Safety and effectiveness of FOLFOXIRI plus molecular target drug therapy for metastatic colorectal cancer: A multicenter retrospective study.

FOLFOXIRI therapy anti-EGFR antibodies anti-VEGF antibodies metastatic colorectal cancer triplet

Journal

Oncotarget
ISSN: 1949-2553
Titre abrégé: Oncotarget
Pays: United States
ID NLM: 101532965

Informations de publication

Date de publication:
01 Feb 2019
Historique:
received: 02 11 2018
accepted: 11 01 2019
entrez: 26 2 2019
pubmed: 26 2 2019
medline: 26 2 2019
Statut: epublish

Résumé

FOLFOXIRI plus bevacizumab has a promising efficacy as first-line systemic chemotherapy for metastatic colorectal cancer (mCRC). This study aimed to evaluate the safety and effectiveness of FOLFOXIRI plus antibodies. Fifty-five patients were enrolled (median age: 60 years, males: 25, females: 30). Twenty-six subjects had RAS mutations and 29 had RAS wild-type. Anti-VEGF and anti-EGFR antibodies were administered to 38 and 17 patients, respectively. The most common severe adverse event was neutropenia (51%). The overall response rate (ORR) was 69% (55% with anti-VEGF antibodies and 100% with anti-EGFR antibodies; We retrospectively collected data from mCRC patients treated with FOLFOXIRI plus antibodies between March 2014 and December 2017. FOLFOXIRI plus antibody therapy was effective in patients with mCRC. The response rate was higher in patients treated with anti-EGFR antibodies than in those treated with anti-VEGF antibodies.

Identifiants

pubmed: 30800219
doi: 10.18632/oncotarget.26626
pii: 26626
pmc: PMC6383688
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1070-1084

Déclaration de conflit d'intérêts

CONFLICTS OF INTEREST The authors declare no conflicts of interest.

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Auteurs

Takatsugu Ogata (T)

Department of Medical Oncology, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

Hironaga Satake (H)

Cancer Treatment Center, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Misato Ogata (M)

Department of Medical Oncology, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

Yukimasa Hatachi (Y)

Department of Medical Oncology, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

Hayato Maruoka (H)

Department of Clinical Laboratory, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

Daisuke Yamashita (D)

Department of Pathology, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

Hiroki Hashida (H)

Department of Surgery, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

Madoka Hamada (M)

Department of Surgery, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Hisateru Yasui (H)

Department of Medical Oncology, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

Classifications MeSH