Randomized Phase II trial of paclitaxel and carboplatin followed by gemcitabine switch-maintenance therapy versus gemcitabine and carboplatin followed by gemcitabine continuation-maintenance therapy in previously untreated advanced non-small cell lung cancer

<p>Abstract</p> <p>Background</p> <p>In recent years, maintenance chemotherapy is increasingly being recognized as a new treatment strategy to improve the outcome of advanced non-small cell lung cancer (NSCLC). However, the optimal maintenance strategy is still controve...

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Main Authors: Minami Seigo, Kijima Takashi, Shiroyama Takayuki, Okafuji Kohei, Hirashima Tomonori, Uchida Junji, Imamura Fumio, Osaki Tadashi, Nakatani Takeshi, Ogata Yoshitaka, Yamamoto Suguru, Namba Yoshinobu, Otsuka Tomoyuki, Tachibana Isao, Komuta Kiyoshi, Kawase Ichiro
Format: Article
Language:English
Published: BMC 2013-01-01
Series:BMC Research Notes
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Online Access:http://www.biomedcentral.com/1756-0500/6/3
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author Minami Seigo
Kijima Takashi
Shiroyama Takayuki
Okafuji Kohei
Hirashima Tomonori
Uchida Junji
Imamura Fumio
Osaki Tadashi
Nakatani Takeshi
Ogata Yoshitaka
Yamamoto Suguru
Namba Yoshinobu
Otsuka Tomoyuki
Tachibana Isao
Komuta Kiyoshi
Kawase Ichiro
author_facet Minami Seigo
Kijima Takashi
Shiroyama Takayuki
Okafuji Kohei
Hirashima Tomonori
Uchida Junji
Imamura Fumio
Osaki Tadashi
Nakatani Takeshi
Ogata Yoshitaka
Yamamoto Suguru
Namba Yoshinobu
Otsuka Tomoyuki
Tachibana Isao
Komuta Kiyoshi
Kawase Ichiro
author_sort Minami Seigo
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>In recent years, maintenance chemotherapy is increasingly being recognized as a new treatment strategy to improve the outcome of advanced non-small cell lung cancer (NSCLC). However, the optimal maintenance strategy is still controversial. Gemcitabine is a promising candidate for single-agent maintenance therapy because of little toxicity and good tolerability. We have conducted a randomized phase II study to evaluate the validity of single-agent maintenance chemotherapy of gemcitabine and to compare continuation- and switch-maintenance.</p> <p>Methods</p> <p>Chemonaïve patients with stage IIIB/IV NSCLC were randomly assigned 1:1 to either arm A or B. Patients received paclitaxel (200 mg/m<sup>2</sup>, day 1) plus carboplatin (AUC 6 mg/mL/min, day 1) every 3 weeks in arm A, or gemcitabine (1000 mg/m<sup>2</sup>, days 1 and 8) plus carboplatin (AUC 5 mg/mL/min, day1) every 3 weeks in arm B. Non-progressive patients following 3 cycles of induction chemotherapy received maintenance gemcitabine (1000 mg/m<sup>2</sup>, days 1 and 8) every 3 weeks. (Trial registration: UMIN000008252)</p> <p>Results</p> <p>The study was stopped because of delayed accrual at interim analysis. Of the randomly assigned 50 patients, 49 except for one in arm B were evaluable. Median progression-free survival (PFS) was 4.6 months for arm A <it>vs</it>. 3.5 months for arm B (HR = 1.03; 95% CI, 0.45–2.27; <it>p</it> = 0.95) and median overall survival (OS) was 15.0 months for arm A <it>vs</it>. 14.8 months for arm B (HR = 0.79; 95% CI, 0.40–1.51; <it>p</it> = 0.60), showing no difference between the two arms. The response rate, disease control rate, and the transit rate to maintenance phase were 36.0% (9/25), 64.0% (16/25), and 48% (12/25) for arm A <it>vs</it>. 16.7% (4/24), 50.0% (12/24), and 33% (8/24) for arm B, which were also statistically similar between the two arms (<it>p</it> = 0.13, <it>p</it> = 0.32, and <it>p</it> = 0.30, respectively). Both induction regimens were tolerable, except that more patients experienced peripheral neuropathy in arm A. Toxicities during the maintenance phase were also minimal.</p> <p>Conclusion</p> <p>Survival and overall response were not significantly different between the two arms. Gemcitabine may be well-tolerable and feasible for maintenance therapy.</p>
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spelling doaj.art-71182083284945f3858ffe491f65f0f82022-12-22T01:49:14ZengBMCBMC Research Notes1756-05002013-01-0161310.1186/1756-0500-6-3Randomized Phase II trial of paclitaxel and carboplatin followed by gemcitabine switch-maintenance therapy versus gemcitabine and carboplatin followed by gemcitabine continuation-maintenance therapy in previously untreated advanced non-small cell lung cancerMinami SeigoKijima TakashiShiroyama TakayukiOkafuji KoheiHirashima TomonoriUchida JunjiImamura FumioOsaki TadashiNakatani TakeshiOgata YoshitakaYamamoto SuguruNamba YoshinobuOtsuka TomoyukiTachibana IsaoKomuta KiyoshiKawase Ichiro<p>Abstract</p> <p>Background</p> <p>In recent years, maintenance chemotherapy is increasingly being recognized as a new treatment strategy to improve the outcome of advanced non-small cell lung cancer (NSCLC). However, the optimal maintenance strategy is still controversial. Gemcitabine is a promising candidate for single-agent maintenance therapy because of little toxicity and good tolerability. We have conducted a randomized phase II study to evaluate the validity of single-agent maintenance chemotherapy of gemcitabine and to compare continuation- and switch-maintenance.