Publications by authors named "Maruyama D"

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  • * New treatment options include targeted drugs like antibody-drug conjugates and small molecules, as well as immune therapies such as CAR T cell therapy and bispecific antibodies, altering how DLBCL and FL are approached therapeutically.
  • * Currently, treatment choices are primarily based on factors like patient history, age, and response to previous therapies rather than randomized trials or a standardized prognostic index, highlighting a need for more comprehensive treatment strategies and future research in this area
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  • Researchers are testing valemetostat, an EZH2 and EZH1 inhibitor, for safety and effectiveness in patients with relapsed or refractory non-Hodgkin lymphoma, due to limited treatment options and poor outcomes.
  • The study involved 90 participants from 19 hospitals across Japan and the USA, who received varying doses of valemetostat in a phase 1 clinical trial to find the right dosage and assess its anti-tumor effects.
  • Initial findings will help determine the most effective dosages and provide insights into the drug's safety profile, with a majority of patients having peripheral T-cell lymphoma.
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  • * The study is a phase III trial testing whether high-dose therapy with autologous stem cell transplantation improves progression-free survival over simply observing patients who have responded well to initial treatment.
  • * A total of 140 patients will participate from 52 hospitals in Japan over a period of 5.5 years, and the trial is officially registered in the Japan Registry of Clinical Trials.
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  • * For patients with limited-stage FL, radiation therapy is preferred and can result in nearly 20 years of median survival, whereas advanced-stage patients with low tumor burden may benefit from a strategy of careful monitoring (watchful waiting).
  • * Advanced-stage patients with high tumor burden typically receive chemoimmunotherapy, while various treatments are being explored for relapsed cases, including new therapies like CAR T-cell and bispecific antibodies.
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Background: Immunofixation electrophoresis (IFE) is the standard method for confirming the presence of a monoclonal protein (M-protein) at multiple myeloma (MM) diagnosis. IFE is also essential at assessment of complete response (CR) and stringent CR during treatment. As the CR assessment is influenced by daratumumab and isatuximab, HYDRASHIFT assays were developed.

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  • Scientists want to understand how blood flows around arteriovenous malformations (AVMs) in the brain to treat them better.
  • They used a special scanning technique called PET to look at how blood and oxygen are working in patients with unruptured AVMs.
  • They found that their new method (DBFM) works well to ensure accurate measurements, making it a promising way to study blood flow changes in patients with AVMs.
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  • A study called JCOG1305 tested a new way to treat young people with advanced classic Hodgkin lymphoma (cHL) using a special PET scan after two treatment cycles.
  • Patients aged 16-60 received specific chemotherapy and then their PET scans determined if they continued the same treatment or switched to a stronger one.
  • The results showed that most patients had a good chance of staying cancer-free for at least two years, making the PET-guided treatment a promising option for younger patients with this type of cancer.
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Gut microbial products are known to act both locally within the intestine and get absorbed into circulation, where their effects can extend to numerous distant organ systems. Short-chain fatty acids (SCFA) are one class of metabolites produced by gut microbes during the fermentation of indigestible dietary fiber. They are now recognized as important contributors to how the gut microbiome influences extra-intestinal organ systems via the gut-lung, gut-brain, and other gut-organ axes throughout the host.

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Background: Multidrug chemotherapy for Ewing sarcoma can lead to severe myelosuppression. We proposed two clinical questions (CQ): CQ #1, "Does primary prophylaxis with G-CSF benefit chemotherapy for Ewing sarcoma?" and CQ #2, "Does G-CSF-based intensified chemotherapy improve Ewing sarcoma treatment outcomes?".

Methods: A comprehensive literature search was conducted in PubMed, Cochrane Library, and Ichushi web databases, including English and Japanese articles published from 1990 to 2019.

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Introduction: Chemotherapy for breast cancer can cause neutropenia, increasing the risk of febrile neutropenia (FN) and serious infections. The use of granulocyte colony-stimulating factors (G-CSF) as primary prophylaxis has been explored to mitigate these risks. To evaluate the efficacy and safety of primary G-CSF prophylaxis in patients with invasive breast cancer undergoing chemotherapy.

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  • G-CSF is a supportive treatment used to prevent severe complications from chemotherapy in patients with non-round cell soft tissue sarcomas (NRC-STS), with two key clinical questions raised about its effectiveness.
  • A literature review found a limited number of studies that addressed these questions, resulting in only a few articles being included for analysis.
  • The conclusion suggests that there is insufficient scientific evidence to confirm the benefits of G-CSF prophylaxis in improving treatment outcomes for NRC-STS, indicating the need for further research.
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There are two main types of clinical trials: industry-sponsored trials and investigator-initiated trials. Both of these, like the two sets of wheels on a car, are essential to development of treatments. Numerous clinical trials have been conducted in multiple myeloma, contributing to the development of new drugs and the current treatment landscape.

