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Experience with dose escalation using CHARTWEL (continuous hyperfractionated accelerated radiotherapy weekend less)
M I Saunders1, A Rojas, B E Lyn
1Marie Curie Research Wing, Mount Vernon Hospital Northwood, Middlesex, UK.
British Journal of Cancer
|November 21, 1998
Summary
Continuous, hyperfractionated, accelerated radiotherapy (CHART) improved survival in non-small-cell lung cancer (NSCLC). A modified CHARTWEL schedule at 60 Gy showed slightly increased, but not clinically significant, toxicity compared to 54 Gy.
Area of Science:
- Radiation Oncology
- Thoracic Oncology
- Clinical Trials
Background:
- Continuous, hyperfractionated, accelerated radiotherapy (CHART) demonstrated improved survival in non-small-cell lung cancer (NSCLC) but had limitations in locoregional control.
- Interest in dose escalation with modified CHART schedules arose to improve treatment efficacy for locally advanced NSCLC.
Purpose of the Study:
- To compare the acute and late morbidity of two modified CHART schedules: CHART WeekEnd Less (CHARTWEL) at 54 Gy in 16 days versus 60 Gy in 18 days.
- To evaluate the feasibility of dose escalation in NSCLC treatment using modified radiotherapy schedules.
Main Methods:
- A comparative study involving patients with locally advanced NSCLC treated with CHARTWEL 54 Gy (16 days) or 60 Gy (18 days).
- Assessment of acute toxicity (dysphagia, analgesia) and late radiation-induced morbidity (pulmonary, spinal cord, oesophageal) using clinical and radiological criteria.
Main Results:
- CHARTWEL 60 Gy resulted in more severe and prolonged acute dysphagia and required more analgesia compared to 54 Gy (P< or = 0.02).
- Oesophagitis at 12 weeks was similar between groups; no consequential damage or significant late toxicities (myelitis, strictures, grade 2/3 lung morbidity) were observed.
- A higher incidence of mild pulmonary toxicity was noted after 6 months with CHARTWEL 60 Gy compared to 54 Gy, which may be clinically relevant if combined with chemotherapy.
Conclusions:
- The CHARTWEL 60 Gy schedule showed a manageable increase in acute toxicity and mild late pulmonary toxicity compared to 54 Gy in locally advanced NSCLC.
- These findings support the potential for further dose escalation or the incorporation of concurrent chemotherapy with modified CHART schedules.