Yu Eun-Mi, Patel Ishan, Hwang Min Woo, Polani Faran, Aragon-Ching Jeanny B
GU Medical Oncology, Inova Schar Cancer Institute, Fairfax, VA, USA.
Division of Hematology and Oncology, Department of Medicine, Inova Schar Cancer Institute, Fairfax, VA, USA.
Clin Med Insights Oncol. 2024 Sep 19;18:11795549241277181. doi: 10.1177/11795549241277181. eCollection 2024.
The management of metastatic hormone-sensitive prostate cancer (mHSPC) or castration-sensitive prostate cancer (mCSPC) has become increasingly complex with the tremendous progress that has been made in this space within the past few decades. In the early days of androgen deprivation therapy (ADT), ADT monotherapy was the mainstay for treatment of advanced prostate cancer. However, novel hormone therapies in the form of androgen receptor pathway inhibitors (ARPI) have emerged; vaccine therapy, chemotherapy with docetaxel and cabazitaxel, and radioactive ligands have shaped the treatment of metastatic prostate cancer in the last decade. Following the initial approval of several drugs for use in metastatic castration-resistant prostate cancer (mCRPC) in combination with primary ADT, these agents were studied and subsequently approved for use in mCSPC. Therefore, ADT monotherapy no longer constitutes an optimal therapeutic option for otherwise fit patients who present with mCSPC. We focus on the treatment of first-line de novo mHSPC or mCSPC and explore frontline doublet and triplet therapy and the pivotal trials that led to their United States Food and Drug Administration approval.
在过去几十年里,转移性激素敏感性前列腺癌(mHSPC)或去势敏感性前列腺癌(mCSPC)的治疗管理变得越来越复杂,这一领域已取得了巨大进展。在雄激素剥夺疗法(ADT)早期,ADT单一疗法是晚期前列腺癌治疗的主要手段。然而,雄激素受体通路抑制剂(ARPI)形式的新型激素疗法出现了;疫苗疗法、多西他赛和卡巴他赛化疗以及放射性配体在过去十年中改变了转移性前列腺癌的治疗方式。在几种用于转移性去势抵抗性前列腺癌(mCRPC)的药物与一线ADT联合使用首次获批后,这些药物经过研究,随后被批准用于mCSPC。因此,对于患有mCSPC的健康患者而言,ADT单一疗法不再是最佳治疗选择。我们专注于一线初发mHSPC或mCSPC的治疗,并探讨一线双联和三联疗法以及使其获得美国食品药品监督管理局批准的关键试验。