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1.
J Clin Oncol ; 30(15): 1805-12, 2012 May 20.
Artículo en Inglés | MEDLINE | ID: mdl-22508807

RESUMEN

PURPOSE: Prolonged and disabling fatigue is prevalent after cancer treatment, but the early natural history of cancer-related fatigue (CRF) has not been systematically examined to document consistent presence of symptoms. Hence, relationships to cancer, surgery, and adjuvant therapy are unclear. PATIENTS AND METHODS: A prospective cohort study of women receiving adjuvant treatment for early-stage breast cancer was conducted. Women (n = 218) were enrolled after surgery and observed at end treatment and at 1, 3, 6, 9, and 12 months as well as 5 years. Structured interviews and self-report questionnaires were used to record physical and psychologic health as well as disability and health care utilization. Patients with CRF persisting for 6 months were assessed to exclude alternative medical and psychiatric causes of fatigue. Predictors of persistent fatigue, mood disturbance, and health care utilization were sought by logistic regression. RESULTS: The case rate for CRF was 24% (n = 51) postsurgery and 31% (n = 69) at end of treatment; it became persistent in 11% (n = 24) at 6 months and 6% (n = 12) at 12 months. At each time point, approximately one third of the patients had comorbid mood disturbance. Persistent CRF was predicted by tumor size but not demographic, psychologic, surgical, or hematologic parameters. CRF was associated with significant disability and health care utilization. CONCLUSION: CRF is common but generally runs a self-limiting course. Much of the previously reported high rates of persistent CRF may be attributable to factors unrelated to the cancer or its treatment.


Asunto(s)
Neoplasias de la Mama/terapia , Fatiga/epidemiología , Mastectomía/efectos adversos , Adulto , Afecto , Neoplasias de la Mama/epidemiología , Neoplasias de la Mama/patología , Quimioradioterapia Adyuvante/efectos adversos , Quimioterapia Adyuvante/efectos adversos , Distribución de Chi-Cuadrado , Comorbilidad , Evaluación de la Discapacidad , Fatiga/diagnóstico , Fatiga/psicología , Femenino , Humanos , Entrevistas como Asunto , Modelos Lineales , Modelos Logísticos , Persona de Mediana Edad , Estadificación de Neoplasias , Nueva Gales del Sur , Oportunidad Relativa , Estudios Prospectivos , Radioterapia Adyuvante/efectos adversos , Medición de Riesgo , Factores de Riesgo , Encuestas y Cuestionarios , Factores de Tiempo , Resultado del Tratamiento , Carga Tumoral
2.
Cancer Invest ; 27(2): 193-200, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19235592

RESUMEN

PURPOSE: To determine the maximal tolerated dose of capecitabine with oxaliplatin + radiotherapy in a phase I study of localized esophageal cancer. PATIENTS AND METHODS: Oxaliplatin (85 mg/m(2)) administered on days 1, 15, and 29. Capecitabine administered twice daily 5 days weekly; dose levels (DL) were 1, 1000; 2, 1250; and 3, 1500 mg/m(2) with 50.4 Gy radiation. RESULTS: Dose-limiting toxicity was reached at DL 3. Carboxylesterase expression in day 2 tumor specimens and induction correlated with response (p

Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Neoplasias Esofágicas/terapia , Adulto , Anciano , Capecitabina , Carboxilesterasa/genética , Terapia Combinada , Citidina Desaminasa/genética , Desoxicitidina/administración & dosificación , Desoxicitidina/efectos adversos , Desoxicitidina/análogos & derivados , Desoxicitidina/farmacocinética , Neoplasias Esofágicas/metabolismo , Femenino , Fluorouracilo/administración & dosificación , Fluorouracilo/efectos adversos , Fluorouracilo/análogos & derivados , Fluorouracilo/farmacocinética , Humanos , Masculino , Persona de Mediana Edad , Compuestos Organoplatinos/administración & dosificación , Compuestos Organoplatinos/efectos adversos , Compuestos Organoplatinos/farmacocinética , Oxaliplatino , Timidina Fosforilasa/genética
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