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1.
Hautarzt ; 68(8): 632-638, 2017 Aug.
Artículo en Alemán | MEDLINE | ID: mdl-28382381

RESUMEN

BACKGROUND: Rating the response of melanoma to immune checkpoint blockade (ICB) by conventional CT proves to be difficult, since response patterns and kinetics differ from the classical responses seen with other therapies. Hence, immune-related response criteria were developed. However, they are mainly based on the alteration of the diameter of lesions over time but do not include metabolic activity. OBJECTIVE: The aim of this study was to search for additional criteria to improve the interpretation of the radiologic images of patients with metastatic melanoma after ICB. MATERIALS AND METHODS: We retrospectively analysed 7 patients with metastatic melanoma over a period of 13-41 months after treatment with ICB using contrast enhanced CT scans from the neck region to the lower abdomen and compared the results in the follow ups with 18F-FDG PET/CT. RESULTS: Metastatic lesions in 5 of 7 patients rated as stable disease (SD) in CT staging showed no metabolic activity in 18F-FDG PET/CT. The size of these lesions did not increase or show metabolic activity in the further follow-up, even after discontinuation of ICB. In contrast, tumor lesions in the other 2 patients rated as SD in CT staging showed metabolic activity in 18F-FDG PET/CT. These tumor lesions expanded significantly in the further course of the disease. CONCLUSION: In addition to the size of a tumor lesion, its metabolic activity adds important information regarding treatment response. Thus, we propose that the metabolic activity assessed with 18F-FDG-PET/CT should be included in the immune response criteria. No FDG uptake in a lesion should be rated as inactive tumor rather than SD and further treatment may not be required.


Asunto(s)
Anticuerpos Monoclonales Humanizados/uso terapéutico , Inmunoterapia/normas , Ipilimumab/uso terapéutico , Melanoma/terapia , Neoplasias Cutáneas/terapia , Adulto , Anciano , Anticuerpos Monoclonales Humanizados/efectos adversos , Anticuerpos Monoclonales Humanizados/farmacología , Femenino , Fluorodesoxiglucosa F18 , Humanos , Inmunoterapia/efectos adversos , Ipilimumab/efectos adversos , Ipilimumab/farmacología , Masculino , Melanoma/diagnóstico por imagen , Melanoma/patología , Melanoma/secundario , Persona de Mediana Edad , Metástasis de la Neoplasia , Estadificación de Neoplasias , Tomografía Computarizada por Tomografía de Emisión de Positrones , Estudios Retrospectivos , Neoplasias Cutáneas/diagnóstico por imagen , Neoplasias Cutáneas/patología , Tomografía Computarizada por Rayos X , Resultado del Tratamiento , Carga Tumoral/efectos de los fármacos
2.
J Eur Acad Dermatol Venereol ; 30(11): 1919-1925, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27581090

RESUMEN

BACKGROUND: Optical coherence tomography (OCT) has become a valuable non-invasive tool in the in vivo diagnosis of non-melanoma skin cancer, especially of basal cell carcinoma (BCC). Due to an updated software-supported algorithm, a new en-face mode - similar to the horizontal en-face mode in high-definition OCT and reflectance confocal microscopy - surface-parallel imaging is possible which, in combination with the established slice mode of frequency domain (FD-)OCT, may offer additional information in the diagnosis of BCC. OBJECTIVES: To define characteristic morphologic features of BCC using the new en-face mode in addition to the conventional cross-sectional imaging mode for three-dimensional imaging of BCC in FD-OCT. METHODS: A total of 33 BCC were examined preoperatively by imaging in en-face mode as well as cross-sectional mode in FD-OCT. Characteristic features were evaluated and correlated with histopathology findings. RESULTS: Features established in the cross-sectional imaging mode as well as additional features were present in the en-face mode of FD-OCT: lobulated structures (100%), dark peritumoral rim (75%), bright peritumoral stroma (96%), branching vessels (90%), compressed fibrous bundles between lobulated nests ('star shaped') (78%), and intranodular small bright dots (51%). These features were also evaluated according to the histopathological subtype. In the en-face mode, the lobulated structures with compressed fibrous bundles of the BCC were more distinct than in the slice mode. CONCLUSION: FD-OCT with a new depiction for horizontal and vertical imaging modes offers additional information in the diagnosis of BCC, especially in nodular BCC, and enhances the possibility of the evaluation of morphologic tumour features.


