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 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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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 |
Author_xml | – sequence: 1 givenname: Taroh surname: Satoh fullname: Satoh, Taroh organization: Medical Oncology, Kinki University Faculty of Medicine – sequence: 2 givenname: Kyung Hee surname: Lee fullname: Lee, Kyung Hee organization: Hemato-Oncology, Internal Medicine, Yeungnam University Hospital – sequence: 3 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 – sequence: 4 givenname: Yasutsuna surname: Sasaki fullname: Sasaki, Yasutsuna organization: Medical Oncology, Saitama Medical University International Medical Center – sequence: 5 givenname: Se Hoon surname: Park fullname: Park, Se Hoon organization: Division of Hematology-Oncology, Department of Medicine, Sungkyunkwan University Samsung Medical Center – sequence: 6 givenname: Yoshito surname: Komatsu fullname: Komatsu, Yoshito organization: Division of Cancer Chemotherapy, Hokkaido University Hospital – sequence: 7 givenname: Hirofumi surname: Yasui fullname: Yasui, Hirofumi organization: Division of GI Oncology, Shizuoka Cancer Center – sequence: 8 givenname: Tae-You surname: Kim fullname: Kim, Tae-You organization: Hematology-Oncology, Internal Medicine, Seoul National University Hospital – sequence: 9 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 |
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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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Keywords | Irinotecan Anti-EGFR Advanced gastric cancer Nimotuzumab Second-line therapy |
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PublicationTitle | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association |
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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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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 |
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