AB050. Novel treatment vs. standard of care in melanoma-associated leptomeningeal metastases: a systematic review & network meta-analysis.

IF 2.1 4区 医学 Q3 ONCOLOGY Chinese clinical oncology Pub Date : 2024-08-01 DOI:10.21037/cco-24-ab050
Jia Jia Teo, Razan Nossier, Angad Chauhan, Tuan Zea Tan, Vincent Diong Weng Nga
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Abstract

Background: Melanoma stands as a prevalent instigator of leptomeningeal disease (LMD) within the realm of cancer. Given the poor prognosis accompanying this condition, ongoing trials explore a spectrum of treatment modalities in pursuit of more effective interventions. To ascertain the most effective therapeutic strategies, we aim to compare novel treatments against the current standard of care for melanoma-associated LMD.

Methods: A comprehensive search was conducted across multiple databases, including PubMed/Medline, EMBASE, Scopus, ScienceDirect and Web of Science for relevant studies published from January 2014 to January 2024. We included primary research studies, including observational studies, randomised control trials, quasi-experimental design studies, clinical trials, and experimental studies focusing on LMD caused by metastatic melanoma. Data extraction was conducted according to PRISMA guidelines and quality assessment/risk of bias is performed individually using the GRADE method. A network meta-analysis is conducted to evaluate the effects of multiple interventions within the study. Overall survival outcomes were quantified using log hazard ratio.

Results: Out of 680 records screened for eligibility, seven carefully chosen studies, meeting our specific inclusion criteria, provide insights into the management of 397 patients grappling with LMD due to metastatic melanoma. These studies vary in design: one observational cohort study with 29 participants, a clinical trial with 25 patients, four retrospective cohort studies ranging from 39 to 190 participants and one experimental study with 24 patients.

Conclusions: Despite the escalating breakthroughs of treatment options in melanoma-associated LMD, further studies may be imperative to conclusively determine whether the newer therapeutic options yield superior outcomes compared to the current standard of care treatments.

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AB050.黑色素瘤相关脑膜转移瘤的新疗法与标准疗法:系统综述与网络荟萃分析。
背景:黑色素瘤是癌症中最常见的脑膜外疾病(LMD)的诱因。鉴于这种疾病的预后较差,目前正在进行的试验探索了一系列治疗方法,以寻求更有效的干预措施。为了确定最有效的治疗策略,我们旨在将新型疗法与目前治疗黑色素瘤相关 LMD 的标准疗法进行比较:我们在多个数据库(包括 PubMed/Medline、EMBASE、Scopus、ScienceDirect 和 Web of Science)中对 2014 年 1 月至 2024 年 1 月期间发表的相关研究进行了全面检索。我们纳入的主要研究包括观察性研究、随机对照试验、准实验设计研究、临床试验和实验研究,重点是由转移性黑色素瘤引起的 LMD。数据提取按照 PRISMA 指南进行,质量评估/偏倚风险采用 GRADE 方法单独进行。进行网络荟萃分析是为了评估研究中多种干预措施的效果。总体生存结果采用对数危险比进行量化:在经过资格筛选的 680 份记录中,有 7 项经过精心挑选的研究符合我们特定的纳入标准,为 397 名因转移性黑色素瘤而患有 LMD 的患者的管理提供了见解。这些研究的设计各不相同:一项观察性队列研究有 29 名参与者,一项临床试验有 25 名患者,四项回顾性队列研究有 39 到 190 名参与者,一项实验研究有 24 名患者:尽管黑色素瘤相关 LMD 的治疗方案不断取得突破性进展,但要最终确定较新的治疗方案是否能产生优于当前标准疗法的疗效,可能还需要进一步的研究。
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来源期刊
CiteScore
3.90
自引率
0.00%
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0
期刊介绍: The Chinese Clinical Oncology (Print ISSN 2304-3865; Online ISSN 2304-3873; Chin Clin Oncol; CCO) publishes articles that describe new findings in the field of oncology, and provides current and practical information on diagnosis, prevention and clinical investigations of cancer. Specific areas of interest include, but are not limited to: multimodality therapy, biomarkers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to cancer. The aim of the Journal is to provide a forum for the dissemination of original research articles as well as review articles in all areas related to cancer. It is an international, peer-reviewed journal with a focus on cutting-edge findings in this rapidly changing field. To that end, Chin Clin Oncol is dedicated to translating the latest research developments into best multimodality practice. The journal features a distinguished editorial board, which brings together a team of highly experienced specialists in cancer treatment and research. The diverse experience of the board members allows our editorial panel to lend their expertise to a broad spectrum of cancer subjects.
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