疗与调强放疗治疗前列腺癌:治疗模式和早期毒性。

Proton versus intensity-modulated radiotherapy for prostate cancer: patterns of care and early toxicity.

机构信息

Yale University School of Medicine, Department of Therapeutic Radiology, 40 Park St, New Haven, CT 06511, USA.

出版信息

J Natl Cancer Inst. 2013 Jan 2;105(1):25-32. doi: 10.1093/jnci/djs463. Epub 2012 Dec 14.

DOI:10.1093/jnci/djs463
PMID:23243199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3536640/
Abstract

BACKGROUND

Proton radiotherapy (PRT) is an emerging treatment for prostate cancer despite limited knowledge of clinical benefit or potential harms compared with other types of radiotherapy. We therefore compared patterns of PRT use, cost, and early toxicity among Medicare beneficiaries with prostate cancer with those of intensity-modulated radiotherapy (IMRT).

METHODS

We performed a retrospective study of all Medicare beneficiaries aged greater than or equal to 66 years who received PRT or IMRT for prostate cancer during 2008 and/or 2009. We used multivariable logistic regression to identify factors associated with receipt of PRT. To assess toxicity, each PRT patient was matched with two IMRT patients with similar clinical and sociodemographic characteristics. The main outcome measures were receipt of PRT or IMRT, Medicare reimbursement for each treatment, and early genitourinary, gastrointestinal, and other toxicity. All statistical tests were two-sided.

RESULTS

We identified 27,647 men; 553 (2%) received PRT and 27,094 (98%) received IMRT. Patients receiving PRT were younger, healthier, and from more affluent areas than patients receiving IMRT. Median Medicare reimbursement was $32,428 for PRT and $18,575 for IMRT. Although PRT was associated with a statistically significant reduction in genitourinary toxicity at 6 months compared with IMRT (5.9% vs 9.5%; odds ratio [OR] = 0.60, 95% confidence interval [CI] = 0.38 to 0.96, P = .03), at 12 months post-treatment there was no difference in genitourinary toxicity (18.8% vs 17.5%; OR = 1.08, 95% CI = 0.76 to 1.54, P = .66). There was no statistically significant difference in gastrointestinal or other toxicity at 6 months or 12 months post-treatment.

CONCLUSIONS

Although PRT is substantially more costly than IMRT, there was no difference in toxicity in a comprehensive cohort of Medicare beneficiaries with prostate cancer at 12 months post-treatment.

摘要

背景

尽管质子放疗 (PRT) 在临床获益或潜在危害方面与其他放疗类型相比所知甚少,但它仍是治疗前列腺癌的一种新兴方法。因此,我们比较了 Medicare 受益人群中接受 PRT 与调强放疗 (IMRT) 的前列腺癌患者的 PRT 使用模式、成本和早期毒性。

方法

我们对在 2008 年和/或 2009 年期间接受 PRT 或 IMRT 治疗的所有年龄大于或等于 66 岁的 Medicare 受益人群进行了回顾性研究。我们使用多变量逻辑回归来确定接受 PRT 的相关因素。为了评估毒性,每位 PRT 患者都与具有相似临床和社会人口统计学特征的两名 IMRT 患者进行了匹配。主要结局指标包括接受 PRT 或 IMRT、每种治疗的 Medicare 报销以及早期泌尿生殖、胃肠道和其他毒性。所有统计检验均为双侧检验。

结果

我们确定了 27647 名男性;553 名(2%)接受了 PRT,27094 名(98%)接受了 IMRT。接受 PRT 的患者比接受 IMRT 的患者年龄更小、更健康、来自更富裕的地区。PRT 的 Medicare 报销中位数为 32428 美元,IMRT 为 18575 美元。尽管与 IMRT 相比,PRT 在 6 个月时泌尿生殖毒性明显降低(5.9% vs 9.5%;比值比 [OR] = 0.60,95%置信区间 [CI] = 0.38 至 0.96,P =.03),但在治疗后 12 个月时,泌尿生殖毒性无差异(18.8% vs 17.5%;OR = 1.08,95% CI = 0.76 至 1.54,P =.66)。在治疗后 6 个月或 12 个月时,胃肠道或其他毒性无统计学差异。

结论

尽管 PRT 的成本明显高于 IMRT,但在接受前列腺癌治疗的 Medicare 受益人群的综合队列中,在治疗后 12 个月时,毒性无差异。