Abstract

Glioblastomas are considered to be one of the most radio resistant tumors. Despite new therapies, the prognosis of this disease remains dismal. Also, the mechanisms of radiation resistance in mammalian cells are more complex than once believed. Experimental studies have indicated that some human cell lines are sensitive to low radiation doses of <1 Gy. This phenomenon has been termed low-dose hyper-radio-sensitivity (HRS), and is more apparent in radio resistant cell lines, such as glioblastoma cells. Sensitivity may result from the inability of low dose radiation to efficiently induce repair mechanisms, whereas higher doses cause enough damage to trigger repair responses for radio resistance. In vitro studies have demonstrated this phenomenon using various human malignant glioma cell lines: (1) daily repeated irradiation of cells with low doses compared to irradiation using a single biologically equivalent dose resulted in significantly higher cell killing; (2) experiments conducted on glioma xenografts demonstrated that repeated irradiation with low doses was more effective for inhibiting tumor growth than a single dose. In order to confirm and validate these promising studies on HRS, a few phase II trials were developed. For translating the experimental observations into the clinic, ultra fractionation protocols (with three daily doses) were tested in glioblastoma patients. Tolerance and toxicity were the primary endpoints, with overall survival as a secondary endpoint. These protocols were initiated before concomitant radio chemotherapy became the standard of care. For these trials, patients with an unfavorable clinical prognostic factor of newly unresectable GBM were included. When comparing the results of these trials with international literature using multivariate analysis for both progression free survival and overall survival, ultra fractionated irradiation showed superiority over radiotherapy alone. In addition, it was found to be equivalent to treatment using radiotherapy and temozolomide. Therefore, ultra fractionated protocols may prolong survival of glioblastoma patients. In this review, we describe the main experimental data regarding low-dose hypersensitivity as well as the findings of clinical trials that have investigated this new radiotherapy regimen.

Highlights

  • Malignant gliomas account for approximately 60% of all primary brain tumors [1,2

  • Treatment consists of neurosurgical resection to the maximal feasible extent, which is followed by combined conformal brain radiotherapy and adjuvant chemotherapy using temozolomide (TMZ) when possible [1–4

  • There was a marked number of long survivors that were reported with this low-dose radiation therapy, and the overall survival rate at 24 months was 15.48%, which compares favorably with data for TMZ–radiation therapy obtained in the EORTC–National Cancer Institute of Canada (NCIC) study (10.42%) [4

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Summary

Introduction

Malignant gliomas account for approximately 60% of all primary brain tumors [1,2. Glioblastoma (GBM) is the most aggressive type of primary brain tumor in adults and is characterized by a high rate of local recurrence due to intrinsic radioresistance [1,2. Radiotherapy is not a curative treatment for GBM, it results in longer survival and optimized quality of life [1–3. It is unclear whether clinical radio resistance in GBM is a result of intrinsic resistance at the cellular level. A few in vitro studies have shown that some human tumor cell lines can be sensitive to low radiation doses of

In Vitro Studies
In Vivo Studies
Mechanisms of HRS
Anti-Neoplastic Agents
De Novo Tumors
Recurrent Tumors
Pulse Reduced Dose Rate Radiotherapy
Findings
Conclusions
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