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女性高危黑色素瘤患者肿瘤微环境和循环中的免疫激活增强,与男性相比,辅助 CTLA4 阻断治疗可改善生存

英文原题:Enhanced immune activation within the tumor microenvironment and circulation of female high-risk melanoma patients and improved survival with adjuvant CTLA4 blockade compared to males.

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Enhanced immune activation within the tumor microenvironment and circulation of female high-risk melanoma patients and improved survival with adjuvant CTLA4 blockade compared to males.

PubMed 2022/06/03(内容时间) J Transl Med Q1 · IF 9.7(JCR 2025)

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研究概要

女性与辅助 CTLA4 阻断临床获益相关,且女性患者更可能在 TME 和循环中具有 1 型免疫激活的证据。试验注册 ClinicalTrials.gov NCT01274338。注册日期 2011 年 1 月 11 日,https://www.

研究思路结论见上方概要

我们假设,与高剂量IFNα(HDI)相比,辅助CTLA4阻断剂ipilimumab的临床反应可能存在性别差异。我们研究了循环和肿瘤微环境(TME)中候选免疫生物标志物的差异。

这项基于性别的分析嵌套在E1609试验中,该试验在高风险已切除黑色素瘤中测试了ipilimumab 3 mg/kg(ipi3)和10 mg/kg(ipi10)对比HDI的辅助治疗。我们在调整年龄、分期、ECOG体能状态(PS)、溃疡、原发肿瘤状态和淋巴结数量后,研究了ipi3和ipi10对比HDI在治疗疗效方面的性别差异。绘制森林图以比较ipi与HDI之间的总生存期(OS)和无复发生存期(RFS)。对718例(454例男性,264例女性)患者的肿瘤进行了基因表达谱分析(GEP)。同样,对血清和外周血单个核细胞(PBMC)样本进行了可溶性和细胞生物标志物检测(N = 321例患者;109例女性和212例男性)。

女性、IIIC期、PS = 1、原发灶溃疡、途中转移等亚组显示,与HDI相比,ipi3在RFS和/或OS方面有显著改善。女性性别在OS和RFS方面均显著,并进一步进行了探索。在RFS比较中,包含显著变量的多变量Cox回归模型显示,性别与治疗之间存在显著交互作用(P = 0.024)。在外周血中,女性CD3+ T细胞百分比(P = 0.024)和CD3+ CD4+辅助T细胞百分比(P = 0.0001)高于男性。女性中还发现IL1β(P = 0.07)和IL6(P = 0.06)循环水平有升高趋势。男性单核细胞百分比更高(P = 0.03),并伴有调节性T细胞(T-reg)百分比升高的趋势。肿瘤GEP分析支持,与男性相比,女性肿瘤中免疫细胞浸润增强,包括γδ T细胞(P = 0.005)、NK细胞(P = 0.01)、树突状细胞(P = 0.01)、CD4+ T细胞(P = 0.03)、CD8+ T细胞(P = 0.03)和T-reg(P = 0.008),并且T效应细胞和IFNγ基因特征评分更高(P = 0.0244)。

展开英文摘要原文

We hypothesized that a gender difference in clinical response may exist to adjuvant CTLA4 blockade with ipilimumab versus high-dose IFNα (HDI). We investigated differences in candidate immune biomarkers in the circulation and tumor microenvironment (TME).

This gender-based analysis was nested within the E1609 trial that tested adjuvant therapy with ipilimumab 3 mg/kg (ipi3) and 10 mg/kg (ipi10) versus HDI in high risk resected melanoma. We investigated gender differences in treatment efficacy with ipi3 and ipi10 versus HDI while adjusting for age, stage, ECOG performance (PS), ulceration, primary tumor status and lymph node number. Forest plots were created to compare overall survival (OS) and relapse free survival (RFS) between ipi and HDI. Gene expression profiling (GEP) was performed on tumors of 718 (454 male, 264 female) patients. Similarly, serum and peripheral blood mononuclear cells (PBMC) samples were tested for soluble and cellular biomarkers (N = 321 patients; 109 female and 212 male).

The subgroups of female, stage IIIC, PS = 1, ulcerated primary, in-transit metastasis demonstrated significant improvement in RFS and/or OS with ipi3 versus HDI. Female gender was significant for both OS and RFS and was further explored. In the RFS comparison, a multivariate Cox regression model including significant variables indicated a significant interaction between gender and treatment (P = 0.024). In peripheral blood, percentages of CD3+ T cells (P = 0.024) and CD3+ CD4+ helper T cells (P = 0.0001) were higher in females compared to males. Trends toward higher circulating levels of IL1β (P = 0.07) and IL6 (P = 0.06) were also found in females. Males had higher percentages of monocytes (P = 0.03) with trends toward higher percentages of regulatory T cells (T-reg). Tumor GEP analysis supported enhanced infiltration with immune cells including gammadelta T cells (P = 0.005), NK cells (P = 0.01), dendritic cells (P = 0.01), CD4+ T cells (P = 0.03), CD8+ T cells (P = 0.03) and T-reg (P = 0.008) in the tumors of females compared to males and a higher T-effector and IFNγ gene signature score (P = 0.0244).

Female gender was associated with adjuvant CTLA4 blockade clinical benefits and female patients were more likely to have evidence of type1 immune activation within the TME and the circulation. Trial registration ClinicalTrials.gov NCT01274338. Registered 11 January 2011, https://www. CLINICALTRIALS: gov/ct2/show/NCT01274338.

论文信息

作者
Saad M、Lee SJ、Tan AC、El Naqa IM、Hodi FS、Butterfield LH、LaFramboise WA、Storkus W
第一作者单位
Departments of Cutaneous Oncology and Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, 33612, USA, 10920 McKinley Dr.United States
通讯作者单位
Departments of Cutaneous Oncology and Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, 33612, USA, 10920 McKinley Dr.. Ahmad.Tarhini@moffitt.org.United States
文献类型
美国 NIH 资助研究
期刊
Journal of translational medicine2022 Jun 3
原文标识
PubMed 35659704 · DOI 10.1186/s12967-022-03450-3