Randomized phase II trial of nimotuzumab plus irinotecan versus irinotecan alone as second-line therapy for patients with advanced gastric cancer

Background This multicenter, randomized phase II trial was conducted to compare the efficacy and safety of nimotuzumab plus irinotecan (N-IRI) versus irinotecan alone (IRI) in patients with advanced gastric cancer (AGC) showing disease progression after previous 5-fluorouracil-based therapy. Methods...

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Published in:Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association Vol. 18; no. 4; pp. 824 - 832
Main Authors: Satoh, Taroh, Lee, Kyung Hee, Rha, Sun Young, Sasaki, Yasutsuna, Park, Se Hoon, Komatsu, Yoshito, Yasui, Hirofumi, Kim, Tae-You, Yamaguchi, Kensei, Fuse, Nozomu, Yamada, Yasuhide, Ura, Takashi, Kim, Si-Young, Munakata, Masaki, Saitoh, Soh, Nishio, Kazuto, Morita, Satoshi, Yamamoto, Eriko, Zhang, Qingwei, Kim, Jung-mi, Kim, Yeul Hong, Sakata, Yuh
Format: Journal Article
Language:English
Published: Tokyo Springer Japan 01-10-2015
Springer Nature B.V
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Abstract Background This multicenter, randomized phase II trial was conducted to compare the efficacy and safety of nimotuzumab plus irinotecan (N-IRI) versus irinotecan alone (IRI) in patients with advanced gastric cancer (AGC) showing disease progression after previous 5-fluorouracil-based therapy. Methods Irinotecan-naive patients ( n  = 82) received N-IRI (nimotuzumab 400 mg weekly plus irinotecan 150 mg/m 2 biweekly) or IRI (irinotecan 150 mg/m 2 biweekly) until disease progression. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were overall survival (OS), response rate (RR), safety, tolerability, and the correlation between efficacy and tumor epidermal growth factor receptor (EGFR) expression. Results Of 83 patients, 40 and 43 patients were randomly assigned to the N-IRI and IRI groups, respectively. In the N-IRI/IRI treatment group, median PFS was 73.0/85.0 days ( P  = 0.5668), and median OS and RR at 18 months were 250.5/232.0 days ( P  = 0.9778) and 18.4/10.3 %, respectively. Median PFS and OS in the EGFR 2+/3+ subgroups were 118.5/59.0 and 358.5/229.5 days, respectively. The RR was 33.3/0.0 % in the N-IRI/IRI treatment group. The incidence of grade 3 or higher adverse events was 77.5/64.3 %. No adverse events of grade 3 or higher skin rash or grade 3 or higher infusion-related reaction were reported. Conclusions There was no superiority of N-IRI over IRI alone in terms of PFS in 5-fluorouracil-refractory AGC patients. However, N-IRI showed potential improvement in the EGFR 2+/3+ subgroup based on improved RR, PFS, and OS.
AbstractList Background This multicenter, randomized phase II trial was conducted to compare the efficacy and safety of nimotuzumab plus irinotecan (N-IRI) versus irinotecan alone (IRI) in patients with advanced gastric cancer (AGC) showing disease progression after previous 5-fluorouracil-based therapy. Methods Irinotecan-naive patients ( n  = 82) received N-IRI (nimotuzumab 400 mg weekly plus irinotecan 150 mg/m 2 biweekly) or IRI (irinotecan 150 mg/m 2 biweekly) until disease progression. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were overall survival (OS), response rate (RR), safety, tolerability, and the correlation between efficacy and tumor epidermal growth factor receptor (EGFR) expression. Results Of 83 patients, 40 and 43 patients were randomly assigned to the N-IRI and IRI groups, respectively. In the N-IRI/IRI treatment group, median PFS was 73.0/85.0 days ( P  = 0.5668), and median OS and RR at 18 months were 250.5/232.0 days ( P  = 0.9778) and 18.4/10.3 %, respectively. Median PFS and OS in the EGFR 2+/3+ subgroups were 118.5/59.0 and 358.5/229.5 days, respectively. The RR was 33.3/0.0 % in the N-IRI/IRI treatment group. The incidence of grade 3 or higher adverse events was 77.5/64.3 %. No adverse events of grade 3 or higher skin rash or grade 3 or higher infusion-related reaction were reported. Conclusions There was no superiority of N-IRI over IRI alone in terms of PFS in 5-fluorouracil-refractory AGC patients. However, N-IRI showed potential improvement in the EGFR 2+/3+ subgroup based on improved RR, PFS, and OS.
