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Survival of patients with symptom- and screening-detected colorectal cancer

BACKGROUND: An increasing proportion of colorectal cancer (CRC) patients are diagnosed by screening rather than symptoms. AIMS: We aimed to assess and compare prognosis of patients with screen-detected CRC and symptom-detected CRC. METHODS: Overall and CRC specific mortality over a median follow-up...

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Detalles Bibliográficos
Autores principales: Brenner, Hermann, Jansen, Lina, Ulrich, Alexis, Chang-Claude, Jenny, Hoffmeister, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5190129/
https://www.ncbi.nlm.nih.gov/pubmed/27213584
http://dx.doi.org/10.18632/oncotarget.9412
Descripción
Sumario:BACKGROUND: An increasing proportion of colorectal cancer (CRC) patients are diagnosed by screening rather than symptoms. AIMS: We aimed to assess and compare prognosis of patients with screen-detected CRC and symptom-detected CRC. METHODS: Overall and CRC specific mortality over a median follow-up of 4.8 years was assessed according to mode of diagnosis (symptoms, screening colonoscopy, fecal occult blood test [FOBT], other) in a multi-center cohort of 2,450 CRC patients aged 50-79 years recruited in Germany in 2003-2010. RESULTS: 68%, 11% and 10% were detected by symptoms, screening colonoscopy and FOBT, respectively. The screen-detected cancers had a more favorable stage distribution than the symptom-detected cancers (68% versus 50% in stage I or II). Age- and sex adjusted hazard ratios (HRs) of total mortality with 95% confidence intervals (95% CIs) compared to symptom-detected cancers were 0.35 (0.24-0.50) and 0.36 (0.25-0.53) for screening colonoscopy and FOBT detected CRCs, respectively. HRs were only slightly attenuated and remained highly significant after adjustment for stage and multiple other covariates (0.50 (0.34-0.73) and 0.54 (0.37-0.80), respectively). Even stronger associations were seen for CRC specific mortality. Patients with screen-detected stage III CRC had as good CRC specific survival as patients with symptom-detected stage I or II CRC. CONCLUSIONS: Patients with screen-detected CRC have a very good prognosis far beyond the level explained by their more favorable stage distribution. Mode of detection is an important, easy-to-obtain proxy indicator for favorable diagnosis beyond earlier stage at diagnosis and as such may be useful for risk stratification in treatment decisions.