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Clinical Trial
. 2016 Oct;18(10):1442-50.
doi: 10.1093/neuonc/now038. Epub 2016 Mar 22.

Phase 2 study of concurrent radiotherapy and temozolomide followed by temozolomide and lomustine in the treatment of children with high-grade glioma: a report of the Children's Oncology Group ACNS0423 study

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Clinical Trial

Phase 2 study of concurrent radiotherapy and temozolomide followed by temozolomide and lomustine in the treatment of children with high-grade glioma: a report of the Children's Oncology Group ACNS0423 study

Regina I Jakacki et al. Neuro Oncol. 2016 Oct.

Abstract

Background: The prognosis for children with malignant glioma is poor. This study was designed to determine whether lomustine and temozolomide following radiotherapy and concurrent temozolomide improves event-free survival (EFS) compared with historical controls with anaplastic astrocytoma (AA) or glioblastoma (GBM) and whether survival is influenced by the expression of O6-methylguanine-DNA-methyltransferase (MGMT).

Methods: Following maximal surgical resection, newly diagnosed children with nonmetastatic high-grade glioma underwent involved field radiotherapy with concurrent temozolomide. Adjuvant chemotherapy consisted of up to 6 cycles of lomustine 90 mg/m(2) on day 1 and temozolomide 160 mg/m(2)/day ×5 every 6 weeks.

Results: Among the 108 eligible patients with AA or GBM, 1-year EFS was 0.49 (95% CI, 0.39-0.58), similar to the original CCG-945-based design model. However, EFS and OS were significantly improved in ACNS0423 compared with the 86 AA or GBM participants treated with adjuvant temozolomide alone in the recent ACNS0126 study (1-sided log-rank P = .019 and .019, respectively). For example, 3-year EFS was 0.22 (95% CI, 0.14-0.30) in ACNS0423 compared with 0.11 (95% CI, 0.05-0.18) in ACNS0126. Stratifying the comparison by resection extent, the addition of lomustine resulted in significantly better EFS and OS in participants without gross-total resection (P = .019 and .00085 respectively). The difference in EFS and OS was most pronounced for participants with GBM (P = .059 and 0.051, respectively), and those with MGMT overexpression (P = .00036 and .00038, respectively).

Conclusion: The addition of lomustine to temozolomide as adjuvant therapy in ACNS0423 was associated with significantly improved outcome compared with the preceding COG ACNS0126 HGG study in which participants received temozolomide alone.

Keywords: astrocytoma; glioblastoma; lomustine; pediatric high-grade glioma; temozolomide.

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Figures

Fig. 1.
Fig. 1.
ACNS0423 EFS (event-free survival) and OS (overall survival) for all participants (n = 108).
Fig. 2.
Fig. 2.
Event-free survival of AA and GBM patients in ACNS0423 (n = 108) versus ACNS0126 (n = 86), 1-sided log-rank P = .019.
Fig. 3.
Fig. 3.
Event-free survival in ACNS0423 compared with ACNS0126 for patients with glioblastoma, 1-sided log-rank P = .059.
Fig. 4.
Fig. 4.
A. Prognostic significance of extent of resection in ACNS0423 in terms of event-free survival (EFS) . B. EFS in ACNS0423 compared with ACNS0126 for patients who had not undergone gross total resection. One-sided log-rank P = .019. C. EFS in ACNS0423 compared with ACNS0126 for patients who had MGMT overexpression. One-sided log-rank P = .00036.

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References

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