Sella Avishay, Sternberg Cora N, Skoneczna Iwona, Kovel Svetlana
Department of Oncology, Assaf Harofeh Medical Center, Zerifin, Israel.
BJU Int. 2008 Dec;102(11):1607-9. doi: 10.1111/j.1464-410X.2008.07873.x. Epub 2008 Oct 2.
To evaluate the prostate-specific antigen (PSA) 'flare' phenomenon in patients with androgen-independent prostate cancer (AIPC) treated with docetaxel, as flare is a known effect of androgen-deprivation therapy in hormone-dependent prostate cancer.
The charts of 56 patients who received docetaxel-based chemotherapy in three different centres from August 1999 to August 2007 were reviewed retrospectively. The biochemical response was characterized according to the Bubley criteria. There was an immediate PSA response (PSA decline >or= 50%) in 23 (41%) patients, PSA stabilization (PSA decline < 50%) in 16 (29%) and PSA progression in nine (16%). There was also a fourth response, i.e. PSA flare, defined as an increase in PSA level with no symptomatic progression, after starting docetaxel-based chemotherapy administered every 3 weeks.
Eight (14%) patients with PSA flare were identified; all had osseous disease and five had additional soft-tissue disease. The PSA flare lasted a median (range) of 21 (21-42) days and it spread over a median of 1 (1-2) cycles. The temporary PSA surge exceeded baseline values by a median (range) of 61.5 (12-404)%. There was a subsequent PSA response in six of the eight patients and PSA stabilized in the remaining two. Patients with flare received a median of 8.5 (5-12) treatment cycles, vs a median of 8 (2-12) in the immediate PSA response group (P = 0.103, Student's t-test). The Response Evaluation Criteria in Solid Tumors criteria evaluation showed one patient with a partial response and six with stable disease. The median survival of patients with PSA flare was 12.5 months, while that of the immediate PSA responders was 20.1 months (not statistically significant, P = 0.168, log-rank test).
Of patients with AIPC, 14% had an initial PSA flare after starting docetaxel-based chemotherapy. The occurrence of PSA flare had no effect on treatment duration or outcome. With lack of clinical progression, docetaxel-based chemotherapy should be administered for at least two 3-week cycles before further decisions are made about efficacy.
评估多西他赛治疗去势抵抗性前列腺癌(AIPC)患者时的前列腺特异性抗原(PSA)“flare”现象,因为flare是激素依赖性前列腺癌中雄激素剥夺治疗的已知效应。
回顾性分析1999年8月至2007年8月在三个不同中心接受以多西他赛为基础化疗的56例患者的病历。根据Bubley标准对生化反应进行特征描述。23例(41%)患者出现即刻PSA反应(PSA下降≥50%),16例(29%)患者PSA稳定(PSA下降<50%),9例(16%)患者PSA进展。还存在第四种反应,即PSA flare,定义为在每3周进行一次以多西他赛为基础的化疗开始后,PSA水平升高且无症状进展。
确定8例(14%)出现PSA flare的患者;所有患者均有骨转移,5例还有软组织转移。PSA flare持续时间的中位数(范围)为21(21 - 42)天,且在中位数为1(1 - 2)个周期内出现。PSA的暂时升高超过基线值的中位数(范围)为61.5(12 - 404)%。8例患者中有6例随后出现PSA反应,其余2例PSA稳定。出现flare的患者接受治疗周期的中位数为8.5(5 - 12)个,而即刻PSA反应组为8(2 - 12)个(P = 0.103,学生t检验)。实体瘤疗效评价标准评估显示1例患者部分缓解,6例病情稳定。出现PSA flare的患者中位生存期为12.5个月,而即刻PSA反应者为20.1个月(无统计学意义,P = 0.168,对数秩检验)。
在AIPC患者中,14%在开始以多西他赛为基础的化疗后最初出现PSA flare。PSA flare的发生对治疗持续时间或结果无影响。在缺乏临床进展的情况下,在对疗效做出进一步决定之前,应以多西他赛为基础的化疗至少进行两个3周周期。