Tomioka Susumu, Shimbo Masashi, Amiya Yoshiyasu, Nakatsu Hiroomi, Murakami Shino, Shimazaki Jun
Department of Urology, Graduate School of Medicine, Chiba University, Inohana, Chuo-ku, Chiba-shi 260-8670, Japan.
Jpn J Clin Oncol. 2008 Jan;38(1):36-42. doi: 10.1093/jjco/hym153.
Most patients with advanced prostate cancer after prostate-specific antigen (PSA) relapse following maximum androgen blockade rapidly progress to death. The present study was aimed to predict the survival of these serious patients after PSA relapse.
Sixty-eight patients with M1b and 20 patients with T3b, who relapsed and died of cancer within a short period, were studied. PSA-doubling time (PSA-DT) at PSA relapse influenced the outcome after PSA relapse [hazard ratio (CI): 2.000 (1.283-3.226)]; thus, on the basis of the median values of PSA-DT (>2 months) and additionally nadir PSA in previous treatment (</=2 ng/ml), patients were stratified into four groups. Outcome in the respective groups was examined.
The patients with PSA-DT of >2 months and nadir PSA of </=2 ng/ml showed the longest survival. The other patients in various classifications proceeded with the similarly worse outcomes, in which PSA-DT still influenced survival [hazard ratio (CI): 0.422 (0.203-0.878)]. In several treatments, estramustine phosphate and dexamethasone were relatively effective. A similar rate of response to these drugs was obtained in all four groups, irrespective of stratifying with PSA-DT and nadir PSA, and this may be possibly due to the intervals between relapse and treatments, in which tumor volume was increased and tumor property was altered. Patients responding to treatment showed prolonged survival.
Both PSA-DT and nadir PSA were predictive factors for subsequent survival at PSA relapse, and the patients with long PSA-DT and low nadir PSA may show long outcome.
大多数晚期前列腺癌患者在接受最大雄激素阻断治疗后前列腺特异性抗原(PSA)复发,随后迅速进展至死亡。本研究旨在预测这些严重患者PSA复发后的生存情况。
研究了68例M1b期患者和20例T3b期患者,这些患者在短期内复发并死于癌症。PSA复发时的PSA倍增时间(PSA-DT)影响PSA复发后的预后[风险比(CI):2.000(1.283 - 3.226)];因此,根据PSA-DT的中位数(>2个月)以及既往治疗中的最低PSA(≤2 ng/ml),将患者分为四组。检查了各组的预后情况。
PSA-DT>2个月且最低PSA≤2 ng/ml的患者生存时间最长。其他各种分类的患者预后同样较差,其中PSA-DT仍影响生存[风险比(CI):0.422(0.203 - 0.878)]。在几种治疗中,磷酸雌莫司汀和地塞米松相对有效。无论根据PSA-DT和最低PSA进行分层,所有四组对这些药物的反应率相似,这可能是由于复发与治疗之间的间隔,在此期间肿瘤体积增大且肿瘤性质发生改变。对治疗有反应的患者生存时间延长。
PSA-DT和最低PSA均为PSA复发后后续生存的预测因素,PSA-DT长且最低PSA低的患者可能有较好的预后。