Cargando…
Rationale and protocol design for the TORG1835/NEXT-SHIP study: a phase II study of carboplatin, etoposide and nintedanib for unresectable limited/extensive disease small cell lung cancer with idiopathic pulmonary fibrosis
BACKGROUND: Interstitial pneumonia (IP) is one of the most common and poor prognostic comorbidities in patients with small cell lung cancer (SCLC). The pharmacotherapy for SCLC occasionally induces fatal acute exacerbation of comorbid IP, especially in patients with idiopathic pulmonary fibrosis (IP...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238300/ https://www.ncbi.nlm.nih.gov/pubmed/32489433 http://dx.doi.org/10.1177/1758835920923431 |
_version_ | 1783536511652724736 |
---|---|
author | Ikeda, Satoshi Ogura, Takashi Kato, Terufumi Kenmotsu, Hirotsugu Iwasawa, Tae Misumi, Toshihiro Yamanaka, Takeharu Okamoto, Hiroaki |
author_facet | Ikeda, Satoshi Ogura, Takashi Kato, Terufumi Kenmotsu, Hirotsugu Iwasawa, Tae Misumi, Toshihiro Yamanaka, Takeharu Okamoto, Hiroaki |
author_sort | Ikeda, Satoshi |
collection | PubMed |
description | BACKGROUND: Interstitial pneumonia (IP) is one of the most common and poor prognostic comorbidities in patients with small cell lung cancer (SCLC). The pharmacotherapy for SCLC occasionally induces fatal acute exacerbation of comorbid IP, especially in patients with idiopathic pulmonary fibrosis (IPF). Safe and effective pharmacotherapy is of greater importance in patients with SCLC and IPF, because SCLC presents a poor prognosis without systemic treatment. Nintedanib is expected to restrain acute exacerbation and present angiogenesis-inhibiting effects. METHODS: The TORG1835/NEXT-SHIP study is the world’s first multi-center, single-arm, phase II trial for unresectable limited or extensive disease SCLC with IPF. The patients receive carboplatin (area under the curve 5, day 1), etoposide (<75 years old: 100 mg/m(2); ⩾75 years old: 80 mg/m(2); days 1–3), and nintedanib (150 mg twice a day) every 3 weeks for four cycles. After completion or discontinuation of carboplatin plus etoposide, the patients continue nintedanib until the discontinuation criteria are met. The primary endpoint is the incidence of acute exacerbation of IPF at 28 days after last administration of cytotoxic anti-cancer agents. We set an expected value of 5% and a threshold value of 20%. Taking statistical points (a/b errors: 0.05/0.75) and ineligible patients into account, the sample size was set at 33. The key secondary endpoints are time to first acute exacerbation of IPF, overall response rate, progression-free survival, overall survival, and toxicities. DISCUSSION: Because there is no clinical trial for unresectable SCLC with IPF, our study would provide a major impact on clinical practice. TRIAL REGISTRATION: Japan Registry of Clinical Trials, jRCTs031190119, registered date: October 18, 2019 – Retrospectively registered, https://jrct.niph.go.jp/en-latest-detail/jRCTs031190119 |
format | Online Article Text |
id | pubmed-7238300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-72383002020-06-01 Rationale and protocol design for the TORG1835/NEXT-SHIP study: a phase II study of carboplatin, etoposide and nintedanib for unresectable limited/extensive disease small cell lung cancer with idiopathic pulmonary fibrosis Ikeda, Satoshi Ogura, Takashi Kato, Terufumi Kenmotsu, Hirotsugu Iwasawa, Tae Misumi, Toshihiro Yamanaka, Takeharu Okamoto, Hiroaki Ther Adv Med Oncol Study Protocol BACKGROUND: Interstitial pneumonia (IP) is one of the most common and poor prognostic comorbidities in patients with small cell lung cancer (SCLC). The pharmacotherapy for SCLC occasionally induces fatal acute exacerbation of comorbid IP, especially in patients with idiopathic pulmonary fibrosis (IPF). Safe and effective pharmacotherapy is of greater importance in patients with SCLC and IPF, because SCLC presents a poor prognosis without systemic treatment. Nintedanib is expected to restrain acute exacerbation and present angiogenesis-inhibiting effects. METHODS: The TORG1835/NEXT-SHIP study is the world’s first multi-center, single-arm, phase II trial for unresectable limited or extensive disease SCLC with IPF. The patients receive carboplatin (area under the curve 5, day 1), etoposide (<75 years old: 100 mg/m(2); ⩾75 years old: 80 mg/m(2); days 1–3), and nintedanib (150 mg twice a day) every 3 weeks for four cycles. After completion or discontinuation of carboplatin plus etoposide, the patients continue nintedanib until the discontinuation criteria are met. The primary endpoint is the