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Biochemical Outcome Following External Beam Radiation Therapy With or Without Androgen Suppression Therapy for Clinically Localized Prostate Cancer. 临床局限性前列腺癌体外放射治疗加或不加雄激素抑制治疗后的生化结果。
Pub Date : 2001-01-01 DOI: 10.1046/J.1525-1411.2001.31007-4.X
T. Gilligan, W. Oh
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引用次数: 0
The Prostate Cancer Continuum: The Role of Bicalutamide (Casodex®) 前列腺癌连续体:比卡鲁胺(Casodex®)的作用
Pub Date : 2001-01-01 DOI: 10.1046/J.1525-1411.2001.003001002.X
G. J. C. M. Kolvenbag
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引用次数: 3
Pilot Study of Oral Eniluracil/5-FU in the Palliation of Hormone-Refractory Prostate Cancer 口服依纽尿嘧啶/5-FU治疗激素难治性前列腺癌的初步研究
Pub Date : 2001-01-01 DOI: 10.1046/J.1525-1411.2001.003001030.X
M. Rosenthal, David M. Thomas, I. Davis, G. Toner, N. Noordin, J. Zalcberg
Objectives: Chemotherapy has an established role in the palliative therapy of patients with hormone-refractory prostate cancer (HRPC). However, optimal chemotherapy for HRPC remains poorly defined. This pilot study examined the activity and toxicity of oral 5-fluorouracil (5-FU) in combination with eniluracil for the treatment of patients with HRPC. Materials and Methods: Eighteen patients with HRPC and painful bone metastases were enrolled, although 1 patient was deemed ineligible because of incidental gastric cancer. The median age was 69 years (range, 57–82 years), median Eastern Cooperative Oncology Group performance status was 1 (range, 0–2) and median prostate specific antigen (PSA) level was 146 μg/l (range 4–2020 μg/l). Eniluracil (10 mg/m2) and 5-FU (1 mg/m2) were given orally, twice daily, for 28 days in 35-day cycles. Results: Two patients (11%) had partial pain responses (95% confidence interval, 0–29%), and 6 patients (35%) had stable pain for a minimum of 8 weeks. A reduction in analgesic use occurred in four patients (23%), and five patients (29%) experienced stable analgesic use. A partial PSA response (>50% reduction on at least two occasions, 5 weeks apart) was achieved in three patients (18%), and eight patients (48%) had stable PSA responses (PSA was rising pretreatment). Grade 4 diarrhea occurred in one patient. Grade 3 toxicities were as follows: anemia, 1 patient; lethargy, 1 patient; and deterioration in liver function, 1 patient. Conclusions: Oral eniluracil/5-FU is well tolerated in this patient population but has only modest activity. Studies in combination with other active agents may be warranted in patients with HRPC.
目的:化疗在激素难治性前列腺癌(HRPC)患者的姑息治疗中已经确立了作用。然而,HRPC的最佳化疗方案仍不明确。本初步研究考察了口服5-氟尿嘧啶(5-FU)联合伊纽尿嘧啶治疗HRPC患者的活性和毒性。材料与方法:纳入了18例HRPC伴疼痛性骨转移患者,其中1例患者因偶发胃癌而被认为不合格。年龄中位数为69岁(范围,57 ~ 82岁),东部肿瘤合作组表现状态中位数为1(范围,0 ~ 2),前列腺特异性抗原(PSA)水平中位数为146 μg/l(范围4 ~ 2020 μg/l)。依纽尿嘧啶(10 mg/m2)和5-FU (1 mg/m2)口服,每日2次,以35天为周期,疗程28天。结果:2例患者(11%)有部分疼痛反应(95%置信区间0-29%),6例患者(35%)至少有8周的稳定疼痛。4例患者(23%)镇痛药使用减少,5例患者(29%)镇痛药使用稳定。3例患者(18%)达到部分PSA缓解(至少两次,间隔5周降低50%),8例患者(48%)具有稳定的PSA缓解(PSA预处理上升)。1例患者出现4级腹泻。3级毒副反应如下:贫血1例;嗜睡1例;肝功能恶化,1例。结论:口服依纽尿嘧啶/5-FU在该患者群体中耐受性良好,但只有适度的活性。HRPC患者联合其他活性药物的研究可能是有必要的。
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引用次数: 1
Anemia Related to Hormonal Ablation Therapy for Prostate Cancer 前列腺癌激素消融治疗相关贫血
Pub Date : 2001-01-01 DOI: 10.1046/J.1525-1411.2001.003001014.X
W. Oh
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引用次数: 3
Bicalutamide Monotherapy Compared with Castration in Patients with Nonmetastatic Locally Advanced Prostate Cancer: 6.3 Years of Follow‐up 比卡鲁胺单药治疗与去势治疗在非转移性局部晚期前列腺癌患者中的比较:6.3年随访
Pub Date : 2001-01-01 DOI: 10.1046/J.1525-1411.2001.003001042.X
T. Gilligan, W. Oh
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引用次数: 51
Prospective Trial of the Herbal Supplement PC‐SPEC in Patients with Progressive Prostate Cancer. 草药补充剂PC‐SPEC在进展性前列腺癌患者中的前瞻性试验。
Pub Date : 2001-01-01 DOI: 10.1046/J.1525-1411.2001.31007-3.X
T. Gilligan, W. Oh
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引用次数: 1
Overall Survival after Prostate‐Specific‐Antigen‐Detected Recurrence Following Conformal Radiation Therapy. 适形放疗后前列腺特异性抗原检测复发后的总生存率。
