Efficacy and safety of PD-1 monoclonal antibody combined with interferon-alpha 1b and anlotinib hydrochloride as the second-line therapy in patients with unresectable advanced melanoma: A retrospective study

IF 2.9 2区 医学 Q2 ONCOLOGY Cancer Medicine Pub Date : 2024-08-21 DOI:10.1002/cam4.70087
Bolun Zhao, Mengyu Zhang, Jingyi Tang, Daopei Zou, Fang Liu, Qiong Shi, Tianwen Gao, Chunying Li, Guannan Zhu
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Abstract

Background

Immune-checkpoint inhibitors are now used more commonly in combination than monotherapy as the first-line choice in patients with unresectable advanced melanoma. Nevertheless, for cases that progressed after the initial combination therapy, the subsequent regimen option can be very difficult. Herein, we reported the efficacy and safety of a triple combination regimen in Chinese unresectable advanced melanoma patients who had poor responses to the first-line immune therapy.

Methods

We reviewed the clinical profiles of patients diagnosed with stage IIIC-IV melanoma between June 1, 2020, and September 30, 2023. The patients who failed the prior immune therapies and received anti-PD-1 mono antibody plus interferon(IFN)-alpha 1b and anlotinib hydrochloride as the second-line therapy were enrolled in the retrospective analysis. Additionally, we examined the exhaustion of T-cells using mIHC staining in available tumor samples.

Results

Fifty-five patients were included in this study. The median follow-up period was 13.6 months. The objective response rate evaluated by the investigators was 9.1%(1CR, 4PR). The disease control rate was 47.3%. The median overall survival was 17.6 months, and the median progression-free survival was 2.8 months. The adverse events rate of any grade was 100%. Grade 3 or 4 irAEs were observed in 29.1% of cases. Multiplex immunohistochemical staining revealed an increased trend of TIM3 expression on tumor-infiltrating T cells in patients without objective response.

Conclusion

PD-1 monoclonal antibody plus interferon-alpha 1b plus anlotinib showed acceptable tolerability and anticancer benefits in Chinese metastatic melanoma patients as a second-line therapy.

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PD-1单克隆抗体联合α-1b干扰素和盐酸安罗替尼作为不可切除的晚期黑色素瘤患者二线疗法的疗效和安全性:一项回顾性研究
背景 目前,免疫检查点抑制剂作为不可切除的晚期黑色素瘤患者的一线选择,其联合疗法比单药疗法更为常用。然而,对于首次联合治疗后出现进展的病例,后续治疗方案的选择可能非常困难。在此,我们报告了三联疗法在中国不可切除的晚期黑色素瘤患者中的疗效和安全性,这些患者对一线免疫疗法反应不佳。 方法 我们回顾了 2020 年 6 月 1 日至 2023 年 9 月 30 日期间确诊的 IIIC-IV 期黑色素瘤患者的临床资料。回顾性分析中纳入了既往免疫疗法失败并接受抗PD-1单抗加干扰素(IFN)-α 1b和盐酸安罗替尼作为二线疗法的患者。此外,我们还使用 mIHC 染色法检测了现有肿瘤样本中 T 细胞的耗竭情况。 结果 本研究共纳入 55 例患者。中位随访时间为 13.6 个月。研究人员评估的客观反应率为 9.1%(1CR,4PR)。疾病控制率为 47.3%。中位总生存期为17.6个月,中位无进展生存期为2.8个月。任何级别的不良事件发生率均为100%。29.1%的病例出现了3级或4级虹膜不良反应。多重免疫组化染色显示,在无客观反应的患者中,肿瘤浸润T细胞上的TIM3表达呈上升趋势。 结论 PD-1单克隆抗体联合α-干扰素1b联合安罗替尼作为二线疗法,在中国转移性黑色素瘤患者中显示出可接受的耐受性和抗癌疗效。
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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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