Long-term outcomes of partial prostate treatment with magnetic resonance imaging-guided brachytherapy for patients with favorable-risk prostate cancer.
Long-term outcomes of partial prostate treatment with magnetic resonance imaging-guided brachytherapy for patients with favorable-risk prostate cancer.
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DOI:
10.1002/cncr.31568
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发表时间:
2018-09-01
期刊:
影响因子:
6.2
通讯作者:
Orio PF 3rd
中科院分区:
文献类型:
--
作者:
King MT;Nguyen PL;Boldbaatar N;Tempany CM;Cormack RA;Beard CJ;Hurwitz MD;Suh WW;D'Amico AV;Orio PF 3rd
Partial prostate treatment has emerged as a potential method for treating favorable-risk prostate cancer while minimizing toxicity. We had previously shown poor rates of biochemical control for National Cancer Center Network (NCCN) intermediate risk disease with partial gland treatment with brachytherapy. Our purpose is to estimate the rates of distant metastasis and prostate cancer specific mortality (PCSM) for this cohort. Between 1997 and 2007, 354 men with clinical T1c, prostate specific antigen (PSA) < 15 ng/mL, Gleason 3+4 or less prostate cancer underwent partial prostate treatment with brachytherapy to the MR defined peripheral zone under 0.5 Tesla MR-guidance. The cumulative incidences of metastasis and PCSM for NCCN very low, low, and intermediate risk groups were estimated. Fine and Gray’s competing risk regression was utilized to evaluate clinical factors associated with times to metastasis. Twenty-two patients developed metastases at a median of 11.0 years (interquartile range: 6.9-13.9). Twelve-year metastasis rates for very low, low, and intermediate risk disease were 0.8% (95% confidence interval) 0.1-4.4%), 8.7% (3.4-17.2), and 15.7% (5.7-30.2), respectively. Respective 12 year PCSM estimates were 1.6% (0.1-7.6), 1.4% (0.1-6.8), and 8.2% (1.9-20.7). On multivariate analysis, NCCN risk category (low risk hazard ratio: 6.34 (1.18-34.06), p = 0.03; intermediate risk: 6.98 (1.23-39.73); p = 0.03) was significantly associated with the time to metastasis. Partial prostate treatment with brachytherapy may be associated with higher rates of distant metastasis and PCSM for intermediate risk disease after long-term follow-up. Treatment of less than the full gland may not be appropriate for this cohort.
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DOI:
10.1200/jco.2015.62.5764
发表时间:
2015-10-20
期刊:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
影响因子:
--
作者:
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通讯作者:
Carter HB
DOI:
10.1016/j.ijrobp.2015.02.047
发表时间:
2015-07-15
影响因子:
7
作者:
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通讯作者:
Ciezki, Jay P.
影响因子:
5.6
作者:
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通讯作者:
Fine, Samson W.
影响因子:
1.9
作者:
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通讯作者:
Vallancien, Guy
影响因子:
19.7
作者:
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通讯作者:
Barentsz, JO