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Radium-223 for primary bone metastases in patients with hormone-sensitive prostate cancer after radical prostatectomy.镭-223用于根治性前列腺切除术后激素敏感性前列腺癌患者的原发性骨转移
Oncotarget. 2017 Jul 4;8(27):44131-44140. doi: 10.18632/oncotarget.17311.
2
An exploratory analysis of alkaline phosphatase, lactate dehydrogenase, and prostate-specific antigen dynamics in the phase 3 ALSYMPCA trial with radium-223.在使用镭-223的3期ALSYMPCA试验中对碱性磷酸酶、乳酸脱氢酶和前列腺特异性抗原动态的探索性分析。
Ann Oncol. 2017 May 1;28(5):1090-1097. doi: 10.1093/annonc/mdx044.
3
Radium-223 and concomitant therapies in patients with metastatic castration-resistant prostate cancer: an international, early access, open-label, single-arm phase 3b trial.镭-223 联合治疗转移性去势抵抗性前列腺癌患者:一项国际性、早期准入、开放标签、单臂 3b 期试验。
Lancet Oncol. 2016 Sep;17(9):1306-16. doi: 10.1016/S1470-2045(16)30173-5. Epub 2016 Jul 26.
4
Molecular Imaging in the Evaluation of 6 Doses of Ra-223 in High-Grade Prostate Cancer: Case Report.分子成像在评估6种剂量镭-223治疗高级别前列腺癌中的应用:病例报告
Clin Genitourin Cancer. 2017 Feb;15(1):e159-e164. doi: 10.1016/j.clgc.2016.05.014. Epub 2016 May 27.
5
Addition of docetaxel, zoledronic acid, or both to first-line long-term hormone therapy in prostate cancer (STAMPEDE): survival results from an adaptive, multiarm, multistage, platform randomised controlled trial.多西他赛、唑来膦酸或两者联合添加至前列腺癌一线长期激素治疗(STAMPEDE):一项适应性、多组、多阶段、平台随机对照试验的生存结果
Lancet. 2016 Mar 19;387(10024):1163-77. doi: 10.1016/S0140-6736(15)01037-5. Epub 2015 Dec 21.
6
Chemohormonal Therapy in Metastatic Hormone-Sensitive Prostate Cancer.转移性激素敏感性前列腺癌的化学激素疗法
N Engl J Med. 2015 Aug 20;373(8):737-46. doi: 10.1056/NEJMoa1503747. Epub 2015 Aug 5.
7
Prognostic Factors in Patients Treated with 223Ra: The Role of Skeletal Tumor Burden on Baseline 18F-Fluoride PET/CT in Predicting Overall Survival.223Ra 治疗患者的预后因素:基线 18F-氟代脱氧葡萄糖 PET/CT 中骨骼肿瘤负荷对总生存的预测作用。
J Nucl Med. 2015 Aug;56(8):1177-84. doi: 10.2967/jnumed.115.158626. Epub 2015 Jun 11.
8
Effect of radium-223 dichloride on symptomatic skeletal events in patients with castration-resistant prostate cancer and bone metastases: results from a phase 3, double-blind, randomised trial.镭-223 二氯化物对去势抵抗性前列腺癌伴骨转移患者症状性骨骼事件的影响:来自一项 3 期、双盲、随机试验的结果。
Lancet Oncol. 2014 Jun;15(7):738-46. doi: 10.1016/S1470-2045(14)70183-4. Epub 2014 May 13.
9
Bone-seeking radiopharmaceuticals for treatment of osseous metastases, Part 1: α therapy with 223Ra-dichloride.用于治疗骨转移的亲骨性放射性药物,第1部分:用二氯化镭-223进行α治疗
J Nucl Med. 2014 Feb;55(2):268-74. doi: 10.2967/jnumed.112.112482. Epub 2013 Dec 16.
10
[Mortality trends and years of potential life lost from prostate cancer in the 32 states and 7 sociecononomic regions of Mexico, 2000-2010].[2000 - 2010年墨西哥32个州和7个社会经济区域前列腺癌的死亡率趋势及潜在寿命损失年数]
Gac Med Mex. 2013 Sep-Oct;149(5):576-85.

