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经典型卡波西肉瘤的管理与未来治疗前景:一项基于证据的综述

Management and Future Therapeutic Perspectives of Classic Kaposi's Sarcoma: An Evidence-Based Review.

作者信息

Denaro Nerina, Indini Alice, Brambilla Lucia, Marzano Angelo Valerio, Garrone Ornella, Tourlaki Athanasia

机构信息

Medical Oncology Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Melanoma Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

出版信息

Onco Targets Ther. 2024 Nov 7;17:961-976. doi: 10.2147/OTT.S468787. eCollection 2024.

Abstract

BACKGROUND

Kaposi sarcoma (KS) is a cutaneous neoplasm of endothelial origin. The causative agent is the human herpes virus-8 (HHV-8) which, combined with an immune system impairment, causes cell proliferation. To date, high-quality evidence and treatment recommendations for the management of KS are confined to the acquired immune deficiency syndrome (AIDS)-related KS, while the clinical approach to the treatment of classic KS (CKS) is based on small retrospective case series and the experience of clinicians in selected referral centers.

MATERIALS AND METHODS

A search of the English literature was conducted through PubMed/MEDLINE databases for studies regarding CKS diagnosis, staging, and treatment, published between January 1990 and September 2023.

RESULTS

Overall, 122 out of 565 articles were selected. Based on the results of this literature review, we proposed indications regarding the recommended flow chart for diagnosis, staging, and follow-up of patients with CKS. We assess available evidences regarding topic, locoregional, and systemic treatments of CKS. We also provide a focus on novel treatment strategies and therapeutic approaches currently under evaluation in clinical trials.

CONCLUSION

CKS is a rare disease and its management requires a multidisciplinary assessment. Treatment in referral centers and enrolment in clinical trials might impact on outcomes.

摘要

背景

卡波西肉瘤(KS)是一种起源于内皮细胞的皮肤肿瘤。其致病因子为人疱疹病毒8型(HHV-8),该病毒与免疫系统损伤共同作用导致细胞增殖。迄今为止,关于KS治疗的高质量证据和治疗建议仅限于与获得性免疫缺陷综合征(AIDS)相关的KS,而经典KS(CKS)的临床治疗方法则基于小型回顾性病例系列以及选定转诊中心临床医生的经验。

材料与方法

通过PubMed/MEDLINE数据库检索1990年1月至2023年9月发表的关于CKS诊断、分期和治疗的英文文献。

结果

总共从565篇文章中筛选出122篇。基于该文献综述的结果,我们提出了关于CKS患者诊断、分期和随访推荐流程图的指征。我们评估了关于CKS局部和全身治疗的现有证据。我们还重点介绍了目前正在临床试验中评估的新型治疗策略和治疗方法。

结论

CKS是一种罕见疾病,其管理需要多学科评估。在转诊中心进行治疗以及参加临床试验可能会影响治疗结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b858/11552409/56db84d08ae9/OTT-17-961-g0001.jpg

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