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1.
Molecules ; 27(10)2022 May 23.
Artículo en Inglés | MEDLINE | ID: mdl-35630817

RESUMEN

Fibroadenomas (FAs) and phyllodes tumors (PTs) are major benign breast tumors, pathologically classified as fibroepithelial tumors. Although the clinical management of PTs differs from FAs, distinction by core needle biopsy diagnoses is still challenging. Here, a combined technique of label-free imaging with multi-photon microscopy and artificial intelligence was applied to detect quantitative signatures that differentiate fibroepithelial lesions. Multi-photon excited autofluorescence and second harmonic generation (SHG) signals were detected in tissue sections. A pixel-wise semantic segmentation method using a deep learning framework was used to separate epithelial and stromal regions automatically. The epithelial to stromal area ratio and the collagen SHG signal strength were investigated for their ability to distinguish fibroepithelial lesions. An image segmentation analysis with a pixel-wise semantic segmentation framework using a deep convolutional neural network showed the accurate separation of epithelial and stromal regions. A further investigation, to determine if scoring the epithelial to stromal area ratio and the SHG signal strength within the stromal area could be a marker for differentiating fibroepithelial tumors, showed accurate classification. Therefore, molecular and morphological changes, detected through the assistance of computational and label-free multi-photon imaging techniques, enable us to propose quantitative signatures for epithelial and stromal alterations in breast tissues.


Asunto(s)
Neoplasias de la Mama , Fibroadenoma , Neoplasias Fibroepiteliales , Inteligencia Artificial , Neoplasias de la Mama/patología , Computadores , Diagnóstico Diferencial , Femenino , Fibroadenoma/diagnóstico por imagen , Fibroadenoma/patología , Humanos , Neoplasias Fibroepiteliales/diagnóstico
2.
Clin Ther ; 40(12): 2170-2179, 2018 12.
Artículo en Inglés | MEDLINE | ID: mdl-30392814

RESUMEN

PURPOSE: The aim of this study was to identify a high-risk or low-risk population for chemotherapy-induced nausea and vomiting among patients with breast cancer treated with a current standard 3-drug antiemetic regimen and receiving anthracycline. METHODS: We analyzed data from chemotherapy-naive Japanese patients with breast cancer, who had received the first cycle of anthracycline-based regimen and were treated with a 3-drug combination of aprepitant, palonosetron, and dexamethasone. This study was carried out at Ehime University Hospital (Toon, Japan) using electronic medical records from May 2011 to June 2017. The primary end point was complete response (CR), which was defined as no emesis and no use of rescue medication. FINDINGS: A total of 103 patients were included in this study. The percentages of patients who had a CR in the overall, acute, and delayed phases were 35.0%, 40.8%, and 50.5%, respectively. Multivariate logistic regression analysis revealed that age <55 years and body mass index <27.5 kg/m2 were significantly associated with an increased risk for CR failure in the overall and acute phases. In contrast, a history of alcohol habit was significantly associated with a decreased risk for CR failure in overall phase. IMPLICATIONS: The present findings suggest that, among patients with breast cancer receiving anthracycline and treated with aprepitant, palonosetron, and dexamethasone, patients younger than 55 years and having a body mass index <27.5 kg/m2 are high-risk populations for chemotherapy-induced nausea and vomiting, whereas those with a history of habitual alcohol consumption is a low-risk one.


Asunto(s)
Antieméticos/uso terapéutico , Antineoplásicos/efectos adversos , Neoplasias de la Mama/tratamiento farmacológico , Náusea/inducido químicamente , Vómitos/inducido químicamente , Antraciclinas/uso terapéutico , Aprepitant/uso terapéutico , Dexametasona/uso terapéutico , Femenino , Humanos , Persona de Mediana Edad , Palonosetrón/uso terapéutico , Estudios Retrospectivos , Factores de Riesgo
3.
Sci Rep ; 8(1): 16232, 2018 11 02.
Artículo en Inglés | MEDLINE | ID: mdl-30389996

RESUMEN

This study aimed to compare the antiemetic efficacy and safety of a four-drug combination with those of a standard three-drug combination in Japanese patients with breast cancer treated with anthracycline. We retrospectively analyzed data from Japanese patients with breast cancer, who had received their first cycle of anthracycline and were treated with aprepitant, palonosetron, and dexamethasone with or without olanzapine. This retrospective observational study was performed at Ehime University Hospital using the electronic medical records. Multivariable and propensity score-adjusted analyses were performed to compare the onset of complete response (CR) failure between the groups. One-hundred and thirty patients were included in this study and the four- and three-drug group had 22 and 108 patients, respectively. Similar to multivariable logistic regression analysis, propensity-adjusted logistic regression analysis revealed that the four-drug group was markedly associated with a decreased odds of CR failure in the overall, acute, and delayed phases (odds ratio [OR]: 0.27, 95% confidence interval [CI]: 0.10-0.73; OR: 0.28, 95% CI: 0.10-0.76; and OR: 0.15, 95% CI: 0.04-0.57, respectively). Additionally, treatment-related adverse events were well tolerated in both the groups. These findings suggest that the antiemetic efficacy of the four-drug combination is superior to that of the standard three-drug combination.


Asunto(s)
Antraciclinas/efectos adversos , Antieméticos/administración & dosificación , Protocolos de Quimioterapia Combinada Antineoplásica/efectos adversos , Neoplasias de la Mama/tratamiento farmacológico , Náusea/prevención & control , Vómitos/prevención & control , Antieméticos/efectos adversos , Aprepitant/administración & dosificación , Aprepitant/efectos adversos , Dexametasona/administración & dosificación , Dexametasona/efectos adversos , Quimioterapia Combinada/métodos , Femenino , Humanos , Incidencia , Persona de Mediana Edad , Náusea/inducido químicamente , Olanzapina/administración & dosificación , Olanzapina/efectos adversos , Palonosetrón/administración & dosificación , Palonosetrón/efectos adversos , Estudios Retrospectivos , Trastornos del Inicio y del Mantenimiento del Sueño/inducido químicamente , Trastornos del Inicio y del Mantenimiento del Sueño/epidemiología , Somnolencia , Resultado del Tratamiento , Vómitos/inducido químicamente
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