TY - JOUR
T1 - Precision medicine for patients with advanced biliary tract cancers
T2 - An effective strategy within the prospective MOSCATO-01 trial
AU - Verlingue, Loic
AU - Malka, David
AU - Allorant, Adrien
AU - Massard, Christophe
AU - Ferté, Charles
AU - Lacroix, Ludovic
AU - Rouleau, Etienne
AU - Auger, Nathalie
AU - Ngo, Maud
AU - Nicotra, Claudio
AU - De Baere, Thierry
AU - Tselikas, Lambros
AU - Ba, Bakar
AU - Michiels, Stefan
AU - Scoazec, Jean Yves
AU - Boige, Valérie
AU - Ducreux, Michel
AU - Soria, Jean Charles
AU - Hollebecque, Antoine
N1 - Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Background Recommended treatments of patients with advanced biliary tract cancer (aBTC) are limited to one chemotherapy doublet. Nevertheless, efficacy of treatment personalisation for aBTCs is supported by accumulating evidences but remains to be evaluated. Patients and methods Patients with aBTCs included in the prospective clinical trial MOSCATO-01 were treated by at least one previous systemic treatment, had an ECOG performance status of 0–1, and at least one tumour site accessible to biopsy. Multiple high-throughput molecular analysis was performed on biopsies to drive the administration of molecular targeted agents (MTAs). Results From November 2011 to March 2016, 43 patients (4%) of the 1035 adult patients included in MOSCATO-01 had aBTCs with a majority of intrahepatic localisation (67%). Successful biopsy procedures and DNA extractions led to molecular portraits for 34 patients (79%). Orientation to an appropriate early clinical trial or accessible MTA(s) was possible for 23 of these patients (68%), and 18 (53%) have received matched MTA(s). Among them, the overall response rate was 33% and the disease control rate was 88%. A PFS ≥6 months was observed in 37% and the PFS ratio was >1.3 for 50% of the patients. These patients had a lower risk for death as compared to the 20 patients not orientated to a matched MTA (HR, 0.29; 95% CI, 0.11–0.76; p = 0.008). Conclusions Within the MOSCATO-01 trial, patients with aBTCs had the highest rate of orientation to matched MTAs and derived a clear clinical benefit. A broader evaluation of these findings may improve future treatments strategies for aBTCs. Trial Registration: NCT01566019.
AB - Background Recommended treatments of patients with advanced biliary tract cancer (aBTC) are limited to one chemotherapy doublet. Nevertheless, efficacy of treatment personalisation for aBTCs is supported by accumulating evidences but remains to be evaluated. Patients and methods Patients with aBTCs included in the prospective clinical trial MOSCATO-01 were treated by at least one previous systemic treatment, had an ECOG performance status of 0–1, and at least one tumour site accessible to biopsy. Multiple high-throughput molecular analysis was performed on biopsies to drive the administration of molecular targeted agents (MTAs). Results From November 2011 to March 2016, 43 patients (4%) of the 1035 adult patients included in MOSCATO-01 had aBTCs with a majority of intrahepatic localisation (67%). Successful biopsy procedures and DNA extractions led to molecular portraits for 34 patients (79%). Orientation to an appropriate early clinical trial or accessible MTA(s) was possible for 23 of these patients (68%), and 18 (53%) have received matched MTA(s). Among them, the overall response rate was 33% and the disease control rate was 88%. A PFS ≥6 months was observed in 37% and the PFS ratio was >1.3 for 50% of the patients. These patients had a lower risk for death as compared to the 20 patients not orientated to a matched MTA (HR, 0.29; 95% CI, 0.11–0.76; p = 0.008). Conclusions Within the MOSCATO-01 trial, patients with aBTCs had the highest rate of orientation to matched MTAs and derived a clear clinical benefit. A broader evaluation of these findings may improve future treatments strategies for aBTCs. Trial Registration: NCT01566019.
KW - Biliary tract carcinoma
KW - Cholangiocarcinoma
KW - Molecular screening
KW - Precision medicine
KW - Targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=85033606592&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2017.10.013
DO - 10.1016/j.ejca.2017.10.013
M3 - Article
C2 - 29145038
AN - SCOPUS:85033606592
SN - 0959-8049
VL - 87
SP - 122
EP - 130
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -