4.6 Article

Combination chemoradiotherapy with temozolomide, vincristine, and interferon-β might improve outcomes regardless of O6-methyl-guanine-DNA-methyltransferase (MGMT) promoter methylation status in newly glioblastoma

Journal

BMC CANCER
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12885-021-08592-z

Keywords

Newly glioblastoma; Combination therapy; Temozolomide; Interferon-beta; MGMT

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This investigator-initiated study aimed to investigate the effectiveness of induction combination chemoradiotherapy and long-term maintenance therapy for glioblastoma. The 2-year overall survival tended to exceed historical controls, but further research may be needed as the lower limit of the 95% confidence interval was below 31.7%.
BackgroundThis investigator-initiated, open-label, single-arm, single-institute study was conducted to investigate the effectiveness of induction combination chemoradiotherapy and long-term maintenance therapy with temozolomide (TMZ) plus interferon (IFN)-beta for glioblastoma.MethodsThe initial induction combination chemoradiotherapy comprised radiotherapy plus TMZ plus vincristine plus IFN-beta. Maintenance chemotherapy comprised monthly TMZ, continued for 24-50cycles, plus weekly IFN-beta continued for as long as possible. The primary endpoint was 2-year overall survival (2y-OS). The study protocol was to be considered valid if the expected 2y-OS was over 38% and the lower limit of the 95% confidence interval (CI) was no less than 31.7% compared with historical controls, using Kaplan-Meier methods. Secondary endpoints were median progression-free survival (mPFS), median OS (mOS), 5-year OS rate (5y-OS), and mPFS and mOS classified according to MGMT promoter methylation status.ResultsForty-seven patients were analyzed. The 2y-OS was 40.7% (95%CI, 27.5-55.4%). The mPFS and mOS were 11.0months and 18.0months, respectively, and 5y-OS was 20.3% (95%CI, 10.9-34.6%). The mPFS in groups with and without MGMT promoter methylation in the tumor was 10.0months and 11.0months (p=0.59), respectively, and mOS was 24.0months and 18.0months (p=0.88), respectively. The frequency of grade 3/4 neutropenia was 19.1%.ConclusionsThe 2y-OS with induction multidrug combination chemoradiotherapy and long-term maintenance therapy comprising TMZ plus IFN-beta tended to exceed that of historical controls, but the lower limit of the 95%CI was below 31.7%. Although the number of cases was small, this protocol may rule out MGMT promoter methylation status as a prognostic factor.Trial registrationUniversity Hospital Medical Information Network (number UMIN000040599).

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