Suvannasankha Attaya, Chirgwin John M
Breast Cancer Res. 2014;16(6):484. doi: 10.1186/s13058-014-0484-9.
Skeletal metastases are an incurable complication afflicting the majority of patients who die from advanced breast cancer. They are most often osteolytic, characterized by net bone destruction and suppressed new bone formation. Life expectancy from first diagnosis of breast cancer bone metastases is several years, during which time skeletal-related events - including pain, fracture, hypercalcemia, and spinal cord compression - significantly degrade quality of life. The bone marrow niche can also confer hormonal and chemo-resistance. Most treatments for skeletal metastases target bone-destroying osteoclasts and are palliative. Recent results from the Breast cancer trials of Oral Everolimus-2 trial suggest that agents such as the mammalian target of rapamycin inhibitor everolimus may have efficacy against breast cancer bone metastases in part via stimulating osteoblasts as well as by inhibiting tumor growth. Selective estrogen receptor modulators similarly inhibit growth of estrogen receptor-positive breast cancers while having positive effects on the skeleton. This review discusses the future role of bone-anabolic agents for the specific treatment of osteolytic breast cancer metastases. Agents with both anti-tumor and bone-anabolic actions have been tested in the setting of multiple myeloma, a hematological malignancy that causes severe osteolytic bone loss and suppression of osteoblastic new bone formation. Stimulation of osteoblast activity inhibits multiple myeloma growth - a strategy that might decrease breast cancer burden in osteolytic bone metastases. Proteasome inhibitors (bortezomib and carfilzomib) inhibit the growth of myeloma directly and are anabolic for bone. Drugs with limited anti-tumor activity but which are anabolic for bone include intermittent parathyroid hormone and antibodies that neutralize the WNT inhibitors DKK1 and sclerostin, as well as the activin A blocker sotatercept and the osteoporosis drug strontium ranelate. Transforming growth factor-beta inhibitors have little tumor antiproliferative activity but block breast cancer production of osteolytic factors and are also anabolic for bone. Some of these treatments are already in clinical trials. This review provides an overview of agents with bone-anabolic properties, which may have utility in the treatment of breast cancer metastatic to the skeleton.
骨转移是一种无法治愈的并发症,折磨着大多数死于晚期乳腺癌的患者。它们大多是溶骨性的,其特征是骨净破坏和新骨形成受抑制。从首次诊断出乳腺癌骨转移开始,患者的预期寿命为数年,在此期间,与骨骼相关的事件——包括疼痛、骨折、高钙血症和脊髓压迫——会显著降低生活质量。骨髓微环境还可赋予激素和化疗抗性。大多数骨转移治疗针对破坏骨骼的破骨细胞,且为姑息性治疗。口服依维莫司 - 2乳腺癌试验的最新结果表明,诸如雷帕霉素靶蛋白抑制剂依维莫司等药物可能部分通过刺激成骨细胞以及抑制肿瘤生长,对乳腺癌骨转移有效。选择性雌激素受体调节剂同样可抑制雌激素受体阳性乳腺癌的生长,同时对骨骼有积极作用。本综述讨论了骨合成代谢药物在溶骨性乳腺癌转移特异性治疗中的未来作用。具有抗肿瘤和骨合成代谢作用的药物已在多发性骨髓瘤的治疗中进行了测试,多发性骨髓瘤是一种血液系统恶性肿瘤,会导致严重的溶骨性骨质流失和成骨细胞新骨形成受抑制。刺激成骨细胞活性可抑制多发性骨髓瘤生长——这一策略可能会减轻溶骨性骨转移中的乳腺癌负担。蛋白酶体抑制剂(硼替佐米和卡非佐米)可直接抑制骨髓瘤生长,且对骨骼有合成代谢作用。抗肿瘤活性有限但对骨骼有合成代谢作用的药物包括间歇性甲状旁腺激素以及中和WNT抑制剂DKK1和硬化蛋白的抗体,还有激活素A阻滞剂索他瑞西普和骨质疏松症药物雷奈酸锶。转化生长因子 - β抑制剂几乎没有肿瘤抗增殖活性,但可阻断乳腺癌溶骨因子的产生,且对骨骼也有合成代谢作用。其中一些治疗方法已在临床试验中。本综述概述了具有骨合成代谢特性的药物,这些药物可能对治疗转移至骨骼的乳腺癌有用。