incidence of acute exacerbation of IPF at 28 days after last administration of cytotoxic anti-cancer agents. We set an expected value of 5% and a threshold value of 20%. Taking statistical points (a/b errors: 0.05/0.75) and ineligible patients into account, the sample size was set at 33. The key secondary endpoints are time to first acute exacerbation of IPF, overall response rate, progression-free survival, overall survival, and toxicities. DISCUSSION: Because there is no clinical trial for unresectable SCLC with IPF, our study would provide a major impact on clinical practice. TRIAL REGISTRATION: Japan Registry of Clinical Trials, jRCTs031190119, registered date: October 18, 2019 – Retrospectively registered, https://jrct.niph.go.jp/en-latest-detail/jRCTs031190119 SAGE Publications 2020-05-18 /pmc/articles/PMC7238300/ /pubmed/32489433 http://dx.doi.org/10.1177/1758835920923431 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Study Protocol Ikeda, Satoshi Ogura, Takashi Kato, Terufumi Kenmotsu, Hirotsugu Iwasawa, Tae Misumi, Toshihiro Yamanaka, Takeharu Okamoto, Hiroaki Rationale and protocol design for the TORG1835/NEXT-SHIP study: a phase II study of carboplatin, etoposide and nintedanib for unresectable limited/extensive disease small cell lung cancer with idiopathic pulmonary fibrosis |
title | Rationale and protocol design for the TORG1835/NEXT-SHIP study: a
phase II study of carboplatin, etoposide and nintedanib for unresectable
limited/extensive disease small cell lung cancer with idiopathic pulmonary
fibrosis |
title_full | Rationale and protocol design for the TORG1835/NEXT-SHIP study: a
phase II study of carboplatin, etoposide and nintedanib for unresectable
limited/extensive disease small cell lung cancer with idiopathic pulmonary
fibrosis |
title_fullStr | Rationale and protocol design for the TORG1835/NEXT-SHIP study: a
phase II study of carboplatin, etoposide and nintedanib for unresectable
limited/extensive disease small cell lung cancer with idiopathic pulmonary
fibrosis |
title_full_unstemmed | Rationale and protocol design for the TORG1835/NEXT-SHIP study: a
phase II study of carboplatin, etoposide and nintedanib for unresectable
limited/extensive disease small cell lung cancer with idiopathic pulmonary
fibrosis |
title_short | Rationale and protocol design for the TORG1835/NEXT-SHIP study: a
phase II study of carboplatin, etoposide and nintedanib for unresectable
limited/extensive disease small cell lung cancer with idiopathic pulmonary
fibrosis |
title_sort | rationale and protocol design for the torg1835/next-ship study: a
phase ii study of carboplatin, etoposide and nintedanib for unresectable
limited/extensive disease small cell lung cancer with idiopathic pulmonary
fibrosis |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238300/ https://www.ncbi.nlm.nih.gov/pubmed/32489433 http://dx.doi.org/10.1177/1758835920923431 |
work_keys_str_mv | AT ikedasatoshi rationaleandprotocoldesignforthetorg1835nextshipstudyaphaseiistudyofcarboplatinetoposideandnintedanibforunresectablelimitedextensivediseasesmallcelllungcancerwithidiopathicpulmonaryfibrosis AT oguratakashi rationaleandprotocoldesignforthetorg1835nextshipstudyaphaseiistudyofcarboplatinetoposideandnintedanibforunresectablelimitedextensivediseasesmallcelllungcancerwithidiopathicpulmonaryfibrosis AT katoterufumi rationaleandprotocoldesignforthetorg1835nextshipstudyaphaseiistudyofcarboplatinetoposideandnintedanibforunresectablelimitedextensivediseasesmallcelllungcancerwithidiopathicpulmonaryfibrosis AT kenmotsuhirotsugu rationaleandprotocoldesignforthetorg1835nextshipstudyaphaseiistudyofcarboplatinetoposideandnintedanibforunresectablelimitedextensivediseasesmallcelllungcancerwithidiopathicpulmonaryfibrosis AT iwasawatae rationaleandprotocoldesignforthetorg1835nextshipstudyaphaseiistudyofcarboplatinetoposideandnintedanibforunresectablelimitedextensivediseasesmallcelllungcancerwithidiopathicpulmonaryfibrosis AT misumitoshihiro rationaleandprotocoldesignforthetorg1835nextshipstudyaphaseiistudyofcarboplatinetoposideandnintedanibforunresectablelimitedextensivediseasesmallcelllungcancerwithidiopathicpulmonaryfibrosis AT yamanakatakeharu rationaleandprotocoldesignforthetorg1835nextshipstudyaphaseiistudyofcarboplatinetoposideandnintedanibforunresectablelimitedextensivediseasesmallcelllungcancerwithidiopathicpulmonaryfibrosis AT okamotohiroaki rationaleandprotocoldesignforthetorg1835nextshipstudyaphaseiistudyofcarboplatinetoposideandnintedanibforunresectablelimitedextensivediseasesmallcelllungcancerwithidiopathicpulmonaryfibrosis |