This multicenter, randomized phase II trial was conducted to compare the efficacy and safety of nimotuzumab plus irinotecan (N-IRI) versus irinotecan alone (IRI) in patients with advanced gastric cancer (AGC) showing disease progression after previous 5-fluorouracil-based therapy. Irinotecan-naive patients (n = 82) received N-IRI (nimotuzumab 400 mg weekly plus irinotecan 150 mg/m(2) biweekly) or IRI (irinotecan 150 mg/m(2) biweekly) until disease progression. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were overall survival (OS), response rate (RR), safety, tolerability, and the correlation between efficacy and tumor epidermal growth factor receptor (EGFR) expression. Of 83 patients, 40 and 43 patients were randomly assigned to the N-IRI and IRI groups, respectively. In the N-IRI/IRI treatment group, median PFS was 73.0/85.0 days (P = 0.5668), and median OS and RR at 18 months were 250.5/232.0 days (P = 0.9778) and 18.4/10.3 %, respectively. Median PFS and OS in the EGFR 2+/3+ subgroups were 118.5/59.0 and 358.5/229.5 days, respectively. The RR was 33.3/0.0 % in the N-IRI/IRI treatment group. The incidence of grade 3 or higher adverse events was 77.5/64.3 %. No adverse events of grade 3 or higher skin rash or grade 3 or higher infusion-related reaction were reported. There was no superiority of N-IRI over IRI alone in terms of PFS in 5-fluorouracil-refractory AGC patients. However, N-IRI showed potential improvement in the EGFR 2+/3+ subgroup based on improved RR, PFS, and OS.
Background This multicenter, randomized phase II trial was conducted to compare the efficacy and safety of nimotuzumab plus irinotecan (N-IRI) versus irinotecan alone (IRI) in patients with advanced gastric cancer (AGC) showing disease progression after previous 5-fluorouracil-based therapy. Methods Irinotecan-naive patients (n = 82) received N-IRI (nimotuzumab 400 mg weekly plus irinotecan 150 mg/m^sup 2^ biweekly) or IRI (irinotecan 150 mg/m^sup 2^ biweekly) until disease progression. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were overall survival (OS), response rate (RR), safety, tolerability, and the correlation between efficacy and tumor epidermal growth factor receptor (EGFR) expression. Results Of 83 patients, 40 and 43 patients were randomly assigned to the N-IRI and IRI groups, respectively. In the N-IRI/IRI treatment group, median PFS was 73.0/85.0 days (P = 0.5668), and median OS and RR at 18 months were 250.5/232.0 days (P = 0.9778) and 18.4/10.3 %, respectively. Median PFS and OS in the EGFR 2+/3+ subgroups were 118.5/59.0 and 358.5/229.5 days, respectively. The RR was 33.3/0.0 % in the N-IRI/IRI treatment group. The incidence of grade 3 or higher adverse events was 77.5/64.3 %. No adverse events of grade 3 or higher skin rash or grade 3 or higher infusion-related reaction were reported. Conclusions There was no superiority of N-IRI over IRI alone in terms of PFS in 5-fluorouracil-refractory AGC patients. However, N-IRI showed potential improvement in the EGFR 2+/3+ subgroup based on improved RR, PFS, and OS.
