Evidence map›Paper›PMID 30425180›Full record

Trial reportThe oncologist2019

aCGH Analysis of Predictive Biomarkers for Response to Bevacizumab plus Oxaliplatin- or Irinotecan-Based Chemotherapy in Patients with Metastatic Colorectal Cancer.

Yoshihiko Fujita, Masataka Taguri, Kentaro Yamazaki, Junji Tsurutani, Kazuko Sakai, Takahiro Tsushima, Michitaka Nagase, Hiroshi Tamagawa, Shinya Ueda, Takao Tamura and 21 more

Open access · bronzeAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in The oncologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
0.3field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 2 syntheses or guidelines pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors at 20 institutions in 1 country.

Yoshihiko FujitaDepartment of Genome Biology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Masataka TaguriDepartment of Biostatistics, Yokohama City University School of Medicine, Japan.
Kentaro YamazakiDivision of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Junji TsurutaniDepartment of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Kazuko SakaiDepartment of Genome Biology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Takahiro TsushimaDivision of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
Michitaka NagaseDepartment of Clinical Oncology, Jichi Medical University, Shimotsuke, Japan.
Hiroshi TamagawaDepartment of Surgery, Osaka General Medical Center, Osaka, Japan.
Shinya UedaDepartment of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Takao TamuraDepartment of Medical Oncology, Nara Hospital Kindai University Faculty of Medicine, Ikoma, Japan.
Yasushi TsujiDepartment of Medical Oncology, Tonan Hospital, Sapporo, Japan.
Kohei MurataDepartment of Surgery, Suita Municipal Hospital, Suita, Japan.
Koichi TairaDepartment of Clinical Oncology, Osaka City General Hospital, Osaka, Japan.
Tadamichi DendaDivision of Gastroenterology, Chiba Cancer Center, Chiba, Japan.
Toshikazu MoriwakiDivision of Gastroenterology, University of Tsukuba, Tsukuba, Japan.
Sadao FunaiDepartment of Surgery, Sakai Hospital Kindai University Faculty of Medicine, Sakai, Japan.
Takako Eguchi NakajimaDepartment of Clinical Oncology, St Marianna University School of Medicine, Kawasaki, Japan.
Kei MuroDepartment of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.
Akihito TsujiDepartment of Medical Oncology, Kochi Health Sciences Center, Kochi, Japan.
Motoki YoshidaDivision of Cancer Chemotherapy Center, Osaka Medical College Hospital, Takatsuki, Japan.
Koichi SuyamaDepartment of Medical Oncology, Toranomon Hospital, Tokyo, Japan.
Takuya KurimotoDepartment of Gastrointestinal Oncology, Nagoya Kyoritsu Hospital, Nagoya, Japan.
Naotoshi SugimotoDepartment of Clinical Oncology, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Japan.
Eishi BabaDepartment of Comprehensive Clinical Oncology, Kyushu University Faculty of Medical Sciences, Fukuoka, Japan.
Nobuhiko SekiDivision of Medical Oncology, Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan.
Mikio SatoDepartment of Gastroenterology and Hepatology, Ryugasaki Saiseikai Hospital, Ryugasaki, Japan.
Takaya ShimuraDepartment of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Narikazu BokuDepartment of Clinical Oncology, St Marianna University School of Medicine, Kawasaki, Japan.
Ichinosuke HyodoDivision of Gastroenterology, University of Tsukuba, Tsukuba, Japan.
Takeharu YamanakaDepartment of Biostatistics, Yokohama City University School of Medicine, Japan.
Kazuto NishioDepartment of Genome Biology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan knishio@med.kindai.ac.jp.
Kindai University · JPShizuoka Cancer Center · JPSt. Marianna University School of Medicine · JPUniversity of Tsukuba · JPYokohama City University · JPAichi Cancer Center · JPChiba Cancer Center · JPHiroshima Kyoritsu Hospital · JPJichi Medical University · JPKindai University Sakai Hospital · JPKochi Medical School Hospital · JPKyushu University · JPNagoya City University · JPNara Medical University Hospital · JPOsaka City General Hospital · JPOsaka Medical and Pharmaceutical University · JPOsaka Medical Center for Cancer and Cardiovascular Diseases · JPOsaka Prefectural Medical Center · JPSuita Municipal Hospital · JPTeikyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe randomized phase III study (WJOG4407G) showed equivalent efficacy between FOLFOX and FOLFIRI in combination with bevacizumab as the first-line treatment for metastatic colorectal cancer (mCRC). We studied whole genome copy number profiles using array-based comparative genomic hybridization (aCGH) analysis of tumor tissue samples obtained in this study. The aim of this study was to identify gene copy number alterations that could aid in selecting either FOLFOX or FOLFIRI in combination with bevacizumab for patients with mCRC. MATERIALS AND

methodsDNA was purified from 154 pretreatment formalin-fixed paraffin-embedded tissue samples (75 from the FOLFOX arm and 79 from the FOLFIRI arm) of 395 patients enrolled in the WJOG4407G trial and analyzed by aCGH. Genomic regions greater than 1.2-fold were regarded as copy number gain (CNG).

resultsPatient characteristics between the treatment arms were well balanced except for tumor laterality (left side; 64% in FOLFOX arm and 80% in FOLFIRI arm,

conclusionChromosome 8q24.1-q24.2 may contain genes that could potentially serve as predictive markers for selecting either FOLFOX or FOLFIRI in combination with bevacizumab for treatment of patients with mCRC. IMPLICATIONS FOR PRACTICE: Bevacizumab has been used as a standard first-line treatment for patients with metastatic colorectal cancer (mCRC) in combination with either oxaliplatin-based or irinotecan-based chemotherapy. Until now, there has been no predictive marker to choose between the two combination chemotherapies. This array-based comparative genomic hybridization analysis revealed that the difference in therapeutic effect between the two combination chemotherapies is prominent in patients with mCRC with gene copy number gain in chromosome 8p24.1-p24.2. Such patients showed more favorable response and survival when treated with irinotecan-based combination chemotherapy. Overlapping genes commonly found in this region may be predictive biomarkers of the efficacy of the combination chemotherapy with bevacizumab.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBevacizumabBiomarkersColorectal NeoplasmsComparative Genomic HybridizationFemaleHumansIrinotecanMaleMiddle AgedNeoplasm MetastasisOxaliplatinPrognosisSurvival AnalysisBevacizumabBiomarkersIrinotecanOxaliplatinaCGH analysisBevacizumabColorectal cancerIrinotecanOxaliplatin

Identifiers

PMID30425180
PMCPMC6519767
OpenAlexW2901770604

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.