TY - JOUR
T1 - Pulsatile Erlotinib in EGFR-Positive Non–Small-Cell Lung Cancer Patients With Leptomeningeal and Brain Metastases
T2 - Review of the Literature
AU - How, Joan
AU - Mann, Janelle
AU - Laczniak, Andrew N.
AU - Baggstrom, Maria Q.
N1 - Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2017/7
Y1 - 2017/7
N2 - Patients with epidermal growth factor receptor (EGFR)-positive (EGFR+) non–small-cell lung cancer (NSCLC) show improved response rates when treated with tyrosine kinase inhibitors (TKIs) such as erlotinib. However, standard daily dosing of erlotinib often does not reach therapeutic concentrations within the cerebrospinal fluid (CSF), resulting in progression of central nervous system (CNS) disease. Intermittent, high-dose administration of erlotinib reaches therapeutic concentrations within the CSF and is well tolerated in patients. Experience with “pulsatile” dosing, however, is limited. We review the literature on the pharmacology and clinical outcomes of pulsatile erlotinib in the treatment of EGFR+ NSCLC with brain and leptomeningeal metastases, and include available data on the use of next-generation TKIs in CNS progression. We also provide our institution's experience with patients treated with pulsatile erlotinib for CNS metastasis, and propose clinical criteria for its use. Pulsatile erlotinib is a reasonable alternative in EGFR+ patients with new or worsening CNS disease, without evidence of systemic progression, and without confirmed T790M resistance mutations within the CNS.
AB - Patients with epidermal growth factor receptor (EGFR)-positive (EGFR+) non–small-cell lung cancer (NSCLC) show improved response rates when treated with tyrosine kinase inhibitors (TKIs) such as erlotinib. However, standard daily dosing of erlotinib often does not reach therapeutic concentrations within the cerebrospinal fluid (CSF), resulting in progression of central nervous system (CNS) disease. Intermittent, high-dose administration of erlotinib reaches therapeutic concentrations within the CSF and is well tolerated in patients. Experience with “pulsatile” dosing, however, is limited. We review the literature on the pharmacology and clinical outcomes of pulsatile erlotinib in the treatment of EGFR+ NSCLC with brain and leptomeningeal metastases, and include available data on the use of next-generation TKIs in CNS progression. We also provide our institution's experience with patients treated with pulsatile erlotinib for CNS metastasis, and propose clinical criteria for its use. Pulsatile erlotinib is a reasonable alternative in EGFR+ patients with new or worsening CNS disease, without evidence of systemic progression, and without confirmed T790M resistance mutations within the CNS.
KW - Blood brain barrier
KW - Central nervous system metastasis
KW - High-dose
KW - Leptomeningeal disease
KW - Tyrosine kinase inhibitor
UR - http://www.scopus.com/inward/record.url?scp=85013743759&partnerID=8YFLogxK
U2 - 10.1016/j.cllc.2017.01.013
DO - 10.1016/j.cllc.2017.01.013
M3 - Review article
C2 - 28245967
AN - SCOPUS:85013743759
SN - 1525-7304
VL - 18
SP - 354
EP - 363
JO - Clinical Lung Cancer
JF - Clinical Lung Cancer
IS - 4
ER -