Department of Nuclear Medicine, Poznan University of Medical Sciences, Poland.
Neoplasma. 2013;60(3):328-33. doi: 10.4149/neo_2013_044.
Bone metastases in prostate cancer constitute the most frequent cause of systemic failure in treatment, which results in numerous complications and finally leads to patient's death. Pain is one of the first and most important clinical symptoms of bone metastases and can be found among more than 80% of patients. Therefore, the most analgetic effective and simultaneously the least toxic treatment is an important point of therapeutic management in this group of patients. The aim of this prospective clinical trial was a comparison of analgetic effectiveness and toxicity of monotherapy with 153Sm isotope to combined therapy (153Sm + EBRT) among patients diagnosed with multiple painful bone metastases due to CRPC (mCRPC). 177 patients with mCRPC were included into the prospective randomised clinical trial in which 89 patients were assigned to the 153Sm isotope monotherapy, while 88 patients were assigned to the combined therapy including 153Sm isotope therapy and EBRT. All patients were diagnosed (bone scan and X-ray or/and CT or/and MRI) with painful bone metastases (bone pain intensity >= 6 according to VAS classification). The following additional inclusion criteria were established: histologically confirmed adenocarcinoma of prostate, multifocal bone metastases, no prior chemotherapy or palliative radiotherapy to bone. All patients signed informed consent.The combination of the isotope therapy with EBRT was more effective analgetic treatment than isotope therapy alone. The highest pain decline was noticed in the first weeks after treatment termination. In the whole group, a total or partial analgesic effect was observed among 154 (87%) patients while among 23 (13%) patients there was a lack of analgesic effect or even pain intensification. The results of this clinical trial demonstrated that for patients with multiple mCRPC it is recommended to combine the 153Sm isotope therapy with local EBRT because of a greater analgetic effect. It is important to note that combined therapy did not intensify the toxicity of treatment.
前列腺癌的骨转移是治疗中全身性失败的最常见原因,导致许多并发症,最终导致患者死亡。疼痛是骨转移的最早和最重要的临床症状之一,80%以上的患者都会出现这种症状。因此,对于这组患者,最有效的止痛治疗同时也是毒性最小的治疗方法是治疗管理的一个重要方面。本前瞻性临床试验的目的是比较 153Sm 同位素单药治疗与联合治疗(153Sm+EBRT)在诊断为多灶性前列腺癌伴多处疼痛性骨转移(mCRPC)患者中的止痛效果和毒性。177 例 mCRPC 患者被纳入前瞻性随机临床试验,其中 89 例患者接受 153Sm 同位素单药治疗,88 例患者接受包括 153Sm 同位素治疗和 EBRT 的联合治疗。所有患者均经骨扫描和 X 线或/和 CT 或/和 MRI 诊断为疼痛性骨转移(根据 VAS 分类,骨痛强度>=6)。还制定了以下纳入标准:组织学证实为前列腺腺癌、多灶性骨转移、无先前的化疗或骨姑息性放疗。所有患者均签署了知情同意书。同位素治疗联合 EBRT 是一种比单独同位素治疗更有效的止痛治疗方法。治疗结束后第一周疼痛下降最明显。在整个组中,154 例(87%)患者观察到完全或部分止痛效果,而 23 例(13%)患者则缺乏止痛效果,甚至疼痛加剧。这项临床试验的结果表明,对于多发性 mCRPC 患者,建议将 153Sm 同位素治疗与局部 EBRT 联合使用,因为这种联合治疗的止痛效果更好。值得注意的是,联合治疗并没有加重治疗的毒性。