</p> <p>Methods</p> <p>Chemonaïve patients with stage IIIB/IV NSCLC were randomly assigned 1:1 to either arm A or B. Patients received paclitaxel (200 mg/m<sup>2</sup>, day 1) plus carboplatin (AUC 6 mg/mL/min, day 1) every 3 weeks in arm A, or gemcitabine (1000 mg/m<sup>2</sup>, days 1 and 8) plus carboplatin (AUC 5 mg/mL/min, day1) every 3 weeks in arm B. Non-progressive patients following 3 cycles of induction chemotherapy received maintenance gemcitabine (1000 mg/m<sup>2</sup>, days 1 and 8) every 3 weeks. (Trial registration: UMIN000008252)</p> <p>Results</p> <p>The study was stopped because of delayed accrual at interim analysis. Of the randomly assigned 50 patients, 49 except for one in arm B were evaluable. Median progression-free survival (PFS) was 4.6 months for arm A <it>vs</it>. 3.5 months for arm B (HR = 1.03; 95% CI, 0.45–2.27; <it>p</it> = 0.95) and median overall survival (OS) was 15.0 months for arm A <it>vs</it>. 14.8 months for arm B (HR = 0.79; 95% CI, 0.40–1.51; <it>p</it> = 0.60), showing no difference between the two arms. The response rate, disease control rate, and the transit rate to maintenance phase were 36.0% (9/25), 64.0% (16/25), and 48% (12/25) for arm A <it>vs</it>. 16.7% (4/24), 50.0% (12/24), and 33% (8/24) for arm B, which were also statistically similar between the two arms (<it>p</it> = 0.13, <it>p</it> = 0.32, and <it>p</it> = 0.30, respectively). Both induction regimens were tolerable, except that more patients experienced peripheral neuropathy in arm A. Toxicities during the maintenance phase were also minimal.</p> <p>Conclusion</p> <p>Survival and overall response were not significantly different between the two arms. Gemcitabine may be well-tolerable and feasible for maintenance therapy.</p>http://www.biomedcentral.com/1756-0500/6/3CarboplatinGemcitabinePaclitaxelSwitch-maintenanceContinuation-maintenanceNon-small cell lung cancer (NSCLC)Randomized phase II
spellingShingle Minami Seigo
Kijima Takashi
Shiroyama Takayuki
Okafuji Kohei
Hirashima Tomonori
Uchida Junji
Imamura Fumio
Osaki Tadashi
Nakatani Takeshi
Ogata Yoshitaka
Yamamoto Suguru
Namba Yoshinobu
Otsuka Tomoyuki
Tachibana Isao
Komuta Kiyoshi
Kawase Ichiro
Randomized Phase II trial of paclitaxel and carboplatin followed by gemcitabine switch-maintenance therapy versus gemcitabine and carboplatin followed by gemcitabine continuation-maintenance therapy in previously untreated advanced non-small cell lung cancer
BMC Research Notes
Carboplatin
Gemcitabine
Paclitaxel
Switch-maintenance
Continuation-maintenance
Non-small cell lung cancer (NSCLC)
Randomized phase II
title Randomized Phase II trial of paclitaxel and carboplatin followed by gemcitabine switch-maintenance therapy versus gemcitabine and carboplatin followed by gemcitabine continuation-maintenance therapy in previously untreated advanced non-small cell lung cancer
title_full Randomized Phase II trial of paclitaxel and carboplatin followed by gemcitabine switch-maintenance therapy versus gemcitabine and carboplatin followed by gemcitabine continuation-maintenance therapy in previously untreated advanced non-small cell lung cancer
title_fullStr Randomized Phase II trial of paclitaxel and carboplatin followed by gemcitabine switch-maintenance therapy versus gemcitabine and carboplatin followed by gemcitabine continuation-maintenance therapy in previously untreated advanced non-small cell lung cancer
title_full_unstemmed Randomized Phase II trial of paclitaxel and carboplatin followed by gemcitabine switch-maintenance therapy versus gemcitabine and carboplatin followed by gemcitabine continuation-maintenance therapy in previously untreated advanced non-small cell lung cancer
title_short Randomized Phase II trial of paclitaxel and carboplatin followed by gemcitabine switch-maintenance therapy versus gemcitabine and carboplatin followed by gemcitabine continuation-maintenance therapy in previously untreated advanced non-small cell lung cancer
title_sort randomized phase ii trial of paclitaxel and carboplatin followed by gemcitabine switch maintenance therapy versus gemcitabine and carboplatin followed by gemcitabine continuation maintenance therapy in previously untreated advanced non small cell lung cancer
topic Carboplatin
Gemcitabine
Paclitaxel
Switch-maintenance
Continuation-maintenance
Non-small cell lung cancer (NSCLC)
Randomized phase II
url http://www.biomedcentral.com/1756-0500/6/3
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