EBioMedicine (Feb 2020)

Near infrared photoimmunotherapy targeting DLL3 for small cell lung cancer

  • Yoshitaka Isobe,
  • Kazuhide Sato,
  • Yuko Nishinaga,
  • Kazuomi Takahashi,
  • Shunichi Taki,
  • Hirotoshi Yasui,
  • Misae Shimizu,
  • Rena Endo,
  • Chiaki Koike,
  • Noriko Kuramoto,
  • Hiroshi Yukawa,
  • Shota Nakamura,
  • Takayuki Fukui,
  • Koji Kawaguchi,
  • Toyofumi F. Chen-Yoshikawa,
  • Yoshinobu Baba,
  • Yoshinori Hasegawa

Journal volume & issue
Vol. 52

Abstract

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Background: Small cell lung cancer (SCLC) has a poor prognosis, and its treatment options are limited. Delta-like protein 3 (DLL3) is expressed specifically in SCLC and is considered a promising therapeutic target for patients with this disease. Rovalpituzumab tesirine (Rova-T) was the first antibody-drug conjugate targeting DLL3. Although Rova-T development was unfortunately terminated, DLL3 remains an ideal target for SCLC. Near infrared photoimmunotherapy (NIR-PIT) is a new form of cancer treatment that employs an antibody-photosensitiser conjugate followed by NIR light exposure and damage target cells specifically. In this study, we demonstrate DLL3-targeted NIR-PIT to develop a novel molecularly targeted treatment for SCLC. Methods: The anti-DLL3 monoclonal antibody rovalpituzumab was conjugated to an IR700 photosensitiser (termed ‘rova-IR700’). SCLC cells overexpressing DLL3 as well as non-DLL3-expressing controls were incubated with rova-IR700 and then exposed to NIR-light. Next, mice with SCLC xenografts were injected with rova-IR700 and irradiated with NIR-light. Findings: DLL3-overexpressing cells underwent immediate destruction upon NIR-light exposure, whereas the control cells remained intact. The xenograft in mice treated with rova-IR700 and NIR-light shrank markedly, whereas neither rova-IR700 injection nor NIR-light irradiation alone affected tumour size. Interpretation: Our data suggest that targeting of DLL3 using NIR-PIT could be a novel and promising treatment for SCLC. Funding: Research supported by grants from the Program for Developing Next-generation Researchers (Japan Science and Technology Agency), KAKEN (18K15923, JSPS), Medical Research Encouragement Prize of The Japan Medical Association, The Nitto Foundation, Kanae Foundation for the Promotion of Medical Science. Keywords: Photoimmunotherapy, DLL3, Small cell lung cancer, Bioluminescence, In vivo imaging