A Phase II Study of Cisplatin Plus Gemcitabine followed by Maintenance Gemcitabine for Advanced Squamous Non-Small-Cell Lung Cancer: Kyoto Thoracic Oncology Research Group 1302

Background: There has been no study so far on gemcitabine continuous maintenance therapy targeting only squamous non-small-cell lung cancer (NSCLC) patients. This study aimed to assess the efficacy and safety of cisplatin plus gemcitabine followed by maintenance gemcitabine for chemotherapy- naïve J...

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Veröffentlicht in:Oncology 2019-12, Vol.97 (6), p.327-333
Hauptverfasser: Ikeda, Satoshi, Yoshioka, Hiroshige, Kaneda, Toshihiko, Yokoyama, Toshihide, Niwa, Takashi, Sone, Naoyuki, Ishida, Tadashi, Morita, Mitsunori, Tomioka, Hiromi, Komaki, Chihito, Hirabayashi, Masataka, Hasegawa, Yoshinori, Noguchi, Tetsuo, Nakano, Yasutaka, Sakaguchi, Chikara, Yoshimura, Kenichi, Hirai, Toyohiro
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container_end_page 333
container_issue 6
container_start_page 327
container_title Oncology
container_volume 97
creator Ikeda, Satoshi
Yoshioka, Hiroshige
Kaneda, Toshihiko
Yokoyama, Toshihide
Niwa, Takashi
Sone, Naoyuki
Ishida, Tadashi
Morita, Mitsunori
Tomioka, Hiromi
Komaki, Chihito
Hirabayashi, Masataka
Hasegawa, Yoshinori
Noguchi, Tetsuo
Nakano, Yasutaka
Sakaguchi, Chikara
Yoshimura, Kenichi
Hirai, Toyohiro
description Background: There has been no study so far on gemcitabine continuous maintenance therapy targeting only squamous non-small-cell lung cancer (NSCLC) patients. This study aimed to assess the efficacy and safety of cisplatin plus gemcitabine followed by maintenance gemcitabine for chemotherapy- naïve Japanese patients with advanced squamous NSCLC. Methods: The patients received 4 cycles of gemcitabine (1,000 mg/m 2 , days 1 and 8) and cisplatin (80 mg/m 2 , day 1) every 3 weeks, followed by gemcitabine alone as maintenance therapy every 3 weeks until disease progression or unacceptable toxicity. The primary end point of the study was progression-free survival (PFS) from the date of registration. Results: From May 2013 to October 2018, 26 patients were enrolled, and 25 patients received ≥1 cycle of planned treatment. Eighteen patients (69.2%) received 4 cycles of cisplatin plus gemcitabine, and 16 patients (61.5%) received ≥1 cycle of maintenance gemcitabine. The median PFS from the date of registration was 5.3 months (95% CI 2.9–7.3 months). In 16 patients who received ≥1 cycle of maintenance gemcitabine, the median PFS from the date of maintenance gemcitabine initiation was 3.8 months (95% CI 2.3–5.2 months). Their median overall survival from the date of registration was 11.9 months (95% CI 7.5–26.5 months). During the maintenance therapy, adverse events (AEs) were mostly Common Terminology Criteria for AE grade 1. Conclusions: While this trial did not meet the primary endpoint, the sufficient efficacy and feasibility of gemcitabine maintenance therapy were suggested.
doi_str_mv 10.1159/000501967
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This study aimed to assess the efficacy and safety of cisplatin plus gemcitabine followed by maintenance gemcitabine for chemotherapy- naïve Japanese patients with advanced squamous NSCLC. Methods: The patients received 4 cycles of gemcitabine (1,000 mg/m 2 , days 1 and 8) and cisplatin (80 mg/m 2 , day 1) every 3 weeks, followed by gemcitabine alone as maintenance therapy every 3 weeks until disease progression or unacceptable toxicity. The primary end point of the study was progression-free survival (PFS) from the date of registration. Results: From May 2013 to October 2018, 26 patients were enrolled, and 25 patients received ≥1 cycle of planned treatment. Eighteen patients (69.2%) received 4 cycles of cisplatin plus gemcitabine, and 16 patients (61.5%) received ≥1 cycle of maintenance gemcitabine. The median PFS from the date of registration was 5.3 months (95% CI 2.9–7.3 months). In 16 patients who received ≥1 cycle of maintenance gemcitabine, the median PFS from the date of maintenance gemcitabine initiation was 3.8 months (95% CI 2.3–5.2 months). Their median overall survival from the date of registration was 11.9 months (95% CI 7.5–26.5 months). During the maintenance therapy, adverse events (AEs) were mostly Common Terminology Criteria for AE grade 1. Conclusions: While this trial did not meet the primary endpoint, the sufficient efficacy and feasibility of gemcitabine maintenance therapy were suggested.</description><identifier>ISSN: 0030-2414</identifier><identifier>EISSN: 1423-0232</identifier><identifier>DOI: 10.1159/000501967</identifier><identifier>PMID: 31412347</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - mortality ; Chemotherapy, Combination ; Cisplatin ; Cisplatin - administration &amp; dosage ; Cisplatin - adverse effects ; Clinical Study ; Deoxycytidine - administration &amp; dosage ; Deoxycytidine - adverse effects ; Deoxycytidine - analogs &amp; derivatives ; Development and progression ; Drug therapy ; Gemcitabine ; Humans ; Lung cancer, Non-small cell ; Lung Neoplasms - drug therapy ; Lung Neoplasms - mortality ; Male ; Methods ; Middle Aged ; Patient outcomes</subject><ispartof>Oncology, 2019-12, Vol.97 (6), p.327-333</ispartof><rights>2019 S. Karger AG, Basel</rights><rights>2019 S. Karger AG, Basel.