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镭-223 二氯化物治疗转移性去势抵抗性前列腺癌男性患者的临床反应。

Clinical response to radium-223 dichloride in men with metastatic castrate-resistant prostate cancer.

机构信息

Department of Radiation Medicine, Northwell Health, Lake Success, NY; Hofstra Northwell School of Medicine, Hempstead, NY.

Biostatistics Unit, Feinstein Institute for Medical Research, Great Neck, NY.

出版信息

Pract Radiat Oncol. 2018 Nov-Dec;8(6):452-457. doi: 10.1016/j.prro.2018.05.003. Epub 2018 May 16.

Abstract

PURPOSE/OBJECTIVE: Radium-223 prolongs survival and decreases symptomatic skeletal events in men with metastatic castrate-resistant prostate cancer and is indicated in patients with painful bone metastases. However, pain responses are rarely reported and often asked about by patients. Further, patients and their physicians are concerned about a lack of pain response portending a poor treatment response and may be inclined to change systemic therapies before completing 6 cycles. We evaluated the likelihood and time course of pain response, potential predictors of response, and its prognostic value in patients receiving radium-223.

MATERIALS AND METHODS

We reviewed the charts of patients who received radium-223 in our department. All patients were planned for 6 cycles with a prescribed dose of 50-55 kBq/kg at each administration. Pain scores, subjective response to pain, analgesic use, treatment toxicities, and laboratory values were recorded at each visit. Symptomatic skeletal events and survival were also recorded.

RESULTS

48 patients received at least one cycle of radium-223 and 27 (56%) received all 6 planned cycles. Median survival from first treatment was 16.0 months (95% CI 8.9 to 19.2 months). 33% experienced at least one symptomatic skeletal event during or after treatment. 62.5% of men reported a decrease in pain from pre-treatment baseline. Of men with improved pain, 96% experienced an improvement before the third cycle. Pain relief was not associated with a decrease in ALK-P or PSA or improved survival.

CONCLUSIONS

Approximately two-thirds of patients who undergo treatment with radium-223 will experience an improvement in pain and, if it occurs, it will most likely occur within the first two cycles. Patients should be counseled about this timeline and, if pain improvement isn't achieved, palliative radiation and oral analgesic readjustment should be considered. Pain response is not associated with survival and should not be used to evaluate the effectiveness of treatment.

摘要

目的

镭-223 可延长转移性去势抵抗性前列腺癌男性患者的生存期并减少有症状的骨骼事件,适用于有疼痛性骨转移的患者。然而,疼痛缓解的报告很少,且常被患者询问。此外,患者及其医生担心缺乏疼痛缓解预示着治疗反应不佳,并且在完成 6 个周期之前可能倾向于改变全身治疗。我们评估了接受镭-223 治疗的患者发生疼痛缓解的可能性和时间过程、缓解的潜在预测因素及其预后价值。

材料和方法

我们回顾了在我们科室接受镭-223 治疗的患者的病历。所有患者均计划接受 6 个周期的治疗,每个周期的给药剂量为 50-55kBq/kg。每次就诊时记录疼痛评分、疼痛主观缓解、镇痛药使用、治疗毒性和实验室值。还记录了有症状的骨骼事件和生存情况。

结果

48 名患者至少接受了一个周期的镭-223 治疗,27 名(56%)接受了所有 6 个计划周期的治疗。从首次治疗开始的中位生存期为 16.0 个月(95%CI 8.9 至 19.2 个月)。33%的患者在治疗期间或之后发生了至少一次有症状的骨骼事件。62.5%的男性报告疼痛较治疗前基线水平有所减轻。在疼痛改善的男性中,96%在第三个周期前就出现了改善。疼痛缓解与碱性磷酸酶或前列腺特异性抗原的降低或生存改善无关。

结论

接受镭-223 治疗的患者中,约有三分之二会出现疼痛改善,如果出现改善,很可能会在头两个周期内发生。应向患者告知这一时程,如果疼痛改善未实现,应考虑姑息性放疗和口服镇痛药调整。疼痛缓解与生存无关,不应作为评估治疗效果的依据。

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