Saroja K R, Oesterling J E, Hendrickson F, Cohen L, Mansell J
Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois.
Urology. 1993 Jun;41(6):540-7. doi: 10.1016/0090-4295(93)90101-f.
Serial serum prostate-specific antigen (PSA) levels were analyzed retrospectively for prognostic implications in 70 patients with locoregional (Stages B2, C, and D1) prostate cancer who were managed with high energy neutron beam therapy. Three groups of patients were identified. Group I included 30 patients whose serum PSA level decreased to the reference range (0-4 ng/mL) following neutron therapy and remained so subsequently: 28 (93%) remained disease-free and 2 (7%) have failed distantly. All 30 patients (100%) had no evidence of locally progressive disease. This group was categorized as having a good prognosis. The mean time for serum PSA value to decline to reference range was six months; calculated mean time to achieve a stable base-line PSA was 53 +/- 37 days. Follow-up period ranged from twelve to fifty-six months (median: 21 months). Group II consisted of 13 patients in whom there was an initial decrease in serum PSA to reference range followed by a subsequent increase: 6 of 13 (46%) have no overt clinical progression of disease; 7 (54%) have either persistent locoregional or distant metastatic disease. Follow-up period was from twelve to seventy-two months (median: 39 months). Calculated mean time to achieve stable baseline PSA for serum PSA in this group was 61 +/- 21 days. Group III patients had a persistently elevated or rising serum PSA concentration. Of 27 patients in this group, only 9 (33%) have no evidence of disease progression, while 18 patients (67%) have failed already, either locoregionally or distantly. Follow-up period ranged from twelve to sixty-nine months (median: 21 months). Mean time to achieve stable baseline of serum PSA in this cohort of patients with a poor prognosis was 108 +/- 76 days. We conclude that PSA has a predictable prognostic value in patients with locally advanced prostate cancer managed with high energy neutron beam therapy. Rapid normalization of PSA after therapy indicates a good prognosis. Persistent elevation signifies either presence of persistent locoregional disease or development of distant metastases. Subsequent elevation of the serum PSA concentration after definitive therapy signals progression of prostate cancer.
对70例接受高能中子束治疗的局限性(B2、C和D1期)前列腺癌患者的系列血清前列腺特异性抗原(PSA)水平进行回顾性分析,以评估其预后意义。确定了三组患者。第一组包括30例患者,其血清PSA水平在中子治疗后降至参考范围(0 - 4 ng/mL)且随后一直保持在该范围:28例(93%)无疾病复发,2例(7%)远处转移失败。所有30例患者(100%)均无局部进展性疾病的证据。该组被归类为预后良好。血清PSA值降至参考范围的平均时间为6个月;计算得出达到稳定基线PSA的平均时间为53±37天。随访期为12至56个月(中位数:21个月)。第二组由13例患者组成,其血清PSA最初降至参考范围,随后又升高:13例中有6例(46%)无明显疾病临床进展;7例(54%)有持续性局部或远处转移性疾病。随访期为12至72个月(中位数:39个月)。该组血清PSA达到稳定基线的计算平均时间为61±21天。第三组患者的血清PSA浓度持续升高或上升。该组27例患者中,只有9例(33%)无疾病进展的证据,而18例患者(67%)已经失败,无论是局部还是远处。随访期为12至69个月(中位数:21个月)。该预后不良的患者队列中血清PSA达到稳定基线的平均时间为108±76天。我们得出结论,PSA在接受高能中子束治疗的局部晚期前列腺癌患者中具有可预测的预后价值。治疗后PSA快速恢复正常表明预后良好。持续升高表明存在持续性局部疾病或远处转移的发生。根治性治疗后血清PSA浓度随后升高表明前列腺癌进展。