Author Satoh, Taroh
Kim, Si-Young
Yamamoto, Eriko
Komatsu, Yoshito
Lee, Kyung Hee
Sasaki, Yasutsuna
Ura, Takashi
Rha, Sun Young
Zhang, Qingwei
Yasui, Hirofumi
Park, Se Hoon
Nishio, Kazuto
Morita, Satoshi
Munakata, Masaki
Yamaguchi, Kensei
Yamada, Yasuhide
Fuse, Nozomu
Kim, Yeul Hong
Kim, Tae-You
Kim, Jung-mi
Sakata, Yuh
Saitoh, Soh
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  givenname: Taroh
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  organization: Medical Oncology, Kinki University Faculty of Medicine
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  givenname: Kyung Hee
  surname: Lee
  fullname: Lee, Kyung Hee
  organization: Hemato-Oncology, Internal Medicine, Yeungnam University Hospital
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  givenname: Sun Young
  surname: Rha
  fullname: Rha, Sun Young
  organization: Medical Oncology, Internal Medicine, Yonsei Cancer Center, Yonsei Cancer Research Institute, Yonsei University College of Medicine
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  givenname: Yasutsuna
  surname: Sasaki
  fullname: Sasaki, Yasutsuna
  organization: Medical Oncology, Saitama Medical University International Medical Center
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  givenname: Se Hoon
  surname: Park
  fullname: Park, Se Hoon
  organization: Division of Hematology-Oncology, Department of Medicine, Sungkyunkwan University Samsung Medical Center
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  givenname: Yoshito
  surname: Komatsu
  fullname: Komatsu, Yoshito
  organization: Division of Cancer Chemotherapy, Hokkaido University Hospital
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  surname: Yasui
  fullname: Yasui, Hirofumi
  organization: Division of GI Oncology, Shizuoka Cancer Center
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  surname: Kim
  fullname: Kim, Tae-You
  organization: Hematology-Oncology, Internal Medicine, Seoul National University Hospital
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  givenname: Kensei
  surname: Yamaguchi
  fullname: Yamaguchi, Kensei
  organization: Department of Gastroenterology, Saitama Cancer Center
– sequence: 10
  givenname: Nozomu
  surname: Fuse
  fullname: Fuse, Nozomu
  organization: Gastrointestinal Oncology, National Cancer Center Hospital East
– sequence: 11
  givenname: Yasuhide
  surname: Yamada
  fullname: Yamada, Yasuhide
  organization: Gastrointestinal Oncology, National Cancer Center Hospital
– sequence: 12
  givenname: Takashi
  surname: Ura
  fullname: Ura, Takashi
  organization: Department of Clinical Oncology, Aichi Cancer Center Hospital
– sequence: 13
  givenname: Si-Young
  surname: Kim
  fullname: Kim, Si-Young
  organization: Department of Medical Oncology and Hematology, Kyung Hee University Hospital
– sequence: 14
  givenname: Masaki
  surname: Munakata
  fullname: Munakata, Masaki
  organization: Internal Medicine, Misawa Municipal Hospital
– sequence: 15
  givenname: Soh
  surname: Saitoh
  fullname: Saitoh, Soh
  organization: Medical Oncology and Gastroenterology, Aomori Prefectural Central Hospital
– sequence: 16
  givenname: Kazuto
  surname: Nishio
  fullname: Nishio, Kazuto
  organization: Department of Genome Biology, Kinki University School of Medicine
– sequence: 17
  givenname: Satoshi
  surname: Morita
  fullname: Morita, Satoshi
  organization: Department of Biostatics and Epidemiology, Yokohama City University
– sequence: 18
  givenname: Eriko
  surname: Yamamoto
  fullname: Yamamoto, Eriko
  organization: Clinical Development Department II, Daiichi Sankyo Co., Ltd
– sequence: 19
  givenname: Qingwei
  surname: Zhang
  fullname: Zhang, Qingwei
  organization: Clinical Data and Biostatistics Department, Daiichi Sankyo Co., Ltd
– sequence: 20
  givenname: Jung-mi
  surname: Kim
  fullname: Kim, Jung-mi
  organization: Medical and Regulatory Affairs Department, Kuhnil Pharm. Co., Ltd
