TY - JOUR
T1 - Treatment rationale and protocol design
T2 - an investigator-initiated phase II study of combination treatment of nivolumab and TM5614, a PAI-1 inhibitor for previously treated patients with non-small cell lung cancer
AU - Masuda, Takeshi
AU - Hirata, Taizo
AU - Sakamoto, Tomohiro
AU - Tsubata, Yukari
AU - Ichihara, Eiki
AU - Kozuki, Toshiyuki
AU - Shoda, Hiroyasu
AU - Motonaga, Masanori
AU - Yoshida, Takako
AU - Fukutani, Miki
AU - Tsuji-Takayama, Kazue
AU - Tamura, Atsushi
AU - Amagase, Harunobu
AU - Fujihara, Hideki
AU - Aoki, Gaku
AU - Akita, Tomoyuki
AU - Orihashi, Yasushi
AU - Miyata, Toshio
AU - Hattori, Noboru
N1 - Publisher Copyright:
© Journal of Thoracic Disease. All rights reserved.
PY - 2024/5/31
Y1 - 2024/5/31
N2 - Background: There is no established standard 3rd line treatment for patients with advanced non-small cell lung cancer (NSCLC). Although cytotoxic chemotherapeutic agents that are not used as 1st or 2nd line treatment are administrated as 3rd line treatment, their anti-tumor efficacy is insufficient. Anti-programmed death ligand-1 (PD-L1)/programmed death-1 (PD1) treatment is more effective and less toxic than chemotherapy in anti-PD-L1/PD-1 treatment-naïve patients with NSCLC. Therefore, anti-PD-L1/ PD-1 therapy is considered an appropriate 3rd line treatment. However, the anti-tumor efficacy is limited in patients previously treated with anti-PD-L1/PD-1 antibody. Today, new drugs are needed to increase the efficacy of anti-PD-L1/PD-1 antibodies. Methods: This open-label, single-arm, investigator-initiated phase II study is designed to evaluate combination treatment of nivolumab and TM5614, a plasminogen activator inhibitor (PAI-1) inhibitor as 3rd or more line treatment in NSCLC patients who underwent standard treatment. The primary endpoint is the objective response rate and the secondary endpoints are progression-free survival (PFS), overall survival (OS), duration of response (DOR) and safety. Recruitment began in September 2023 and is expected to continue for approximately three years. Discussion: Currently, there is no standard 3rd line treatment for advanced NSCLC, and we hope that the findings of this study will facilitate more effective treatments in this setting. Ethics and dissemination: the study protocol conformed to the ethical principles outlined in the Declaration of Helsinki. All patients will provide written informed consent prior to enrollment. Results will be published in a peer-reviewed publication. Trial Registration: This study is registered to Japan Registry of Clinical Trials with number: jRCT2061230039 (19/July/2023).
AB - Background: There is no established standard 3rd line treatment for patients with advanced non-small cell lung cancer (NSCLC). Although cytotoxic chemotherapeutic agents that are not used as 1st or 2nd line treatment are administrated as 3rd line treatment, their anti-tumor efficacy is insufficient. Anti-programmed death ligand-1 (PD-L1)/programmed death-1 (PD1) treatment is more effective and less toxic than chemotherapy in anti-PD-L1/PD-1 treatment-naïve patients with NSCLC. Therefore, anti-PD-L1/ PD-1 therapy is considered an appropriate 3rd line treatment. However, the anti-tumor efficacy is limited in patients previously treated with anti-PD-L1/PD-1 antibody. Today, new drugs are needed to increase the efficacy of anti-PD-L1/PD-1 antibodies. Methods: This open-label, single-arm, investigator-initiated phase II study is designed to evaluate combination treatment of nivolumab and TM5614, a plasminogen activator inhibitor (PAI-1) inhibitor as 3rd or more line treatment in NSCLC patients who underwent standard treatment. The primary endpoint is the objective response rate and the secondary endpoints are progression-free survival (PFS), overall survival (OS), duration of response (DOR) and safety. Recruitment began in September 2023 and is expected to continue for approximately three years. Discussion: Currently, there is no standard 3rd line treatment for advanced NSCLC, and we hope that the findings of this study will facilitate more effective treatments in this setting. Ethics and dissemination: the study protocol conformed to the ethical principles outlined in the Declaration of Helsinki. All patients will provide written informed consent prior to enrollment. Results will be published in a peer-reviewed publication. Trial Registration: This study is registered to Japan Registry of Clinical Trials with number: jRCT2061230039 (19/July/2023).
KW - anti-programmed death-1 antibody
KW - nivolumab
KW - Non-small cell lung cancer (NSCLC)
KW - plasminogen activator inhibitor-1 (PAI-1)
KW - TM5614
UR - http://www.scopus.com/inward/record.url?scp=85195033080&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85195033080&partnerID=8YFLogxK
U2 - 10.21037/jtd-23-1858
DO - 10.21037/jtd-23-1858
M3 - Article
AN - SCOPUS:85195033080
SN - 2072-1439
VL - 16
SP - 3381
EP - 3388
JO - Journal of Thoracic Disease
JF - Journal of Thoracic Disease
IS - 5
ER -