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European journal of cancer (Oxford, England : 1990) · 2019

Brainstem biopsy in pediatric diffuse intrinsic pontine glioma in the era of precision medicine: the INFORM study experience.

СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Pfaff Elke, El Damaty Ahmed, Balasubramanian Gnana Prakash, Blattner-Johnson Mirjam, Worst Barbara C, Stark Sebastian, Witt Hendrik, Pajtler Kristian W, van Tilburg Cornelis M, Witt Ruth, Milde Till, Jakobs Martin, Fiesel Petra, Frühwald Michael C, Hernáiz Driever Pablo, Thomale Ulrich W, Schuhmann Martin U, Metzler Markus, Bochennek Konrad, Simon Thorsten, Dürken Matthias, Karremann Michael, Knirsch Stephanie, Ebinger Martin, von Bueren André O, Pietsch Torsten, Herold-Mende Christel, Reuss David E, Kiening Karl, Lichter Peter, Eggert Angelika, Kramm Christof M, Pfister Stefan M, Jones David T W, Bächli Heidi, Witt Olaf

Аннотация

PURPOSE: Diffuse intrinsic pontine glioma (DIPG) is a highly aggressive paediatric brain tumour with fatal outcome. The Individualised Therapy For Relapsed Malignancies In Childhood (INFORM) registry study offers comprehensive molecular profiling of high-risk tumours to identify target alterations for potential precision therapy. We analysed molecular characteristics and clinical data after brainstem biopsy of all enrolled newly diagnosed DIPGs.

PATIENTS AND METHODS: From -February 2015 to February 2018, 21 subsequent primary DIPG cases were enrolled in the nation-wide multicentre INFORM registry study after brainstem biopsy. Whole-genome, whole-exome sequencing and DNA methylation analysis were performed, and RNA-sequencing was added in case of sufficient material. Clinical data were obtained from standardised questionnaires and the INFORM clinical data bank.

RESULTS: Tumour material obtained from brainstem biopsy was sufficient for DNA analysis in all cases and RNA analysis in 16 of 21 cases. In 16 of 21 cases (76%), potential targetable alterations were identified including highly relevant MET and NTRK1 fusions as well as an EZH2 alteration not previously described in DIPG. In 5 of 21 cases, molecular information was used for initiation of targeted treatment. The majority of patients (19/21) presented with neurological deficits at diagnosis. Newly arising or worsening of neurological deficits post-biopsy occurred in nine patients. Symptoms were reversible or improved notably in eight cases.

CONCLUSION: In this multicentre study setting, brainstem biopsy of DIPG was feasible and yielded sufficient material for comprehensive molecular profiling. Relevant molecular targets were identified impacting clinical management in a substantial subset. Death or severe bleeding occurred in none of the cases. One of 20 patients experienced unilateral paraesthesia possibly related to biopsy.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты