Publications by authors named "Junko Eba"

The new national guidelines for clinical research, the Ethical Guidelines for Medical and Biological Research Involving Human Subjects, were implemented in Japan in June 2021. The guidelines were developed by integrating two ethical guidelines: Ethical Guidelines for Medical and Health Research Involving Human Subjects and Ethical Guidelines for Human Genome/Gene Analysis Research. The Ethical Guidelines for Clinical Research were originally developed as three separate guidelines: Ethical Guidelines for Human Genome/Gene Analysis Research formulated in 2001, Ethical Guidelines for Epidemiological Research in 2002 and Ethical Guidelines for Clinical Research in 2003.

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  • - The study aimed to examine how the timing of ureteral ligation (either early or late) during radical nephroureterectomy affects intravesical recurrence and overall survival in patients with upper urinary tract urothelial carcinoma.
  • - A review of 664 patients showed that while the timing of ureteral ligation did not significantly affect the rate of intravesical recurrence, patients with early ureteral ligation had worse survival outcomes compared to those with late ligation.
  • - The results suggest that early ureteral ligation is associated with higher cancer-specific mortality and overall mortality, indicating it may be a critical factor to consider in surgical planning for this type of cancer.
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  • The Clinical Trials Act was enacted in April 2018 to address research misconduct and build trust in clinical trials in Japan.
  • "Specified clinical trials" involve tests using unapproved pharmaceuticals or medical devices, often funded by manufacturers with approved products.
  • Key requirements for these trials include adherence to standards, approval from a certified review board, submission of plans to health authorities, and agreements with funding manufacturers.
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  • The study aimed to compare two chemotherapy regimens—irinotecan plus cisplatin and etoposide plus cisplatin—as post-surgery treatments for lung neuroendocrine carcinoma patients.
  • Over 221 patients were enrolled in the study, which ran from 2013 to 2018, but the trial was ended early due to lack of significant results.
  • Ultimately, etoposide plus cisplatin showed no significant difference in relapse-free survival compared to irinotecan plus cisplatin, confirming etoposide plus cisplatin as the standard treatment option.
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This report summarizes the presentations and discussion in the first Japan Clinical Oncology Group-European Organisation for Research and Treatment of Cancer Quality of Life/Patient-Reported Outcome workshop funded by the National Cancer Center Hospital that was held on Saturday, 1 September 2018 in Tokyo, Japan. The infrastructure and understanding regarding the Quality of Life/Patient-Reported Outcome assessment of cancer patients in Japan is still immature, in spite of the increased demand for oncological Patient-Reported Outcome research felt not only by researchers but also by patients or other stakeholders of cancer drug development. The workshop aimed to share each perspective, common issues to be considered and future perspectives regarding the strong alliance between the European Organisation for Research and Treatment of Cancer Quality of Life Group and the Japan Clinical Oncology Group for Quality of Life/Patient-Reported Outcome research as well as explore the possibility of conducting collaborative research.

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Purpose: We investigated the impact of previous, simultaneous or subsequent bladder cancer on the clinical outcomes of upper urinary tract urothelial carcinoma.

Materials And Methods: We retrospectively collected data on 2,668 patients who underwent radical nephroureterectomy of nonmetastatic upper urinary tract urothelial carcinoma in 1995 to 2009. We evaluated the impact of bladder cancer on overall mortality and the factors predictive of subsequent bladder cancer.

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  • A randomized phase III trial aimed at evaluating the effectiveness of preoperative denosumab for treating resizable giant cell tumors of bone (GCTB) is set to begin in October 2017 across 34 institutions in Japan.
  • The study will involve 106 patients and focuses on improving relapse-free survival (RFS), given previous local recurrence rates of 24.6-30.8% after standard treatment.
  • Besides RFS, the trial will also assess various secondary endpoints, including overall survival, joint preservation, and adverse events, and is registered with the UMIN Clinical Trials Registry under UMIN000029451.
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For stage I/II tongue cancer patients, it is controversial whether prophylactic neck dissection should be performed with partial glossectomy. Based on the evidence of the primary tumor's depth of invasion as a predictive factor of occult lymph node metastases and a prognostic factor of disease-free survival, randomized phase III trial was initiated in November 2017 to evaluate the omission value for prophylactic neck dissection for stage I/II tongue cancer with 3-10 mm of depth of invasion. In 5 years, 440 patients will be accrued from 28 institutions.

