Berruti A, Cerutti S, Fasolis G, Sperone P, Tarabuzzi R, Bertetto O, Pagani G, Zolfanelli R, Pallotti S, Bumma C, Fontana D, Rosseti S R, Dogliotti L, Angeli A
Dipartimento di Scienze Cliniche e Biologiche, Universita di Torino, Italy.
Anticancer Res. 1997 Nov-Dec;17(6D):4697-702.
A transient rise in serum alkaline phosphatase (ALP) activity (ALP flare) after androgen deprivation in prostate cancer patients with bone metastases has been previously correlated with both response to therapy and poor prognosis. In the present study we analyzed data coming from an Italian multicenter phase III, trial aimed to compare the efficacy of treatment with goserelin alone with that of goserelin plus mitomycin C. Sixty-seven bone metastatic patients were enrolled: 32 were treated with goserelin and 35 with and goserelin plus mitomycin. 58 cases had ALP measured every month; and were considered for flare assessment. Remarkably elevated ALP and PSA levels at baseline were significantly correlated with poor prognosis. The addition of mitomycin to goserelin resulted in a greater percent reduction of PSA values with respect to goserelin alone but did not augment the time to progression and overall survival. The monthly profile of ALP serum levels was superimposable in patients assigned to hormone therapy or chemotherapy plus hormone therapy. Patients showing a flare in ALP activity (transient rise > 15% in ALP values with respect to baseline at the first month) were classified as responders to therapy or as having stable disease upon PSA evaluation and/or at bone pain assessment, but had a shorter time to progression (median 12 months) in comparison to those showing a different ALP pattern (median 23 months). The measurement of flare in ALP activity during androgen suppression with or without concomitant mitomycin administration, may permit the early identification of patients who are likely to progress rapidly, and hence be candidate for more aggressive treatments.
在患有骨转移的前列腺癌患者中,雄激素剥夺后血清碱性磷酸酶(ALP)活性短暂升高(ALP 激增),此前已被证明与治疗反应和不良预后相关。在本研究中,我们分析了来自一项意大利多中心 III 期试验的数据,该试验旨在比较单独使用戈舍瑞林与戈舍瑞林加丝裂霉素 C 的治疗效果。67 例骨转移患者入组:32 例接受戈舍瑞林治疗,35 例接受戈舍瑞林加丝裂霉素治疗。58 例患者每月测量 ALP;并用于激增评估。基线时显著升高的 ALP 和 PSA 水平与不良预后显著相关。与单独使用戈舍瑞林相比,戈舍瑞林加丝裂霉素可使 PSA 值降低的百分比更大,但并未延长疾病进展时间和总生存期。接受激素治疗或化疗加激素治疗的患者中,ALP 血清水平的月度变化情况是重叠的。在 PSA 评估和/或骨痛评估中,ALP 活性出现激增(第一个月时 ALP 值相对于基线短暂升高>15%)的患者被分类为治疗反应者或疾病稳定,但与 ALP 模式不同的患者相比,其疾病进展时间较短(中位 12 个月)(中位 23 个月)。在雄激素抑制期间,无论是否同时给予丝裂霉素,测量 ALP 活性的激增情况,可能有助于早期识别可能迅速进展的患者,因此这些患者可能是更积极治疗的候选者。