Jul 2026· Anti-Cancer Agents in Medicinal Chemistry· 0 citations
Medicine
Abstract
Chimeric antigen receptor (CAR)-T cells are synthetic receptors used for the recognition of specific antigens expressed by reprogrammed T cells for targeting tumors. CAR-T cell therapy has gained remarkable clinical success for the treatment of hematological malignancies such as chronic lymphocytic leukemia (CLL), mantle cell lymphoma (MCL), diffuse large B-cell lymphoma (DLBCL), lymphoplasmacytic lymphoma (LPL), and primary intraocular lymphoma (PIL). The increasing number of preclinical investigations and clinical trials is focusing on extending CAR-T cell therapy to solid tumors due to its remarkable success in leukemia and lymphoma cancers. However, some limitations of CAR-T therapy still exist, including a lack of targetable antigen diversity, heterogeneous antigen expression, insufficient T-cell trafficking efficiency, and an immunosuppressive tumor microenvironment. This review explores the role of CAR-T cell therapy, current challenges, and emerging solutions for solid tumor malignancies. To overcome the existing limitations of CAR-T cell therapy, innovative strategies, including the optimization of novel CAR vectors with checkpoint inhibitors, have been designed to enhance the antitumor activity of CAR-T cells against solid tumors. It also explores the design of novel CAR-T cells and strategies for improving antitumor activity against solid tumors. Among the emerging strategies, universal CARs and combination approaches with checkpoint inhibitors are especially promising for extending CAR-T therapy to solid tumors.
Next-generation engineering strategies are being designed to overcome the obstacles that constrain CAR-T-cell efficacy in solid tumors and to guide the development of safer and more effective therapeutic platforms.
Ziyan Kong, Jinke Wang· Frontiers in Immunology· 0 citations
Continued efforts to identify highly specific target antigens, optimize manufacturing processes, enhance safety, and integrate CAR-T therapy with complementary immunotherapeutic approaches are expected to improve clinical outcomes and broaden the application of CAR-T therapy to T-cell malignancies and potentially other solid and hematologic cancers.
H. Hetta, Fawaz E Alanazi, Mahmoud H. El-Maghrabey et al.· Journal of Pharmaceutical In...· 0 citations
This review aims to provide a comprehensive overview of recent advances in the design of innovative CAR architectures to expand the targetable antigen landscape and discusses innovative CARs in four main categories.
Umida Yoziyeva, Alexey Yumashev, Shakhodat Kobilova et al.· Transplantation and Cellular...· 0 citations
Breast cancer is one of the most common malignancies worldwide and remains a leading cause of cancer-related mortality. Over the past decades, advances in multimodal treatment have significantly improved patient survival. However, disease recurrence, metastatic progression, and therapeutic resistance continue to limit long-term outcomes, underscoring the need for more effective therapies. Among emerging immunotherapeutic approaches, chimeric antigen receptor T (CAR-T) cell therapy has attracted considerable attention. CAR-T therapy has achieved remarkable success in hematologic malignancies, prompting its investigation in breast cancer. However, translating this success to solid tumors remains challenging because of fundamental biological differences between hematologic and solid malignancies. Major barriers include antigen heterogeneity, limited tumor trafficking and infiltration, an immunosuppressive tumor microenvironment, and therapy-related toxicities. Numerous preclinical and clinical studies are currently evaluating CAR-T cell therapy in solid tumors, including breast cancer. These efforts incorporate next-generation CAR designs and novel engineering strategies with the goal of reproducing the clinical success achieved in hematologic malignancies. Although the available clinical evidence is still largely limited to early-phase trials, current findings suggest that CAR-T therapy in breast cancer is feasible and generally well tolerated. Most reported adverse events have been low-grade inflammatory toxicities, whereas severe neurotoxicity and dose-limiting toxicities have been infrequent. Despite this favorable safety profile, clinical responses remain modest, with stable disease representing the most common outcome and durable objective responses being uncommon. These findings underscore the need to overcome the major biological barriers that continue to limit CAR-T cell therapy in solid tumors. This review summarizes recent advances in CAR-T cell engineering, discusses the major target antigens investigated to date, provides a comprehensive overview of the available clinical evidence, and examines the key biological and clinical challenges that must be addressed to improve future therapeutic outcomes.
Ahmad Farajzadeh, Mahmoud Mahmoudi, Soroush Yazdani et al.· International Immunopharmaco...· 0 citations
This review comprehensively examines the current landscape of CAR-T cell therapy for colon cancer, focusing on its underlying mechanisms, recent clinical advances, major challenges, and future perspectives.
Arifa Raza, M. Raza, Junaid Khan et al.· Pathology, Research and Prac...· 0 citations