Mollica Veronica, Nuvola Giacomo, Tassinari Elisa, Nigro Maria Concetta, Marchetti Andrea, Rosellini Matteo, Rizzo Alessandro, Errani Costantino, Massari Francesco
Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Struttura Semplice Dipartimentale di Oncologia Medica per la Presa in Carico Globale del Paziente Oncologico 'Don Tonino Bello', IRCCS Istituto Tumori 'Giovanni Paolo II', Viale Orazio Flacco 65, 70124 Bari, Italy.
Curr Oncol. 2022 Mar 5;29(3):1709-1722. doi: 10.3390/curroncol29030142.
Bone metastases are the most frequent site of secondary localization of prostate cancer (PCa) and are present in about 90% of cases of advanced disease. Consequently, an adequate management of bone involvement is of pivotal importance in the therapeutic approach and skeletal-related events (SREs) need to be closely monitored and promptly assessed and treated. Bone targeting agents (BTAs), consisting in bisphosphonates and denosumab, are an essential part of the treatment of metastatic prostate cancer that accompanies systemic treatments throughout the most part of the history of the disease. Activity and safety of bone targeting agents: These treatments are correlated to better outcomes in terms of reduction of SREs and, in metastatic castration resistant setting, of increased overall survival (OS), but several important adverse events have to be managed and prevented. Of these, osteonecrosis of the jaw (ONJ) is extremely invalidating and should be managed with a special attention.
The role of BTAs in prostate cancer is pivotal throughout many stages of the disease, but several toxicities should be quickly recognized and treated. We aim at recollecting evidence on clinical benefit of BTAs, common and specific toxicities, and explore the pathophysiology and clinical aspects of osteonecrosis of the jaw. We present a review of the literature to report the role of the different types of bone targeting agents in the management of prostate cancer with bone metastases with a particular focus on common toxicities and ONJ to recollect current evidences on the activity of these compounds and the correct management of their adverse events.
骨转移是前列腺癌(PCa)最常见的继发性转移部位,约90%的晚期病例会出现骨转移。因此,对骨转移的恰当处理在治疗方案中至关重要,需要密切监测、及时评估和治疗骨相关事件(SREs)。骨靶向药物(BTAs),包括双膦酸盐和地诺单抗,是转移性前列腺癌治疗的重要组成部分,在该疾病大部分治疗历程中都与全身治疗联合使用。骨靶向药物的活性和安全性:这些治疗与减少SREs以及在转移性去势抵抗情况下提高总生存期(OS)方面的更好结局相关,但必须处理和预防一些重要的不良事件。其中,颌骨骨坏死(ONJ)极具致残性,应予以特别关注。
BTAs在前列腺癌疾病的多个阶段都起着关键作用,但应迅速识别并治疗几种毒性反应。我们旨在收集关于BTAs临床获益、常见及特殊毒性的证据,并探讨颌骨骨坏死的病理生理学和临床方面。我们对文献进行综述,以报告不同类型骨靶向药物在伴有骨转移的前列腺癌治疗中的作用,特别关注常见毒性和ONJ,以收集关于这些化合物活性及不良事件正确处理的当前证据。