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  • * S-1 has been previously shown to be effective with mild side effects in advanced cases and has benefited patients with resected gastric and pancreatic cancers.
  • * This Phase III trial, started in September 2013, aims to enroll 440 patients over four years, with a primary goal of measuring overall survival, and has been updated to enhance its statistical power.
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  • Observation is the standard treatment for Stage 0a-III upper tract urothelial carcinoma after surgery called radical nephroureterectomy.
  • A randomized Phase III trial started in Japan in October 2016 to compare the effectiveness of a single dose intravesical treatment with pirarubicin against observation for improving relapse-free survival.
  • The trial aims to enroll 310 patients over 5 years from 43 institutions, measuring primary outcomes like relapse-free survival and secondary outcomes such as overall survival and adverse effects.
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  • - The study focuses on a trial for treating advanced maxillary sinus cancer by using high-dose cisplatin via a specific method while also applying radiotherapy.
  • - During the dose-finding phase, researchers aimed to identify any serious side effects and establish how many treatment cycles of cisplatin patients should receive.
  • - Out of 18 patients, most completed 7 treatment cycles, and the therapy was found to be safe and tolerable, establishing 7 cycles as the recommended approach for these cancer patients.
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  • The study aimed to assess whether lymph node dissection (LND) during radical nephroureterectomy (RNU) improves outcomes for patients with upper urinary tract urothelial cancer (UTUC).
  • Data was collected from 2037 patients who underwent RNU between 1995-2009, distinguishing between those who had LND and those who did not; results showed no significant difference in overall survival or cancer-specific mortality between the two groups.
  • The findings suggest that while having positive lymph nodes indicates a worse prognosis, performing LND does not provide additional therapeutic benefits in this context.
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A randomized Phase III trial commenced in Japan in February 2016. Currently, 42 Gy in four fractions of stereotactic body radiotherapy prescribed at the D of the planning target volume, which is considered equal to the commonly used 48 Gy in four fractions at the isocenter using an old dose calculation algorithm, is the standard treatment in Japan for medically inoperable Stage IA non-small cell lung cancer and small lung lesions clinically diagnosed as primary lung cancer. This study aims to examine the superiority of 55 Gy in four fractions over 42 Gy in four fractions.

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  • The study aimed to compare survival outcomes between stereotactic body radiotherapy and lobectomy for early-stage non-small-cell lung cancer, as no randomized trials had been previously conducted.
  • It included patients from two clinical trials, selecting those with operable, early-stage adenocarcinoma, and used propensity score analysis to assess survival rates.
  • Results indicated that lobectomy may have better outcomes, especially in patients aged 75 or younger, highlighting the need for more rigorous randomized controlled trials for a reliable comparison.
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A randomized Phase III trial commenced in Japan in September 2014. Endoscopic local steroid injection has been commonly used and considered acceptable as the current standard treatment for the prevention of esophageal stricture after endoscopic submucosal dissection for superficial esophageal cancer. The purpose of this study is to confirm the superiority of prophylactic oral steroid administration following endoscopic submucosal dissection in terms of stricture-free survival over endoscopic local steroid injection for patients with superficial esophageal cancer.

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A randomized Phase II/III trial commenced in May 2014. Endoscopic balloon dilation with steroid injection is the current standard treatment for patients with refractory anastomotic stricture after esophagectomy. The purpose of this study is to confirm the superiority of radial incision and cutting with steroid injection in terms of both restricture-free survival and number of dilations within 24 weeks compared with endoscopic balloon dilation with steroid injection for these patients.

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  • A randomized Phase II/III trial started in Japan in December 2013 to compare the effectiveness of carboplatin plus irinotecan versus the standard treatment of carboplatin plus etoposide for elderly patients with extensive-disease small-cell lung cancer.
  • The study aims to confirm whether carboplatin plus irinotecan can improve overall survival rates in these patients, with 370 participants expected from 38 institutions over 5 years.
  • Key measures assessed include response rates and adverse events in Phase II, while Phase III focuses on overall survival along with other endpoints like progression-free survival and symptom scores.
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  • A Phase III trial, launched in Japan in March 2013, aims to compare the efficacy of irinotecan plus cisplatin against the standard treatment of etoposide plus cisplatin for patients with resected pulmonary high-grade neuroendocrine carcinoma.
  • The study involves 220 patients and focuses on overall survival as the primary endpoint, alongside secondary endpoints like relapse-free survival and treatment-related adverse events.
  • It is registered under UMIN000010298 in the UMIN Clinical Trials Registry, reflecting its commitment to rigorous clinical research standards.
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