Regorafenib in combination with FOLFOX or FOLFIRI as first- or second-line treatment of colorectal cancer: results of a multicenter, phase Ib study

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • B Schultheis - , Ruhr University Bochum (Author)
  • G Folprecht - , Department of internal Medicine I (Author)
  • J Kuhlmann - , University Medical Center Freiburg (Author)
  • R Ehrenberg - (Author)
  • U T Hacker - (Author)
  • C H Köhne - (Author)
  • M Kornacker - (Author)
  • O Boix - (Author)
  • J Lettieri - (Author)
  • J Krauss - (Author)
  • R Fischer - , MVZ Medizinisches Versorgungszentrum Dreiländereck - Onkologische Schwerpunktpraxis Lörrach (Author)
  • S Hamann - , University Hospital Carl Gustav Carus Dresden (Author)
  • D Strumberg - (Author)
  • K B Mross - (Author)

Abstract

BACKGROUND: Metastatic colorectal cancer (mCRC) is commonly treated with 5-fluorouracil, folinic acid, and oxaliplatin or irinotecan. The multitargeted kinase inhibitor, regorafenib, was combined with chemotherapy as first- or second-line treatment of mCRC to assess safety and pharmacokinetics (primary objectives) and tumor response (secondary objective).

PATIENTS AND METHODS: Forty-five patients were treated every 2 weeks with 5-fluorouracil 400 mg/m(2) bolus then 2400 mg/m(2) over 46 h, folinic acid 400 mg/m(2), and either oxaliplatin 85 mg/m(2) or irinotecan 180 mg/m(2). On days 4-10, patients received regorafenib 160 mg orally once daily.

RESULTS: The median duration of treatment was 108 (range 2-345 days). Treatment was stopped for adverse events or death (17 patients), disease progression (11 patients), and consent withdrawal or investigator decision (11 patients). Six patients remained on regorafenib at data cutoff (two without chemotherapy). Drug-related adverse events occurred in 44 patients [grade ≥ 3 in 32 patients: mostly neutropenia (17 patients) and leukopenia, hand-foot skin reaction, and hypophosphatemia (four patients each)]. Thirty-three patients achieved disease control (partial response or stable disease) for a median of 126 (range 42-281 days).

CONCLUSION: Regorafenib had acceptable tolerability in combination with chemotherapy, with increased exposure of irinotecan and SN-38 but no significant effect on 5-fluorouracil or oxaliplatin pharmacokinetics.

Details

Original languageEnglish
Pages (from-to)1560-1567
Number of pages8
JournalAnnals of Oncology
Volume24
Issue number6
Publication statusPublished - Jun 2013
Peer-reviewedYes

External IDs

Scopus 84878442416
PubMed 23493136
PubMedCentral PMC3660081
ORCID /0000-0002-9321-9911/work/142251945

Keywords

Sustainable Development Goals

Keywords

  • Adolescent, Adult, Aged, Aged, 80 and over, Antineoplastic Combined Chemotherapy Protocols/administration & dosage, Camptothecin/administration & dosage, Colorectal Neoplasms/drug therapy, Female, Fluorouracil/administration & dosage, Humans, Leucovorin/administration & dosage, Male, Middle Aged, Organoplatinum Compounds/administration & dosage, Phenylurea Compounds/administration & dosage, Pyridines/administration & dosage, Treatment Outcome, Young Adult