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1.
BMC Gastroenterol ; 22(1): 516, 2022 Dec 13.
Artículo en Inglés | MEDLINE | ID: mdl-36513968

RESUMEN

BACKGROUND: T1 colorectal cancer (CRC) without histological high-risk factors for lymph node metastasis (LNM) can potentially be cured by endoscopic resection, which is associated with significantly lower morbidity, mortality and costs compared to radical surgery. An important prerequisite for endoscopic resection as definite treatment is the histological confirmation of tumour-free resection margins. Incomplete resection with involved (R1) or indeterminate (Rx) margins is considered a strong risk factor for residual disease and local recurrence. Therefore, international guidelines recommend additional surgery in case of R1/Rx resection, even in absence of high-risk factors for LNM. Endoscopic full-thickness resection (eFTR) is a relatively new technique that allows transmural resection of colorectal lesions. Local scar excision after prior R1/Rx resection of low-risk T1 CRC could offer an attractive minimal invasive strategy to achieve confirmation about radicality of the previous resection or a second attempt for radical resection of residual luminal cancer. However, oncologic safety has not been established and long-term data are lacking. Besides, surveillance varies widely and requires standardization. METHODS/DESIGN: In this nationwide, multicenter, prospective cohort study we aim to assess feasibility and oncological safety of completion eFTR following incomplete resection of low-risk T1 CRC. The primary endpoint is to assess the 2 and 5 year luminal local tumor recurrence rate. Secondary study endpoints are to assess feasibility, percentage of curative eFTR-resections, presence of scar tissue and/or complete scar excision at histopathology, safety of eFTR compared to surgery, 2 and 5 year nodal and/or distant tumor recurrence rate and 5-year disease-specific and overall-survival rate. DISCUSSION: Since the implementation of CRC screening programs, the diagnostic rate of T1 CRC is steadily increasing. A significant proportion is not recognized as cancer before endoscopic resection and is therefore resected through conventional techniques primarily reserved for benign polyps. As such, precise histological assessment is often hampered due to cauterization and fragmentation and frequently leads to treatment dilemmas. This first prospective trial will potentially demonstrate the effectiveness and oncological safety of completion eFTR for patients who have undergone a previous incomplete T1 CRC resection. Hereby, substantial surgical overtreatment may be avoided, leading to treatment optimization and organ preservation. Trial registration Nederlands Trial Register, NL 7879, 16 July 2019 ( https://trialregister.nl/trial/7879 ).


Asunto(s)
Neoplasias Colorrectales , Recurrencia Local de Neoplasia , Humanos , Cicatriz/complicaciones , Cicatriz/patología , Neoplasias Colorrectales/patología , Metástasis Linfática , Estudios Multicéntricos como Asunto , Recurrencia Local de Neoplasia/patología , Estadificación de Neoplasias , Neoplasia Residual/patología , Estudios Prospectivos , Estudios Retrospectivos , Resultado del Tratamiento
2.
Neth J Med ; 74(6): 240-6, 2016 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-27571721

RESUMEN

BACKGROUND: Criteria assessing biochemical response to ursodeoxycholic acid (UDCA) are established risk stratification tools in primary biliary cholangitis (PBC). We aimed to evaluate to what extent liver tests influenced patient management during a three decade period, and whether this changed over time. METHODS: 851 Dutch PBC patients diagnosed between 1988 and 2012 were reviewed to assess patient management in relation to liver test results during UDCA treatment. To do so, biochemical response at one year was analysed retrospectively according to Paris-1 criteria. RESULTS: Response was assessable for 687/851 (81%) patients; 157/687 non-responders. During a follow-up of 8.8 years (IQR 4.8-13.9), 141 died and 30 underwent liver transplantation. Transplant-free survival of non-responders (60%) was significantly worse compared with responders (87%) (p < 0.0001). Management was modified in 46/157 (29%) non-responders. The most frequent change observed, noted in 26/46 patients, was an increase in UDCA dosage. Subsequently, 9/26 (35%) non-responders became responders within the next two years. Steroid treatment was started in one patient; 19 patients were referred to a tertiary centre. No trend towards more frequent changes in management over time was observed (p = 0.10). CONCLUSION: Changes in medical management occurred in a minority of non-responders. This can largely be explained by the lack of accepted response criteria and of established second-line treatments for PBC. Nevertheless, the observation that response-guided management did not increase over time suggests that awareness of the concept of biochemical response requires further attention,particularly since new treatment options for PBC will soon become available.


Asunto(s)
Colagogos y Coleréticos/uso terapéutico , Cirrosis Hepática Biliar/tratamiento farmacológico , Ácido Ursodesoxicólico/uso terapéutico , Adulto , Anciano , Fosfatasa Alcalina , Aspartato Aminotransferasas/sangre , Bilirrubina/sangre , Manejo de la Enfermedad , Femenino , Estudios de Seguimiento , Humanos , Cirrosis Hepática Biliar/sangre , Trasplante de Hígado/estadística & datos numéricos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Albúmina Sérica/metabolismo , Resultado del Tratamiento
3.
Neth J Med ; 70(8): 381-5, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23065990

RESUMEN

In 2008, the Netherlands Association of Gastroenterologists and Hepatologists (Nederlands Vereniging van Maag-Darm-Leverartsen) published the Dutch national guidelines for the treatment of chronic hepatitis B virus infection. New insights into the treatment of chronic hepatitis B with relevance for clinical practice have been adopted in these concise, revised guidelines. The most important changes include the choice of initial antiviral therapy, licensing of tenofovir for the treatment of chronic hepatitis B and the management of antiviral resistance.


Asunto(s)
Adenina/análogos & derivados , Aprobación de Drogas , Farmacorresistencia Viral/efectos de los fármacos , Guanina/análogos & derivados , Hepatitis B Crónica/tratamiento farmacológico , Organofosfonatos/uso terapéutico , Guías de Práctica Clínica como Asunto , Complicaciones Infecciosas del Embarazo/tratamiento farmacológico , Adenina/administración & dosificación , Adenina/normas , Adenina/uso terapéutico , Antivirales/administración & dosificación , Antivirales/normas , Antivirales/uso terapéutico , Femenino , Guanina/administración & dosificación , Guanina/normas , Guanina/uso terapéutico , Hepatitis B Crónica/complicaciones , Humanos , Transmisión Vertical de Enfermedad Infecciosa/prevención & control , Lamivudine/normas , Lamivudine/uso terapéutico , Leche Humana/efectos de los fármacos , Países Bajos , Nucleósidos/administración & dosificación , Nucleósidos/uso terapéutico , Organofosfonatos/administración & dosificación , Organofosfonatos/normas , Embarazo , Insuficiencia Renal/tratamiento farmacológico , Insuficiencia Renal/etiología , Telbivudina , Tenofovir , Timidina/análogos & derivados , Timidina/normas , Timidina/uso terapéutico
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