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1.
Br J Cancer ; 112(6): 963-70, 2015 Mar 17.
Artículo en Inglés | MEDLINE | ID: mdl-25742472

RESUMEN

BACKGROUND: Mutations affecting RAS genes are now established predictive markers of nonresponse to anti-EGFR antibodies in advanced CRC. This analysis assessed the prognostic and predictive impact of extended RAS and PIK3CA gene mutation status in patients receiving capecitabine plus or minus bevacizumab (±mitomycin C) in the randomised phase III MAX study. METHODS: DNA was extracted from archival macrodissected formalin-fixed paraffin-embedded tumour tissue. Mutation status was determined using pyrosequencing, confirmed with Sanger sequencing (for equivocal RAS) and correlated with efficacy outcomes. Predictive analyses were undertaken using a test for interaction involving both C vs CB+CBM. RESULTS: Of the available 280 of the 471 (59.4%) patients, mutations in KRAS exons 2, 3 and 4 and NRAS 2, 3 and 4 were as follows: 32%, 2.9%, 2.2%, 1.4%, 0.7% and 0% (total RAS MT 39%). The PIK3CA MT rate was 7.5% exon 9 and 3.6% exon 20. Extended RAS gene mutation status (WT vs MT) had no prognostic impact for PFS (HR 0.91 (0.71-1.17)) or OS (HR 0.95 (0.71-1.25)). The RAS gene mutation status was not predictive of the effectiveness of bevacizumab for PFS (HR 0.56 (0.37-0.85) for RAS MT and HR 0.69 (0.5-0.97) for RAS WT; P for interaction 0.50). The PIK3CA mutation was neither predictive for bevacizumab effect nor prognostic. CONCLUSION: Of KRAS exon 2 WT patients, 10% had additional RAS mutations. Neither all RAS gene mutation status nor PIK3CA mutation status was prognostic for PFS or OS, or predictive of bevacizumab outcome in patients with advanced CRC.


Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Neoplasias Colorrectales/tratamiento farmacológico , Neoplasias Colorrectales/genética , Genes ras , Mutación , Fosfatidilinositol 3-Quinasas/genética , Adulto , Anciano , Anciano de 80 o más Años , Anticuerpos Monoclonales Humanizados/administración & dosificación , Bevacizumab , Capecitabina , Fosfatidilinositol 3-Quinasa Clase I , Neoplasias Colorrectales/patología , ADN de Neoplasias/química , ADN de Neoplasias/genética , Desoxicitidina/administración & dosificación , Desoxicitidina/análogos & derivados , Femenino , Fluorouracilo/administración & dosificación , Fluorouracilo/análogos & derivados , Humanos , Masculino , Mitomicina/administración & dosificación , Pronóstico
2.
Ugeskr Laeger ; 152(49): 3711-3, 1990 Dec 03.
Artículo en Danés | MEDLINE | ID: mdl-2264176

RESUMEN

With the object of reducing the high of vacuum extraction in deliveries with lumbar epidural analgesia, we introduced "late pushing" in these deliveries in 1988. By this is understood that the parturient women is first encouraged to push when the orifice is completely dilated and the infant's head is visible at introitus. Before the "late pushing" was introduced, the frequency of vacuum extractions in deliveries with lumbar epidural analgesia was 44% of the vaginal deliveries. During the period of investigation, the frequency was 43%. Introduction of the "late pushing" thus did not result in any alteration (p greater than 0.4). Parturient women with lumbar epidural analgesia and slow progression of labour differed from the remainder of the parturient women with lumbar epidiral analgesia by significantly higher birth weights (4,000 g as compared with 3,400 g) and this may explain the increased frequency of vacuum extraction in this particular group of parturient women. The authors consider that lumbar epidural analgesia has the advantage that delivery is less painful for the mother without any simultaneous increased risk for the infant.


Asunto(s)
Analgesia Epidural , Analgesia Obstétrica , Extracción Obstétrica por Aspiración/estadística & datos numéricos , Femenino , Humanos , Segundo Periodo del Trabajo de Parto/fisiología , Embarazo , Estudios Prospectivos
3.
Eur J Cancer ; 49(7): 1627-33, 2013 May.
Artículo en Inglés | MEDLINE | ID: mdl-23274198

RESUMEN

BACKGROUND AND AIM: Significant tumour progression was observed during waiting time for treatment of head and neck cancer. To reduce waiting times, a Danish national policy of fast track accelerated clinical pathways was introduced in 2007. This study describes changes in waiting time and the potential influence of fast track by comparing waiting times in 2010 to 2002 and 1992. METHODS: Charts of all new patients diagnosed with squamous cell carcinoma of the oral cavity, pharynx and larynx at the five Danish head and neck oncology centres from January to April 2010 (n=253) were reviewed and compared to similar data from 2002 (n=211) and 1992 (n=168). RESULTS: The median time to diagnosis was 13 days (2010) versus 17 days (2002; p<0.001) and 20 days (1992; p<0.001). Median days from diagnosis to treatment start were 25 (2010) versus 47 (2002; p<0.001) and 31 (1992; p<0.001). Total pre-treatment time was median 41 days in 2010 versus 69 days (2002) (p<0.001) and 50 days (1992; p<0.001). Significantly more diagnostic imaging was done in 2010 compared to 2002 and 1992. When compared to current fast track standards the adherence to diagnosis improved slightly from 47% (1992) to 51% (2002) and 64% (2010); waiting time for radiotherapy was within standards for 7%, 1% and 22% of cases, respectively; waiting time for surgery was within standards for 17%, 22% and 48%, respectively. CONCLUSION: The study showed a significant reduction in delay of diagnosis and treatment of head and neck cancer in 2010, but still less than half of all patients start treatment within the current standards.


Asunto(s)
Carcinoma de Células Escamosas/diagnóstico , Carcinoma de Células Escamosas/terapia , Neoplasias de Cabeza y Cuello/diagnóstico , Neoplasias de Cabeza y Cuello/terapia , Dinamarca , Femenino , Humanos , Masculino , Persona de Mediana Edad , Programas Nacionales de Salud/normas , Programas Nacionales de Salud/tendencias , Atención Individual de Salud/normas , Atención Individual de Salud/tendencias , Factores de Tiempo , Listas de Espera
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