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Spots Global Cancer Trial Database for Second Line Therapy in Advanced Biliary Tract Cancer

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Trial Identification

Brief Title: Second Line Therapy in Advanced Biliary Tract Cancer

Official Title: A Randomized Phase II Trial of Second Line Therapy in Advanced Biliary Tract Cancer: Capecitabine or Capecitabine Plus Mitomycin C

Study ID: NCT01530503

Study Description

Brief Summary: The purpose of this study is to assess the therapeutic activity of capecitabine alone or in combination with mitomycin C as second-line therapy in patients with advanced/metastatic biliary adenocarcinoma in progression after gemcitabine and platinum compounds

Detailed Description: Biliary tract adenocarcinoma is an uncommon tumor with a poor prognosis and a median overall survival (OS) rarely exceeding 6 months. Less than 25% of patients are resectable at diagnosis and, even in this subset of patients, relapse rate is high. An improvement of OS and quality of life for patients receiving chemotherapy versus best supportive care was demonstrated in advanced disease. Recently, cisplatin and gemcitabine combination was identified as the new standard first-line chemotherapy, yielding a median progression free survival (PFS) and median OS of 8.5 and 11.7 months, respectively. Despite the outcome improvement, disease progression is a constant and approximately half of patients failing upfront treatment has a good performance status and are willing to undergo further treatment. No standard salvage chemotherapy regimen has been identified. Clinical trials are difficult to perform due to the rarity and heterogeneity of these tumors and to the lack of interest of the pharmaceutical industry. Fluoropyrimidines and mitomycin C have been considered the basis of palliative chemotherapy for a long time. The investigators decided to explore the activity, in terms of PFS, of capecitabine alone or combined with mitomycin C as second-line therapy in patients with pathological diagnosis of advanced biliary tract cancer and progressive disease after gemcitabine and cisplatin, by means of an open label randomized multicentric phase II trial.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

ASUR zona territoriale N. 6 FABRIANO, Fabriano, Ancona, Italy

Fondazione Istituto San Raffaele G. Giglio, Cefalù, Palermo, Italy

Azienda Ospedaliero Universitaria Ospedali Riuniti Umberto I - G.M. Lancisi - G Salesi, Ancona, , Italy

A.O. Ospedali Riuniti, Bergamo, , Italy

Azienda Ospedaliero-Universitaria Policlinico S. Orsola-Malpighi, Bologna, , Italy

Fondazione Piemontese Per la Ricerca sul Cancro, Candiolo (Torino), , Italy

Azienda Ospedaliera di Rilievo Nazionale e di Alta Specializzazione Garibaldi, Catania, , Italy

Ospedale San Raffaele, Milan, , Italy

Istituto Oncologico Veneto I.R.C.C.S., Padova, , Italy

Azienda Ospedaliero-Universitaria Pisana, Pisa, , Italy

Azienda Ospedaliera Regionale San Carlo, Potenza, , Italy

Istituto Nazionale dei Tumori Regina Elena, Roma, , Italy

Ospedale Generale Provinciale, Saronno (VA), , Italy

Azienda Ospedaliera Universitaria San Giovanni Battista di Torino, Torino, , Italy

Azienda Ospedaliero Universitaria Santa Maria della Misericordia, Udine, , Italy

Azienda Ospedaliera Universitaria Integrata, Verona, , Italy

Contact Details

Name: stefano cereda, MD

Affiliation: Ospedale San Raffaele (Milan, Italy)

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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