Pub Date : 2001-01-01 DOI: 10.1046/J.1525-1411.2001.31007-2.X
T. Gilligan, W. Oh
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引用次数: 26
Comparative Analysis of the Role of Prostate Specific Antigen Parameters in Clinical Practice 前列腺特异性抗原参数在临床应用中的比较分析
Pub Date : 2000-12-01 DOI: 10.1046/J.1525-1411.2000.24009.X
N.N.K. Lynn, G. N. Collins, K. Alexandrou, S. Brown, P. Brooman, P. O’Reilly
Introduction: Serum prostate specific antigen at the cutoff levels of 4 ng/ml has low specificity for prostate cancer. We evaluated various PSA parameters (i.e., total PSA density [tPSAD], free PSA density [fPSAD], the ratio of free to total PSA [f/t ratio], and age-specific PSA) in terms of cancer diagnosis and reducing the number of negative results for prostatic biopsies. Materials and Methods: A series of 305 patients was studied. Serum tPSA and fPSA levels were measured. Prostate volume was measured with transrectal ultrasound, and sextant biopsies were performed. The f/t ratio, tPSAD, and fPSAD were calculated. Sensitivity and specificity were calculated for age-specific PSA. Receiver operating characteristic curve analysis was used to analyze the diagnostic performance of these PSA parameters. A subpopulation of patients with serum PSA levels between 4 and 10 ng/ml also was analyzed with a specific view to reducing negative results of biopsies. The Mann-Whitney U test was used to analyze the difference in these parameters between patients with benign and malignant histologies. Results: There was significant difference in these PSA parameters between patients with benign and malignant histologies (p < 0.05). tPSAD had the largest area under the curve for total population as well as for patients with tPSA levels between 4 and 10 ng/ml. Although the f/t ratio had a larger area under the curve than did tPSA assay in patients with PSA levels between 4 and 10 ng/ml, the difference was not statistically significant. Using a tPSAD of 0.12 ng/ml/ml as the cutoff level of negative results of prostate biopsies could be reduced by 37% in patients with PSA levels between 4 and 10 ng/ml. Although the f/t ratio could reduce negative results of biopsies by 33.8% at the cutoff value of 0.26, 15.6% of cancers would be missed. Age-specific PSA could reduce 31% of negative prostatic biopsies, but 28% of cancers would be missed. Using combined tPSAD and the f/t ratio did not improve reductions of negative biopsy results. Conclusion: tPSA density has the highest sensitivity and specificity in differentiating benign from malignant prostates. By using tPSA density, negative results of prostate biopsies can be reduced by 37%, while missing only a small number of cancers.
前言:血清前列腺特异性抗原在临界值为4 ng/ml时对前列腺癌的特异性较低。我们评估了各种PSA参数(即总PSA密度[tPSAD]、游离PSA密度[fPSAD]、游离PSA与总PSA之比[f/t ratio]和年龄特异性PSA)在癌症诊断和减少前列腺活检阴性结果数量方面的作用。材料与方法:对305例患者进行研究。测定血清tPSA和fPSA水平。经直肠超声测量前列腺体积,并进行六分仪活检。计算f/t比值、tPSAD、fPSAD。计算年龄特异性PSA的敏感性和特异性。采用受试者工作特征曲线分析,分析这些PSA参数的诊断效能。还分析了血清PSA水平在4至10 ng/ml之间的患者亚群,以减少活检的阴性结果。使用Mann-Whitney U检验来分析这些参数在良性和恶性组织学患者之间的差异。结果:良性与恶性组织学患者PSA指标差异有统计学意义(p < 0.05)。总体人群以及tPSA水平在4 - 10 ng/ml之间的患者的tPSAD曲线下面积最大。虽然在PSA水平为4 ~ 10 ng/ml的患者中,f/t比曲线下面积比tPSA法大,但差异无统计学意义。在PSA水平在4 - 10 ng/ml之间的患者中,使用0.12 ng/ml的tPSAD作为前列腺活检阴性结果的临界值可降低37%。虽然f/t比值在截断值为0.26时可使活检阴性结果减少33.8%,但仍会遗漏15.6%的癌症。年龄特异性PSA可以减少31%的前列腺活检阴性,但28%的癌症将被遗漏。联合使用tPSAD和f/t比值并没有改善阴性活检结果的减少。结论:tPSA密度对鉴别前列腺良恶性具有最高的敏感性和特异性。通过使用tPSA密度,前列腺活检的阴性结果可以减少37%,同时只遗漏了少数癌症。
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引用次数: 4
Benefit of Adjuvant Radiation Therapy for Localized Prostate Cancer with a Positive Surgical Margin. 手术切缘阳性的局限性前列腺癌辅助放射治疗的益处。
Pub Date : 2000-12-01 DOI: 10.1046/J.1525-1411.2000.24005-2.X
G. Bubley
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引用次数: 14
Therapy of Advanced Prostate Cancer Part II: Response End Points and the Use of Chemotherapy 晚期前列腺癌的治疗第二部分:反应终点和化疗的使用
Pub Date : 2000-12-01 DOI: 10.1046/J.1525-1411.2000.24001.X
D. Reese, E. Small
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引用次数: 0
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The open prostate cancer journal
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