释放铂类耐药卵巢癌免疫疗法的潜力:原理、挑战和新策略。

IF 4.6 Q1 ONCOLOGY 癌症耐药(英文) Pub Date : 2024-10-15 eCollection Date: 2024-01-01 DOI:10.20517/cdr.2024.67
Joanna Kefas, Michael Flynn
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引用次数: 0

摘要

卵巢癌是全球健康面临的重大挑战,细胞修复手术和铂类化疗是公认的主要治疗方法。遗憾的是,大多数患者会复发并最终对铂类药物产生耐药性,此时有效的治疗方案十分有限。鉴于免疫疗法在诱导其他几种癌症的持久治疗反应方面取得了成功,目前正在研究其在铂类耐药卵巢癌(PROC)中的潜力。然而,在未经选择的晚期卵巢癌人群中,研究人员发现免疫检查点抑制的反应率很低,而且到目前为止,还没有有效的生物标志物可以预测反应。了解铂耐药性、免疫识别和肿瘤微环境(TME)之间错综复杂的相互作用至关重要。在这篇综述中,我们将探讨迄今为止所遇到的研究挑战、免疫疗法的生物学原理、免疫耐受的内在机制以及克服耐药性的新策略。
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Unlocking the potential of immunotherapy in platinum-resistant ovarian cancer: rationale, challenges, and novel strategies.

Ovarian cancer is a significant global health challenge, with cytoreductive surgery and platinum-based chemotherapy serving as established primary treatments. Unfortunately, most patients relapse and ultimately become platinum-resistant, at which point there are limited effective treatment options. Given the success of immunotherapy in inducing durable treatment responses in several other cancers, its potential in platinum-resistant ovarian cancer (PROC) is currently being investigated. However, in unselected advanced ovarian cancer populations, researchers have reported low response rates to immune checkpoint inhibition, and thus far, no validated biomarkers are predictive of response. Understanding the intricate interplay between platinum resistance, immune recognition, and the tumour microenvironment (TME) is crucial. In this review, we examine the research challenges encountered thus far, the biological rationale for immunotherapy, the underlying mechanisms of immune resistance, and new strategies to overcome resistance.

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Exploring resistance to immune checkpoint inhibitors and targeted therapies in melanoma. NFE2L2 and ferroptosis resistance in cancer therapy. The BET inhibitor sensitivity is associated with the expression level of CDC25B in pancreatic cancer models. Unlocking the potential of immunotherapy in platinum-resistant ovarian cancer: rationale, challenges, and novel strategies. Emerging roles of small extracellular vesicles in metabolic reprogramming and drug resistance in cancers.
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