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Preoperative nivolumab to evaluate pathological response in patients with stage I non-small cell lung cancer: a study protocol of phase II trial (POTENTIAL).

AbstractINTRODUCTION:
Recently, inhibition of programmed cell death 1 or its ligand has shown therapeutic effects on non-small cell lung cancer (NSCLC). However, the effectiveness of preoperative nivolumab monotherapy for stage I NSCLC remains unknown. The present study aimed to investigate the pathological response of preoperative treatment with nivolumab for clinically node negative but having a high risk of NSCLC recurrence.
METHODS AND ANALYSIS:
The Preoperative Nivolumab (Opdivo) to evaluate pathologic response in patients with stage I non-small cell lung cancer: a phase 2 trial (POTENTIAL) study is a multicentre phase II trial investigating efficacy of preoperative nivolumab for clinical stage I patients at high risk of recurrence. This study includes histologically or cytologically confirmed NSCLC patients with clinical N0 who were found on preoperative high-resolution CT to have a pure solid tumour without a ground-glass opacity component (clinical T1b, T1c or T2a) or a solid component measuring 2-4 cm in size (clinical T1c or T2a). Patients with epidermal growth factor receptor (EGFR) mutation (deletion of exon 19 or point mutation on exon21, L858R), anaplastic lymphoma kinase (ALK) translocation or c-ros oncogene 1 (ROS-1) translocation are excluded from this study. Nivolumab (240 mg/body) is administrated intravenously as preoperative therapy every 2 weeks for three cycles. Afterward, lobectomy and mediastinal lymph node dissection (ND 2a-1 or ND 2a-2) are performed. The primary endpoint is a pathological complete response in the resected specimens. The secondary endpoints are safety, response rates and major pathological response. The planed sample size is 50 patients. Patients have been enrolled since April 2019.
ETHICS AND DISSEMINATION:
This trial was approved by the Institutional Review Board of Hiroshima University Hospital and other participating institutions. This trial will help examine the efficacy of preoperative nivolumab therapy for clinical stage I NSCLC.
TRIAL REGISTRATION NUMBER:
jRCT2061180016.
AuthorsAtsushi Kagimoto, Yasuhiro Tsutani, Takahiro Mimae, Yoshihiro Miyata, Norihiko Ikeda, Hiroyuki Ito, Yoshimasa Maniwa, Kenji Suzuki, Masahiro Tsuboi, Kenichi Yoshimura, Seiji Umemoto, Morihito Okada
JournalBMJ open (BMJ Open) Vol. 11 Issue 3 Pg. e043234 (03 17 2021) ISSN: 2044-6055 [Electronic] England
PMID33737428 (Publication Type: Clinical Trial Protocol, Journal Article, Research Support, Non-U.S. Gov't)
Copyright© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Chemical References
  • Antineoplastic Agents, Immunological
  • Nivolumab
Topics
  • Antineoplastic Agents, Immunological (therapeutic use)
  • Antineoplastic Combined Chemotherapy Protocols
  • Carcinoma, Non-Small-Cell Lung (drug therapy)
  • Clinical Trials, Phase II as Topic
  • Humans
  • Lung Neoplasms (drug therapy)
  • Neoplasm Recurrence, Local (drug therapy)
  • Nivolumab (therapeutic use)

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