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1.
J Eur Acad Dermatol Venereol ; 31(4): 636-642, 2017 Apr.
Article in English | MEDLINE | ID: mdl-27633490

ABSTRACT

BACKGROUND: To date, lactate dehydrogenase (LDH) and S100B remain the most useful biomarkers for follow-up of melanoma patients. In recent years, indoleamine 2,3-dioxygenase (IDO), an immunosuppressive enzyme, has been proposed as a new potential tumour biomarker for melanoma. However, further studies are needed to confirm the usefulness of IDO expression as an independent prognostic factor. OBJECTIVE: To explore the potential association between serum IDO levels and melanoma stage at diagnosis and recurrence, and to compare the results to those obtained with LDH and S100B. In addition, we also investigated a possible cut off for IDO level as a prognostic factor for overall survival. METHODS: IDO, LDH and S100B levels were measured in serum samples of 186 patients in all melanoma stages at diagnosis and twice a year thereafter. A cut-off point for IDO levels was calculated using receiver operating characteristic curves to explore the association between these levels and the likelihood of lymphatic spread. Survival curves were estimated for patient groups stratified by IDO level (higher or lower than the cut off), using the Kaplan-Meier method. RESULTS: At diagnosis, serum IDO levels were significantly higher in stages IB, II, III and IV, whereas S100B levels were significantly higher in stages III and IV, and LDH levels were only higher in stage IV. In relapsed patients, significant increases were found in levels of all three markers. Finally, overall survival was significantly longer in patients with IDO levels below a cut off of 1.65 µM at diagnosis than in those with higher levels (91.3 vs. 71.0% at 36 months). CONCLUSION: In melanoma patients, serum IDO levels are significantly associated with disease stage, relapses and overall survival. These results indicate IDO could be a useful serum prognostic marker for melanoma.


Subject(s)
Indoleamine-Pyrrole 2,3,-Dioxygenase/blood , Melanoma/blood , Melanoma/secondary , Neoplasm Recurrence, Local/blood , Skin Neoplasms/blood , Skin Neoplasms/pathology , Adult , Aged , Aged, 80 and over , Biomarkers, Tumor/blood , Female , Humans , L-Lactate Dehydrogenase/blood , Male , Melanoma/diagnosis , Middle Aged , Neoplasm Metastasis , Neoplasm Staging , Prognosis , ROC Curve , S100 Calcium Binding Protein beta Subunit/blood , Skin Neoplasms/diagnosis , Survival Rate , Young Adult
2.
An Sist Sanit Navar ; 29(3): 349-56, 2006.
Article in Spanish | MEDLINE | ID: mdl-17224938

ABSTRACT

INTRODUCTION: Pre and post-operative oncological therapy in patients with breast cancer is determined, amongst other factors, by hormone receptor status and by c-erbB2 expression. The aim of this study is to determine the influence of neoadjuvant therapy on the expression of oestrogen receptor (OR), progesterone receptor (PR) and c-erbB2. METHODS: Fifty-three patients with breast cancer diagnosed by tru-cut biopsy were studied. Patients with locally advanced carcinoma (20) had preoperative treatment. All patients underwent surgical resection. Expression of OR, PR and c-erbB2 in both the tru-cut biopsy and the gross specimen was compared. RESULTS: We found significant differences in OR, PR expression in both biopsy and gross specimen, between the group of patients who underwent neoadjuvant treatment and the group without pre-surgical treatment. Changes in PR, OR and c-erbB2 status were found between the tru-cut biopsy and the gross specimen, in about 10 to 40% of the cases who received neoadjuvant therapy. These changes had no statistical significance.


Subject(s)
Breast Neoplasms , Carcinoma , Genes, erbB-2/genetics , Neoadjuvant Therapy/methods , Receptors, Estrogen/immunology , Receptors, Progesterone/immunology , Breast Neoplasms/genetics , Breast Neoplasms/immunology , Breast Neoplasms/therapy , Carcinoma/genetics , Carcinoma/immunology , Carcinoma/therapy , Female , Humans , Immunohistochemistry
3.
An Sist Sanit Navar ; 28(3): 367-77, 2005.
Article in Spanish | MEDLINE | ID: mdl-16421615

ABSTRACT

Primary cerebral lymphoma (Primary CNS Lymphoma, PCNSL) is an aggressive non-Hodgkin lymphoma that originates in the central nervous system without evidence of lymphoma in any other localization at the time of diagnosis. Primary cerebral lymphomas are less well-known and are characterized than their homologues the systemic lymphomas, as they are an entity whose frequency was scarce until a few decades ago. However, the great rise in incidence that this pathology has undergone over the last three decades, and which is still unexplained, makes more studies necessary to better understand the etiopathology of this entity. Thanks to the new systems of treatment, the prognosis of this pathology has improved significantly in recent years. Nonetheless, treatment of primary cerebral lymphoma continues to give rise to numerous controversies at present due to its high neurotoxicity in patients over 60 years of age, a group of patients frequently affected by this pathology. To resolve these and other questions it is necessary to deep in the study of primary cerebral lymphoma and to carry out high quality clinical trials.


Subject(s)
Brain Neoplasms , Lymphoma, Non-Hodgkin , Brain Neoplasms/complications , Brain Neoplasms/diagnosis , Brain Neoplasms/therapy , Female , Hospitals , Humans , Lymphoma, AIDS-Related , Lymphoma, Non-Hodgkin/complications , Lymphoma, Non-Hodgkin/diagnosis , Lymphoma, Non-Hodgkin/therapy , Male , Middle Aged , Spain
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