TY - JOUR
T1 - MODUL—a multicenter randomized clinical trial of biomarker-driven maintenance therapy following first-line standard induction treatment of metastatic colorectal cancer
T2 - an adaptable signal-seeking approach
AU - Schmoll, Hans Joachim
AU - Arnold, Dirk
AU - de Gramont, Aimery
AU - Ducreux, Michel
AU - Grothey, Axel
AU - O’Dwyer, Peter J.
AU - Van Cutsem, Eric
AU - Hermann, Frank
AU - Bosanac, Ivan
AU - Bendahmane, Belguendouz
AU - Mancao, Christoph
AU - Tabernero, Josep
N1 - Publisher Copyright:
© 2018, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2018/6/1
Y1 - 2018/6/1
N2 - Purpose: The old approach of one therapeutic for all patients with mCRC is evolving with a need to target specific molecular aberrations or cell-signalling pathways. Molecular screening approaches and new biomarkers are required to fully characterize tumours, identify patients most likely to benefit, and predict treatment response. Methods: MODUL is a signal-seeking trial with a design that is highly adaptable, permitting modification of different treatment cohorts and inclusion of further additional cohorts based on novel evidence on new compounds/combinations that emerge during the study. Results: MODUL is ongoing and its adaptable nature permits timely and efficient recruitment of patients into the most appropriate cohort. Recruitment will take place over approximately 5 years in Europe, Asia, Africa, and South America. The design of MODUL with ongoing parallel/sequential treatment cohorts means that the overall size and duration of the trial can be modified/prolonged based on accumulation of new data. Conclusions: The early success of the current trial suggests that the design may provide definitive leads in a patient-friendly and relatively economical trial structure. Along with other biomarker-driven trials that are currently underway, it is hoped that MODUL will contribute to the continuing evolution of clinical trial design and permit a more ‘tailored’ approach to the treatment of patients with mCRC.
AB - Purpose: The old approach of one therapeutic for all patients with mCRC is evolving with a need to target specific molecular aberrations or cell-signalling pathways. Molecular screening approaches and new biomarkers are required to fully characterize tumours, identify patients most likely to benefit, and predict treatment response. Methods: MODUL is a signal-seeking trial with a design that is highly adaptable, permitting modification of different treatment cohorts and inclusion of further additional cohorts based on novel evidence on new compounds/combinations that emerge during the study. Results: MODUL is ongoing and its adaptable nature permits timely and efficient recruitment of patients into the most appropriate cohort. Recruitment will take place over approximately 5 years in Europe, Asia, Africa, and South America. The design of MODUL with ongoing parallel/sequential treatment cohorts means that the overall size and duration of the trial can be modified/prolonged based on accumulation of new data. Conclusions: The early success of the current trial suggests that the design may provide definitive leads in a patient-friendly and relatively economical trial structure. Along with other biomarker-driven trials that are currently underway, it is hoped that MODUL will contribute to the continuing evolution of clinical trial design and permit a more ‘tailored’ approach to the treatment of patients with mCRC.
KW - Biomarker
KW - FOLFOX + bevacizumab
KW - MODUL
KW - Metastatic colorectal cancer
KW - Signal seeking
KW - Switch maintenance therapy
UR - http://www.scopus.com/inward/record.url?scp=85046854671&partnerID=8YFLogxK
U2 - 10.1007/s00432-018-2632-6
DO - 10.1007/s00432-018-2632-6
M3 - Article
C2 - 29644408
AN - SCOPUS:85046854671
SN - 0171-5216
VL - 144
SP - 1197
EP - 1204
JO - Journal of Cancer Research and Clinical Oncology
JF - Journal of Cancer Research and Clinical Oncology
IS - 6
ER -