Clinical implications of monitoring nivolumab immunokinetics in non–small cell lung cancer patients

Akio Osa(The University of Osaka), Takeshi Uenami(Toneyama National Hospital), Shohei Koyama(The University of Osaka), Kosuke Fujimoto(Osaka City University), Daisuke Okuzaki(The University of Osaka), Takayuki Takimoto(The University of Osaka), Haruhiko Hirata(The University of Osaka), Yukihiro Yano(Toneyama National Hospital), Soichiro Yokota(Toneyama National Hospital), Yuhei Kinehara(The University of Osaka), Yujiro Naito(The University of Osaka), Tomoyuki Otsuka(The University of Osaka), Masaki Kanazu(Toneyama National Hospital), Muneyoshi Kuroyama(The University of Osaka), Masanari Hamaguchi(The University of Osaka), Taro Koba(The University of Osaka), Yu Futami(The University of Osaka), Mikako Ishijima(Toneyama National Hospital), Yasuhiko Suga(The University of Osaka), Yuki Akazawa(Toneyama National Hospital), Hirotomo Machiyama(The University of Osaka), Kota Iwahori(The University of Osaka), Hyota Takamatsu(The University of Osaka), Izumi Nagatomo(The University of Osaka), Yoshito Takeda(The University of Osaka), Hiroshi Kida(The University of Osaka), Esra A. Akbay(The University of Texas Southwestern Medical Center), Peter S. Hammerman(Novartis (United States)), Kwok‐Kin Wong(NYU Langone Health), Glenn Dranoff(Novartis (United States)), Masahide Mori(Toneyama National Hospital), Takashi Kijima(The University of Osaka), Atsushi Kumanogoh(The University of Osaka)
JCI Insight
October 3, 2018
Cited by 233Open Access
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Abstract

BACKGROUND: The PD-1-blocking antibody nivolumab persists in patients several weeks after the last infusion. However, no study has systematically evaluated the maximum duration that the antibody persists on T cells or the association between this duration and residual therapeutic efficacy or potential adverse events. METHODS: To define the duration of binding and residual efficacy of nivolumab after discontinuation, we developed a simplified strategy for T cell monitoring and used it to analyze T cells from peripheral blood from 11 non-small cell lung cancer patients previously treated with nivolumab. To determine the suitability of our method for other applications, we compared transcriptome profiles between nivolumab-bound and nivolumab-unbound CD8 T cells. We also applied T cell monitoring in 2 nivolumab-treated patients who developed progressive lung tumors during long-term follow-up. RESULTS: Prolonged nivolumab binding was detected more than 20 weeks after the last infusion, regardless of the total number of nivolumab infusions (2-15 doses) or type of subsequent treatment, in 9 of the 11 cases in which long-term monitoring was possible. Ki-67 positivity, a proliferation marker, in T cells decreased in patients with progressive disease. Transcriptome profiling identified the signals regulating activation of nivolumab-bound T cells, which may contribute to nivolumab resistance. In 2 patients who restarted nivolumab, T cell proliferation markers exhibited the opposite trend and correlated with clinical response. CONCLUSIONS: Although only a few samples were analyzed, our strategy of monitoring both nivolumab binding and Ki-67 in T cells might help determine residual efficacy under various types of concurrent or subsequent treatment. TRIAL REGISTRATION: University Hospital Medical Information Network Clinical Trials Registry, UMIN000024623. FUNDING: This work was supported by Japan Society for the Promotion of Science KAKENHI (JP17K16045, JP18H05282, and JP15K09220), Japan Agency for Medical Research and Development (JP17cm0106310, JP18cm0106335 and JP18cm059042), and Core Research for Evolutional Science and Technology (JPMJCR16G2).


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