TY - JOUR
T1 - Immunotherapeutic and Targeted Strategies for Managing Brain Metastases from Common Cancer Origins
T2 - A State-of-the-Art Review
AU - Podder, Vivek
AU - Bellur, Shreyas
AU - Margolin, Kim
AU - Advani, Pooja
AU - Mahtani, Reshma L
AU - Subbiah, Vivek
AU - Novo, Gabriella B
AU - Ranjan, Tulika
AU - Ahluwalia, Manmeet S
N1 - © 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2024/12
Y1 - 2024/12
N2 - PURPOSE OF REVIEW: This review examines contemporary strategies for managing brain metastases (BM) from common cancers such as lung, breast, and melanoma. We evaluate the efficacy and applicability of targeted therapies and immunotherapies, exploring their potential to cross the blood-brain barrier and improve patient outcomes.RECENT FINDINGS: Recent studies have shown that tyrosine kinase inhibitors, immune checkpoint inhibitors, and ADCs effectively treat BM. These treatments can overcome the challenges posed by the blood-brain barrier and improve therapeutic outcomes. ADCs are promising because they can deliver cytotoxic agents directly to tumor cells, which reduces systemic toxicity and increases drug delivery efficiency to the brain. Personalized medicine is becoming increasingly significant in treatment decisions, with biomarkers playing an essential role. Advances in molecular genetics and drug development have led to more refined treatments, emphasizing the precision medicine framework. The management of BM is evolving, driven by drug efficacy, resistance mechanisms, and the need for personalized medicine. Integrating ADCs into treatment regimens represents a significant advancement in targeting metastatic brain tumors. Despite these advances, BM management still presents considerable challenges, requiring ongoing research and multi-institutional trials to optimize therapeutic strategies. This review outlines the current state and future directions in treating BM, highlighting the critical need for continued innovation and comprehensive clinical evaluations to improve survival rates and quality of life for affected patients.
AB - PURPOSE OF REVIEW: This review examines contemporary strategies for managing brain metastases (BM) from common cancers such as lung, breast, and melanoma. We evaluate the efficacy and applicability of targeted therapies and immunotherapies, exploring their potential to cross the blood-brain barrier and improve patient outcomes.RECENT FINDINGS: Recent studies have shown that tyrosine kinase inhibitors, immune checkpoint inhibitors, and ADCs effectively treat BM. These treatments can overcome the challenges posed by the blood-brain barrier and improve therapeutic outcomes. ADCs are promising because they can deliver cytotoxic agents directly to tumor cells, which reduces systemic toxicity and increases drug delivery efficiency to the brain. Personalized medicine is becoming increasingly significant in treatment decisions, with biomarkers playing an essential role. Advances in molecular genetics and drug development have led to more refined treatments, emphasizing the precision medicine framework. The management of BM is evolving, driven by drug efficacy, resistance mechanisms, and the need for personalized medicine. Integrating ADCs into treatment regimens represents a significant advancement in targeting metastatic brain tumors. Despite these advances, BM management still presents considerable challenges, requiring ongoing research and multi-institutional trials to optimize therapeutic strategies. This review outlines the current state and future directions in treating BM, highlighting the critical need for continued innovation and comprehensive clinical evaluations to improve survival rates and quality of life for affected patients.
KW - Humans
KW - Brain Neoplasms/secondary
KW - Immunotherapy/methods
KW - Precision Medicine
KW - Molecular Targeted Therapy
KW - Immune Checkpoint Inhibitors/therapeutic use
KW - Blood-Brain Barrier
KW - Melanoma/drug therapy
KW - Lung Neoplasms/secondary
KW - Breast Neoplasms/pathology
U2 - 10.1007/s11912-024-01593-8
DO - 10.1007/s11912-024-01593-8
M3 - Review article
C2 - 39514054
SN - 1523-3790
VL - 26
SP - 1612
EP - 1638
JO - Current oncology reports
JF - Current oncology reports
IS - 12
ER -