Publications by authors named "Masahiro Yoshioka"

Article Synopsis
  • In 2022, a survey was conducted to understand how hospitals in Japan handle secondary findings from genetic tests, updating information from a 2020 survey.
  • About 82% of hospitals replied, and they mostly used a specific guideline (CTGPMRSF) for sharing secondary findings.
  • The results showed that many hospitals had challenges like insurance issues and different levels of understanding of secondary findings, but the rates for confirmatory tests (tests to double-check findings) were improving, especially in places with genetic experts.
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Dysregulation of mesenchymal-epithelial transition factor () gene due to amplification, mutation, and fusion has been reported in various types of human cancers. Recently, the efficacy of small-molecule tyrosine kinase inhibitors (TKIs) targeting MET has been demonstrated in a wide range of -dysregulated tumors. The majority of biliary tract cancers including intrahepatic cholangiocarcinoma (iCCA) are diagnosed at an advanced stage, and the utility of conventional chemotherapy is limited.

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Neuroendocrine carcinoma (NEC) of the gallbladder origin is particularly rare, accounting for only 0.38% of primary malignancies of the gallbladder, and standard therapies are limited. The gene encodes the tyrosine kinase receptor, c-Met.

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Article Synopsis
  • The study assesses the clinical utility of comprehensive genomic profiling (CGP) using next-generation sequencing for patients with previously untreated metastatic or recurrent solid tumors, highlighting the need for more evidence on its effectiveness before standard treatment.
  • Conducted in Japan, the multicenter observational study enrolled 180 patients with various types of advanced cancers to examine outcomes after CGP.
  • Results showed that all analyzed patients had actionable genomic alterations, with 63.4% identified as druggable, indicating CGP may help guide personalized treatment options.
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Article Synopsis
  • The study investigates the distinction between somatic and germline variants in circulating tumor DNA (ctDNA) testing, which typically requires analyzing non-tumor samples to identify germline variants.
  • A cohort of 106 patients with advanced solid tumors was analyzed using ctDNA tests, revealing that 223 pathogenic variants were identified, with varying variant allele fractions (VAFs) across samples.
  • The findings indicate that higher VAFs (≥30%) are more likely to correspond to germline variants, suggesting that VAF values can assist in selecting presumed germline variants during clinical ctDNA testing.
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Article Synopsis
  • - The ESMO-PMWG provided guidelines for confirmatory germline testing for presumed germline pathogenic variants (PGPVs) found in tumor-only genomic profiling, but these recommendations hadn't been tested in real-world settings until now.
  • - A study reviewed records of 143 patients who underwent tumor-only genomic profiling, identifying 195 variants, of which 12 were confirmed as germline variants, while filtering through ESMO-PMWG criteria revealed that 6 out of 7 selected PGPVs were of germline origin.
  • - The findings suggest that ESMO-PMWG criteria effectively help clinicians choose PGPVs likely to originate from germline sources, enhancing the validity of genomic testing in clinical practice.
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Background: Tumor heterogeneity has been known to cause inter-assay discordance among next-generation sequencing (NGS) results. However, whether preclinical factors such as sample type, sample quality and analytical features of gene panel can affect the concordance between two different assays remains largely unexplored.

Methods: Replicate sets of DNA samples extracted from formalin-fixed paraffin-embedded tissues (FFPE) (n = 20) and fresh frozen (FF) tissues (n = 10) were herein analyzed using a tumor-only (TO) and paired tumor-normal (TN) gene panel in laboratories certified by the Clinical Laboratory Improvement Amendment.

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In June 2019, the Japanese National Health Insurance (NHI) system introduced coverage for two types of tumor genomic profiling (TGP): FoundationOne CDx (F1) and OncoGuide™ NCC OncoPanel System (NCCOP). TGP sometimes reveals germline variants that are potentially pathogenic as secondary findings (SFs). We conducted a questionnaire-based survey to find out the operational statuses of F1 and NCCOP at institutions where TGP was performed to elucidate issues related to SFs.

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In Japan, 2 comprehensive genome profiling(CGP)tests for cancer was covered by national health insurance in June 2019, and cancer genome medicine was introduced at a total of 225 hospitals designated by the Ministry of Health, Labor and Welfare as"core center hospitals for cancer genome medicine(12 hospitals)"," core hospitals for cancer genome medicine (33 hospitals)", and"collaborative hospitals for cancer genome medicine(180 hospitals)". On the other hand, the interpretation of the results of the cancer CGP test must be discussed by an expert panel conducted at the core center hospitals for cancer genome medicine or the core hospitals for cancer genome medicine, and the results must be explained to patients in order to be covered by insurance. In other words, these hospitals are required to review not only their own cases but also those of collaborating hospitals.

