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Métodos Terapéuticos y Terapias MTCI
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1.
J Thorac Cardiovasc Surg ; 160(1): 261-271.e1, 2020 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-31924363

RESUMEN

OBJECTIVES: To examine guideline concordance across a national sample and determine the relationship between socioeconomic factors, use of recommended postoperative adjuvant therapy, and outcomes for patients with resected pN1 or pN2 non-small cell lung cancer. METHODS: All margin-negative pT1-3 N1-2 M0 non-small cell lung cancers treated with lobectomy or pneumonectomy without induction therapy in the National Cancer Database between 2006 and 2013 were included. Use of guideline-concordant adjuvant treatment, defined as chemotherapy for pN1 disease and chemotherapy with or without radiation for pN2 disease, was examined. Multivariable regression models were developed to determine associations of clinical factors with guideline adherence. Survival was estimated using Kaplan-Meier and Cox proportional hazard analyses. RESULTS: Of 13,462 patients, 10,113 had pN1 disease and 3349 had pN2 disease. Guideline-concordant adjuvant therapy was used in 6844 (67.7%) patients with pN1 disease and 2622 (78.3%) patients with pN2 disease. After multivariable adjustment, insurance status, older age, pneumonectomy, readmission, and longer postoperative stays were associated with lower likelihood of guideline concordance. Conversely, increased education level, later year of diagnosis, and greater nodal stage were associated with greater concordance. Overall, patients treated with guideline-concordant therapy had superior survival (5-year survival: 51.6 vs 36.0%; hazard ratio, 0.66; 95% confidence interval, 0.62-0.70, P < .001). CONCLUSIONS: Socioeconomic factors, including insurance status and geographic region, are associated with disparities in use of adjuvant therapy as recommended by National Comprehensive Cancer Network guidelines. These disparities significantly impact patient survival. Future work should focus on improving access to appropriate adjuvant therapies among the under insured and socioeconomically disadvantaged.


Asunto(s)
Carcinoma de Pulmón de Células no Pequeñas , Adhesión a Directriz/estadística & datos numéricos , Disparidades en Atención de Salud/estadística & datos numéricos , Neoplasias Pulmonares , Cuidados Posoperatorios , Anciano , Carcinoma de Pulmón de Células no Pequeñas/epidemiología , Carcinoma de Pulmón de Células no Pequeñas/mortalidad , Carcinoma de Pulmón de Células no Pequeñas/terapia , Femenino , Humanos , Neoplasias Pulmonares/epidemiología , Neoplasias Pulmonares/mortalidad , Neoplasias Pulmonares/terapia , Masculino , Persona de Mediana Edad , Neumonectomía , Cuidados Posoperatorios/mortalidad , Cuidados Posoperatorios/estadística & datos numéricos , Estudios Retrospectivos
2.
J Immunother ; 32(8): 870-4, 2009 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-19752747

RESUMEN

A patient with metastatic melanoma who had progressive disease after prior surgical resections, high dose interleukin-2, and anti-cytotoxic T lymphocyte antigen-4 antibody received sequential treatments with autologous tumor infiltrating lymphocytes that recognized the gp100 melanocyte differentiation antigen. Although no clinical response was seen when cells were administered alone, an objective clinical response to therapy was seen with tumor infiltrating lymphocytes administered together with a highly immunogenic fowlpox vaccine expressing a gp100: 209-217 (210M) epitope. Persistence of the transferred antigen-specific lymphocytes in the peripheral blood was observed only after adoptive cell therapy plus administration of vaccine. Cell proliferation in vitro was further stimulated by additional vaccine and interleukin-2. The patient has an ongoing partial response at 10 months after the last treatment.


Asunto(s)
Neoplasias Faciales/inmunología , Neoplasias Faciales/terapia , Virus de la Viruela de las Aves de Corral , Inmunoterapia Adoptiva , Linfocitos Infiltrantes de Tumor/metabolismo , Melanoma/inmunología , Melanoma/terapia , Transfusión de Sangre Autóloga , Proliferación Celular , Progresión de la Enfermedad , Epítopos de Linfocito T/genética , Epítopos de Linfocito T/metabolismo , Neoplasias Faciales/patología , Humanos , Linfocitos Infiltrantes de Tumor/patología , Masculino , Melanoma/patología , Glicoproteínas de Membrana/genética , Glicoproteínas de Membrana/metabolismo , Persona de Mediana Edad , Metástasis de la Neoplasia , Vacunas Virales/genética , Antígeno gp100 del Melanoma
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