Ghanshyam Kumawat, SS Yadav, Sanjeev Jaiswal, Ramdayal Sahu, Anurag Garg, V. Tomar
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Univariate and multivariate analyses of potential factors were done, and data analysis was done with SPSS (Statistical Package for the Social Sciences) version 21.0. In this study, after univariate analysis, seven factors were associated with longer duration of response to abiraterone. These were PSA at diagnosis (hazard ratio (HR) = −1.011 (95% confidence interval (CI) = 1.003–1.020), p-value = 0.008), PSA at start of abiraterone (HR = −1.018 (95% CI = 1.011–1.025), p-value = 0.0001), nadir PSA (HR = −1.063 (95% CI = 1.024–1.104), p-value = 0.001), prostate-specific antigen doubling (PSAD) time (HR = −0.745 (95% CI = 0.672–0.827), p-value = 0.001), raised alkaline phosphatase (ALP) (HR = −1.002 (95% CI = 1.001–1.003), p-value = 0.001), neutrophil/lymphocyte ratio (NLR) (HR = −2.16 (95% CI = 1.672–2.81), p-value = 0.001) and <5 bone metastasis (HR = −0.235 (95% CI = 0.130–0.422), p-value = 0.01). But after multivariate analysis, nadir PSA achieved, PSAD, NLR and ⩽5 bone metastasis were predictors of better response to abiraterone. This study had identified that less nadir PSA achieved, long PSAD time, low NLR and limited number of skeletal metastases were potential factors for better PSA response to abiraterone. 1","PeriodicalId":15471,"journal":{"name":"Journal of Clinical Urology","volume":" ","pages":""},"PeriodicalIF":0.2000,"publicationDate":"2022-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of factors predicting response to abiraterone acetate in metastatic castration-resistant prostate cancer: A prospective study\",\"authors\":\"Ghanshyam Kumawat, SS Yadav, Sanjeev Jaiswal, Ramdayal Sahu, Anurag Garg, V. 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In this study, after univariate analysis, seven factors were associated with longer duration of response to abiraterone. These were PSA at diagnosis (hazard ratio (HR) = −1.011 (95% confidence interval (CI) = 1.003–1.020), p-value = 0.008), PSA at start of abiraterone (HR = −1.018 (95% CI = 1.011–1.025), p-value = 0.0001), nadir PSA (HR = −1.063 (95% CI = 1.024–1.104), p-value = 0.001), prostate-specific antigen doubling (PSAD) time (HR = −0.745 (95% CI = 0.672–0.827), p-value = 0.001), raised alkaline phosphatase (ALP) (HR = −1.002 (95% CI = 1.001–1.003), p-value = 0.001), neutrophil/lymphocyte ratio (NLR) (HR = −2.16 (95% CI = 1.672–2.81), p-value = 0.001) and <5 bone metastasis (HR = −0.235 (95% CI = 0.130–0.422), p-value = 0.01). But after multivariate analysis, nadir PSA achieved, PSAD, NLR and ⩽5 bone metastasis were predictors of better response to abiraterone. 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引用次数: 0
摘要
在当今时代,醋酸阿比特龙是去势抵抗性前列腺癌的主要治疗策略,并被证明可以延长总生存期。我们的目的是前瞻性地确定与阿比特龙反应持续时间相关的因素。2019年2月至2020年3月期间,所有符合阿比特龙治疗条件的转移性去势抵抗性前列腺癌患者均被纳入研究。所有基线数据和潜在相关因素的记录和随访与前列腺特异性抗原(PSA),并在1个月的间隔进行必要的调查。记录PSA反应持续时间,根据反应持续时间将患者分为五组。对潜在因素进行单因素和多因素分析,使用SPSS (Statistical Package for Social Sciences) 21.0版本进行数据分析。在这项研究中,经过单因素分析,七个因素与阿比特龙反应持续时间较长有关。诊断时PSA(风险比(HR) = - 1.011(95%可信区间(CI) = 1.003-1.020), p值= 0.008),阿比龙开始时PSA (HR = - 1.018 (95% CI = 1.011 - 1.025), p值= 0.0001),最低点PSA (HR = - 1.063 (95% CI = 1.024-1.104), p值= 0.001),前列腺特异性抗原加倍(PSAD)时间(HR = - 0.745 (95% CI = 0.672-0.827), p值= 0.001),碱性磷酸酶(ALP)升高(HR = - 1.002 (95% CI = 1.001-1.003), p值= 0.001),嗜中性粒细胞和淋巴细胞比率(NLR) (HR =−2.16 (95% CI = 1.672 - -2.81),假定值= 0.001)和< 5骨转移(HR =−0.235 (95% CI = 0.130 - -0.422),假定值= 0.01)。但在多因素分析后,最低PSA达到,PSAD, NLR和骨转移≥5是阿比特龙治疗效果更好的预测因素。本研究发现,较低的最低PSA,较长的PSAD时间,较低的NLR和有限的骨骼转移是阿比特龙对PSA更好的潜在因素。1
Evaluation of factors predicting response to abiraterone acetate in metastatic castration-resistant prostate cancer: A prospective study
In the current era, abiraterone acetate is mainstay of the treatment strategies of castration-resistant prostate cancer and proven to prolong overall survival. We aimed to prospectively identify factors associated with duration of response to abiraterone. All metastatic castration-resistant prostate cancer patients eligible for abiraterone were included in the study from February 2019 till March 2020. All baseline data and potential factors associated recorded and follow-up with prostate-specific antigen (PSA), and required investigations were done at 1 month interval. Duration of PSA response was recorded, and patients were divided in five groups on the basis of duration of response. Univariate and multivariate analyses of potential factors were done, and data analysis was done with SPSS (Statistical Package for the Social Sciences) version 21.0. In this study, after univariate analysis, seven factors were associated with longer duration of response to abiraterone. These were PSA at diagnosis (hazard ratio (HR) = −1.011 (95% confidence interval (CI) = 1.003–1.020), p-value = 0.008), PSA at start of abiraterone (HR = −1.018 (95% CI = 1.011–1.025), p-value = 0.0001), nadir PSA (HR = −1.063 (95% CI = 1.024–1.104), p-value = 0.001), prostate-specific antigen doubling (PSAD) time (HR = −0.745 (95% CI = 0.672–0.827), p-value = 0.001), raised alkaline phosphatase (ALP) (HR = −1.002 (95% CI = 1.001–1.003), p-value = 0.001), neutrophil/lymphocyte ratio (NLR) (HR = −2.16 (95% CI = 1.672–2.81), p-value = 0.001) and <5 bone metastasis (HR = −0.235 (95% CI = 0.130–0.422), p-value = 0.01). But after multivariate analysis, nadir PSA achieved, PSAD, NLR and ⩽5 bone metastasis were predictors of better response to abiraterone. This study had identified that less nadir PSA achieved, long PSAD time, low NLR and limited number of skeletal metastases were potential factors for better PSA response to abiraterone. 1