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Temozolomide monotherapy versus combination therapies in melanoma: a meta-analysis of efficacy and safety

替莫唑胺 医学 内科学 肿瘤科 联合疗法 达卡巴嗪 荟萃分析 黑色素瘤 白细胞减少症 相对风险 药理学 置信区间 毒性 化疗 癌症研究
作者
Lu Chen,Beichen Cai,Xuejun Ni,Qian Lin,Ruonan Ke,Xiaofen Wan,Tao Huang,Xiuying Shan,Biao Wang
出处
期刊:Melanoma Research [Lippincott Williams & Wilkins]
卷期号:35 (2): 87-101
标识
DOI:10.1097/cmr.0000000000001021
摘要

Temozolomide is used in melanoma therapy, but the comparative efficacy and safety of monotherapy vs combination therapies are unclear. This meta-analysis evaluates temozolomide monotherapy vs combination therapies in melanoma patients. PubMed, Embase, and Cochrane Library were searched up to August 2024 for studies comparing temozolomide monotherapy with combination therapies in melanoma. Primary outcomes were 1-year survival and objective response rates (RR); secondary outcomes included hematologic and non-hematologic toxicities. Data were pooled using risk ratios with 95% confidence intervals (CIs). Seven studies were included. Combination therapies improved objective RR over temozolomide monotherapy (risk ratio 0.68, 95% CI: 0.53–0.88). One-year survival did not differ significantly between groups (risk ratio 0.81, 95% CI: 0.59–1.12). Temozolomide monotherapy was associated with reduced incidence of leukopenia (risk ratio 0.54, 95% CI: 0.30–0.95). Adding interferon-alpha (IFN-α) to temozolomide significantly improved 1-year survival (risk ratio 0.54, 95% CI: 0.35–0.84) and objective RR (risk ratio 0.57, 95% CI: 0.42–0.78) compared to temozolomide alone, without significantly increasing toxicity. Combination therapies enhance objective RR over temozolomide monotherapy, with similar 1-year survival. Temozolomide monotherapy offers a better hematologic safety profile. Combining temozolomide with IFN-α significantly improves survival and RR without increasing toxicity. Clinicians should balance efficacy and safety when choosing melanoma treatments.
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