Tu Shi-Ming, Trikannad Anup K, Vellanki Sruthi, Hussain Munawwar, Malik Nazish, Singh Sunny R, Jillella Anusha, Obulareddy Sri, Malapati Sindhu, Bhatti Sajjad A, Arnaoutakis Konstantinos, Atiq Omar T
Division of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Cancers (Basel). 2024 Mar 14;16(6):1151. doi: 10.3390/cancers16061151.
Although immunotherapy has revolutionized cancer care, there is still an urgent need to enhance its efficacy and ensure its safety. A correct cancer theory and proper scientific method empower pertinent cancer research and enable effective and efficient drug versus therapy development for patient care. In this perspective, we revisit the concept of immune privilege in a cancer cell versus normal cell, as well as in a cancer stem cell versus normal stem cell. We re-examine whether effective immunotherapies are efficacious due to their anti-cancer and/or immune modulatory mechanisms. We reassess why checkpoint inhibitors (CPIs) are not equal. We reconsider whether one can attribute the utility of immunotherapy to specific cancer subtypes and its futility to certain tumor/immune compartments, components, and microenvironments. We propose ways and means to advance immunotherapy beyond CPIs by combining anti-PD1/L1 with various other treatment modalities according to an appropriate scientific theory, e.g., stem cell origin of cancer, and based on available clinical evidence, e.g., randomized clinical trials. We predict that a stem cell theory of cancer will facilitate the design of better and safer immunotherapy with improved selection of its use for the right patient with the right cancer type at the right time to optimize clinical benefits and minimize potential toxic effects and complications.
尽管免疫疗法彻底改变了癌症治疗方式,但仍迫切需要提高其疗效并确保其安全性。正确的癌症理论和恰当的科学方法有助于开展相关癌症研究,并推动开发有效且高效的药物及疗法以治疗患者。从这一角度出发,我们重新审视癌细胞与正常细胞、癌症干细胞与正常干细胞中免疫豁免的概念。我们重新审视有效的免疫疗法是否因其抗癌和/或免疫调节机制而有效。我们重新评估为什么检查点抑制剂(CPIs)并不相同。我们重新考虑是否可以将免疫疗法的效用归因于特定的癌症亚型,而将其无效归因于某些肿瘤/免疫区室、成分和微环境。我们提出了根据适当的科学理论(例如癌症的干细胞起源)并基于现有临床证据(例如随机临床试验),通过将抗PD1/L1与各种其他治疗方式相结合,推动免疫疗法超越CPIs的方法和途径。我们预测,癌症的干细胞理论将有助于设计出更好、更安全的免疫疗法,在正确的时间为患有正确癌症类型的合适患者更好地选择使用该疗法,以优化临床效益并将潜在的毒性作用和并发症降至最低。