</rights><rights>COPYRIGHT 2019 S. Karger AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-fdf93ff34cb81ccafb7ac5cf9e4585e824721ecfd0a57e71b757133249d8f6d53</citedby><orcidid>0000-0001-5203-7911 ; 0000-0001-7724-0481</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2423,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31412347$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikeda, Satoshi</creatorcontrib><creatorcontrib>Yoshioka, Hiroshige</creatorcontrib><creatorcontrib>Kaneda, Toshihiko</creatorcontrib><creatorcontrib>Yokoyama, Toshihide</creatorcontrib><creatorcontrib>Niwa, Takashi</creatorcontrib><creatorcontrib>Sone, Naoyuki</creatorcontrib><creatorcontrib>Ishida, Tadashi</creatorcontrib><creatorcontrib>Morita, Mitsunori</creatorcontrib><creatorcontrib>Tomioka, Hiromi</creatorcontrib><creatorcontrib>Komaki, Chihito</creatorcontrib><creatorcontrib>Hirabayashi, Masataka</creatorcontrib><creatorcontrib>Hasegawa, Yoshinori</creatorcontrib><creatorcontrib>Noguchi, Tetsuo</creatorcontrib><creatorcontrib>Nakano, Yasutaka</creatorcontrib><creatorcontrib>Sakaguchi, Chikara</creatorcontrib><creatorcontrib>Yoshimura, Kenichi</creatorcontrib><creatorcontrib>Hirai, Toyohiro</creatorcontrib><title>A Phase II Study of Cisplatin Plus Gemcitabine followed by Maintenance Gemcitabine for Advanced Squamous Non-Small-Cell Lung Cancer: Kyoto Thoracic Oncology Research Group 1302</title><title>Oncology</title><addtitle>Oncology</addtitle><description>Background: There has been no study so far on gemcitabine continuous maintenance therapy targeting only squamous non-small-cell lung cancer (NSCLC) patients. This study aimed to assess the efficacy and safety of cisplatin plus gemcitabine followed by maintenance gemcitabine for chemotherapy- naïve Japanese patients with advanced squamous NSCLC. Methods: The patients received 4 cycles of gemcitabine (1,000 mg/m 2 , days 1 and 8) and cisplatin (80 mg/m 2 , day 1) every 3 weeks, followed by gemcitabine alone as maintenance therapy every 3 weeks until disease progression or unacceptable toxicity. The primary end point of the study was progression-free survival (PFS) from the date of registration. Results: From May 2013 to October 2018, 26 patients were enrolled, and 25 patients received ≥1 cycle of planned treatment. Eighteen patients (69.2%) received 4 cycles of cisplatin plus gemcitabine, and 16 patients (61.5%) received ≥1 cycle of maintenance gemcitabine. The median PFS from the date of registration was 5.3 months (95% CI 2.9–7.3 months). In 16 patients who received ≥1 cycle of maintenance gemcitabine, the median PFS from the date of maintenance gemcitabine initiation was 3.8 months (95% CI 2.3–5.2 months). Their median overall survival from the date of registration was 11.9 months (95% CI 7.5–26.5 months). During the maintenance therapy, adverse events (AEs) were mostly Common Terminology Criteria for AE grade 1. 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This study aimed to assess the efficacy and safety of cisplatin plus gemcitabine followed by maintenance gemcitabine for chemotherapy- naïve Japanese patients with advanced squamous NSCLC. Methods: The patients received 4 cycles of gemcitabine (1,000 mg/m 2 , days 1 and 8) and cisplatin (80 mg/m 2 , day 1) every 3 weeks, followed by gemcitabine alone as maintenance therapy every 3 weeks until disease progression or unacceptable toxicity. The primary end point of the study was progression-free survival (PFS) from the date of registration. Results: From May 2013 to October 2018, 26 patients were enrolled, and 25 patients received ≥1 cycle of planned treatment. Eighteen patients (69.2%) received 4 cycles of cisplatin plus gemcitabine, and 16 patients (61.5%) received ≥1 cycle of maintenance gemcitabine. The median PFS from the date of registration was 5.3 months (95% CI 2.9–7.3 months). In 16 patients who received ≥1 cycle of maintenance gemcitabine, the median PFS from the date of maintenance gemcitabine initiation was 3.8 months (95% CI 2.3–5.2 months). Their median overall survival from the date of registration was 11.9 months (95% CI 7.5–26.5 months). During the maintenance therapy, adverse events (AEs) were mostly Common Terminology Criteria for AE grade 1. Conclusions: While this trial did not meet the primary endpoint, the sufficient efficacy and feasibility of gemcitabine maintenance therapy were suggested.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>31412347</pmid><doi>10.1159/000501967</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-5203-7911</orcidid><orcidid>https://orcid.org/0000-0001-7724-0481</orcidid></addata></record>
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source Karger Journals; MEDLINE
subjects Aged
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Carcinoma, Non-Small-Cell Lung - drug therapy
Carcinoma, Non-Small-Cell Lung - mortality
Chemotherapy, Combination
Cisplatin
Cisplatin - administration & dosage
Cisplatin - adverse effects
Clinical Study
Deoxycytidine - administration & dosage
Deoxycytidine - adverse effects
Deoxycytidine - analogs & derivatives
Development and progression
Drug therapy
Gemcitabine
Humans
Lung cancer, Non-small cell
Lung Neoplasms - drug therapy
Lung Neoplasms - mortality
Male
Methods
Middle Aged
Patient outcomes
title A Phase II Study of Cisplatin Plus Gemcitabine followed by Maintenance Gemcitabine for Advanced Squamous Non-Small-Cell Lung Cancer: Kyoto Thoracic Oncology Research Group 1302
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