Asunto(s)
Carcinoma Basocelular/patología , Neoplasias Cutáneas/patología , Tomografía de Coherencia Óptica , Cara/patología , Femenino , Humanos , Masculino
4.
J Eur Acad Dermatol Venereol ; 29(9): 1816-21, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25712452

RESUMEN

BACKGROUND: Folliculitis decalvans leads to scarring alopecia through inflammatory destruction of the hair follicle. Currently, antibiotics are most commonly used to treat this disease. However, treatment regimens with antibiotics feature a high relapse rate and encourage the development of resistant bacteria. OBJECTIVE: To evaluate the outcome of different treatment options for folliculitis decalvans. METHODS: Retrospective study to compare the efficacy of different treatment regimens in 28 patients with folliculitis decalvans. RESULTS: The success of treatment with clindamycin and rifampicin, clarithromycin, dapsone and isotretinoin was analysed. The evaluation of the combination of clindamycin and rifampicin showed the lowest success rate in achieving long-term remission, since 80% of the patients relapsed shortly after end of treatment. Clarithromycin and dapsone were more successful with long-term and stable remission rates of 33% and 43% respectively. Treatment with isotretinoin was the most successful oral treatment in our analysis with 90% of the patients experiencing stable remission during and up to two years after cessation of the treatment. CONCLUSION: The common use of antibiotics as first-line therapy in folliculitis decalvans needs to be re-evaluated critically and oral isotretinoin should be considered as valid treatment alternative.


Asunto(s)
Clindamicina/administración & dosificación , Foliculitis/tratamiento farmacológico , Isotretinoína/administración & dosificación , Rifampin/administración & dosificación , Dermatosis del Cuero Cabelludo/tratamiento farmacológico , Administración Oral , Adulto , Antibacterianos/administración & dosificación , Fármacos Dermatológicos/administración & dosificación , Quimioterapia Combinada , Femenino , Foliculitis/diagnóstico , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Dermatosis del Cuero Cabelludo/diagnóstico , Resultado del Tratamiento , Adulto Joven
5.
Dtsch Med Wochenschr ; 139(28-29): 1462-7, 2014 Jul.
Artículo en Alemán | MEDLINE | ID: mdl-24983194

Asunto(s)
Antineoplásicos/uso terapéutico , Melanoma/tratamiento farmacológico , Terapia Molecular Dirigida , Neoplasias Cutáneas/tratamiento farmacológico , Anticuerpos Monoclonales/efectos adversos , Anticuerpos Monoclonales/uso terapéutico , Antineoplásicos/efectos adversos , Ensayos Clínicos como Asunto , Análisis Mutacional de ADN , Progresión de la Enfermedad , Supervivencia sin Enfermedad , Resistencia a Antineoplásicos , Quimioterapia Combinada , GTP Fosfohidrolasas/antagonistas & inhibidores , GTP Fosfohidrolasas/genética , Humanos , Imidazoles/efectos adversos , Imidazoles/uso terapéutico , Inmunoterapia , Indoles/efectos adversos , Indoles/uso terapéutico , Ipilimumab , MAP Quinasa Quinasa 1/antagonistas & inhibidores , MAP Quinasa Quinasa 1/genética , MAP Quinasa Quinasa 2/antagonistas & inhibidores , MAP Quinasa Quinasa 2/genética , Melanoma/genética , Melanoma/mortalidad , Melanoma/patología , Proteínas de la Membrana/antagonistas & inhibidores , Proteínas de la Membrana/genética , Estadificación de Neoplasias , Oximas/efectos adversos , Oximas/uso terapéutico , Inhibidores de Proteínas Quinasas/efectos adversos , Inhibidores de Proteínas Quinasas/uso terapéutico , Proteínas Proto-Oncogénicas B-raf/antagonistas & inhibidores , Proteínas Proto-Oncogénicas B-raf/genética , Neoplasias Cutáneas/genética , Neoplasias Cutáneas/mortalidad , Neoplasias Cutáneas/patología , Sulfonamidas/efectos adversos , Sulfonamidas/uso terapéutico , Vemurafenib
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