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接受抗癌治疗患者的贫血:聚焦新型治疗方法。

Anemia in patients receiving anticancer treatments: focus on novel therapeutic approaches.

作者信息

Bozzini Claudia, Busti Fabiana, Marchi Giacomo, Vianello Alice, Cerchione Claudio, Martinelli Giovanni, Girelli Domenico

机构信息

Department of Medicine, Section of Internal Medicine, University of Verona, Verona, Italy.

EuroBloodNet Referral Center, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.

出版信息

Front Oncol. 2024 Apr 2;14:1380358. doi: 10.3389/fonc.2024.1380358. eCollection 2024.

Abstract

Anemia is common in cancer patients and impacts on quality of life and prognosis. It is typically multifactorial, often involving different pathophysiological mechanisms, making treatment a difficult task. In patients undergoing active anticancer treatments like chemotherapy, decreased red blood cell (RBC) production due to myelosuppression generally predominates, but absolute or functional iron deficiency frequently coexists. Current treatments for chemotherapy-related anemia include blood transfusions, erythropoiesis-stimulating agents, and iron supplementation. Each option has limitations, and there is an urgent need for novel approaches. After decades of relative immobilism, several promising anti-anemic drugs are now entering the clinical scenario. Emerging novel classes of anti-anemic drugs recently introduced or in development for other types of anemia include activin receptor ligand traps, hypoxia-inducible factor-prolyl hydroxylase inhibitors, and hepcidin antagonists. Here, we discuss their possible role in the treatment of anemia observed in patients receiving anticancer therapies.

摘要

贫血在癌症患者中很常见,会影响生活质量和预后。它通常是多因素的,常常涉及不同的病理生理机制,这使得治疗成为一项艰巨的任务。在接受化疗等积极抗癌治疗的患者中,骨髓抑制导致的红细胞(RBC)生成减少通常占主导,但绝对或功能性缺铁常常并存。目前治疗化疗相关贫血的方法包括输血、促红细胞生成剂和铁补充剂。每种选择都有局限性,因此迫切需要新的方法。在经历了几十年的相对停滞之后,几种有前景的抗贫血药物现在正进入临床阶段。最近引入或正在开发用于其他类型贫血的新型抗贫血药物包括激活素受体配体陷阱、缺氧诱导因子脯氨酰羟化酶抑制剂和铁调素拮抗剂。在此,我们讨论它们在接受抗癌治疗的患者中所观察到的贫血治疗中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87c0/11018927/015bd2346329/fonc-14-1380358-g001.jpg

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