Advancements in current one-size-fits-all therapies compared to future treatment innovations for better improved chemotherapeutic outcomes: a step-toward personalized medicine.

IF 2.4 4区 医学 Q1 MEDICINE, GENERAL & INTERNAL Current Medical Research and Opinion Pub Date : 2024-11-01 Epub Date: 2024-10-21 DOI:10.1080/03007995.2024.2416985
Nadia M Hamdy, Emad B Basalious, Mona G El-Sisi, Maha Nasr, Ahmed M Kabel, Eman S Nossier, Ashraf H Abadi
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Abstract

The development of therapies followed a generalized approach for a long time, assuming that a single treatment could effectively address various patient populations. However, recent breakthroughs have revealed the limitations of this one-size-fits-all paradigm. More recently, the field of therapeutics has witnessed a shift toward other modules, including cell therapies, high molecular weight remedies, personalized medicines, and gene therapies. Such advancements in therapeutic modules have the potential to revolutionize healthcare and pave the way for medicines that are more efficient and with minimal side effects. Cell therapies have gained considerable attention in regenerative medicine. Stem cell-based therapies, for instance, hold promise for tissue repair and regeneration, with ongoing research focusing on enhancing their efficacy and safety. High molecular weight drugs like peptides and proteins emerged as promising therapeutics because of their high specificity and diverse biological functions. Engineered peptides and proteins are developed for targeted drug delivery, immunotherapy, and disease-modulation. In personalized medicine, tailored treatments to individuals based on specific genetic profiling, lifestyle, biomarkers, and disease characteristics are all implemented. Clinicians have tailored treatments to optimize outcomes and minimize adverse effects, using targeted therapies based on specific mutations, yielding remarkable results. Gene therapies have revolutionized the treatment of genetic disorders by directly targeting the underlying genetic abnormalities. Innovative techniques, such as CRISPR-Cas9 have allowed precise gene editing, opening up possibilities for curing previously incurable conditions. In conclusion, advancements in therapeutic modules have the potential to revolutionize healthcare and pave the way for medicines that are more efficient and with minimal side effects.

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当前 "一刀切 "疗法的进步与未来治疗创新的比较,以更好地改善化疗效果:迈向个性化医疗的一步。
长期以来,治疗方法的开发一直遵循着一种通用的方法,即假设一种治疗方法可以有效地解决不同患者群体的问题。然而,最近的突破揭示了这种 "一刀切 "模式的局限性。最近,治疗领域出现了向其他模块的转变,包括细胞疗法、高分子量疗法、个性化药物和基因疗法。这些治疗模块的进步有可能彻底改变医疗保健,并为开发更高效、副作用最小的药物铺平道路。细胞疗法在再生医学领域备受关注。例如,以干细胞为基础的疗法有望实现组织修复和再生,目前的研究重点是提高其疗效和安全性。肽和蛋白质等高分子量药物具有高度特异性和多种生物功能,因此成为前景广阔的疗法。工程肽和蛋白质被开发用于靶向给药、免疫疗法和疾病调节。在个性化医疗中,根据特定的基因图谱、生活方式、生物标志物和疾病特征,为个人量身定制治疗方案。临床医生根据特定的基因突变使用靶向疗法,为患者量身定制治疗方案,以优化治疗效果,减少不良反应,取得了显著成效。基因疗法直接针对潜在的基因异常,彻底改变了遗传性疾病的治疗方法。CRISPR-Cas9 等创新技术实现了精确的基因编辑,为治愈以前无法治愈的疾病提供了可能。总之,治疗模块的进步有可能彻底改变医疗保健,并为开发更高效、副作用最小的药物铺平道路。
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来源期刊
Current Medical Research and Opinion
Current Medical Research and Opinion 医学-医学:内科
CiteScore
4.40
自引率
4.30%
发文量
247
审稿时长
3-8 weeks
期刊介绍: Current Medical Research and Opinion is a MEDLINE-indexed, peer-reviewed, international journal for the rapid publication of original research on new and existing drugs and therapies, Phase II-IV studies, and post-marketing investigations. Equivalence, safety and efficacy/effectiveness studies are especially encouraged. Preclinical, Phase I, pharmacoeconomic, outcomes and quality of life studies may also be considered if there is clear clinical relevance
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