2000
DOI: 10.1016/s0360-3016(00)80455-1
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Treatment breaks caused by toxicity from concurrent chemoradiation for limited small cell lung cancer decrease survival and local control

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Cited by 2 publications
(3 citation statements)
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“…While mucositis-mediated intestinal febrile bacteremia associated with HSCT contributes 3,412 annual deaths, the remaining 38,089 deaths arise from mucositis-dependent unplanned treatment interruptions and doses reductions lower [28,29] which unavoidably lowers the "kill dose intensity" required for optimal survival and remission. Lowered dose intensity prompts early disease recurrence and lowered 5 year survival [28,[30][31][32][33][34][35].…”
Section: The Problem With Toxic Mucositis: Increased Morbidity Costsmentioning
confidence: 99%
“…While mucositis-mediated intestinal febrile bacteremia associated with HSCT contributes 3,412 annual deaths, the remaining 38,089 deaths arise from mucositis-dependent unplanned treatment interruptions and doses reductions lower [28,29] which unavoidably lowers the "kill dose intensity" required for optimal survival and remission. Lowered dose intensity prompts early disease recurrence and lowered 5 year survival [28,[30][31][32][33][34][35].…”
Section: The Problem With Toxic Mucositis: Increased Morbidity Costsmentioning
confidence: 99%
“…Two reports analysing the time-dose relationship for local control of disease in patients with advanced head and neck cancer treated by concomitant radio-chemotherapy delivered on alternate schedules show that it does not result in loss of local control [65,66]. In contrast, Tomiak and coworkers found an impact on survival and local control of interruptions in treatment to palliate acute morbidity of concurrent chemoradiation for limited small-cell lung cancer [67]. More clinical data are needed to study this problem in detail.…”
Section: Radio-chemotherapymentioning
confidence: 99%
“…A rate of loss of survival probability with an increase in treatment duration for non-small-cell lung cancer has been calculated as being as fast as for the rate of loss of local control with treatment prolongation in head and neck cancer [36]. Much less data regarding the effect of treatment duration are available for other sites such as medulloblastoma [37,38], anal carcinoma [39][40][41][42], oesophageal cancer [43][44][45], vaginal cancer [46] or limited stage small-cell lung cancer [47,48]. In bladder cancer, the results are conflicting.…”
Section: Introductionmentioning
confidence: 99%