Galalae Razvan M, Kovács Gyoergy, Schultze Juergen, Loch Tillmann, Rzehak Peter, Wilhelm Roland, Bertermann Hagen, Buschbeck Britta, Kohr Peter, Kimmig Bernhard
Interdisciplinary Brachytherapy Center, Clinic for Radiation Therapy (Radio-oncology), University Hospital, Christian-Albrechts-University, Kiel, Germany.
Int J Radiat Oncol Biol Phys. 2002 Jan 1;52(1):81-90. doi: 10.1016/s0360-3016(01)01758-8.
To report the 8-year outcome of local dose escalation using high-dose-rate conformal brachytherapy combined with elective irradiation of the pelvic lymphatics for localized prostate cancer.
One hundred forty-four consecutively treated men (1986-1992) were recorded prospectively. Twenty-nine (20.14%) patients had T1b-2a tumors, and 115 (79.86%) patients had T2b-3 tumors according to, respectively, American Joint Committee on Cancer/Union Internationale Contre le Cancer 1992. All patients had a negative nodal status, proven by CT or MRI. The mean initial PSA value was 25.61 ng/mL (Initial value for 41.66% of patients was <10 ng/mL, for 21.52% was 10-20 ng/mL, and for 32.63% was >20 ng/mL). The total dose applied by external beam radiotherapy was 50 Gy in the pelvis and 40 Gy in the prostate. The high-dose-rate brachytherapy was delivered in two fractions, which were incorporated into the external beam treatment (after 20-Gy and 40-Gy external beam radiotherapy dose). The dose per fraction was 15 Gy for the PTV1 (peripheral prostate zone) and 9 Gy for the PTV2 (entire prostatic gland). Any patient free of clinical or biochemical evidence of disease was termed bNED. Actuarial rates of outcome were calculated by Kaplan-Meier and compared using the log-rank. Cox regression models were used to establish prognostic factors of the various measures of outcome.
The median follow-up was 8 years (range 60-171 months). The overall survival rate was 71.5%, and the disease-free survival rate was 82.6%. The bNED survival rate was 72.9%. Freedom from local recurrence for T3 stage was 91.3%, whereas for G3 lesions it was 88.23%. Freedom from distant recurrence for T3 stage was 82.6% and for G3 lesions 70.59%. Univariate survival analyses revealed that low stage (T1-2), low grade (G1-2), no hormonal therapy, initial PSA value less than 40 ng/mL, and PSA normalization <1.0 ng/mL after irradiation were associated with long survival. In multivariate analyses, initial PSA value, PSA kinetics after radiation therapy, and no adjuvant hormonal treatment were independent prognostic factors. Grade 3 late radiation toxicity (according to RTOG/EORTC scoring scheme) was 2.3% for the genitourinary system in terms of cystitis and 4.10% for the gastrointestinal system in terms of proctitis. Grades 4 and 5 genitourinary/gastrointestinal morbidity was not observed. A history of transurethral resection of the prostate with a median interval of less than 6 months from radiotherapy was associated with a high risk of genitourinary toxicity.
The 8-year results confirm the feasibility and effectiveness of combined elective irradiation of the pelvic lymphatics and local dose escalation using high-dose-rate brachytherapy for cure of localized and especially high-risk prostate cancer.
报告采用高剂量率适形近距离放射治疗联合盆腔淋巴结选择性照射对局限性前列腺癌进行局部剂量递增的8年治疗结果。
前瞻性记录了1986年至1992年间连续治疗的144例男性患者。根据美国癌症联合委员会/国际抗癌联盟1992年标准,29例(20.14%)患者为T1b - 2a期肿瘤,115例(79.86%)患者为T2b - 3期肿瘤。所有患者经CT或MRI证实淋巴结阴性。初始PSA值的平均值为25.61 ng/mL(41.66%的患者初始值<10 ng/mL,21.52%为10 - 20 ng/mL,32.63%>20 ng/mL)。外照射放疗在盆腔给予的总剂量为50 Gy,在前列腺给予40 Gy。高剂量率近距离放射治疗分两次进行,并入外照射治疗(分别在外照射放疗剂量达到20 Gy和40 Gy后)。PTV1(前列腺外周区)每分次剂量为15 Gy,PTV2(整个前列腺腺体)为9 Gy。任何无疾病临床或生化证据的患者称为bNED。采用Kaplan - Meier法计算精算结局率,并使用对数秩检验进行比较。使用Cox回归模型建立各种结局指标的预后因素。
中位随访时间为8年(范围60 - 171个月)。总生存率为71.5%,无病生存率为82.6%。bNED生存率为72.9%。T3期患者局部无复发生存率为91.3%,G3级病变患者为88.23%。T3期患者远处无复发生存率为82.6%,G3级病变患者为70.59%。单因素生存分析显示,低分期(T1 - 2)、低分级(G1 - 2)、未接受激素治疗、初始PSA值小于40 ng/mL以及放疗后PSA正常化<1.0 ng/mL与长期生存相关。多因素分析中,初始PSA值、放疗后PSA动力学以及未进行辅助激素治疗是独立的预后因素。根据RTOG/EORTC评分方案,3级晚期放射毒性在泌尿系统中因膀胱炎为2.3%,在胃肠道系统中因直肠炎为4.10%。未观察到4级和5级泌尿生殖系统/胃肠道并发症。前列腺经尿道切除术史且距放疗的中位间隔时间小于6个月与泌尿生殖系统毒性高风险相关。
8年结果证实了盆腔淋巴结选择性照射联合高剂量率近距离放射治疗进行局部剂量递增治疗局限性尤其是高危前列腺癌的可行性和有效性。