Publications by authors named "Shin-Ichi Nihira"

Article Synopsis
  • Clinical studies for regulatory drug approval must show the drug's clinical benefits in the target population, following a stepwise process of safety, dose determination, and efficacy evaluation.
  • The clinical evaluation guidelines for anti-cancer drugs in Japan, established in 1991 and revised in 2006, are now updated to reflect advancements in immunotherapy and cancer genomic medicine.
  • Due to the challenges in conducting studies for rare molecular subtypes, global collaboration is essential, and updated guidelines now include provisions for using surrogate endpoints and accommodate differences in pharmacokinetics across ethnic groups.
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Gastrointestinal tract cancers constitute a group of highest morbidity both in and outside Japan, and the prognosis still remains unfavorable when the disease has progressed to the unresectable stage. Since the late 1990s, a novel category of anti-cancer drugs, 'molecular-targeted drugs', has become available, and angiogenesis has been considered as one of the most important molecular targets for antitumor therapy since it is essential for tumor growth. Anti-angiogenic therapy inhibits tumor angiogenesis and promotes apoptosis of existing tumor blood vessels, thereby intercepting the supply of oxygen and nutrition essential for tumor growth and metastasis.

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HER2 is a member of the human epidermal growth factor receptor family, possessing protein kinase activity in its cytoplasmic domain. There were evidences indicating that (1) amplification of HER2/neu gene and HER2 protein over-expression in tumor cells was observed in 25-30% of human breast cancer and (2) amplification of HER2/neu correlated with poor prognosis, including shorter disease-free and overall survival. These evidences suggested HER2 was a promising candidate for novel molecular targets of breast cancer therapy.

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