1997
DOI: 10.1016/s0360-3016(97)00390-8
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Impact of clinical and therapeutic factors on major late complications after radiotherapy with or without concomitant chemotherapy for anal carcinoma

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Cited by 65 publications
(34 citation statements)
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“…The most important prognostic factors have been defined by several studies: a tumor originating from the anal canal is more aggressive than one originating from peri-anal skin; the size of the tumor is also important, with higher T stage correlating with worse prognosis [2,[19][20][21]; differentiation and histologic type also play roles-epidermoid carcinoma has a better prognosis than adenocarcinoma; finally, prognosis is better in females than in males [2,4].…”
Section: Prognostic Factors Tumor Location and Sizementioning
confidence: 99%
See 1 more Smart Citation
“…The most important prognostic factors have been defined by several studies: a tumor originating from the anal canal is more aggressive than one originating from peri-anal skin; the size of the tumor is also important, with higher T stage correlating with worse prognosis [2,[19][20][21]; differentiation and histologic type also play roles-epidermoid carcinoma has a better prognosis than adenocarcinoma; finally, prognosis is better in females than in males [2,4].…”
Section: Prognostic Factors Tumor Location and Sizementioning
confidence: 99%
“…According to some investigators, younger aged patients have worse prognoses. Treatment delay may also have an adverse effect [21].…”
Section: Lymph Node Involvementmentioning
confidence: 99%
“…Thus, alternative radiation treatment schedules tailored to reduce toxicities without compromise of disease control have been investigated, including the delivery of lower dose radiotherapy [12], continuous vs. split course treatments [13], brachytherapy [14], and the introduction of Intensity-modulated radiation therapy (IMRT) as an alternative to the conventional conformal radiation therapy (CRT) [15,16]. The current clinical practice guidelines for anal cancer recommend radiation doses of at least 45-50 Gray (Gy) with boost doses between 15 and 20 Gy , thus the study and management of late toxicities is clearly pertinent [11].…”
Section: Introduction Backgroundmentioning
confidence: 99%
“…Dermatologic and gastrointestinal late toxicities were also reported in 122 (42%) of 292 patients receiving chemoradiation in the UKCCCR trial 6. Allal et al reported that morbidity correlated significantly with anatomic location of tumor and prescribed external-beam dose 20. In addition, Hung et al reported only a 2% (3 patients) chronic toxicity in patients treated with cisplatin-based chemoradiation 21.…”
Section: Discussionmentioning
confidence: 99%