CONKO-006: A randomised double-blinded phase IIb-study of additive therapy with gemcitabine + sorafenib/placebo in patients with R1 resection of pancreatic cancer - Final results.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
10 2020
Historique:
received: 20 03 2020
revised: 16 06 2020
accepted: 26 06 2020
pubmed: 6 9 2020
medline: 26 1 2021
entrez: 5 9 2020
Statut: ppublish

Résumé

CONKO-006 was designed for patients with pancreatic adenocarcinoma with postsurgical R1 residual status to evaluate the efficacy and safety of the combination of gemcitabine and sorafenib (GemSorafenib) compared with those of gemcitabine + placebo (GemP) for 12 cycles. This randomised, double-blind, placebo-controlled, multicenter study was planned to detect an improvement in recurrence-free survival (RFS) from 42% to 60% after 18 months. Secondary objectives were overall survival (OS), safety and duration of treatment. 122 patients were included between 02/2008 and 09/2013; 57 were randomised to GemSorafenib and 65 to GemP. Patient characteristics were wellbalanced (GemSorafenib/GemP) in terms of median age (63/63 years), tumour size (T3/T4: 97/97%), and nodal positivity (86/85%). Grade 3/4 toxicities comprised diarrhoea (GemSorafenib: 12%; GemP: 2%), elevated gamma-glutamyl transferase (GGT) (19%; 9%), fatigue (5%; 2%) and hypertension (5%; 2%), as well as neutropenia (18%; 25%) and thrombocytopenia (9%; 2%). By August 2017, 118 (97%) RFS event had occurred. There were no difference in RFS (median GemSorafenib: 8.5 versus GemP: 9.4 months; p = 0.730) nor OS (median GemSorafenib: 17.6 versus GemP: 17.5 months; p = 0.481). Landmark analyses suggest that patients who received more than six cycles of postoperative chemotherapy had significantly longer OS (p = 0.021). CONKO-006 is the first randomised clinical trial to include exclusively patients with PDAC with postsurgical R1 status thus far. Sorafenib added to gemcitabine did neither improve RFS nor OS. However, postoperative treatment exceeding six months seemed to prolong survival and should be further investigated in these high-risk patients. German Tumor Study Registry (Deutsches Krebsstudienregister), DRKS00000242.

Sections du résumé

BACKGROUND
CONKO-006 was designed for patients with pancreatic adenocarcinoma with postsurgical R1 residual status to evaluate the efficacy and safety of the combination of gemcitabine and sorafenib (GemSorafenib) compared with those of gemcitabine + placebo (GemP) for 12 cycles.
PATIENTS AND METHODS
This randomised, double-blind, placebo-controlled, multicenter study was planned to detect an improvement in recurrence-free survival (RFS) from 42% to 60% after 18 months. Secondary objectives were overall survival (OS), safety and duration of treatment.
RESULTS
122 patients were included between 02/2008 and 09/2013; 57 were randomised to GemSorafenib and 65 to GemP. Patient characteristics were wellbalanced (GemSorafenib/GemP) in terms of median age (63/63 years), tumour size (T3/T4: 97/97%), and nodal positivity (86/85%). Grade 3/4 toxicities comprised diarrhoea (GemSorafenib: 12%; GemP: 2%), elevated gamma-glutamyl transferase (GGT) (19%; 9%), fatigue (5%; 2%) and hypertension (5%; 2%), as well as neutropenia (18%; 25%) and thrombocytopenia (9%; 2%). By August 2017, 118 (97%) RFS event had occurred. There were no difference in RFS (median GemSorafenib: 8.5 versus GemP: 9.4 months; p = 0.730) nor OS (median GemSorafenib: 17.6 versus GemP: 17.5 months; p = 0.481). Landmark analyses suggest that patients who received more than six cycles of postoperative chemotherapy had significantly longer OS (p = 0.021).
CONCLUSION
CONKO-006 is the first randomised clinical trial to include exclusively patients with PDAC with postsurgical R1 status thus far. Sorafenib added to gemcitabine did neither improve RFS nor OS. However, postoperative treatment exceeding six months seemed to prolong survival and should be further investigated in these high-risk patients.
CLINICAL TRIAL INFORMATION
German Tumor Study Registry (Deutsches Krebsstudienregister), DRKS00000242.

Identifiants

pubmed: 32890813
pii: S0959-8049(20)30365-8
doi: 10.1016/j.ejca.2020.06.032
pii:
doi:

Substances chimiques

Deoxycytidine 0W860991D6
Sorafenib 9ZOQ3TZI87
Gemcitabine 0

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

172-181

Informations de copyright

Copyright © 2020. Published by Elsevier Ltd.

Auteurs

M Sinn (M)

Charité Universitätsmedizin Berlin, Campus Virchow Klinikum, Department of Medical Oncology and Hematology, Berlin, Germany; Universitätsklinikum Hamburg-Eppendorf, Department of Medical Oncology, Hamburg, Germany. Electronic address: ma.sinn@uke.de.

T Liersch (T)

University of Göttingen, Department of General, Visceral and Pediatric Surgery, Göttingen, Germany.

H Riess (H)

Charité Universitätsmedizin Berlin, Campus Virchow Klinikum, Department of Medical Oncology and Hematology, Berlin, Germany.

K Gellert (K)

Sana Klinikum Lichtenberg, Department of General and Visceral Surgery, Berlin, Germany.

P Stübs (P)

Otto-Guericke-University of Magdeburg, Department of General, Visceral and Vascular Surgery, Magdeburg, Germany.

D Waldschmidt (D)

University of Köln, Department of Gastroenterology and Hepatology, Köln, Germany.

F Lammert (F)

Universitätskliniken des Saarlandes, Department of Internal Medicine, Gastroenterology and Endocrinology, Homburg, Germany.

G Maschmeyer (G)

Ernst von Bergmann Klinikum, Department of Hematology, Oncology and Palliative Care, Potsdam, Germany.

W Bechstein (W)

Universitätsklinikum Frankfurt, Department of General and Visceral Surgery, Frankfurt, Germany.

M Bitzer (M)

Eberhard-Karls-Universität Tübingen, Department of Internal Medicine, Tübingen, Germany.

C Denzlinger (C)

Marienhospital Stuttgart, Department of Hematology, Oncology and Palliative Care, Stuttgart Germany.

R Hofheinz (R)

Universitätsklinikum Mannheim, Department of Medical Oncology, Mannheim, Germany.

U Lindig (U)

Universitätsklinikum Jena, Department of Hematology and Oncology, Jena, Germany.

M Ghadimi (M)

University of Göttingen, Department of General, Visceral and Pediatric Surgery, Göttingen, Germany.

A Hinke (A)

CCRC, Düsseldorf, Germany.

J K Striefler (JK)

Charité Universitätsmedizin Berlin, Campus Virchow Klinikum, Department of Medical Oncology and Hematology, Berlin, Germany.

U Pelzer (U)

Charité Universitätsmedizin Berlin, Campus Virchow Klinikum, Department of Medical Oncology and Hematology, Berlin, Germany.

S Bischoff (S)

Charité Universitätsmedizin Berlin, Campus Virchow Klinikum, Department of Medical Oncology and Hematology, Berlin, Germany.

M Bahra (M)

Charité Universitätsmedizin Berlin, Campus Virchow Klinikum, Department of Surgery, Berlin, Germany.

H Oettle (H)

Outpatient Department of Hematology/Oncology, Friedrichshafen, Germany.

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Classifications MeSH