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...
Gespeichert in:
Veröffentlicht in: | Oncology 2019-12, Vol.97 (6), p.327-333 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>gale_karge</sourceid><recordid>TN_cdi_gale_healthsolutions_A643566482</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A643566482</galeid><sourcerecordid>A643566482</sourcerecordid><originalsourceid>FETCH-LOGICAL-c432t-fdf93ff34cb81ccafb7ac5cf9e4585e824721ecfd0a57e71b757133249d8f6d53</originalsourceid><addsrcrecordid>eNpt0s-LEzEUB_BBFLeuHryLBATRw6z5NZPWWxnWWqx2set5yCQvbTSTdJOZlf5X_olOaa2uLDkEHp_3ki-8LHtO8AUhxeQdxrjAZFKKB9mIcMpyTBl9mI0wZjinnPCz7ElK3wcmCl4-zs4Y4YQyLkbZrym62sgEaD5Hq67XOxQMqmzaOtlZj65cn9AMWmU72VgPyATnwk_QqNmhz9L6Drz0Cv4zEU317b6u0eqml20YpnwJPl-10rm8AufQovdrVO1NfI8-7UIX0PUmRKmsQkuvggvrHfoKCWRUGzSLod8iwjB9mj0y0iV4drzPs28fLq-rj_liOZtX00WuOKNdbrSZMGMYV82YKCVNI6QqlJkAL8YFjCkXlIAyGstCgCCNKARhjPKJHptSF-w8e3OYu43hpofU1a1Navi59DDEqSkVTBQloXv66kDX0kFtvQndkGPP62nJWVGWfEwHdXGPGo6G1qrgwdihfqfh9T8NG5Cu26Tg-s4Gn-7CtweoYkgpgqm30bYy7mqC6_2C1KcFGezLY6y-aUGf5J-N-Bvmh4xriCewrBaHEfVWm0G9uFcdX_kN7VnJCQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2273756125</pqid></control><display><type>article</type><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><source>Karger Journals</source><source>MEDLINE</source><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</creator><creatorcontrib>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</creatorcontrib><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.</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 & 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</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. Conclusions: While this trial did not meet the primary endpoint, the sufficient efficacy and feasibility of gemcitabine maintenance therapy were suggested.</description><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - mortality</subject><subject>Chemotherapy, Combination</subject><subject>Cisplatin</subject><subject>Cisplatin - administration & dosage</subject><subject>Cisplatin - adverse effects</subject><subject>Clinical Study</subject><subject>Deoxycytidine - administration & dosage</subject><subject>Deoxycytidine - adverse effects</subject><subject>Deoxycytidine - analogs & derivatives</subject><subject>Development and progression</subject><subject>Drug therapy</subject><subject>Gemcitabine</subject><subject>Humans</subject><subject>Lung cancer, Non-small cell</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - mortality</subject><subject>Male</subject><subject>Methods</subject><subject>Middle Aged</subject><subject>Patient outcomes</subject><issn>0030-2414</issn><issn>1423-0232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0s-LEzEUB_BBFLeuHryLBATRw6z5NZPWWxnWWqx2set5yCQvbTSTdJOZlf5X_olOaa2uLDkEHp_3ki-8LHtO8AUhxeQdxrjAZFKKB9mIcMpyTBl9mI0wZjinnPCz7ElK3wcmCl4-zs4Y4YQyLkbZrym62sgEaD5Hq67XOxQMqmzaOtlZj65cn9AMWmU72VgPyATnwk_QqNmhz9L6Drz0Cv4zEU317b6u0eqml20YpnwJPl-10rm8AufQovdrVO1NfI8-7UIX0PUmRKmsQkuvggvrHfoKCWRUGzSLod8iwjB9mj0y0iV4drzPs28fLq-rj_liOZtX00WuOKNdbrSZMGMYV82YKCVNI6QqlJkAL8YFjCkXlIAyGstCgCCNKARhjPKJHptSF-w8e3OYu43hpofU1a1Navi59DDEqSkVTBQloXv66kDX0kFtvQndkGPP62nJWVGWfEwHdXGPGo6G1qrgwdihfqfh9T8NG5Cu26Tg-s4Gn-7CtweoYkgpgqm30bYy7mqC6_2C1KcFGezLY6y-aUGf5J-N-Bvmh4xriCewrBaHEfVWm0G9uFcdX_kN7VnJCQ</recordid><startdate>20191201</startdate><enddate>20191201</enddate><creator>Ikeda, Satoshi</creator><creator>Yoshioka, Hiroshige</creator><creator>Kaneda, Toshihiko</creator><creator>Yokoyama, Toshihide</creator><creator>Niwa, Takashi</creator><creator>Sone, Naoyuki</creator><creator>Ishida, Tadashi</creator><creator>Morita, Mitsunori</creator><creator>Tomioka, Hiromi</creator><creator>Komaki, Chihito</creator><creator>Hirabayashi, Masataka</creator><creator>Hasegawa, Yoshinori</creator><creator>Noguchi, Tetsuo</creator><creator>Nakano, Yasutaka</creator><creator>Sakaguchi, Chikara</creator><creator>Yoshimura, Kenichi</creator><creator>Hirai, Toyohiro</creator><general>S. Karger AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5203-7911</orcidid><orcidid>https://orcid.org/0000-0001-7724-0481</orcidid></search><sort><creationdate>20191201</creationdate><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><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-fdf93ff34cb81ccafb7ac5cf9e4585e824721ecfd0a57e71b757133249d8f6d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - mortality</topic><topic>Chemotherapy, Combination</topic><topic>Cisplatin</topic><topic>Cisplatin - administration & dosage</topic><topic>Cisplatin - adverse effects</topic><topic>Clinical Study</topic><topic>Deoxycytidine - administration & dosage</topic><topic>Deoxycytidine - adverse effects</topic><topic>Deoxycytidine - analogs & derivatives</topic><topic>Development and progression</topic><topic>Drug therapy</topic><topic>Gemcitabine</topic><topic>Humans</topic><topic>Lung cancer, Non-small cell</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - mortality</topic><topic>Male</topic><topic>Methods</topic><topic>Middle Aged</topic><topic>Patient outcomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ikeda, Satoshi</au><au>Yoshioka, Hiroshige</au><au>Kaneda, Toshihiko</au><au>Yokoyama, Toshihide</au><au>Niwa, Takashi</au><au>Sone, Naoyuki</au><au>Ishida, Tadashi</au><au>Morita, Mitsunori</au><au>Tomioka, Hiromi</au><au>Komaki, Chihito</au><au>Hirabayashi, Masataka</au><au>Hasegawa, Yoshinori</au><au>Noguchi, Tetsuo</au><au>Nakano, Yasutaka</au><au>Sakaguchi, Chikara</au><au>Yoshimura, Kenichi</au><au>Hirai, Toyohiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Oncology</jtitle><addtitle>Oncology</addtitle><date>2019-12-01</date><risdate>2019</risdate><volume>97</volume><issue>6</issue><spage>327</spage><epage>333</epage><pages>327-333</pages><issn>0030-2414</issn><eissn>1423-0232</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 0030-2414 |
ispartof | Oncology, 2019-12, Vol.97 (6), p.327-333 |
issn | 0030-2414 1423-0232 |
language | eng |
recordid | cdi_gale_healthsolutions_A643566482 |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T18%3A08%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_karge&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Phase%20II%20Study%20of%20Cisplatin%20Plus%20Gemcitabine%20followed%20by%20Maintenance%20Gemcitabine%20for%20Advanced%20Squamous%20Non-Small-Cell%20Lung%20Cancer:%20Kyoto%20Thoracic%20Oncology%20Research%20Group%201302&rft.jtitle=Oncology&rft.au=Ikeda,%20Satoshi&rft.date=2019-12-01&rft.volume=97&rft.issue=6&rft.spage=327&rft.epage=333&rft.pages=327-333&rft.issn=0030-2414&rft.eissn=1423-0232&rft_id=info:doi/10.1159/000501967&rft_dat=%3Cgale_karge%3EA643566482%3C/gale_karge%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2273756125&rft_id=info:pmid/31412347&rft_galeid=A643566482&rfr_iscdi=true |