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
相关论文
共 50 条
  • [1] Retrospective analysis of combination carboplatin and vinblastine for pediatric low-grade glioma
    Anandani Nellan
    Erin Wright
    Kristen Campbell
    Kurtis D. Davies
    Andrew M. Donson
    Vladimir Amani
    Alexis Judd
    Molly S. Hemenway
    Jennifer Raybin
    Nicholas K. Foreman
    Sarah Rush
    Kathleen Dorris
    Journal of Neuro-Oncology, 2020, 148 : 569 - 575
  • [2] Single agent carboplatin for pediatric low-grade glioma: A retrospective analysis shows equivalent efficacy to multiagent chemotherapy
    Dodgshun, Andrew J.
    Maixner, Wirginia J.
    Heath, John A.
    Sullivan, Michael J.
    Hansford, Jordan R.
    INTERNATIONAL JOURNAL OF CANCER, 2016, 138 (02) : 481 - 488
  • [3] Carboplatin Rechallenge After Hypersensitivity Reactions in Pediatric Patients With Low-Grade Glioma
    Shah, Amish C.
    Minturn, Jane E.
    Li, Yimei
    Belasco, Jean B.
    Phillips, Peter C.
    Kang, Tammy I.
    Cole, Kristina A.
    Waanders, Angela J.
    Pollack, Rosanna
    Didomenico, Concetta
    Wildes, Cynthia
    Fisher, Michael J.
    PEDIATRIC BLOOD & CANCER, 2016, 63 (01) : 21 - 26
  • [4] Weekly vinblastine in pediatric low-grade glioma patients with carboplatin allergic reaction
    Lafay-Cousin, L
    Holm, S
    Qaddoumi, I
    Nicolin, G
    Bartels, U
    Tabori, U
    Huang, A
    Bouffet, E
    CANCER, 2005, 103 (12) : 2636 - 2642
  • [5] Phase II Study of Weekly Vinblastine in Recurrent or Refractory Pediatric Low-Grade Glioma
    Bouffet, Eric
    Jakacki, Regina
    Goldman, Stewart
    Hargrave, Darren
    Hawkins, Cynthia
    Shroff, Manohar
    Hukin, Juliette
    Bartels, Ute
    Foreman, Nicholas
    Kellie, Stewart
    Hilden, Joanne
    Etzl, Michael
    Wilson, Beverly
    Stephens, Derek
    Tabori, Uri
    Baruchel, Sylvain
    JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (12) : 1358 - 1363
  • [6] Clinical features and management of carboplatin-related hypersensitivity reactions in pediatric low-grade glioma
    Genc, Dildar Bahar
    Canpolat, Cengiz
    Berrak, Su Gulsun
    SUPPORTIVE CARE IN CANCER, 2012, 20 (02) : 385 - 393
  • [7] Efficacy of different salvage regimens in progressive unresectable pediatric low-grade glioma
    El-Hemaly, Ahmed
    Taha, Hala
    Refaat, Amal
    Adel, Fatima
    Elbeltagy, Mohamed
    Arafah, Omar
    ONCOLOGY LETTERS, 2022, 24 (05)
  • [8] Chemotherapy in pediatric low-grade gliomas (PLGG)
    Lassaletta, Alvaro
    Zapotocky, Michal
    Bouffet, Eric
    CHILDS NERVOUS SYSTEM, 2024, 40 (10) : 3229 - 3239
  • [9] Increased risk of pseudoprogression among pediatric low-grade glioma patients treated with proton versus photon radiotherapy
    Ludmir, Ethan B.
    Mahajan, Anita
    Paulino, Arnold C.
    Jones, Jeremy Y.
    Ketonen, Leena M.
    Su, Jack M.
    Grosshans, David R.
    McAleer, Mary Frances
    McGovern, Susan L.
    Lassen-Ramshad, Yasmin A.
    Adesina, Adekunle M.
    Dauser, Robert C.
    Weinberg, Jeffrey S.
    Chintagumpala, Murali M.
    NEURO-ONCOLOGY, 2019, 21 (05) : 686 - 695
  • [10] Tumor Volumetric Measurements in Surgically Inaccessible Pediatric Low-grade Glioma
    Kilday, John-Paul
    Branson, Helen
    Rockel, Conrad
    Laughlin, Suzanne
    Mabbott, Donald
    Bouffet, Eric
    Bartels, Ute
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2015, 37 (01) : E31 - E36