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Low-dose fractionated radiotherapy and concomitant chemotherapy in glioblastoma multiforme with poor prognosis: a feasibility study

机译:预后不良的多形性胶质母细胞瘤小剂量分次放疗和伴随化疗的可行性研究

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摘要

We explored the feasibility of concurrent palliative chemotherapy and low-dose fractionated radiotherapy (LD-FRT) in glioblastoma multiforme (GBM). Patients with recurrent/progressive GBM at least 3 months after the end of primary radiotherapy received 0.3 Gy twice daily with cisplatin and fotemustine if progressing on temozolomide, or 0.4 Gy twice daily with temozolomide if recurrent 4–6 months later (retreatment group). Newly diagnosed GBM with gross residual mass received 30 Gy with concomitant and adjuvant temozolomide and 0.4 Gy twice daily from the second adjuvant cycle (naive group) for 2–4 cycles. Twenty-six patients were enrolled. In the retreatment group (n = 17; median LD-FRT total dose 7.2 Gy [range 2.4–11.6]), grade 3 or 4 hematological toxicity was observed in 5.9% of patients. Median follow-up time was 20 months (range 4–35). Median progression-free survival (PFS) and overall survival (OS) from the time of recurrence or progression were 4 and 8 months, respectively (OS at 6 months, 69%; at 12 months, 16.7%). In the naive group (n = 9; median LD-FRT total dose 8 Gy [range 3.2–16]), grade 3 or 4 hematological toxicity was observed in 11.1% of patients. Median follow-up time was 17 months (range 8–20)—median PFS was 9 months, with PFS at 6 months and at 1 year of 66.7% and 26.7%, respectively; and median OS was 12 months, with OS at 6 months and at 1 year of 77.8% and 34.6%, respectively. LD-FRT with concurrent chemotherapy was well tolerated.
机译:我们探讨了在多形性胶质母细胞瘤(GBM)中同时进行姑息化疗和低剂量分次放疗(LD-FRT)的可行性。复发/进行性GBM的患者至少在初次放疗结束后3个月接受替莫唑胺治疗的患者每天两次接受0.3 Gy顺铂和铁莫司汀治疗;如果4-6个月后复发,则接受替莫唑胺治疗每天0.4 Gy两次(治疗组)。新诊断的总残留量为GBM的伴有替莫唑胺和辅助替莫唑胺30 Gy,从第二个辅助周期(未治疗组)每天两次,每次2〜4个周期,每次0.4 Gy。纳入26位患者。在再治疗组中(n = 17; LD-FRT中位总剂量为7.2 Gy [范围2.4-11.6]),在5.9%的患者中观察到3或4级血液学毒性。中位随访时间为20个月(范围4–35)。复发或进展时的中位无进展生存期(PFS)和总体生存期(OS)分别为4个月和8个月(6个月时OS为69%; 12个月时为16.7%)。天真的组(n = 9;中位数LD-FRT总剂量为8 Gy [范围3.2–16]),在11.1%的患者中观察到3或4级血液学毒性。中位随访时间为17个月(范围8-20)-中位PFS为9个月,其中PFS为6个月和1年的分别为66.7%和26.7%;中位OS为12个月,其中6个月和1年的OS分别为77.8%和34.6%。 LD-FRT并发化疗耐受性良好。

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