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1.
Front Oncol ; 12: 1062389, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36703782

RESUMEN

Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is a rare T-cell lymphoma associated with textured breast implants. The most common presentation is a periprosthetic seroma that occurs at least 1 year after an aesthetic or reconstructive implantation, and in these cases, the surgical treatment seems to be successful. More rarely, BIA-ALCL presents with locally advanced mass-formed disease and a related regional lymph node involvement. In all these cases with worse prognosis, a multidisciplinary approach is required, including adjuvant chemotherapy, radiation therapy, and surgery. We present a clinical case of a 49-year-old woman who developed on the left side of the breast a mass-formed stage 3 BIA-ALCL 15 years after a bilateral breast augmentation with textured silicone implant. Our multidisciplinary team (MDT) scheduled the patient for a "reverse-strategy" sequential approach consisting of induction chemotherapy, hematopoietic stem cell mobilization, and harvest followed by autologous stem cell transplant (ASCT). After 100 days from the stem cell transplant, the patient showed a complete pathologic response and was a candidate for radical surgery. She underwent removal of both implants with total en bloc capsulectomy. On the left site, the periprosthetic mass was also en bloc removed. We did not perform any axillary dissection. Our surgical and hemato-oncological teams followed the patient every 3 months, and no local or systemic recurrences were observed 24 months after surgery. This case report has demonstrated the effectiveness of neoadjuvant chemotherapy as part of a "reverse strategy" in selected cases of advanced-stage BIA-ALCL in which it was not possible to perform an immediate radical surgery. Furthermore, in our case, the de-escalation strategy adopted permitted a less demolitic surgery with good functional and aesthetic results.

2.
J Cell Physiol ; 230(8): 1708-12, 2015 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-25510909

RESUMEN

Genomic and trascriptomic profiling has recently contributed details to the characterization of luminal B breast cancer. We explored the contribution of anthropometric, metabolic, and molecular determinants to the multifaceted heterogeneity of this breast cancer subtype, with a specific focus on the association between body mass index (BMI), pre-treatment fasting glucose, hormone receptors, and expression of human epidermal growth factor receptor 2 (HER2). Extensively annotated specimens were obtained from 154 women with luminal B breast cancer diagnosed at two Italian comprehensive cancer centres. Participants' characteristics were descriptively analyzed overall and by HER2 status (positive vs. negative). BMI (<25 vs ≥25), pre-treatment fasting glucose (

Asunto(s)
Neoplasias de la Mama/genética , Neoplasias de la Mama/metabolismo , Receptor ErbB-2/biosíntesis , Adulto , Anciano , Antropometría , Glucemia/análisis , Índice de Masa Corporal , Femenino , Humanos , Inmunohistoquímica , Persona de Mediana Edad , Receptores de Estrógenos/biosíntesis
3.
In Vivo ; 20(6A): 739-42, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-17203758

RESUMEN

BACKGROUND: Hyperthermic isolation limb perfusion (HILP) with tumor necrosis factor alpha (TNFalpha) and IFNgamma was pioneered by Liénard and Lejeune in 1988. The TNFalpha was empirically employed at a dosage of 3-4 mg, that is ten times the systemic maximum tolerated dose (MTD). After eighteen years from its first clinical application, more than 300 patients have been treated. The aim of this study is to clarify two major arguments: the TNFalpha dose and eligibility criteria for patient selection. PATIENTS AND METHODS: A phase I-II study has previously been conducted in 20 patients with in-transit melanoma metastases using a combination of melphalan and TNFalpha at dosages ranging from 0.5 to 3.3 mg. Twenty patients were treated and a complete pathological response of 70% was recorded, with no correlation between tumor response and TNFalpha. The dose of 1 mg of TNFalpha provided the best results regarding efficacy and toxicity. On the basis of this results a large phase II SITILO study was undertaken. Patients with stage IIIA - IIIAB (presence of in transit metastases and/or regional node involvement) were considered eligible; a total of 113 patients were enrolled in the study. The disease was bulky (> 10 nodules or fewer nodules with a diameter > or = 3 cm) in 42.5% of the patients and unresectable in 33%. Forty patients were treated with a TNFalpha dosage > 1 mg and 73 with 1 mg. All the patients were submitted to HILP via axillary and iliac vessels for tumor of upper and lower limb, respectively. TNFalpha was injected in the extracorporal circuit at the pre-established dose, followed after 30 minutes by melphalan (13 and 10 mg/L of limb volume for upper and lower limbs, respectively). RESULTS: A grade 1 and 2 limb toxicity was found in 52.9% and 30.1% of the patients, respectively, 5.5% of patients exhibited a grade 3 and 4, whereas grade 5 limb toxicity was not found. The complete and partial responses were 63% and 24.5%, respectively, with an objective response of 87.5%. We tried to correlate the typed tumor response (CR or not CR) and the TNFalpha dosage < or = 1 mg or > 1 mg, but no statistically significant difference was found between the two groups. The bulky disease was the only prognostic factor able to influence the tumor response. CONCLUSION: Only patients with bulky melanoma disease can benefit from HILP with TNFalpha at a low dose of 1 mg.


Asunto(s)
Hipertermia Inducida , Melanoma/terapia , Neoplasias Cutáneas/terapia , Factor de Necrosis Tumoral alfa/administración & dosificación , Adulto , Anciano , Anciano de 80 o más Años , Antineoplásicos Alquilantes/administración & dosificación , Quimioterapia del Cáncer por Perfusión Regional , Terapia Combinada , Quimioterapia Combinada , Extremidades , Femenino , Humanos , Masculino , Melanoma/secundario , Melfalán/administración & dosificación , Persona de Mediana Edad , Estadificación de Neoplasias , Neoplasias Cutáneas/patología
4.
Rev. paul. med ; 108(1): 21-5, jan.-fev. 1990. ilus
Artículo en Portugués | LILACS | ID: lil-85489

RESUMEN

Os autores, através de uma revisäo da literatura, propöem-se a verificar os parâmetros oncológicos para a definiçäo dos casos "candidatáveis" a yna reconstruçäo imediata após mastectomia de Patey. Em relaçäo ao problema das recidivas locais, pelos resultados observados, evidencia-se que a hipótese de uma prótese sob o músculo grande peitoral mascarar essas recidivas näo é estatisticamente quantificável. A reconstrçäo näo interfere também com o carcinoma mamário, seja em termos de sobrevida ou de intervalo livre da doença. Consideramos que o tempo médio de aparecimento da recidiva, também nos casos N+, é de cerca de dois anos; achamos que estas pacientes com linfonodos positivos, se motivadas e candidatas a uma mastectomia modificada, näo devem ser excluídas de um programa reconstrutivo imediato. A baixa morbidade, os custos limitados, as vantagens psicológicas e o rápido início das terapias complementares fazem da reconstruçäo imediata um recurso fundamental. Conseqüentemente, há uma melhora da qualidade de vida também para os casos com limitadas perspectivas de sobrevida


Asunto(s)
Humanos , Femenino , Mama/cirugía , Neoplasias de la Mama/cirugía , Mastectomía Radical Modificada , Recurrencia Local de Neoplasia/diagnóstico , Factores de Tiempo
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