Castration resistant prostate cancer: recent advances in novel therapeutic treatments

Hareer Fatima, Hussain Sohail Rangwala, Faiza Riaz, Laiba Ali, S. R. Abbas, Shajee-Ul -Haque
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Abstract

Prostate cancer is a prevalent and deadly malignancy that poses challenges in diagnosis and treatment. It is the second most common cancer in men worldwide and the fifth leading cause of cancer-related deaths. This abstract provides an overview of current treatments and recent advances in the field of prostate cancer treatment, with a focus on metastatic castration-resistant prostate cancer (mCRPC). Current treatments for mCRPC include chemotherapy, endocrine therapy, and bone-targeting therapy. Chemotherapy drugs such as docetaxel and cabazitaxel are commonly used, but their efficacy is limited. Endocrine therapy, particularly androgen-receptor signaling inhibitors like abiraterone acetate, has shown significant clinical benefits. Bone-targeting therapies such as bisphosphonates and denosumab provide symptomatic relief for bone metastases. Recent advances in novel treatments have shown promise in improving outcomes for patients with mCRPC. Trials investigating the PARP inhibitor rucaparib have demonstrated longer progression-free survival, particularly in patients with BRCA mutations. The combination of talazoparib and enzalutamide has also shown improved progression-free survival and delayed the need for chemotherapy. Another promising treatment is darolutamide, which has been shown to reduce the risk of metastasis or death and extend metastasis-free survival. Immunotherapy, particularly sipuleucel-T and PROSTVAC, has shown potential in reducing mortality risk and increasing overall survival (OS) in mCRPC patients. The combination of sipuleucel-T with abiraterone acetate or enzalutamide has been found to be effective and safe. The introduction of lutetium Lu 177 vipivotide tetraxetan, a PSMA-targeted therapy, has shown improved OS in PSMA-positive mCRPC patients. Radium-223, a radioactive drug targeting bone metastasis, has also demonstrated improved OS and delayed skeletal-related events. These recent advances in prostate cancer treatment offer hope for improved outcomes for patients with mCRPC. Further research and clinical trials are needed to validate these findings and explore additional treatment options.
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阉割抵抗性前列腺癌:新型疗法的最新进展
前列腺癌是一种常见的致命恶性肿瘤,给诊断和治疗带来了挑战。它是全球第二大男性常见癌症,也是癌症相关死亡的第五大原因。本摘要概述了前列腺癌治疗领域的当前治疗方法和最新进展,重点关注转移性抗性前列腺癌(mCRPC)。目前治疗mCRPC的方法包括化疗、内分泌治疗和骨靶向治疗。多西他赛和卡巴他赛等化疗药物是常用药物,但其疗效有限。内分泌治疗,尤其是雄激素受体信号转导抑制剂,如醋酸阿比特龙,已显示出显著的临床疗效。双膦酸盐和地诺单抗等骨靶向疗法可缓解骨转移的症状。新型疗法的最新进展显示,有望改善 mCRPC 患者的治疗效果。研究 PARP 抑制剂 rucaparib 的试验表明,无进展生存期更长,尤其是在 BRCA 基因突变的患者中。talazoparib和enzalutamide的联合治疗也改善了无进展生存期,并推迟了化疗需求。另一种很有前景的治疗方法是达罗他胺(darolutamide),它已被证明可以降低转移或死亡风险,延长无转移生存期。免疫疗法,尤其是sipuleucel-T和PROSTVAC,在降低mCRPC患者的死亡风险和提高总生存期(OS)方面已显示出潜力。研究发现,sipuleucel-T与醋酸阿比特龙或恩杂鲁胺联合使用既有效又安全。镥Lu 177 vipivotide tetraxetan是一种PSMA靶向疗法,它的引入改善了PSMA阳性mCRPC患者的OS。镭-223是一种针对骨转移的放射性药物,它也改善了患者的生存期并延缓了骨骼相关事件的发生。前列腺癌治疗领域的这些最新进展为改善 mCRPC 患者的预后带来了希望。要验证这些发现并探索更多的治疗方案,还需要进一步的研究和临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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