– sequence: 21
  givenname: Yeul Hong
  surname: Kim
  fullname: Kim, Yeul Hong
  email: yhk0215@korea.ac.kr
  organization: Department of Internal Medicine, Section of Hemato-Oncology, Korea University Anam Hospital
– sequence: 22
  givenname: Yuh
  surname: Sakata
  fullname: Sakata, Yuh
  organization: Internal Medicine, Misawa Municipal Hospital
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25185971$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright The Author(s) 2014
The International Gastric Cancer Association and The Japanese Gastric Cancer Association 2015
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Issue 4
Keywords Irinotecan
Anti-EGFR
Advanced gastric cancer
Nimotuzumab
Second-line therapy
Language English
License Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
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OpenAccessLink http://link.springer.com/10.1007/s10120-014-0420-9
PMID 25185971
PQID 1712725188
PQPubID 43697
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ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_4572054
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crossref_primary_10_1007_s10120_014_0420_9
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PublicationDate 2015-10-01
PublicationDateYYYYMMDD 2015-10-01
PublicationDate_xml – month: 10
  year: 2015
  text: 2015-10-01
  day: 01
PublicationDecade 2010
PublicationPlace Tokyo
PublicationPlace_xml – name: Tokyo
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PublicationTitle Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association
PublicationTitleAbbrev Gastric Cancer
PublicationTitleAlternate Gastric Cancer
PublicationYear 2015
Publisher Springer Japan
Springer Nature B.V
Publisher_xml – name: Springer Japan
– name: Springer Nature B.V
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Snippet Background This multicenter, randomized phase II trial was conducted to compare the efficacy and safety of nimotuzumab plus irinotecan (N-IRI) versus...
This multicenter, randomized phase II trial was conducted to compare the efficacy and safety of nimotuzumab plus irinotecan (N-IRI) versus irinotecan alone...
Background This multicenter, randomized phase II trial was conducted to compare the efficacy and safety of nimotuzumab plus irinotecan (N-IRI) versus...
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StartPage 824
SubjectTerms Abdominal Surgery
Adenocarcinoma - drug therapy
Adenocarcinoma - genetics
Adenocarcinoma - mortality
Adult
Aged
Antibodies, Monoclonal, Humanized - administration & dosage
Antibodies, Monoclonal, Humanized - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Camptothecin - administration & dosage
Camptothecin - adverse effects
Camptothecin - analogs & derivatives
Cancer Research
Disease-Free Survival
DNA Mutational Analysis
Female
Gastric cancer
Gastroenterology
Genes, ras - genetics
Humans
Immunohistochemistry
In Situ Hybridization, Fluorescence
Kaplan-Meier Estimate
Male
Medicine
Medicine & Public Health
Middle Aged
Neoplasm Recurrence, Local - drug therapy
Neoplasm Recurrence, Local - genetics
Neoplasm Recurrence, Local - mortality
Oncology
Original
Original Article
Polymerase Chain Reaction
Receptor, Epidermal Growth Factor - biosynthesis
Receptor, Epidermal Growth Factor - genetics
Receptor, ErbB-2 - biosynthesis
Salvage Therapy - methods
Stomach Neoplasms - drug therapy
Stomach Neoplasms - genetics
Stomach Neoplasms - mortality
Surgical Oncology
Treatment Outcome
Title Randomized phase II trial of nimotuzumab plus irinotecan versus irinotecan alone as second-line therapy for patients with advanced gastric cancer
URI https://link.springer.com/article/10.1007/s10120-014-0420-9
https://www.ncbi.nlm.nih.gov/pubmed/25185971
https://www.proquest.com/docview/1712725188
https://pubmed.ncbi.nlm.nih.gov/PMC4572054
Volume 18
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