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Background: Talaporfin sodium photodynamic therapy (tPDT) is an effective salvage treatment for local failure after chemoradiotherapy for esophageal cancer. Repeated tPDT could also be indicated for local recurrence or residue after the first salvage tPDT. However, the safety and efficacy of repeated tPDT have not been elucidated.

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Article Synopsis
  • Comprehensive genomic profiling (CGP) testing is used in precision cancer medicine to help select targeted therapies, but its utility during first-line chemotherapy is uncertain.
  • A study involving 197 chemotherapy-naïve patients with stage III/IV gastrointestinal cancer found that CGP testing had a success rate of 76.6%, with actionable genomic alterations detected in 73.6% of patients.
  • The research indicates that CGP testing could be a valuable method to identify effective first-line chemotherapy options, particularly showing the highest detection rate in colorectal cancer.
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Background: Although endoscopic resection is increasingly performed to treat submucosal invasive colorectal cancer (T1CRC), approximately 10% are at risk of lymph node metastasis. The Japanese Society for Cancer of the Colon and Rectum guideline indicates that the following risk factors should be considered when deciding whether to perform additional surgical resection with lymph node dissection: depth of T1 invasion, lymphovascular invasion, poor histological grade, and budding grade 2/3. However, there is little information about the prognosis of T1CRC patients, or factors to consider when deciding subsequent treatment of high-risk T1CRC.

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Background: Epidermal growth factor receptor (EGFR) plays a pivotal role in the pathophysiology of esophageal squamous cell carcinoma (ESCC). However, the clinical effects of EGFR inhibitors on ESCC are controversial. This study sought to identify the factors determining the therapeutic efficacy of EGFR inhibitors in ESCC cells.

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5-Fluorouracil (5-FU) is a key drug for the treatment of esophageal squamous cell carcinoma (ESCC); however, resistance to it remains a critical limitation to its clinical use. To clarify the mechanisms of 5-FU resistance of ESCC, we originally established 5-FU-resistant ESCC cells, TE-5R, by step-wise treatment with continuously increasing concentrations of 5-FU. The half maximal inhibitory concentration of 5-FU showed that TE-5R cells were 15.

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Context: Intraductal papillary mucinous neoplasm (IPMN) of the pancreas occasionally penetrates to others organs. We present a case of IPMN penetrating to the stomach and the common bile duct.

Case Report: A 75-year-old man was admitted to the hospital because of epigastric pain.

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Background: Vaccinium uliginosum L. is a type of blueberry found in the Chinese Changbai Mountains. We extracted Vaccinium uliginosum Anthocyanins (A(V.

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A 74-year-old woman presented with abducens nerve palsy, postganglionic Horner syndrome and sensory disturbance in the territory of the ophthalmic nerve on the left side. Cranial magnetic resonance imaging demonstrated a gadolinium-enhanced lesion within the left cavernous sinus. Thereafter, uterine cervical cancer was detected as the origin of this intra-cavernous sinus metastasis.

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We examined therapeutic superiority of induction therapy with twice-daily IFN-beta (3X2=6 million units/day) onto 6-months consensus interferon monotherapy for chronic hepatitis C. Patients were randomly assigned to monotherapy without (group I, n=16) and with induction therapy (group II, n=12). The mean age of group II was older than that of group I, and other baseline condition was not statistically significant.

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Background/aims: We previously reported that intravenous interferon-beta administration was effective in treating patients with chronic hepatitis C and that there was no significant correlation between the response to therapy and host in vitro immunoglobulin production. The aims of this study were to evaluate the additive effect of a liver extract preparation and flavin adenine dinucleotide mixture and to reevaluate the correlation.

Methodology: 65 patients with chronic hepatitis C received intravenously 6 million units of interferon-beta and 2 mL of a liver extract preparation and flavin adenine dinucleotide mixture.

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Background: The Chinese herbal dietary supplements Chaso and Onshido are marketed for weight loss in Japan. The safety of these weight loss aids is unknown.

Objective: To describe patients who developed liver injury while taking Chaso or Onshido.

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