镭-223治疗转移性激素敏感性高级别前列腺癌:初步经验

Radium-223 IN metastatic hormone-sensitive high-grade prostate cancer: initial experience.

作者信息

Osvaldo García-Pérez Francisco, Salvador Medina-Ornelas Sevastián, Zael Santana-Ríos, Nora Sobrevilla-Moreno

机构信息

Nuclear Medicine and Molecular Imaging Department, Instituto Nacional de CancerologíaMexico City, Mexico.

Urologic Malignances Department, Instituto Nacional de CancerologíaMexico City, Mexico.

出版信息

Am J Nucl Med Mol Imaging. 2017 Nov 1;7(5):236-245. eCollection 2017.

PMID:29181271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5698617/
Abstract

Our study evaluates the feasibility of compassionate exemption of Radium-223 (Ra) treatment in metastatic hormone-sensitive high-grade prostate cancer (mHSHGPC) patients with concomitant androgen deprivation-therapy (ADT). Seven patients with mHSHGPC, were treated with six cycles of Ra plus ADT. All patients had undergone to F-NaF-PET/CT. A qualitative analyses of the F-NaF-PET/CT was performed in conjunction with Alkaline Phosphatase (ALP), Lactate-dehydrogenase (LDH) and Prostatic-Specific Antigen (PSA) values. The mean of SUVmax values were used as a quantitative measure of tumoral burden. Changes in PSA, ALP, LDH from baseline were evaluated, and were defined as increase or decrease of at least 30%. Clinical response was achieved if there was pain reduction using visual analogic scale. Four patients showed a significant reduction in mean SUVmax after 3 cycles of Ra, and one after 6 cycles. Patients who showed reductions in mean SUVmax after Ra-223 also showed reductions in PSA, ALP and LDH. Four weeks after the last cycle of Ra all patients had decreased total PSA, ALP and LDH values ≥ 30% also significant improvement on pain. No progress disease was documented after 14 ± 4 weeks. We found slight to moderate decreases in neutrophils and hemoglobin in two patients. We concluded that Ra plus ADT can be useful in mHSHGPC; the semi-quantitative F-NaF-PET/CT as a method effective to monitor the treatment response. Due to concomitant administration of ADT, F-NaF-PET/CT cannot differentiate whether the findings were due to androgen blockade or the Ra; nevertheless, data supporting the efficacy of Ra is the significant improvement on pain.

摘要

我们的研究评估了在接受雄激素剥夺治疗(ADT)的转移性激素敏感性高级别前列腺癌(mHSHGPC)患者中给予镭-223(Ra)治疗同情用药豁免的可行性。7例mHSHGPC患者接受了6个周期的Ra联合ADT治疗。所有患者均接受了F-NaF-PET/CT检查。结合碱性磷酸酶(ALP)、乳酸脱氢酶(LDH)和前列腺特异性抗原(PSA)值对F-NaF-PET/CT进行定性分析。SUVmax值的平均值用作肿瘤负荷的定量指标。评估了PSA、ALP、LDH相对于基线的变化,定义为至少增加或减少30%。如果使用视觉模拟量表疼痛减轻,则达到临床缓解。4例患者在接受3个周期的Ra治疗后平均SUVmax显著降低,1例在接受6个周期治疗后降低。接受Ra-223治疗后平均SUVmax降低的患者,其PSA、ALP和LDH也降低。在最后一个周期的Ra治疗后4周,所有患者的总PSA、ALP和LDH值均降低≥30%,疼痛也有显著改善。在14±4周后未记录到疾病进展。我们发现2例患者的中性粒细胞和血红蛋白有轻度至中度下降。我们得出结论,Ra联合ADT可用于mHSHGPC;半定量F-NaF-PET/CT是监测治疗反应的有效方法。由于同时给予ADT,F-NaF-PET/CT无法区分这些发现是由于雄激素阻断还是Ra所致;然而,支持Ra疗效的数据是疼痛有显著改善。