Abstract

IntroductionROBO1 is a membrane protein that contributes to tumor metastasis and angiogenesis. We previously reported that 90Y-labeled anti-ROBO1 monoclonal antibody (90Y-anti-ROBO1 IgG) showed an antitumor effect against ROBO1-positive tumors. In this study, we performed a biodistribution study and radioimmunotherapy (RIT) against ROBO1-positive small cell lung cancer (SCLC) models.MethodsFor the biodistribution study, 111In-labeled anti-ROBO1 monoclonal antibody (111In-anti-ROBO1 IgG) was injected into ROBO1-positive SCLC xenograft mice via the tail vein. To evaluate antitumor effects, an RIT study was performed, and SCLC xenograft mice were treated with 90Y-anti-ROBO1 IgG. Tumor volume and body weight were periodically measured throughout the experiments. The tumors and organs of mice were then collected, and a pathological analysis was carried out.ResultsAs a result of the biodistribution study, we observed tumor uptake of 111In-anti-ROBO1 IgG. The liver, kidney, spleen, and lung showed comparably high accumulation of 111In-labeled anti-ROBO1. In the RIT study, 90Y-anti-ROBO1 IgG significantly reduced tumor volume compared with baseline. Pathological analyses of tumors revealed coagulation necrosis and fatal degeneration of tumor cells, significant reduction in the number of Ki-67-positive cells, and an increase in the number of apoptotic cells. A transient reduction of hematopoietic cells was observed in the spleen, sternum, and femur.ConclusionsThese results suggest that RIT with 90Y-anti-ROBO1 IgG is a promising treatment for ROBO1-positive SCLC.

Highlights

  • ObjectivesWe did not performed a dose escalation study because our objective was not optimization of injection dose but an evaluation of the antitumor effect on small cell lung cancer (SCLC) xenografts, and determination of whether 90Y-B5209B causes damage to organs in terms of pathology

  • ROBO1 is a membrane protein that contributes to tumor metastasis and angiogenesis

  • A transient reduction of hematopoietic cells was observed in the spleen, sternum, and femur. These results suggest that RIT with 90Y-anti-ROBO1 IgG is a promising treatment for ROBO1-positive small cell lung cancer (SCLC)

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Summary

Objectives

We did not performed a dose escalation study because our objective was not optimization of injection dose but an evaluation of the antitumor effect on SCLC xenografts, and determination of whether 90Y-B5209B causes damage to organs in terms of pathology

Methods
Results
Conclusion
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