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1.
Chinese Journal of Oncology ; (12): 88-94, 2023.
Artículo en Chino | WPRIM | ID: wpr-969810

RESUMEN

Objective: To explore the application and efficacy of paclitaxel liposome in the treatment of advanced breast cancer among Chinese population in the real world. Methods: The clinical characteristics of patients with advanced breast cancer who received paclitaxel liposome as salvage treatment from January 1, 2016 to August 31, 2019 in 11 hospitals were collected and retrospectively analyzed. The primary outcome was progression free survival (PFS), and the secondary outcome included objective response rate (ORR) and safety. The survival curve was drawn by Kaplan-Meier analysis and the Cox regression model were used for the multivariate analysis. Results: Among 647 patients with advanced breast cancer who received paclitaxel liposome, the first-line treatment accounted for 43.3% (280/647), the second-line treatment accounted for 27.7% (179/647), and the third-line and above treatment accounted for 29.1% (188/647). The median dose of first-line and second-line treatment was 260 mg per cycle, and 240 mg in third line and above treatment. The median period of paclitaxel liposome alone and combined chemotherapy or targeted therapy is 4 cycles and 6 cycles, respectively. In the whole group, 167 patients (25.8%) were treated with paclitaxel liposome combined with capecitabine±trastuzumab (TX±H), 123 patients (19.0%) were treated with paclitaxel liposome alone (T), and 119 patients (18.4%) were treated with paclitaxel liposome combined with platinum ± trastuzumab (TP±H), 108 patients (16.7%) were treated with paclitaxel liposome combined with trastuzumab ± pertuzumab (TH±P). The median PFS of first-line and second-line patients (5.5 and 5.5 months, respectively) were longer than that of patients treated with third line and above (4.9 months, P<0.05); The ORR of the first line, second line, third line and above patients were 46.7%, 36.8% and 28.2%, respectively. Multivariate analysis showed that event-free survival (EFS) and the number of treatment lines were independent prognostic factors for PFS. The common adverse events were myelosuppression, gastrointestinal reactions, hand foot syndrome and abnormal liver function. Conclusion: Paclitaxel liposomes is widely used and has promising efficacy in multi-subtype advanced breast cancer.


Asunto(s)
Humanos , Femenino , Neoplasias de la Mama/inducido químicamente , Paclitaxel/efectos adversos , Liposomas/uso terapéutico , Estudios Retrospectivos , Resultado del Tratamiento , Trastuzumab/uso terapéutico , Capecitabina/uso terapéutico , Protocolos de Quimioterapia Combinada Antineoplásica/efectos adversos
2.
Chinese Journal of Oncology ; (12): 660-663, 2004.
Artículo en Chino | WPRIM | ID: wpr-331237

RESUMEN

<p><b>OBJECTIVE</b>To identify molecular markers of lung squamous cell carcinoma by cDNA microarray technique.</p><p><b>METHODS</b>cDNA expression profiles were examined by microarrays of 6 surgical specimens of stage I lung squamous cell carcinomas. Those genes, either up-regulated or down-regulated in every specimen studied, were identified. The expression levels of nm23 and BRCA2 by the squamous cell carcinoma of the lung were further examined by immunohistochemical techniques.</p><p><b>RESULTS</b>A total of 107 genes were identified, of which 26 were up-regulated and 81 were down-regulated in all six specimens. Immunohistochemical staining showed that, compared with normal lung tissues, the intensity of nm23 expression by the squamous cell carcinoma of lung was significantly increased while that of BRCA-2 was decreased.</p><p><b>CONCLUSION</b>cDNA microarrays can be used to identify gene expression profile of lung cancer, some of which may be used as markers of lung squamous cell carcinoma.</p>


Asunto(s)
Humanos , Masculino , Proteína BRCA2 , Metabolismo , Biomarcadores de Tumor , Carcinoma de Células Escamosas , Genética , Metabolismo , Perfilación de la Expresión Génica , Neoplasias Pulmonares , Genética , Metabolismo , Nucleósido Difosfato Quinasas NM23 , Nucleósido-Difosfato Quinasa , Metabolismo , Análisis de Secuencia por Matrices de Oligonucleótidos
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