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Bone quality is an essential factor determining bone strength. However, the relationship between physical activity (PA) and bone quality remains unclear. This study aimed to ascertain the relationship between bone quality and PA using a cortical bone quantitative ultrasound device that measures components of bone quality.

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  • Relapsed or refractory acute myeloid leukemia (AML) has poor outcomes, and the impact of granulocyte colony-stimulating factor (G-CSF) combined with chemotherapy is still debated.
  • A systematic literature review and meta-analysis were conducted, assessing 11 studies, which suggested that G-CSF priming did not significantly improve response rates or overall survival for AML patients, although there was a slight trend towards lower relapse rates.
  • Certain groups, particularly those with intermediate cytogenetic risk and those receiving high-dose cytarabine, showed prolonged overall survival with G-CSF priming, indicating the need for further research to find the most suitable patients for this treatment approach.*
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Background: Febrile neutropenia represents a critical oncologic emergency, and its management is pivotal in cancer therapy. In several guidelines, the use of granulocyte colony-stimulating factor (G-CSF) in patients with chemotherapy-induced febrile neutropenia is not routinely recommended except in high-risk cases. The Japan Society of Clinical Oncology has updated its clinical practice guidelines for the use of G-CSF, incorporating a systematic review to address this clinical question.

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  • Granulocyte colony-stimulating factor (G-CSF) is used to prevent febrile neutropenia (FN) in cancer patients, with two types available in Japan: long-lasting PEG G-CSF and short-term non-PEG G-CSF.
  • A systematic review of studies found that PEG G-CSF significantly reduces the incidence of FN compared to non-PEG G-CSF, based on a thorough analysis of 23 articles.
  • The study concludes that a single dose of PEG G-CSF is preferred for primary prevention of FN, as it shows stronger evidence compared to multiple doses of non-PEG G-CSF.
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Follicular lymphoma (FL) is an indolent lymphoma that becomes aggressive due to histological transformation (HT), leading to reduced survival. Patients with FL have different clinical courses and various treatment options. Some patients exhibit shorter survival and experience disease progression within 24 months of diagnosis/treatment (POD24); the optimal treatment remains an unmet needs.

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  • Granulocyte colony-stimulating factor (G-CSF) is used to reduce the risk of neutropenia and infections during cancer chemotherapy, but its effectiveness for digestive system tumors is still uncertain.
  • A systematic review was conducted to evaluate the effectiveness of G-CSF as primary prophylaxis and its impact on the intensity of chemotherapy for various digestive system tumors.
  • The findings indicated that while G-CSF's use in colorectal cancer chemotherapy is inappropriate, there wasn't enough data to make strong recommendations for other types of digestive cancers.
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Background: Docetaxel (DTX) is commonly used as a primary chemotherapy, and cabazitaxel (CBZ) has shown efficacy in patients who are DTX resistant. Primary prophylactic granulocyte colony stimulating factor (G-CSF) therapy is currently used with CBZ treatment in routine clinical care in Japan.

Methods: In this study, we performed a systematic review following the Minds guidelines to investigate the effectiveness and safety of primary prophylaxis with G-CSF during chemotherapy for prostate cancer and to construct G-CSF guidelines for primary prophylaxis use during chemotherapy.

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High-risk cytogenetic abnormalities (HRCAs) influence the prognosis of multiple myeloma (MM). However, additional cytogenetic aberrations can lead to poor outcomes. This study aimed to clarify whether HRCAs and additional chromosomal abnormalities affect MM prognosis.

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  • The review examines the optimal timing for administering prophylactic pegylated granulocyte colony-stimulating factor (G-CSF) during cancer chemotherapy, focusing mainly on Day 2 versus Days 3-5.
  • Out of 300 studies initially reviewed, only four met the criteria, suggesting a potential increase in febrile neutropenia when G-CSF is given on Days 3-5 compared to Day 2, but no significant differences in overall survival or infection-related mortality were found.
  • The findings indicate weak recommendations for both timing options and emphasize the need for more research to make clearer guidelines for pegylated G-CSF administration.
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Granulocyte colony-stimulating factor (G-CSF) decreases the incidence, duration, and severity of febrile neutropenia (FN); however, dose reduction or withdrawal is often preferred in the management of adverse events in the treatment of urothelial cancer. It is also important to maintain therapeutic intensity in order to control disease progression and thereby relieve symptoms, such as hematuria, infection, bleeding, and pain, as well as to prolong the survival. In this clinical question, we compared treatment with primary prophylactic administration of G-CSF to maintain therapeutic intensity with conventional standard therapy without G-CSF and examined the benefits and risks as major outcomes.

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