The Role of Immune Checkpoint Inhibitors in Leptomeningeal Disease: A Systematic Review

被引:11
作者
Palmisciano, Paolo [1 ]
Haider, Ali S. [2 ]
Nwagwu, Chibueze D. [3 ]
Wahood, Waseem [4 ]
Yu, Kenny [5 ]
Ene, Chibawanye I. [6 ]
O'Brien, Barbara J. [7 ]
Aoun, Salah G. [8 ]
Cohen-Gadol, Aaron A. [9 ]
El Ahmadieh, Tarek Y. [8 ]
机构
[1] Cannizzaro Hosp, Dept Neurosurg, Ctr Trauma, Gamma Knife Ctr, Catania, Italy
[2] Texas A&M Univ Houston, Coll Med, Houston, TX USA
[3] Emory Univ, Sch Med, Atlanta, GA USA
[4] Nova Southeastern Univ, Dr Kiran C Patel Coll Allopath Med, Davie, FL USA
[5] Mem Sloan Kettering Canc Ctr, Dept Neurosurg Surg, 1275 York Ave, New York, NY 10021 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Neurosurg, Houston, TX 77030 USA
[7] Univ Texas MD Anderson Canc Ctr, Dept Neurooncol, Houston, TX USA
[8] Univ Texas South Western, Dept Neurol Surg, Med Ctr, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[9] Indiana Univ Sch Med, Dept Neurol Surg, Indianapolis, IN 46202 USA
关键词
Brain metastasis; corticosteroids; immunotherapy; leptomeningeal disease; review; immune checkpoint inhibitors; CELL LUNG-CANCER; WHOLE-BRAIN RADIOTHERAPY; BREAST-CANCER; STEREOTACTIC RADIOSURGERY; PROGNOSTIC-FACTORS; OPEN-LABEL; METASTASIS; NIVOLUMAB; PEMBROLIZUMAB; MELANOMA;
D O I
10.21873/anticanres.15346
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Leptomeningeal disease (LMD) is a debilitating complication of advanced malignancies. Immune checkpoint inhibitors (ICIs) may alter disease course. We analyzed the role and toxicity of ICIs in LMD. Materials and Methods: We systematically reviewed the literature reporting on outcome data of patients with LMD treated with ICIs. Results: We included 14 studies encompassing 61 patients. Lung-cancer (44.3%), breast-cancer (27.9%), and melanoma (23.0%) were the most frequent primary tumors. Median duration of ICI treatment was 7-months (range=0.5-58.0): pembrolizumab (49.2%), nivolumab (32.8%), ipilimumab (18.0%). Radiological responses included complete response (33.3%), partial response (12.5%), stable disease (33.3%), progressive disease (20.8%). Twenty-two patients developed ICI-related adverse-events, mild (100%) and/or severe (15.6%). Median progression-free and overall survival were 5.1 and 6.3 months, and 12-month survival was 32.1%. Survival correlated with ICI agents (p=0.042), but not with primary tumors (p=0.144). Patients receiving concurrent steroids showed worse survival (p=0.040). Conclusion: ICI therapy is well-tolerated in patients with LMD, but concurrent steroids may worsen survival.
引用
收藏
页码:5333 / 5342
页数:10
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