Leptomeningeal Metastasis from Non-Small Cell Lung Cancer and Current Landscape of Treatments

被引:74
作者
Ozcan, Gonca [1 ,3 ]
Singh, Meghana [1 ]
Vredenburgh, James J. [2 ]
机构
[1] Univ Connecticut Hlth Ctr, Dept Med, Farmington, CT USA
[2] St Francis Hosp & Med Ctr, Dept Med, Div Hematol Oncol, Hartford, CT USA
[3] Univ Connecticut, Dept Internal Med, 263 Farmington Ave, Farmington, CT 06030 USA
关键词
CENTRAL-NERVOUS-SYSTEM; CEREBROSPINAL-FLUID CYTOLOGY; TYROSINE KINASE INHIBITORS; CIRCULATING TUMOR-CELLS; EGFR-MUTANT NSCLC; CARCINOMATOUS MENINGITIS; SURGICAL RESECTION; BRAIN METASTASES; CNS METASTASES; SOLID TUMORS;
D O I
10.1158/1078-0432.CCR-22-1585
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Leptomeningeal metastasis (LM), also known as leptomenin-geal carcinomatosis (LC), is a devastating complication of metastatic cancer that occurs when neoplastic cells invade the meningeal space. Diagnosis of LM remains challenging given the heterogeneous signs and symptoms at presentation and requires thorough neurological examination, cerebrospinal fluid (CSF) analysis, and MRI of the brain and spine with gadolinium. Detecting neoplastic cells in the CSF is the gold standard for diagnosing leptomeningeal metastases; however, it has low sensitivity and may require multiple CSF samples. New emerging technologies, such as liquid biopsy of CSF, have increased sensitivity and specificity for detecting circulating tumor cells in CSF. The management of LM in patients with NSCLC requires an individualized multidisciplinary approach. Treatment options include surgery for ventricular shunt placement, radiation therapy to bulky or symptomatic disease sites, systemic or intrathecal chemotherapy, molecularly targeted agents, and, more recently, immunotherapy. Targeting actionable mutations in LM from NSCLC, such as EGFR tyrosine kinase inhibitors or anaplastic lymphoma kinase gene rearrangement inhibitors, has shown encouraging results in terms of disease control and survival. Although there are limited data regarding the use of immuno-therapy in LM, immunotherapy has produced promising results in several case reports. In this review, we focused on the epidemiology, pathophysiology, clinical presentation, diagnosis, and current treatment strategies, with a special emphasis on novel agents, including targeted therapies and immunotherapy of LM in patients with NSCLC.
引用
收藏
页码:11 / 29
页数:19
相关论文
共 156 条
[1]   ALK inhibitor crizotinib combined with intrathecal methotrexate treatment for non-small cell lung cancer with leptomeningeal carcinomatosis [J].
Ahn, Hee Kyung ;
Han, Boram ;
Lee, Su Jin ;
Lim, Taekyu ;
Sun, Jong-Mu ;
Ahn, Jin Seok ;
Ahn, Myung-Ju ;
Park, Keunchil .
LUNG CANCER, 2012, 76 (02) :253-254
[2]   Osimertinib for Patients With Leptomeningeal Metastases Associated With EGFR T790M-Positive Advanced NSCLC: The AURA Leptomeningeal Metastases Analysis [J].
Ahn, Myung-Ju ;
Chiu, Chao-Hua ;
Cheng, Ying ;
Han, Ji-Youn ;
Goldberg, Sarah B. ;
Greystoke, Alastair ;
Crawford, Jeffrey ;
Zhao, Yanqiu ;
Huang, Xiangning ;
Johnson, Martin ;
Vishwanathan, Karthick ;
Yates, James W. T. ;
Brown, Andrew P. ;
Mendoza-Naranjo, Ariadna ;
Mok, Tony .
JOURNAL OF THORACIC ONCOLOGY, 2020, 15 (04) :637-648
[3]   Activity and safety of AZD3759 in EGFR-mutant non-small-cell lung cancer with CNS metastases (BLOOM): a phase 1, open-label, dose-escalation and dose-expansion study [J].
Ahn, Myung-Ju ;
Kim, Dong-Wan ;
Cho, Byoung Chul ;
Kim, Sang-We ;
Lee, Jong Seok ;
Ahn, Jin-Seok ;
Kim, Tae Min ;
Lin, Chia-Chi ;
Kim, Hye Ryun ;
John, Thomas ;
Kao, Steven ;
Goldman, Jonathan W. ;
Su, Wu-Chou ;
Natale, Ronald ;
Rabbie, Sarit ;
Harrop, Bryony ;
Overend, Philip ;
Yang, Zhenfan ;
Yang, James Chih-Hsin .
LANCET RESPIRATORY MEDICINE, 2017, 5 (11) :891-902
[4]   Leptomeningeal Metastases in Non-small Cell Lung Cancer: Optimal Systemic Management in NSCLC With and Without Driver Mutations [J].
Alexander, Mariam ;
Lin, Emily ;
Cheng, Haiying .
CURRENT TREATMENT OPTIONS IN ONCOLOGY, 2020, 21 (09)
[5]  
[Anonymous], 2022, 2 NCCNCNSCV
[6]   Efficacy of bevacizumab and erlotinib combination for leptomeningeal carcinomatosis after failure of erlotinib [J].
Ariyasu, Ryo ;
Horiike, Atsushi ;
Koyama, Junji ;
Saiki, Masafumi ;
Sonoda, Tomoaki ;
Kawashima, Yosuke ;
Takano, Natsuki ;
Oguri, Tomoyo ;
Nishikawa, Shingo ;
Kitazono, Satoru ;
Yanagitani, Noriko ;
Ohyanagi, Fumiyoshi ;
Nishio, Makoto .
ANTI-CANCER DRUGS, 2017, 28 (05) :565-567
[7]   LDK378 Compassionate Use for Treating Carcinomatous Meningitis in an ALK Translocated Non-Small-Lung Cancer [J].
Arrondeau, Jennifer ;
Ammari, Samy ;
Besse, Benjamin ;
Soria, Jean-Charles .
JOURNAL OF THORACIC ONCOLOGY, 2014, 9 (08) :E62-E63
[8]   Cerebrospinal fluid diversion for leptomeningeal metastasis: palliative, procedural and oncologic outcomes [J].
Bander, Evan D. ;
Yuan, Melissa ;
Reiner, Anne S. ;
Garton, Andrew L. A. ;
Panageas, Katherine S. ;
Brennan, Cameron W. ;
Tabar, Viviane ;
Moss, Nelson S. .
JOURNAL OF NEURO-ONCOLOGY, 2021, 154 (03) :301-313
[9]   Brain Penetration of Lorlatinib: Cumulative Incidences of CNS and Non-CNS Progression with Lorlatinib in Patients with Previously Treated ALK-Positive Non-Small-Cell Lung Cancer [J].
Bauer, Todd M. ;
Shaw, Alice T. ;
Johnson, Melissa L. ;
Navarro, Alejandro ;
Gainor, Justin F. ;
Thurm, Holger ;
Pithavala, Yazdi K. ;
Abbattista, Antonello ;
Peltz, Gerson ;
Felip, Enriqueta .
TARGETED ONCOLOGY, 2020, 15 (01) :55-65
[10]   Intrathecal chemotherapy for treatment of leptomeningeal dissemination of metastatic tumours [J].
Beauchesne, Patrick .
LANCET ONCOLOGY, 2010, 11 (09) :871-879