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阿比特龙治疗的去势抵抗性前列腺癌患者中前列腺特异性抗原激增的长期临床影响

Long-term clinical impact of PSA surge in castration-resistant prostate cancer patients treated with abiraterone.

作者信息

Conteduca Vincenza, Caffo Orazio, Lolli Cristian, Aieta Michele, Scarpi Emanuela, Bianchi Emanuela, Maines Francesca, Schepisi Giuseppe, Salvi Samanta, Massari Francesco, Carrozza Francesco, Veccia Antonello, Chiuri Vincenzo E, Campadelli Enrico, Facchini Gaetano, De Giorgi Ugo

机构信息

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, Meldola, Italy.

Medical Oncology Department, Santa Chiara Hospital, Trento, Italy.

出版信息

Prostate. 2017 Jun;77(9):1012-1019. doi: 10.1002/pros.23357. Epub 2017 Apr 20.

Abstract

BACKGROUND

Early changes in PSA have been evaluated in association to treatment outcome. The aim of this study was to assess PSA surge phenomenon in castration-resistant prostate cancer (CRPC) patients treated with abiraterone and to correlate those variations with long-term treatment outcome.

PATIENTS AND METHODS

We retrospectively evaluated 330 CRPC patients in 11 Italian hospitals, monitoring PSA levels at baseline and every 4 weeks. Other clinical, biochemical and molecular parameters were determined at baseline. We considered PSA surge as PSA increase within the first 8 weeks from starting abiraterone more than 1% from baseline followed by a PSA decline. The log-rank test was applied to compare survival between groups of patients according to PSA surge. The impact of PSA surge on survival was evaluated by Cox regression analyses.

RESULTS

A total of 330 patients with CRPC, median age 74 years (range, 45-90), received abiraterone (281 chemotherapy-treated and 49 chemotherapy-naïve). PSA surge was observed in 20 (7%) post-chemotherapy and 2 (4%) chemotherapy-naïve patients. For overall patients presenting PSA surge, timing of PSA peak from baseline was 5 ± 1.8 weeks and PSA rise from baseline was 21 ± 18.4%. The overall median follow-up was 23 months (range 1-62). No significant differences in progression-free survival and overall survival were observed between patients with and without PSA surge (P = 0.16 and =0.86, respectively). In addition, uni- and multivariate analyses showed no baseline factors related to PSA surge.

CONCLUSION

PSA surge occurs in both chemotherapy-treated and chemotherapy-naïve patients treated with abiraterone resulting, however, in no long-term impact on outcome. Physicians and patients should be aware of PSA surge challenge to prevent a premature discontinuation of potentially effective therapy with abiraterone. Further larger and prospective studies are warranted to investigate this not infrequent phenomenon.

摘要

背景

已对前列腺特异性抗原(PSA)的早期变化与治疗结果的相关性进行了评估。本研究的目的是评估接受阿比特龙治疗的去势抵抗性前列腺癌(CRPC)患者中的PSA激增现象,并将这些变化与长期治疗结果相关联。

患者与方法

我们回顾性评估了意大利11家医院的330例CRPC患者,在基线时以及每4周监测一次PSA水平。在基线时确定其他临床、生化和分子参数。我们将PSA激增定义为从开始使用阿比特龙的前8周内PSA较基线升高超过1%,随后PSA下降。应用对数秩检验比较根据PSA激增分组的患者之间的生存率。通过Cox回归分析评估PSA激增对生存的影响。

结果

共有330例CRPC患者,中位年龄74岁(范围45 - 90岁),接受了阿比特龙治疗(281例接受过化疗,49例未接受过化疗)。在20例(7%)接受化疗后的患者和2例(4%)未接受过化疗的患者中观察到PSA激增。对于出现PSA激增的所有患者,PSA从基线达到峰值的时间为5±1.8周,PSA较基线升高为21±18.4%。总体中位随访时间为23个月(范围1 - 62个月)。在有和没有PSA激增的患者之间,无进展生存期和总生存期均未观察到显著差异(P分别为0.16和0.86)。此外,单因素和多因素分析均未显示与PSA激增相关的基线因素。

结论

接受阿比特龙治疗的接受过化疗和未接受过化疗的患者中均会出现PSA激增,但对结局无长期影响。医生和患者应意识到PSA激增带来的挑战,以防止过早停用可能有效的阿比特龙治疗。有必要进行进一步更大规模的前瞻性研究来调查这种并非罕见的现象。

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