TY - JOUR
T1 - Central nervous system metastases and oligoprogression during treatment with tyrosine kinase inhibitors in oncogene-addicted non-small cell lung cancer
T2 - how to treat and when?
AU - Schoenmaekers, Janna Josephus Anna Oda
AU - Paats, Marthe Sentijna
AU - Dingemans, Anne-Marie Clasina
AU - Hendriks, Lizza Elisabeth Lucia
N1 - Funding Information:
ICMJE uniform disclosure form (available at http:// dx.doi.org/10.21037/tlcr-20-459). The series “Looking for Chimeras in NSCLC: Widen Therapeutic Options Targeting Oncogenic Fusions” was commissioned by the editorial office without any funding or sponsorship. MSP reports consulting fees from Lilly, Roche, and Takeda, outside the submitted work; AMCD reports grants from Bristol-Myers-Squibb, personal fees from Roche, Bristol-Myers-Squibb, Eli Lily, Takeda, and Boehringer Ingelheim, non-financial support from Abbvie, outside the submitted work; LELH reports receiving other fees from Boehringer Ingelheim for advisory board, other fees from BMS for travel support and advisory board, other fees from Roche for travel support and advisory board, grants from Roche and Boehringer Ingelheim, other fees from AstraZeneca for mentorship program with key opinion leaders, personal fees from Quadia for educational webinars, grants from Astra Zeneca, other fees from Lilly, Roche, Pfizer and Takeda for advisory board, other fees from MSD as speaker and advisory board, outside the submitted work. The other
Publisher Copyright:
© Translational Lung Cancer Research. All rights reserved.
PY - 2020/12
Y1 - 2020/12
N2 - Up to 70% of non-small cell lung cancer (NSCLC) patients develop central nervous system (CNS) metastases during the course of their disease, especially those with oncogenic drivers treated with a first-generation tyrosine kinase inhibitor (TKI), because of the relatively poor CNS penetration. CNS metastases are associated with a negative impact on quality of life and survival. As, with the introduction of newer generation TKIs, the survival rates are increasing in this particular population, treatment and/or prevention of CNS metastases becomes even more relevant and the TKI with the best CNS efficacy should be selected. Unfortunately, CNS efficacy data in clinical trials are not fully comparable. Furthermore, oligoprogression to the brain without extracranial progression regularly occurs in the oncogenic driver population and both local therapy and switch of systemic therapy are possible treatment options. However, the best order of systemic and local therapy is still not precisely known. In this narrative review, we will summarize incidence and treatment of CNS metastases in oncogene driven NSCLC, including the optimal treatment of CNS oligometastatic disease (synchronous as well as oligoprogressive).
AB - Up to 70% of non-small cell lung cancer (NSCLC) patients develop central nervous system (CNS) metastases during the course of their disease, especially those with oncogenic drivers treated with a first-generation tyrosine kinase inhibitor (TKI), because of the relatively poor CNS penetration. CNS metastases are associated with a negative impact on quality of life and survival. As, with the introduction of newer generation TKIs, the survival rates are increasing in this particular population, treatment and/or prevention of CNS metastases becomes even more relevant and the TKI with the best CNS efficacy should be selected. Unfortunately, CNS efficacy data in clinical trials are not fully comparable. Furthermore, oligoprogression to the brain without extracranial progression regularly occurs in the oncogenic driver population and both local therapy and switch of systemic therapy are possible treatment options. However, the best order of systemic and local therapy is still not precisely known. In this narrative review, we will summarize incidence and treatment of CNS metastases in oncogene driven NSCLC, including the optimal treatment of CNS oligometastatic disease (synchronous as well as oligoprogressive).
KW - Non-small cell lung cancer (NSCLC)
KW - central nervous system metastases (CNS metastases)
KW - oligometastatic disease
KW - tyrosine kinase inhibitors (TKIs)
KW - DABRAFENIB PLUS TRAMETINIB
KW - POSITIVE SOLID TUMORS
KW - EML4-ALK FUSION GENE
KW - HIGH-DOSE ERLOTINIB
KW - BRAIN METASTASES
KW - OPEN-LABEL
KW - EGFR-MUTATION
KW - LEPTOMENINGEAL METASTASES
KW - CEREBROSPINAL-FLUID
KW - 1ST-LINE TREATMENT
U2 - 10.21037/tlcr-20-459
DO - 10.21037/tlcr-20-459
M3 - (Systematic) Review article
C2 - 33489821
SN - 2218-6751
VL - 9
SP - 2599
EP - 2617
JO - Translational Lung Cancer Research
JF - Translational Lung Cancer Research
IS - 6
ER -