PGV001, a multi-peptide personalized neoantigen vaccine platform: Phase I study in patients with solid and hematological malignancies in the adjuvant setting

IF 33.3 1区 医学 Q1 ONCOLOGY Cancer discovery Pub Date : 2025-03-17 DOI:10.1158/2159-8290.cd-24-0934
Mansi Saxena, Thomas U. Marron, Julia Kodysh, John P. Finnigan, Sayali Onkar, Anna Kaminska, Kevin Tuballes, Ruiwei Guo, Rachel Lubong. Sabado, Marcia Meseck, Timothy J. O'Donnell, Robert P. Sebra, Samir Parekh, Matthew D. Galsky, Ana Blasquez, Gustavo Gimenez, Mesude Bicak, Cansu Cimen Bozkus, Daniela Delbeau-Zagelbaum, Denise Rodriguez, Ana Acuna-Villaorduna, Krzysztof J. Misiukiewicz, Marshall R. Posner, Brett A. Miles, Hanna Y. Irie, Amy Tiersten, Deborah B. Doroshow, Andrea Wolf, John Mandeli, Rachel Brody, Andres M. Salazar, Sacha Gnjatic, Jeff Hammerbacher, Eric Schadt, Philip Friedlander, Alexander Rubinsteyn, Nina Bhardwaj
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Abstract

Immunotherapies like immune checkpoint inhibitors (ICIs) have changed the standard of care for cancer patients, often leading to durable responses. However, many patients remain or become refractory to ICIs owing to factors such as a lack of primed neoantigen-reactive T cells. We developed a peptide-based vaccination platform that utilizes fully personalized genome vaccines (PGV) and targets neoantigens predicted by our OpenVax computational pipeline. Here we report results from PGV001 study (NCT02721043) targeting up to 10 neoantigens, administered in the adjuvant setting to patients with both solid and hematological malignancies who have high risk of recurrence. Our data indicates that PGV001 is feasible and safe, with 13 out of 14 enrolled patients receiving the vaccine and 11 completing the treatment. 100% of vaccinated patients developed targeted T cell and B cell responses highlighting the capacity of OpenVax to predict immunogenic neoantigens and the potential of PGV001 for safely inducing targeted immunity.
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PGV001,一种多肽个体化新抗原疫苗平台:在实体和血液系统恶性肿瘤患者中进行辅助治疗的I期研究
免疫检查点抑制剂(ICIs)等免疫疗法已经改变了癌症患者的治疗标准,通常会产生持久的反应。然而,由于缺乏启动的新抗原反应性T细胞等因素,许多患者对ICIs仍然或变得难治性。我们开发了一个基于多肽的疫苗接种平台,该平台利用完全个性化的基因组疫苗(PGV),并针对我们的OpenVax计算管道预测的新抗原。在此,我们报告了PGV001研究(NCT02721043)的结果,该研究针对多达10种新抗原,在辅助环境下给予复发风险高的实体和血液系统恶性肿瘤患者。我们的数据表明PGV001是可行和安全的,14名入组患者中有13名接受了疫苗,11名完成了治疗。100%接种疫苗的患者产生了靶向T细胞和B细胞应答,这突出了OpenVax预测免疫原性新抗原的能力,以及PGV001安全诱导靶向免疫的潜力。
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来源期刊
Cancer discovery
Cancer discovery ONCOLOGY-
CiteScore
22.90
自引率
1.40%
发文量
838
审稿时长
6-12 weeks
期刊介绍: Cancer Discovery publishes high-impact, peer-reviewed articles detailing significant advances in both research and clinical trials. Serving as a premier cancer information resource, the journal also features Review Articles, Perspectives, Commentaries, News stories, and Research Watch summaries to keep readers abreast of the latest findings in the field. Covering a wide range of topics, from laboratory research to clinical trials and epidemiologic studies, Cancer Discovery spans the entire spectrum of cancer research and medicine.
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