Publications by authors named "Kan Ito"

Background: Assessing the response to neoadjuvant chemotherapy is crucial for determining surgical treatment strategies and optimizing personalized postoperative care in osteosarcoma patients. The apparent diffusion coefficient, derived from diffusion-weighted imaging, reflects tumor aggressiveness; however, its role in evaluating neoadjuvant chemotherapy response remains unclear. This study aimed to evaluate the utility of apparent diffusion coefficient maps in assessing chemotherapy-induced necrosis and prognosis in osteosarcoma.

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Liquid nitrogen-treated autografts are used to reconstruct bone defects after wide resection of malignant bone tumours. However, the lack of blood supply makes them prone to infection, which is traditionally treated with systemic antibiotics and infected bone removal. Continuous local antibiotic perfusion (CLAP) therapy, delivering high-dose antibiotics directly to the infection site, is a promising alternative.

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Background/aim: The role of chemotherapy for malignant peripheral nerve sheath tumors (MPNSTs) remains controversial, particularly in neurofibromatosis type 1 (NF1)-related MPNST (NF1-MPNST). This study aimed to assess the clinical outcomes of patients with NF1-MPNST who underwent curative treatment comprising neoadjuvant chemotherapy followed by wide resection.

Patients And Methods: We retrospectively analyzed data from patients with NF1-MPNST who received preoperative chemotherapy.

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Multiple osteochondromas (MO) occur in approximately 1 in 50,000 people/yr. One in 3 patients with MO will develop valgus knee deformity (VKD), but the predictive factors for VKD are unclear. The purpose of this study was to examine the factors associated with VKD in patients with MO.

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NTRK-rearranged spindle cell neoplasm is a group of tumors characterized by NTRK1/2/3 gene fusion. Recently, tumors with other kinase fusion genes were reported to exhibit similar morphologies. Herein, we discuss an adult-onset soft tissue tumor with similar histologic patterns as kinase gene fusion-related tumors but with BRAF and NRAS mutations.

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Background As desmoid-type fibromatosis (DF) exhibits a high recurrence rate after surgery, initial active surveillance followed by medical therapy is the mainstay of the treatment. However, there are few effective drugs with acceptable side effects. Methodology Among drugs that have been used for a long period and possess a known safety profile, auranofin was observed to be effective in suppressing DF using the drug repositioning method in our laboratory.

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  • * The study found that ipriflavone reduced KIAA1199 activity, which is linked to OA progression, and preserved vital components like hyaluronan (HA) in cartilage tissue.
  • * Results suggest that ipriflavone could serve as a potential treatment for OA by inhibiting factors that lead to its development and progression.
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  • The study investigates the surgical outcomes and complications of removing deep-seated nodular plexiform neurofibromas in patients with neurofibromatosis type 1, based on a review of cases from 2015 to 2021.
  • Surgical methods included enucleation to preserve nerves and en bloc resection when nerves were entrapped, involving 24 tumors in 15 patients.
  • Post-surgery, all patients experienced symptom resolution, though some faced new but mild neurological deficits, suggesting the procedure is generally safe with a low risk of severe complications.
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Background: The treatment of choice for desmoid-type fibromatosis (DF) has been changed to active surveillance (AS). However, few studies have reported clinical outcomes of AS modality in Asian countries. This study aimed to clarify the significance of AS as a DF treatment modality.

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Anticancer drugs and molecular targeted therapies are used for refractory desmoid-type fibromatosis (DF), but occasionally cause severe side effects. The purpose of this study was to identify an effective drug with fewer side effects against DF by drug repositioning, and evaluate its efficacy. FDA-approved drugs that inhibit the proliferation of DF cells harboring S45F mutations of CTNNB1 were screened.

