全组织自体治疗疫苗人体试验中的自身免疫风险、癌症播种和不良事件

Garrett Gianneschi , Anthony Scolpino , James Oleske
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引用次数: 0

摘要

背景:全组织自体治疗性疫苗(WATVs)是一种利用患者自身病理组织的癌症免疫疗法。对WATVs诱导自身免疫或癌症扩散的可能性存在担忧;然而,它们的不良事件(ae)尚未得到充分的研究。本文献综述的主要目的是评估在人体临床试验中使用WATVs相关的自身免疫和癌症播种的风险。次要目标包括使用不良事件通用术语标准v5.0评估1-5级ae的发生率。方法纳入标准是任何使用人类受试者的临床试验,其中至少部分癌症疫苗来自患者自身的肿瘤组织,可能保留了患者肿瘤(即整个组织)中存在的独特肿瘤相关抗原(TAAs)。排除了使用有限TAAs或高度加工肿瘤抗原的肿瘤疫苗试验。使用b谷歌Scholar检索已发表的临床试验,直至2024年3月。如所示,作者详细阐述了这种情况下的偏见风险。对所有被审查的出版物进行检索,以寻找自身免疫、癌症播种和其他不良事件的证据。《2020年系统评价和荟萃分析首选报告项目》声明指导了本次评价。研究人员分析了55项人类临床试验、摘要、病例报告和未发表的数据,包括3323例接受WATVs治疗的各种癌症患者。主要结局是:(1)没有记录的watv诱导的自身免疫病例,(2)没有记录的watv诱导的非传染性癌症扩散或播种的病例,(3)观察到的0.24%(2/838)的传染性癌症扩散或播种的风险归因于消毒不充分。次要结局为:(1)无死亡归因于WATV治疗,(2)4级ae发生率0.18%(6/3323),(3)3级ae发生率0.42%(14/3323),(4)1 - 2级ae发生率52.21%(478/916)。结论经适当灭菌处理的watv无自身免疫诱导风险,基本无癌苗风险。WATVs也表现出与常规疫苗相当的副作用,具有常见,轻微和短暂的不良反应。3级和4级ae的合并风险为0.60%(20/3323)。没有死亡与WATV治疗有因果关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Risk of autoimmunity, cancer seeding, and adverse events in human trials of whole-tissue autologous therapeutic vaccines

Risk of autoimmunity, cancer seeding, and adverse events in human trials of whole-tissue autologous therapeutic vaccines

Background

Whole-tissue autologous therapeutic vaccines (WATVs) are a form of cancer immunotherapy that use a patient's own pathological tissue. Concerns exist regarding the potential of WATVs to induce autoimmunity or the spread of cancer; however, their adverse events (AEs) have not been adequately studied. This literature review primarily aimed to evaluate the risks of autoimmunity and cancer seeding associated with using WATVs in human clinical trials. Its secondary objectives included assessing the incidence of AEs graded 1–5 using the Common Terminology Criteria for Adverse Events v5.0.

Methods

The inclusion criteria were any clinical trial using human subjects in which at least part of the cancer vaccine was derived from the patient's own tumor tissue, which likely preserved the unique tumor-associated antigens (TAAs) present in the patient's tumor (i.e., whole-tissue). Tumor vaccine trials that used limited TAAs or highly processed tumor antigens were excluded. Published clinical trials were searched using Google Scholar until March 2024. The authors elaborated on the risk of bias in such cases, as indicated. All reviewed publications were searched for evidence of autoimmunity, cancer seeding, and other AEs. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2020 statement guided the review.

Results

Data from 55 human clinical trials, abstracts, case reports, and unpublished data were analyzed, including 3323 patients treated with WATVs for various cancers. The primary outcomes were: (1) no documented cases of WATV-induced autoimmunity, (2) no documented cases of WATV-induced spreading or seeding of noninfectious cancers, and (3) the observed 0.24% (2/838) risk of spreading or seeding infectious cancers was attributed to inadequate sterilization. The secondary outcomes were: (1) no deaths were attributed to WATV therapy, (2) 0.18% (6/3323) incidence of grade 4 AEs, (3) 0.42% (14/3323) incidence of grade 3 AEs, (4) the incidence of grades 1–2 AEs was 52.21% (478/916).

Conclusions

WATVs carry no risk of inducing autoimmunity and essentially no risk of cancer seeding if properly sterilized. WATVs also exhibit a side effect profile comparable to that of routine vaccinations, with common, mild, and transient adverse effects. The combined risk of grade 3 and 4 AEs was 0.60% (20/3323). No deaths were causally associated with WATV treatment.
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来源期刊
Cancer pathogenesis and therapy
Cancer pathogenesis and therapy Surgery, Radiology and Imaging, Cancer Research, Oncology
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