The purpose of the present study is to investigate the benefit of anti-cancer therapy administered on the basis of drug sensitivity testing. This concerns colorectal cancer patients who have previously received standard treatment.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
90
* 5FU, infusional * Capecitabine * Oxaliplatin (FOLFOX) * Irinotecan (FOLFIRI) * FOLFOXIRI (triplet) * Bevacizumab * Panitumumab * Cetuximab * Regorafenib * Tas-102 * Ramucirumab * Aflibercept * Pembrolizumab * Nivolumab * Vinorelbine and capecitabine * Sorafenib * Gemcitabine and capecitabine * Olaparib * Epirubicin
Department of Oncology, Aalborg University Hospital
Aalborg, Denmark
Department of Oncology, Rigshospitalet
Copenhagen, Denmark
Departmen of Oncology, Vejle Hospital
Vejle, Denmark
Universitätsklinikum Hamburg - Eppendorf, Universitäres Cancer Center Hamburg (UCCH)
Hamburg, Germany
Progression free survival 8 weeks after start of treatment
Time frame: 42-63 days after start of treatment
Progression free survival
Time frame: Every 8 weeks until progression or death up to 2.5 years
Overall survival
Time frame: Every 3 months up to 2.5 years
Response rate
Time frame: Every 8 weeks until progression up to 2.5 years
Quality of life as measured by questionnaire EQ-5D-5L
Time frame: Every 8 weeks up to 2.5 years
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