Morphologic response to chemotherapy containing bevacizumab in patients with colorectal liver metastases: A post hoc analysis of the WJOG4407G phase III study.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
04 Sep 2020
Historique:
entrez: 9 9 2020
pubmed: 10 9 2020
medline: 20 9 2020
Statut: ppublish

Résumé

The phase III West Japan Oncology Group (WJOG) 4407G study showed noninferiority of folinic acid, bolus/continuous fluorouracil, and irinotecan plus bevacizumab to modified folinic acid, bolus/continuous fluorouracil, and oxaliplatin 6 plus bevacizumab in progression-free survival (PFS) as first-line chemotherapy for patients with metastatic colorectal cancer. The aim of this study was to evaluate the predictive and prognostic value of morphologic response in patients with colorectal liver metastases (CLM) as a post hoc analysis of the WJOG4407G study.Morphologic response was assessed by comparing contrast-enhanced computed tomography (CT) images at baseline and week 8. Three blinded radiologists evaluated CT images and classified their response as optimal, incomplete, or no response according to the morphologic criteria. Response evaluation criteria in solid tumors (RECIST) response, early tumor shrinkage (ETS), and depth of response (DpR) were also evaluated.Among 395 patients who were eligible for efficacy analysis in the WJOG4407G study, 70 patients had liver-limited disease. We finally evaluated 55 of these patients. Optimal morphologic response was identified in 19 of 55 patients (34.5%). The median PFS was 10.7 months for patients with optimal response and 10.1 months in those with incomplete/no response (log-rank, P = .96). The median overall survival (OS) was 26.2 and 35.5 months, respectively (log-rank, P = .062). According to univariate analysis, morphologic response was not associated with PFS or OS, whereas RECIST response was significantly associated with both PFS and OS, with ETS and DpR being associated with significantly longer PFS.Morphologic response might be neither a predictive nor a prognostic factor in patients with CLM undergoing chemotherapy containing bevacizumab, whereas RECIST response was significantly associated with both PFS and OS.

Identifiants

pubmed: 32899071
doi: 10.1097/MD.0000000000022060
pii: 00005792-202009040-00083
pmc: PMC7478588
doi:

Substances chimiques

Antimetabolites, Antineoplastic 0
Antineoplastic Agents, Immunological 0
Topoisomerase I Inhibitors 0
Oxaliplatin 04ZR38536J
Vitamin B Complex 12001-76-2
Bevacizumab 2S9ZZM9Q9V
Irinotecan 7673326042
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e22060

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Auteurs

Ayumu Hosokawa (A)

Department of Clinical Oncology, University of Miyazaki Hospital, Miyazaki.

Kentaro Yamazaki (K)

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka.

Chu Matsuda (C)

Department of Surgery, Osaka General Medical Center, Osaka.

Shinya Ueda (S)

Department of Medical Oncology, Kindai University Nara Hospital, Nara.

Hitoshi Kusaba (H)

Department of Hematology, Oncology and Cardiovascular Medicine, Kyushu University Hospital, Fukuoka.

Shu Okamura (S)

Department of Surgery, Suita Municipal Hospital, Suita.

Masahiro Tsuda (M)

Department of Gastroenterological Oncology, Hyogo Cancer Center, Hyogo.

Takao Tamura (T)

Department of Medical Oncology, Kindai University Faculty of Medicine, Osakasayama.

Katsunori Shinozaki (K)

Division of Clinical Oncology, Hiroshima Prefectural Hospital, Hiroshima.

Takahiro Tsushima (T)

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka.

Takashi Tsuda (T)

Department of Clinical Oncology, St Marianna University School of Medicine, Kawasaki.

Tsuyoshi Shirakawa (T)

Department of Chemotherapy, Miyazaki Prefectural Miyazaki Hospital, Miyazaki.

Haruhiro Yamashita (H)

Department of Clinical Oncology, National Hospital Organization, Okayama Medical Center, Okayama.

Satoshi Morita (S)

Department of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine, Kyoto.

Shuichi Hironaka (S)

Department of Medical Oncology and Hematology, Oita University Faculty of Medicine, Yufu.

Kei Muro (K)

Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.

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Classifications MeSH