卵巢癌对PARPi和含铂化疗的耐药性。

IF 4.6 Q1 ONCOLOGY 癌症耐药(英文) Pub Date : 2022-06-22 eCollection Date: 2022-01-01 DOI:10.20517/cdr.2021.146
Rebekah Summey, Denise Uyar
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引用次数: 2

摘要

上皮性卵巢癌仍然是最致命的女性恶性肿瘤,尽管系统治疗的选择和靶向治疗的出现。虽然观察到对治疗的初始反应,但复发和最终的化疗耐药导致整体治疗失败。自20世纪80年代以来,这种模式在铂疗法中已经很明显。随着个性化医疗的出现,人们对聚(adp -核糖)聚合酶抑制(PARPi)作为一种新的治疗选择的批准感到非常兴奋,但对这些治疗的耐药性也同样出现了。人们不断寻找新的药物,但如果化学耐药性的障碍仍然存在,反应的持久性将仍然是脆弱的。揭示铂和PARPi耐药的多因素机制越来越重要,因为目前的治疗策略几乎肯定会失败。将更多的精力集中在扩大目前对铂和PARPi化疗耐药复杂性的理解上,对于改善临床结果具有巨大的潜力。
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Ovarian cancer resistance to PARPi and platinum-containing chemotherapy.

Epithelial ovarian cancer remains the most lethal female malignancy despite options for systemic therapy and the emergence of targeted therapies. Although initial response to therapy is observed, recurrence and ultimately chemoresistance result in overall therapeutic failure. This pattern has been evident with platinum therapy since the 1980s. Significant excitement surrounded the approval of poly (ADP-ribose) polymerase inhibition (PARPi) as a novel therapeutic option, especially with the advent of personalized medicine, but resistance has similarly developed to these treatments. Novel agents are constantly being sought, but if the obstacle of chemoresistance remains, the durability of responses will remain tenuous. Unraveling the multifactorial mechanisms of platinum and PARPi resistance is increasingly important as a therapeutic failure with current strategies is almost assured. Focusing greater efforts on expanding the current understanding of the complex nature of platinum and PARPi chemoresistance has tremendous potential to improve clinical outcomes.

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