Joshi Deeksha, Khursheed Rubiya, Gupta Saurabh, Wadhwa Diksha, Singh Thakur Gurjeet, Sharma Sumit, Porwal Sejal, Gauniyal Swati, Vishwas Sukriti, Goyal Sanjay, Gupta Gaurav, Eri Rajaraman D, Williams Kylie A, Dua Kamal, Singh Sachin Kumar
Chitkara College of Pharmacy, Chitkara University, Rajpura 140401, India.
School of Pharmaceutical Sciences, Lovely Professional University, Phagwara 144411, India.
Pharmaceutics. 2022 Dec 5;14(12):2721. doi: 10.3390/pharmaceutics14122721.
Biologic-based medicines are used to treat a variety of diseases and account for around one-quarter of the worldwide pharmaceutical market. The use of biologic medications among cancer patients has resulted in substantial advancements in cancer treatment and supportive care. Biosimilar medications (or biosimilars) are very similar to the reference biologic drugs, although they are not identical. As patent protection for some of the most extensively used biologics begins to expire, biosimilars have the potential to enhance access and provide lower-cost options for cancer treatment. Initially, regulatory guidelines were set up in Europe in 2003, and the first biosimilar was approved in 2006 in Europe. Many countries, including the United States of America (USA), Canada, and Japan, have adopted Europe's worldwide regulatory framework. The use of numerous biosimilars in the treatment and supportive care of cancer has been approved and, indeed, the count is set to climb in the future around the world. However, there are many challenges associated with biosimilars, such as cost, immunogenicity, lack of awareness, extrapolation of indications, and interchangeability. The purpose of this review is to provide an insight into biosimilars, which include various options available for oncology, and the associated adverse events. We compare the regulatory guidelines for biosimilars across the world, and also present the latest trends and challenges in medical oncology both now and in the future, which will assist healthcare professionals, payers, and patients in making informed decisions, increasing the acceptance of biosimilars in clinical practice, increasing accessibility, and speeding up the health and economic benefits associated with biosimilars.
基于生物制剂的药物用于治疗多种疾病,约占全球制药市场的四分之一。在癌症患者中使用生物药物已使癌症治疗和支持性护理取得了重大进展。生物类似药与参照生物药物非常相似,尽管并非完全相同。随着一些使用最广泛的生物制剂的专利保护开始到期,生物类似药有可能增加可及性,并为癌症治疗提供低成本选择。最初,欧洲在2003年制定了监管指南,2006年欧洲批准了首个生物类似药。包括美国、加拿大和日本在内的许多国家都采用了欧洲的全球监管框架。多种生物类似药已获批用于癌症的治疗和支持性护理,而且实际上,未来全球范围内生物类似药的数量还会增加。然而,生物类似药存在许多挑战,如成本、免疫原性、认知不足、适应症外推和可互换性等。本综述的目的是深入探讨生物类似药,包括肿瘤学领域的各种可用选择以及相关不良事件。我们比较了全球生物类似药的监管指南,并介绍了当前及未来医学肿瘤学的最新趋势和挑战,这将有助于医疗保健专业人员、支付方和患者做出明智的决策,提高临床实践中对生物类似药的接受度,增加可及性,并加速与生物类似药相关的健康和经济效益。