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      Advancements in clinical aspects of targeted therapy and immunotherapy in breast cancer

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          Abstract

          Breast cancer is the second leading cause of death for women worldwide. The heterogeneity of this disease presents a big challenge in its therapeutic management. However, recent advances in molecular biology and immunology enable to develop highly targeted therapies for many forms of breast cancer. The primary objective of targeted therapy is to inhibit a specific target/molecule that supports tumor progression. Ak strain transforming, cyclin-dependent kinases, poly (ADP-ribose) polymerase, and different growth factors have emerged as potential therapeutic targets for specific breast cancer subtypes. Many targeted drugs are currently undergoing clinical trials, and some have already received the FDA approval as monotherapy or in combination with other drugs for the treatment of different forms of breast cancer. However, the targeted drugs have yet to achieve therapeutic promise against triple-negative breast cancer (TNBC). In this aspect, immune therapy has come up as a promising therapeutic approach specifically for TNBC patients. Different immunotherapeutic modalities including immune-checkpoint blockade, vaccination, and adoptive cell transfer have been extensively studied in the clinical setting of breast cancer, especially in TNBC patients. The FDA has already approved some immune-checkpoint blockers in combination with chemotherapeutic drugs to treat TNBC and several trials are ongoing. This review provides an overview of clinical developments and recent advancements in targeted therapies and immunotherapies for breast cancer treatment. The successes, challenges, and prospects were critically discussed to portray their profound prospects.

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          Atezolizumab and Nab-Paclitaxel in Advanced Triple-Negative Breast Cancer

          Unresectable locally advanced or metastatic triple-negative (hormone-receptor-negative and human epidermal growth factor receptor 2 [HER2]-negative) breast cancer is an aggressive disease with poor outcomes. Nanoparticle albumin-bound (nab)-paclitaxel may enhance the anticancer activity of atezolizumab.
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            Olaparib for Metastatic Breast Cancer in Patients with a Germline BRCA Mutation.

            Olaparib is an oral poly(adenosine diphosphate-ribose) polymerase inhibitor that has promising antitumor activity in patients with metastatic breast cancer and a germline BRCA mutation.
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              Pembrolizumab plus chemotherapy versus placebo plus chemotherapy for previously untreated locally recurrent inoperable or metastatic triple-negative breast cancer (KEYNOTE-355): a randomised, placebo-controlled, double-blind, phase 3 clinical trial

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                Author and article information

                Contributors
                tapanbehl31@gmail.com
                Saurabh.jha@sharda.ac.in
                tanghl@sysucc.org.cn
                Journal
                Mol Cancer
                Mol Cancer
                Molecular Cancer
                BioMed Central (London )
                1476-4598
                6 July 2023
                6 July 2023
                2023
                : 22
                : 105
                Affiliations
                [1 ]GRID grid.12981.33, ISNI 0000 0001 2360 039X, State Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, ; Guangzhou, China
                [2 ]GRID grid.216499.1, ISNI 0000 0001 0722 3459, Advanced Pharmacognosy Research Laboratory, Department of Pharmaceutical Technology, , Jadavpur University, ; Kolkata, 700032 India
                [3 ]GRID grid.412017.1, ISNI 0000 0001 0266 8918, Department of Medical Oncology, , the First Affiliated Hospital, Hengyang Medical School, University of South China, ; Hengyang, China
                [4 ]GRID grid.412017.1, ISNI 0000 0001 0266 8918, Institute of Pathogenic Biology, Hengyang Medical College, , University of South China, ; Hengyang, China
                [5 ]GRID grid.412552.5, ISNI 0000 0004 1764 278X, Department of Biotechnology, School of Engineering and Technology, , Sharda University, ; Greater Noida, India
                [6 ]GRID grid.449005.c, School of Bioengineering & Biosciences, , Lovely Professional University, ; Phagwara, 144411 India
                [7 ]GRID grid.264091.8, ISNI 0000 0001 1954 7928, Department of Pharmaceutical Sciences, , College of Pharmacy and Health Sciences, St. John’s University, ; New York, 11439 USA
                [8 ]GRID grid.512718.8, ISNI 0000 0004 5928 727X, Pharmaceutical and Health Sciences, , Career Point University, ; Hamirpur, Himachal Pradesh India
                [9 ]GRID grid.444415.4, ISNI 0000 0004 1759 0860, School of Health Sciences and Technology, , University of Petroleum and Energy Studies, ; Bidholi, Dehradun, Uttarakhand India
                [10 ]GRID grid.448792.4, ISNI 0000 0004 4678 9721, Department of Biotechnology Engineering and Food Technology, , Chandigarh University, ; Mohali, 140413 India
                [11 ]GRID grid.449906.6, ISNI 0000 0004 4659 5193, Department of Biotechnology, School of Applied & Life Sciences (SALS), , Uttaranchal University, ; Dehradun, 248007 India
                Article
                1805
                10.1186/s12943-023-01805-y
                10324146
                37415164
                664cc1cb-20ce-412f-ae2a-7480f3584f0f
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 27 February 2023
                : 8 June 2023
                Funding
                Funded by: This work was supported by funds from the National Natural Science Foundation of China (82203130, Feng Ye), the Science and Technology Program of Guangzhou (2023A04J1785, Feng Ye), the Key Research Project of Hunan Provincial Education Department (21A0270, Yuehua Li), and China Postdoctoral Science Foundation (2022M711541, Yuehua Li).
                Award ID: 82203130
                Categories
                Review
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2023

                Oncology & Radiotherapy
                breast cancer,clinical trials,immune-checkpoint inhibitors,immunotherapy,targeted therapies

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