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DOI 10.1200/jco.2016.68.1585

Медицинская библиотека · Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2016

Phase II Weekly Vinblastine for Chemotherapy-Naïve Children With Progressive Low-Grade Glioma: A Canadian Pediatric Brain Tumor Consortium Study.

Lassaletta Alvaro, Scheinemann Katrin, Zelcer Shayna M, Hukin Juliette, Wilson Beverley A, Jabado Nada, Carret Anne Sophie, Lafay-Cousin Lucie, Larouche Valerie, Hawkins Cynthia E, Pond Gregory Russell, Poskitt Ken, Keene Daniel, Johnston Donna L, Eisenstat David D, Krishnatry Rahul, Mistry Matthew, Arnoldo Anthony, Ramaswamy Vijay, Huang Annie, Bartels Ute, Tabori Uri, Bouffet Eric

Клиническое исследование II фазыСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Purpose Vinblastine monotherapy has shown promising activity and a low-toxicity profile in patients with pediatric low-grade glioma (PLGG) who experienced treatment failure after initial treatment with chemotherapy and/or radiation. The aim of this study was to assess the activity of vinblastine in therapy-naïve children. Patients and Methods Patients < 18 years old with unresectable and/or progressive therapy-naïve PLGG were eligible. Vinblastine was administered once per week at a dose of 6 mg/m2 intravenously over a period of 70 weeks. Vision, quality of life, neurofibromatosis type 1 (NF1) status, and BRAF mutation/fusion status were also determined and correlated with outcome. Results Fifty-four patients were enrolled onto the study, with a median age of 8 years (range, 0.7 to 17.2 years). Most patients had chiasmatic/hypothalamic tumors (55.5%), and 13 patients (24.1%) had NF1. The most common histology was pilocytic astrocytoma (46.3%). Seventeen patients were diagnosed using radiologic criteria alone. Best response to chemotherapy was centrally reviewed with a response rate (complete, partial, or minor response) of 25.9%. Disease stabilization (complete, partial, or minor response or stable disease) was achieved in 47 patients (87.0%). Visual improvement was observed in 20% of patients with optic pathway glioma. Five-year overall survival and progression-free survival (PFS) rates were 94.4% (95% CI, 88.5% to 100%) and 53.2% (95% CI, 41.3% to 68.5%), respectively, for the entire cohort. Patients with NF1 had a significantly better PFS (85.1%; 95% CI, 68.0% to 100%) when compared with patients without NF1 (42.0%; 95% CI, 29.1% to 60.7%; P = .012). Age< 3 years or > 10 years was not associated with poor outcome. Treatment was well tolerated, and quality of life was not affected during treatment. In this trial, there was no correlation between BRAF alterations and outcome. Conclusion Vinblastine administered once per week is well tolerated in children with treatment naïve PLGG. Overall survival and PFS are comparable to current therapies, with a favorable toxicity profile and a maintained quality of life.

Для цитирования: Lassaletta Alvaro, Scheinemann Katrin, Zelcer Shayna M, Hukin Juliette, Wilson Beverley A, Jabado Nada, Carret Anne Sophie, Lafay-Cousin Lucie, Larouche Valerie, Hawkins Cynthia E, Pond Gregory Russell, Poskitt Ken, Keene Daniel, Johnston Donna L, Eisenstat David D, Krishnatry Rahul, Mistry Matthew, Arnoldo Anthony, Ramaswamy Vijay, Huang Annie, Bartels Ute, Tabori Uri, Bouffet Eric. Phase II Weekly Vinblastine for Chemotherapy-Naïve Children With Progressive Low-Grade Glioma: A Canadian Pediatric Brain Tumor Consortium Study.. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2016. DOI: 10.1200/jco.2016.68.1585.

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