Bouvet Michael, Reid Tony R, Larson Chris, Oronsky Bryan, Carter Corey, Morris John C
Department of Surgery, University of California San Diego, La Jolla, CA, USA.
EpicentRx, Inc., La Jolla, CA, USA.
Oxf Med Case Reports. 2019 Dec 9;2019(11):461-463. doi: 10.1093/omcr/omz105. eCollection 2019 Nov.
Neoantigen vaccines involving multi-peptides and poly-epitope-encoding RNA or DNA have undergone early phase clinical testing with modest reported antitumor effects [ 1]. The less-than-expected activity of these neoantigenic vaccines may correspond with the development of immune escape mechanisms. One permutation on neoantigen vaccines, which may counter or prevent these adaptive immune escape mechanisms, are 'personalized' oncolytic viruses that encode one or more tumor-specific transgenes. Herein, positive therapeutic effects for MY-NEOVAX™, personalized neoantigen-enhanced oncolytic adenoviruses, are described for two heavily pretreated end-stage patients, one with high-grade metastatic neuroendocrine carcinoma of the pancreas and the other with colorectal cancer metastatic to the brain, liver and lungs. To date, treatment benefit has exceeded 12 months without dose-limiting toxicities or related serious adverse events and with documented radiologic stabilization and improved performance status.
包含多种肽以及编码多表位的RNA或DNA的新抗原疫苗已进入早期临床试验阶段,据报道具有一定的抗肿瘤效果[1]。这些新抗原疫苗活性低于预期,可能与免疫逃逸机制的形成有关。新抗原疫苗的一种变体——可对抗或预防这些适应性免疫逃逸机制的“个性化”溶瘤病毒,可编码一种或多种肿瘤特异性转基因。本文描述了MY-NEOVAX™(个性化新抗原增强型溶瘤腺病毒)对两名经过大量前期治疗的终末期患者的积极治疗效果,其中一名患有胰腺高级别转移性神经内分泌癌,另一名患有转移至脑、肝和肺的结直肠癌。迄今为止,治疗获益已超过12个月,未出现剂量限制性毒性或相关严重不良事件,且有影像学稳定和功能状态改善的记录。