Yashi Masahiro, Nishihara Daisaku, Mizuno Tomoya, Yuki Hideo, Masuda Akinori, Kambara Tsunehito, Betsunoh Hironori, Abe Hideyuki, Fukabori Yoshitatsu, Muraishi Osamu, Kamai Takao
Department of Urology, Dokkyo Medical University, Tochigi, Japan.
Department of Urology, Dokkyo Medical University, Tochigi, Japan.
Clin Genitourin Cancer. 2014 Oct;12(5):e197-203. doi: 10.1016/j.clgc.2014.02.007. Epub 2014 Mar 2.
INTRODUCTION/BACKGROUND: Castration-resistant prostate cancer remains a therapeutic challenge, even after establishing the survival benefits of docetaxel chemotherapy. Metronomic chemotherapy stabilizes various cancers through antiangiogenic and immunomodulatory effects. We evaluate the activity of metronomic oral cyclophosphamide chemotherapy in metastatic CRPC patients, and assess predictive factors for clinical outcomes.
Twenty-four patients with metastatic CRPC received an oral cyclophosphamide and dexamethasone regimen. Of those, 11 patients (45.8%) had been exposed and resistant to previous docetaxel chemotherapy. Six patients had refused to receive docetaxel chemotherapy, and 7 patients could not receive the therapy because of deteriorated performance status. All patients had already shown resistance to continuous dexamethasone therapy. Demographic and clinical data were collected prospectively.
A total of 16 patients (66.7%) experienced a reduction in PSA levels, and PSA decrease ≥ 50% was observed in 8 patients (33.3%). The median PSA progression-free and overall survival were 5.0 months and 19.0 months, respectively. The favorable PSA decrease had no associations with the progression-free and overall survival, but 7 patients (29.2%) in whom response had exceeded 8 months achieved long overall survival of 28 months in median. None of the patients discontinued therapy because of the presence of toxicities.
Metronomic cyclophosphamide is an active and well tolerated chemotherapy and can be an option for metastatic CRPC patients. The benefit of this regimen could not always be evaluated according to a favorable PSA decrease; thus, we must identify the predictive factors of response other than known clinical factors.
引言/背景:即使在确立了多西他赛化疗的生存益处之后,去势抵抗性前列腺癌仍然是一个治疗难题。节拍化疗通过抗血管生成和免疫调节作用使各种癌症病情稳定。我们评估了口服环磷酰胺节拍化疗在转移性去势抵抗性前列腺癌(CRPC)患者中的活性,并评估了临床结局的预测因素。
24例转移性CRPC患者接受了口服环磷酰胺和地塞米松方案。其中,11例患者(45.8%)曾接受过多西他赛化疗且对其耐药。6例患者拒绝接受多西他赛化疗,7例患者因身体状况恶化无法接受该治疗。所有患者均已对持续的地塞米松治疗产生耐药。前瞻性收集了人口统计学和临床数据。
共有16例患者(66.7%)前列腺特异性抗原(PSA)水平下降,8例患者(33.3%)PSA下降≥50%。PSA无进展生存期和总生存期的中位数分别为5.0个月和19.0个月。PSA下降情况良好与无进展生存期和总生存期无关,但7例缓解期超过8个月的患者(29.2%)中位总生存期达到28个月。没有患者因毒性反应而停止治疗。
口服环磷酰胺节拍化疗是一种有效的且耐受性良好的化疗方法,可作为转移性CRPC患者的一种选择。该方案的益处不能总是根据PSA的良好下降情况来评估;因此,我们必须识别出除已知临床因素之外的反应预测因素。