Long-Term Follow-Up of Gemogenovatucel-T (Vigil) Survival and Molecular Signals of Immune Response in Recurrent Ovarian Cancer.

Long-Term Follow-Up of Gemogenovatucel-T (Vigil) Survival and Molecular Signals of Immune Response in Recurrent Ovarian Cancer.
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DOI:
10.3390/vaccines9080894
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发表时间:
2021-08-12
期刊:
影响因子:
7.8
通讯作者:
Nemunaitis J
Nemunaitis J
中科院分区:
医学3区
文献类型:
--
作者:
Rocconi RP;Stanbery L;Madeira da Silva L;Barrington RA;Aaron P;Manning L;Horvath S;Wallraven G;Bognar E;Walter A;Nemunaitis J

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目的:确定 Vigil 治疗后 NanoString 基因表达谱 (GEP) 与总生存期 (OS) 之间的关系。患者和方法:复发性卵巢癌患者 (n = 21) 参加了先前的临床试验。结果:按 TISHIGH 与 TISLOW 分层的 GEP 证明了 OS 优势(NR 与 5.8 个月 HR 0.23;p = 0.0379),特别是,MHC-II 基线表达升高与 OS 优势相关(p = 0.038)。此外,TISHIGH 患者的 1 年 OS 为 75%,而 TISLOW 患者的 1 年 OS 为 25% (p = 0.03795)。 OS 还与 γ-IFN ELISPOT 阳性反应相关,分别为 36.8 个月与 23.0 个月(HR 0.19,p = 0.0098)。结论:Vigil 证明,复发性卵巢癌患者的 OS 获益与 TISHIGH 评分、MHC-II 表达升高和 γ-IFN ELISPOT 阳性相关。
Aim: To determine the relationship between gene expression profile (GEP) and overall survival (OS) by NanoString following treatment with Vigil. Patients and Methods: Recurrent ovarian cancer patients (n = 21) enrolled in prior clinical trials. Results: GEP stratified by TISHIGH vs. TISLOW demonstrated OS benefit (NR vs. 5.8 months HR 0.23; p = 0.0379), and in particular, MHC-II elevated baseline expression was correlated with OS advantage (p = 0.038). Moreover, 1-year OS was 75% in TISHIGH patients vs. 25% in TISLOW (p = 0.03795). OS was also correlated with positive γ-IFN ELISPOT response, 36.8 vs. 23.0 months (HR 0.19, p = 0.0098). Conclusion: Vigil demonstrates OS benefit in correlation with TISHIGH score, elevated MHC-II expression and positive γ-IFN ELISPOT in recurrent ovarian cancer patients.
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发表时间: 2018-06-22
影响因子: 10.9
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