Jereczek-Fossa Barbara Alicja, Fanetti Giuseppe, Fodor Cristiana, Ciardo Delia, Santoro Luigi, Francia Claudia Maria, Muto Matteo, Surgo Alessia, Zerini Dario, Marvaso Giulia, Timon Giorgia, Romanelli Paola, Rondi Elena, Comi Stefania, Cattani Federica, Golino Federica, Mazza Stefano, Matei Deliu Victor, Ferro Matteo, Musi Gennaro, Nolè Franco, de Cobelli Ottavio, Ost Piet, Orecchia Roberto
Department of Radiotherapy, European Institute of Oncology, Milan, Italy; Department of Oncology and Hemato-oncology, University of Milan, Milan, Italy.
Department of Radiotherapy, European Institute of Oncology, Milan, Italy; Department of Oncology and Hemato-oncology, University of Milan, Milan, Italy.
Clin Genitourin Cancer. 2017 Aug;15(4):e623-e632. doi: 10.1016/j.clgc.2017.01.004. Epub 2017 Jan 11.
The purpose of the study was to evaluate the prostate serum antigen (PSA) response, local control, progression-free survival (PFS), and toxicity of stereotactic body radiotherapy (SBRT) for lymph node (LN) oligorecurrent prostate cancer.
Between May 2012 and October 2015, 124 lesions were treated in 94 patients with a median dose of 24 Gy in 3 fractions. Seventy patients were treated for a single lesion and 25 for > 1 lesion. In 34 patients androgen deprivation (AD) was combined with SBRT. We evaluated biochemical response according to PSA level every 3 months after SBRT: a 3-month PSA decrease from pre-SBRT PSA of more than 10% identified responder patients. In case of PSA level increase, imaging was performed to evaluate clinical progression. Toxicity was assessed every 6 to 9 months after SBRT.
Median follow-up was 18.5 months. In 13 patients (14%) Grade 1 to 2 toxicity was reported without any Grade 3 to 4 toxicity. Biochemical response, stabilization, and progression were observed in 64 (68%), 10 (11%), and 20 (21%) of 94 evaluable patients. Clinical progression was observed in 31 patients (33%) after a median time of 8.1 months. In-field progression occurred in 12 lesions (9.7%). Two-year local control and PFS rates were 84% and 30%, respectively. Age older than 75 years correlated with better biochemical response rate. Age older than 75 years, concomitant AD administered up to 12 months, and pelvic LN involvement correlated with longer PFS.
SBRT is safe and offers good in-field control. At 2 years after SBRT, 1 of 3 patients is progression-free. Further investigation is warranted to identify patients who benefit most from SBRT and to define the optimal combination with AD.
本研究的目的是评估立体定向体部放疗(SBRT)治疗淋巴结(LN)寡转移复发性前列腺癌的前列腺血清抗原(PSA)反应、局部控制、无进展生存期(PFS)和毒性。
2012年5月至2015年10月期间,对94例患者的124个病灶进行了治疗,中位剂量为24 Gy,分3次给予。70例患者治疗单个病灶,25例患者治疗1个以上病灶。34例患者将雄激素剥夺(AD)与SBRT联合应用。SBRT后每3个月根据PSA水平评估生化反应:SBRT前PSA水平下降超过10%的患者为反应者。如果PSA水平升高,则进行影像学检查以评估临床进展。SBRT后每6至9个月评估毒性。
中位随访时间为18.5个月。13例患者(14%)报告有1至2级毒性,无3至4级毒性。94例可评估患者中,64例(68%)出现生化反应、10例(11%)病情稳定、20例(21%)病情进展。中位时间8.1个月后,31例患者(33%)出现临床进展。12个病灶(9.7%)出现野内进展。两年局部控制率和PFS率分别为84%和30%。75岁以上患者生化反应率较好。75岁以上、同时给予AD达12个月以及盆腔LN受累与更长的PFS相关。
SBRT安全且能提供良好的野内控制。SBRT后2年,3例患者中有1例无进展。有必要进一步研究以确定最能从SBRT中获益的患者,并确定与AD的最佳联合方案。