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  • Hyaluronan (HA) is important for maintaining cartilage, but its changes in osteoarthritis (OA) and osteonecrosis of the femoral head (ONFH) need more research.
  • The study focused on how KIAA1199, a hyaluronidase, affects HA metabolism in OA and ONFH by analyzing human cartilage samples.
  • Findings revealed that KIAA1199 is overexpressed in OA, leading to changes in HA levels, while ONFH showed lower KIAA1199 expression and a less active HA metabolism.
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  • - Fibrous dysplasia is a rare condition that can cause fractures, pain, and other disabilities but lacks effective medical treatments; surgery is sometimes impractical due to the extent of the lesions.
  • - A 27-year-old woman with right buttock pain was diagnosed with cystic fibrous dysplasia, and initial tests showed no associated syndromes or abnormal blood values, although her acid phosphatase level was elevated.
  • - The patient was treated with denosumab, resulting in pain relief and improved bone density, and this positive effect lasted for 9 months after the treatment ended, highlighting the potential of denosumab for off-label use in fibrous dysplasia cases.
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  • The study investigates how diffusion-weighted imaging (DWI) can help differentiate between benign plexiform neurofibromas (pNF) and malignant peripheral nerve sheath tumors (MPNST) in patients with neurofibromatosis type 1 (NF1).
  • Researchers analyzed 29 NF1 cases, comparing diagnostic features and apparent diffusion coefficient (ADC) values using magnetic resonance imaging (MRI).
  • Results showed significant differences in tumor characteristics between pNF and MPNST, with DWI providing a valuable tool for differentiation, increasing diagnostic accuracy when used alongside standard MRI evaluations.
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The mainstay of treatment for desmoid has been shifted to active surveillance (AS). However, surgery is still being performed on abdominal wall desmoid with a wide surgical margin. The purposes of this study are to clarify the treatment results of less-invasive, fascia preserving surgery for patients with abdominal wall desmoid, and to propose a new treatment modality.

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A 52-year-old man, with a history of diabetic nephropathy and renal cancer, had been treated with peritoneal dialysis for four months before consulting our hospital. At the time of imaging evaluation, three years after surgery for renal cancer, fluorodeoxyglucose accumulation was found at the distal metaphysis of the left radius. After the biopsy, he was diagnosed with giant cell tumor of bone (GCTB), and surgery was scheduled.

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Background: Hyaluronan (HA) has been shown to play important roles in the growth, invasion, and metastasis of malignant tumors. KIAA1199, which has potent HA-degrading activity, has been reported to be expressed in various malignancies and associated with patient prognosis. However, there are no reports on the expression of KIAA1199 in osteosarcoma.

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  • - Desmoid-type fibromatosis (DF) is a non-metastatic tumor known for its aggressive local growth and is often identified by positive nuclear staining for beta-catenin—a result of CTNNB1 mutations.
  • - A study found that even some DFs that don’t show nuclear beta-catenin can still have CTNNB1 mutations, emphasizing variability in test results based on the specific antibody used.
  • - The research compared the effectiveness of three commonly used antibodies for detecting nuclear beta-catenin in diagnosing DF, revealing notable differences in sensitivity and specificity, which could enhance diagnostic accuracy.
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Previous studies have not clearly identified a prognostic factor for desmoid tumours (DT). Whole-exome sequencing (WES) and/or RNA sequencing (RNA-seq) were performed in 64 cases of DT to investigate the molecular profiles in combination with the clinicopathological characteristics. CTNNB1 mutations with specific hotspots were identified in 56 cases (87.

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  • This study assessed the efficacy of PET/CT imaging in distinguishing between benign and malignant neurogenic tumors in patients with Neurofibromatosis Type 1 (NF1), focusing on plexiform neurofibromas (pNF) and malignant peripheral nerve sheath tumors (MPNST).
  • The results showed that MPNSTs had a significantly higher PET/CT uptake (SUVmax) compared to pNFs, indicating that SUVmax can help differentiate between these tumor types, with a sensitivity of 78.6% and specificity of 88.9%.
  • Additionally, the study identified other tumor types unrelated to neurogenic tumors through PET/CT, but it emphasized the need for ongoing research to monitor the progression of pNF
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  • Low-dose methotrexate (MTX) combined with vinblastine (VBL) has been found effective in treating desmoid-type fibromatosis (DF), and this study examined a biweekly regimen as opposed to a weekly one.
  • Out of 38 patients treated prospectively, 51% showed a partial response, with a high clinical benefit rate of 95% and a 5-year progression-free survival (PFS) of 80.8%.
  • The biweekly approach was well tolerated, had fewer severe side effects, and might take longer to show results, suggesting that treatment plans should consider both tumor conditions and patient preferences.
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Hyaluronan (HA) has been shown to play crucial roles in the tumorigenicity of malignant tumors. Chondrosarcoma, particularly when low-grade, is characterized by the formation of an extracellular matrix (ECM) containing abundant HA, and its drug/radiation resistance has become a clinically relevant problem. This study aimed to evaluate the effects of a novel hyaluronidase, KIAA1199, on ECM formation as well as antitumor effects on chondrosarcoma.

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