Craniospinal irradiation with concurrent temozolomide and nimotuzumab in a child with primary metastatic diffuse intrinsic pontine glioma A compassionate use treatment

被引:0
|
作者
Mueller, K. [1 ]
Schlamann, A. [1 ]
Seidel, C. [1 ]
Warmuth-Metz, M. [2 ]
Christiansen, H. [3 ]
Vordermark, D. [4 ]
Kortmann, R. -D. [1 ]
Kramm, C. M. [5 ]
von Bueren, A. O. [5 ]
机构
[1] Univ Med Ctr Leipzig, Dept Radiat Oncol, D-04103 Leipzig, Germany
[2] Univ Med Ctr Wurzburg, Dept Neuroradiol, Wurzburg, Germany
[3] Univ Med Ctr Leipzig, Dept Pediat Hematol & Oncol, D-04103 Leipzig, Germany
[4] Univ Med Ctr Halle, Dept Radiat Oncol, Halle, Germany
[5] Univ Med Ctr Goettingen, Div Pediat Hematol & Oncol, Dept Pediat & Adolescent Med, Gottingen, Germany
关键词
Case reports; Child; Neoplasm metastasis; Antibodies; monoclonal; humanized; Radiotherapy; BRAIN-STEM GLIOMAS;
D O I
10.1007/s00066-013-0370-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Primary metastatic diffuse intrinsic pontine glioma (DIPG) is relatively rare and associated with a dismal prognosis. Combining craniospinal irradiation (CSI) with concurrent temozolomide and nimotuzumab therapy may slightly improve tumor control and overall survival. However, little is known about the feasibility and toxicity of this treatment approach. Here, we describe the case of an 8-year-old girl with primary metastatic DIPG who received craniospinal radiotherapy, a local boost, and concurrent temozolomide and nimotuzumab treatment based on an individual therapy recommendation. Radiotherapy could be completed without any interruption. However, concurrent temozolomide had to be disrupted several times due to considerable acute myelotoxicity (grade III-IV).Maintenance immunochemotherapy could be started with a delay of 5 days and was performed according to treatment schedule. The disease could be stabilized for a few months. A routine MRI scan finally depicted disease progression 5.7 months after the start of irradiation. The patient died 1.9 months later.
引用
收藏
页码:693 / 696
页数:4
相关论文
共 28 条
  • [21] Treatment-Related Noncontiguous Radiologic Changes in Children With Diffuse Intrinsic Pontine Glioma Treated With Expanded Irradiation Fields and Antiangiogenic Therapy
    Patay, Zoltan
    Merchant, Thomas E.
    Rosa Nguyen
    Pierson, Christopher R.
    Onar-Thomas, Arzu
    Broniscer, Alberto
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2017, 99 (05): : 1295 - 1305
  • [22] The use of facial nerve fasciculus motor evoked potential (MEP) as intraoperative neurophysiological monitoring modality in a child with a diffuse intrinsic pontine glioma: A case report
    Al-Salihi, Mohammed Maan
    Ayyad, Ali
    Al-Jebur, Maryam Sabah
    Khan, Robert Ahmed
    Rahman, Md Moshiur
    Rahman, Sabrina
    INTERNATIONAL JOURNAL OF SURGERY CASE REPORTS, 2021, 88
  • [23] TREATMENT-RELATED NON-CONTIGUOUS RADIOLOGICAL CHANGES IN CHILDREN WITH DIFFUSE INTRINSIC PONTINE GLIOMA TREATED WITH EXPANDED IRRADIATION FIELDS AND ANTIANGIOGENIC THERAPY
    Broniscer, Alberto
    Merchant, Thomas
    Nguyen, Rosa
    Onar-Thomas, Arzu
    Gajjar, Amar
    Patay, Zoltan
    NEURO-ONCOLOGY, 2016, 18 : 61 - 61
  • [24] Importance of immune monitoring approaches and the use of immune checkpoints for the treatment of diffuse intrinsic pontine glioma: From bench to clinic and vice versa (Review)
    Scutti, Jorge Augusto Borin
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2018, 52 (04) : 1041 - 1056
  • [25] Craniospinal irradiation with concurrent temozolomide for primary metastatic pediatric high-grade or diffuse intrinsic pontine gliomasA first report from the GPOH-HIT-HGG Study GroupKraniospinale Bestrahlung mit simultanem Temozolomid bei primär metastasierten hochgradigen Gliomen oder diffus intrinsischen Ponsgliomen des KindesaltersErste Erfahrungen der GPOH-HIT-HGG-Studiengruppe
    K. Müller
    A. Schlamann
    M. Guckenberger
    M. Warmuth-Metz
    A. Glück
    S. Pietschmann
    A. Wawer
    R.-D. Kortmann
    C. Kramm
    A.O. von Bueren
    Strahlentherapie und Onkologie, 2014, 190 (4) : 377 - 381
  • [26] A murine model of suicide gene therapy in the brainstem demonstrates efficacy without toxic inflammation, suggesting possible use as a treatment for diffuse intrinsic pontine glioma (DIPG)
    Schuelke, Matt
    Evgin, Laura
    Thompson, Jill
    Daniels, David
    Rao, Amulya Nageswara
    Bram, Richard J.
    Kasahara, Noriyuki
    Vile, Richard
    JOURNAL OF IMMUNOLOGY, 2017, 198 (01):
  • [27] FEASIBILITY AND EARLY RESULTS OF PHASE 2 OPEN LABEL RANDOMIZED STUDY OF RADIOTHERAPY(RT), CONCOMITANT NIMOTUZUMAB AND VINORELBINE AND RE-IRRADIATION AT RELAPSE, VERSUS MULTIPLE ELECTIVE RADIOTHERAPY COURSES WITH CONCOMITANT VINORELBINE AND NIMOTUZUMAB FOR NEWLY DIAGNOSED CHILDHOOD AND ADOLESCENCE DIFFUSE INTRINSIC PONTINE GLIOMA (DIPG)
    Massimino, Maura
    Biassoni, Veronica
    Mastronuzzi, Angela
    Schiavello, Elisabetta
    Barretta, Francesco
    Quaglietta, Lucia
    Milanaccio, Claudia
    Pecori, Emilia
    Cacchione, Antonella
    Boschetti, Luna
    Di Ruscio, Valentina
    Chiesa, Silvia
    Scimone, Giuseppe
    Barra, Salvina
    De Martino, Lucia
    Ramaglia, Antonia
    Picariello, Stefania
    Verrico, Antonio
    Alessandro, Ombretta
    Vennarini, Sabina
    Podda, Marta
    Gattuso, Giovanna
    Cinalli, Giuseppe
    Antonelli, Manila
    Modena, Piergiorgio
    De Cecco, Loris
    Buttarelli, Francesca R.
    Gandola, Lorenza
    NEURO-ONCOLOGY, 2022, 24 : 17 - 18
  • [28] A PHASE 2 STUDY OF SAFETY AND EFFICACY OF CONCURRENT ACT001 AND RADIATION TREATMENT FOLLOWED BY ACT001 MAINTENANCE THERAPY IN NEWLY DIAGNOSED PEDIATRIC PATIENTS WITH DIFFUSE INTRINSIC PONTINE GLIOMA (DIPG)
    Wang, Yang
    Liu, Yanwei
    Zhang, Jing
    Wang, Gang
    Tao, Rongjie
    Cai, Linbo
    Wang, Liang
    Liu, Yanhui
    Cai, Doug
    Qiu, Xiaoguang
    NEURO-ONCOLOGY, 2024, 26