Retrospective analysis of combination carboplatin and vinblastine for pediatric low-grade glioma

被引:15
|
作者
Nellan, Anandani [1 ,4 ]
Wright, Erin [2 ]
Campbell, Kristen [1 ]
Davies, Kurtis D. [3 ]
Donson, Andrew M. [1 ]
Amani, Vladimir [1 ]
Judd, Alexis [2 ]
Hemenway, Molly S. [1 ]
Raybin, Jennifer [1 ]
Foreman, Nicholas K. [1 ]
Rush, Sarah [2 ]
Dorris, Kathleen [1 ]
机构
[1] Univ Colorado, Dept Pediat, Morgan Adams Fdn Pediat, Childrens Hosp Colorado,Brain Tumor Res Program, Anschutz Med Campus, Aurora, CO 80045 USA
[2] Akron Childrens Hosp, Div Hematol Oncol, One Perkins Sq, Akron, OH 44308 USA
[3] Univ Colorado, Dept Pathol, Anschutz Med Campus, Aurora, CO USA
[4] Univ Colorado, Ctr Canc & Blood Disorders, Morgan Adams Fdn, Pediat Brain Tumor Res Program,Sch Med, 13123 East 16th Ave,Box B115, Aurora, CO 80045 USA
关键词
Low-grade glioma; Pediatrics; Brain tumor; Chemotherapy; PHASE-II; CHILDREN; VINCRISTINE; ONCOLOGY; CHEMOTHERAPY; RADIOTHERAPY; ADOLESCENTS; RECURRENT; CANCER;
D O I
10.1007/s11060-020-03549-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Low-grade glioma (LGG) represent the most common pediatric central nervous system tumor. When total surgical resection is not feasible, chemotherapy is first-line therapy in children. Multiple pediatric LGG chemotherapy regimens have been investigated with variable 2-year event free survival (EFS) rates of 39-69%. To date, treatment of pediatric LGG with a carboplatin and vinblastine (C/VBL) chemotherapy regimen has only been evaluated in a phase 1 dose-finding study. Methods A retrospective review of pediatric patients with LGG who were treated with C/VBL at Children's Hospital of Colorado or Akron Children's Hospital from 2011 to 2017 was conducted. Data collected included patient demographics, tumor location, disease response, neurofibromatosis 1 (NF1) status, therapy duration and toxicities. Response to therapy was determined by objective findings on imaging and treating physicians' evaluation. Results Forty-six patients were identified for analysis, all of whom were chemotherapy-naive. Only five patients treated in this cohort had NF1. BRAF fusion was identified in 65% (22/34) of tested tumors. Best therapy response was partial response in nine patients and stable disease in twenty-five patients. Twelve patients had progressive disease. One-year, 3-year, and 5-year EFS probabilities for all patients were 69.6%, 39.4%, and 34.5%, respectively. Nine patients had admissions for febrile neutropenia and seven patients experienced one delay in chemotherapy due to neutropenia. Only two patients had to discontinue this chemotherapy regimen because of treatment-related toxicities [carboplatin allergy (n = 1) and vinblastine neuropathy (n = 1)]. Conclusion C/VBL achieves similar EFS rates to other single-agent and combination cytotoxic chemotherapy regimens for pediatric LGG with manageable toxicities.
引用
收藏
页码:569 / 575
页数:7
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