Poor prognosis outcome tumors, bacteria-infected tumors and nanodrugs: current evidence and hypotheses towards a paradigm change for treatment.

IF 12.4 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Henk J Busscher, David W Grainger, JinPu Yu, Da-Yuan Wang
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Abstract

New therapies and supportive care have converted several cancer types into chronic conditions. Yet, some tumors exhibit features reproducibly correlated with poor prognosis outcome (PPO-tumors). Bacteria in a tumor environment can inactivate chemotherapeutics and are a feature of PPO-tumors, although standard diagnostic tests for tumor infections do not exist. Optimism is high for nanotechnologic innovations but nanoparticulate chemotherapeutics based on enhanced permeability and retention in a human tumor environment have only shown limited treatment benefits. Moreover, treatment of infected tumors in animals with stimuli-responsive nanocarriers loaded with an antibiotic/chemotherapeutic combination has demonstrated limited benefits compared to treatment with combinations of carrier-free antibiotics and chemotherapeutics. Development of nanoparticulate chemotherapeutics with significant benefits in human clinical use is estimated to take several decades, which is too long for patients with PPO-tumors. Herein we hypothesize the following: 1-all diagnosed PPO-tumors are infected with bacteria; 2-all PPO-tumors in mice and humans exhibit enhanced permeability to chemotherapeutics; and 3-all diagnosed PPO-tumors must be treated from the onset with a combination of carrier-free antibiotics and chemotherapeutics. Each hypothesis was critically evaluated and judged plausible and clinically acceptable. Potential clinical treatment of PPO-tumors, presuming bacterial infection without diagnosis, with an approved antibiotic and chemotherapeutic free drug combination requires a paradigm change in treatment concept towards more lenient antibiotic use. However, many cancer patients already require antibiotics during chemotherapeutic treatment and combined carrier-free antibiotic/chemotherapeutic treatment may provide an immediate pathway to re-sensitize PPO-tumors to clinically used chemotherapeutics and alter the prognosis to a more favourable outcome.

预后不良的肿瘤、细菌感染的肿瘤和纳米药物:目前的证据和治疗模式改变的假设。
新的治疗方法和支持性护理已经将几种癌症类型转化为慢性疾病。然而,一些肿瘤表现出与预后不良相关的特征(ppo -肿瘤)。肿瘤环境中的细菌可以使化疗药物失活,并且是ppo肿瘤的一个特征,尽管不存在肿瘤感染的标准诊断测试。人们对纳米技术的创新持高度乐观态度,但基于增强人类肿瘤环境渗透性和滞留性的纳米颗粒化疗药物仅显示出有限的治疗效果。此外,与无载体抗生素和化疗药物联合治疗相比,使用刺激反应性纳米载体装载抗生素/化疗药物联合治疗动物感染肿瘤的疗效有限。据估计,在人类临床应用中具有显著益处的纳米颗粒化疗药物的开发需要几十年的时间,这对患有ppo肿瘤的患者来说太长了。在此,我们假设:1-所有诊断的ppo -肿瘤都感染了细菌;2 .小鼠和人类的所有ppo -肿瘤对化疗药物的渗透性增强;3-所有诊断为ppo的肿瘤必须从一开始就联合使用无载体抗生素和化疗药物进行治疗。每个假设都经过严格的评估,判断为合理和临床可接受的。假定未经诊断的细菌感染,使用批准的抗生素和无化疗药物联合治疗ppo -肿瘤的潜在临床治疗需要在治疗概念上的范式改变,转向更宽松的抗生素使用。然而,许多癌症患者在化疗期间已经需要抗生素,无载体抗生素/化疗联合治疗可能提供一个直接途径,使ppo肿瘤对临床使用的化疗药物重新敏感,并将预后改变为更有利的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer Biology & Medicine
Cancer Biology & Medicine Medicine-Oncology
CiteScore
9.80
自引率
3.60%
发文量
1143
审稿时长
12 weeks
期刊介绍: Cancer Biology & Medicine (ISSN 2095-3941) is a peer-reviewed open-access journal of Chinese Anti-cancer Association (CACA), which is the leading professional society of oncology in China. The journal quarterly provides innovative and significant information on biological basis of cancer, cancer microenvironment, translational cancer research, and all aspects of clinical cancer research. The journal also publishes significant perspectives on indigenous cancer types in China.
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