Laverdière J, Gomez J L, Cusan L, Suburu E R, Diamond P, Lemay M, Candas B, Fortin A, Labrie F
Department of Radiation Oncology, L'Hôtel-Dieu de Québec, Canada.
Int J Radiat Oncol Biol Phys. 1997 Jan 15;37(2):247-52. doi: 10.1016/s0360-3016(96)00513-5.
The aim of the present study is to investigate whether combined androgen blockade associated with radiation therapy for localized prostate cancer decreases at 12 and 24 months the rate of positive follow-up biopsies and serum PSA compared to radiation therapy alone. This is the report of an interim analysis.
One hundred and twenty patients with clinical Stage B1-T2a, B2-T2b/T2c, and C-T3/T4, adenocarcinoma of the prostate were entered in a prospective randomized study. After written informed consent, the subjects were randomly allocated between external beam radiation therapy (EBRT) alone (group 1), 3 months of neoadjuvant combination therapy (LHRH-agonist + Flutamide) prior to EBRT (group 2), and a third group receiving combination therapy 3 months before, during, and 6 months after EBRT. There is no significant difference between the three groups concerning age, stage of disease, grade of tumor, and pretreatment PSA levels. Control transrectal ultrasound (TRUS)-guided needle biopsies (one core was taken from the initial cancer site regardless of the presence or absence of TRUS abnormalities) were done 12 and 24 months after the end of EBRT. Serum PSA measurements were done on schedule visits.
Ninety-two and 68 patients underwent biopsies at 12 and 24 months, respectively, after the end of radiation therapy. While 62% of control patients at 12 months in Group 1 disclosed residual neoplasm, only 30% and 4% showed residual disease in groups 2 and 3, respectively (p = 0.00005). When looking at 24 months, 65, 28, and 5% showed residual cancer for groups 1, 2, and 3, respectively (p = 0.00001). The PSA measurements indicate also at 12 months a difference between the three groups (p < 0.0001), except at 24 months, the difference between the group 2 and 3 is no longer significant.
The preliminary analysis of this clinical trial indicates that patients treated with radiation therapy alone show a significantly higher rate of positive biopsies at 12 and 24 months after the end of radiation therapy as compared with those treated with total antiandrogen blockade (TAB) and radiation therapy. When analyzing the median PSA serum levels, we found the same advantage at 12 months, but, at the time of the analysis at 24 months, the PSA levels are not different between groups 2 and 3.
本研究旨在探讨与单纯放疗相比,局部前列腺癌患者在接受放疗的同时联合雄激素阻断治疗,在12个月和24个月时,随访活检阳性率和血清前列腺特异抗原(PSA)水平是否降低。这是一项中期分析报告。
120例临床分期为B1-T2a、B2-T2b/T2c和C-T3/T4期的前列腺腺癌患者进入一项前瞻性随机研究。在获得书面知情同意后,受试者被随机分配至单纯外照射放疗组(第1组)、放疗前接受3个月新辅助联合治疗(促性腺激素释放激素激动剂+氟他胺)组(第2组),以及在放疗前3个月、放疗期间及放疗后6个月接受联合治疗的第3组。三组在年龄、疾病分期、肿瘤分级和治疗前PSA水平方面无显著差异。在放疗结束后12个月和24个月进行对照经直肠超声(TRUS)引导下穿刺活检(无论TRUS有无异常,均从初始癌灶取1个组织芯)。按计划访视时测定血清PSA水平。
放疗结束后,分别有92例和68例患者在12个月和24个月时接受了活检。第1组12个月时62%的对照患者显示有残留肿瘤,而第2组和第3组分别仅有30%和4%显示有残留疾病(p = 0.00005)。在24个月时,第1组、第2组和第3组分别有65%、28%和5%显示有残留癌(p = 0.00001)。PSA测定结果显示,在12个月时三组之间也存在差异(p < 0.0001),但在24个月时,第2组和第3组之间的差异不再显著。
该临床试验的初步分析表明,与接受全雄激素阻断(TAB)联合放疗的患者相比,单纯接受放疗的患者在放疗结束后12个月和24个月时活检阳性率显著更高。在分析PSA血清中位水平时,我们发现在12个月时也有同样的优势,但在24个月分析时,第2组和第3组之间的PSA水平无差异。