SBRT: an opportunity to improve quality of life for oligometastatic prostate cancer

被引:16
作者
Azzam, Gregory [1 ]
Lanciano, Rachelle [1 ,2 ]
Arrigo, Steve [1 ,2 ]
Lamond, John [1 ,2 ]
Ding, William [2 ]
Yang, Jun [1 ,2 ]
Hanlon, Alexandra [3 ]
Good, Michael [2 ]
Brady, Luther [1 ,2 ]
机构
[1] Drexel Univ, Dept Radiat Oncol, Coll Med, Philadelphia, PA 19104 USA
[2] Delaware Cty Mem Hosp, Philadelphia CyberKnife Ctr, Havertown, PA USA
[3] Univ Penn, Off Nursing Res, Philadelphia, PA 19104 USA
关键词
SBRT; oligometastases; prostate cancer; androgen deprivation therapy; docetaxel; STEREOTACTIC BODY RADIOTHERAPY; ANDROGEN-DEPRIVATION THERAPY; RADIATION-THERAPY; MITOXANTRONE; PREDNISONE; DOCETAXEL;
D O I
10.3389/fonc.2015.00101
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Oligometastatic prostate cancer is a limited metastatic disease state in which potential long-term control is still possible with the use of targeted therapies such as surgery or stereotactic body radiation therapy (SBRT). SBRT may as well potentially prolong the time before the initiation of androgen deprivation therapy (ADT) and docetaxel chemotherapy for oligometastatic prostate cancer. The goal of this study is to outline prognostic factors associated with improved outcome with SBRT for metastatic prostate cancer and to quantify the effect of prior systemic treatments such as ADT and docetaxel on survival after SBRT. Methods: Twenty-four prostate cancer patients were treated with SBRT at the Philadelphia CyberKnife Center between August 2007 and April 2014. Retrospective data collection and analysis were performed for these patients on this Institutional Review Board approved study. Kaplan Meier methodology was utilized to estimate and visually assess overall survival (OS) at the patient level, with comparisons accomplished using the log-rank test. Unadjusted hazard ratios were estimated using Cox proportional hazards regression modeling. Results: An improved median survival was noted for patients with oligometastatic disease defined as <= 4 lesions with median survival of >3 years compared with 11 months for polymetastases (p = 0.02). The use of docetaxel at some time in follow-up either before or after SBRT was associated with decreased survival with median survival of 9 months vs. >3 years (p = 0.01). Conclusion: Prognosis was better for men with recurrent prostate cancer treated with SBRT if they had <= 4 metastases (oligometastases) or if docetaxel was not necessary for salvage treatment. The prolonged median OS for men with oligometastases in this population of heavily pretreated prostate cancer patients following SBRT may allow for improved quality of life because of a delay of more toxic salvage therapies.
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页数:6
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