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1.
Ann Hematol ; 96(7): 1069-1075, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28451802

ABSTRACT

We investigated the frequency, predictors, and evolution of acute lymphoblastic leukemia (ALL) in patients with CNS relapse and introduced a novel method for studying BCR-ABL1 protein variants in cDNA from bone marrow (BM) and cerebrospinal fluid (CSF) blast cells. A total of 128 patients were analyzed in two PETHEMA clinical trials. All achieved complete remission after imatinib treatment. Of these, 30 (23%) experienced a relapse after achieving complete remission, and 13 (10%) had an isolated CNS relapse or combined CNS and BM relapses. We compared the characteristics of patients with and without CNS relapse and further analyzed CSF and BM samples from two of the 13 patients with CNS relapse. In both patients, classical sequencing analysis of the kinase domain of BCR-ABL1 from the cDNA of CSF blasts revealed the pathogenic variant p.L387M. We also performed ultra-deep next-generation sequencing (NGS) in three samples from one of the relapsed patients. We did not find the mutation in the BM sample, but we did find it in CSF blasts with 45% of reads at the time of relapse. These data demonstrate the feasibility of detecting BCR-ABL1 mutations in CSF blasts by NGS and highlight the importance of monitoring clonal evolution over time.


Subject(s)
Central Nervous System/pathology , Fusion Proteins, bcr-abl/genetics , Mutation , Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics , Proto-Oncogene Proteins c-abl/genetics , Adult , Aged , Aged, 80 and over , Feasibility Studies , Female , Fusion Proteins, bcr-abl/blood , Fusion Proteins, bcr-abl/cerebrospinal fluid , High-Throughput Nucleotide Sequencing/methods , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Models, Molecular , Outcome Assessment, Health Care , Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology , Precursor Cell Lymphoblastic Leukemia-Lymphoma/therapy , Protein Structure, Tertiary , Proto-Oncogene Proteins c-abl/cerebrospinal fluid , Proto-Oncogene Proteins c-abl/chemistry , Recurrence
2.
Psicothema ; 25(4): 452-60, 2013.
Article in English | MEDLINE | ID: mdl-24124777

ABSTRACT

BACKGROUND: Cognitive impairment in multiple sclerosis (MS) is common (45-65%).Deficits occur in speed of information processing (SIP), memory, attention, executive functions (EF) and visuoconstruction.Involvement of cognitive functions like language and gnosis is rare and lesser known. Our aim is to describe the cognitive function and the clinical and radiological features of five patients with MS and with neuropsychological syndromes (NPS). METHOD: Retrospective review of MS patients with NPS studied, using specific tests of SIP, memory, attention, EF, visuo-spatial abilities, praxis and language. RESULTS: The sample included four women (3 relapsing-remitting MS/1 secondary progressive MS) and one man with primary progressive MS (aged between 30-55 years). Cognitive symptoms were the initial complaint in three cases. Three cases presented apperceptive agnosia and constructive apraxia, one case presented alexia with agraphia and the fifth patient presented motor aphasia. Four patients suffered cognitive dysfunction considered typical of MS. Magnetic resonance imaging (MR) in all cases showed high lesion volumes in T1 and T2-weighted sequences. A good correlation was observed between cognitive deficits and the location of the lesions in four patients. CONCLUSIONS: NPS may be the initial complaint in MS patients, often associated with other cognitive deficits, and it shows a close relationship with lesion location.


Subject(s)
Cognition Disorders/etiology , Multiple Sclerosis/psychology , Adult , Agnosia/etiology , Agnosia/pathology , Agraphia/etiology , Agraphia/pathology , Anxiety/etiology , Anxiety/pathology , Aphasia, Broca/etiology , Aphasia, Broca/pathology , Apraxias/etiology , Apraxias/pathology , Brain/pathology , Cognition Disorders/pathology , Depression/etiology , Depression/pathology , Dyslexia/etiology , Dyslexia/pathology , Female , Humans , Intelligence Tests , Magnetic Resonance Imaging , Male , Middle Aged , Multiple Sclerosis/pathology , Neuropsychological Tests , Retrospective Studies
4.
Arch. esp. urol. (Ed. impr.) ; 60(10): 1167-1174, dic. 2007. graf
Article in Spanish | IBECS | ID: ibc-135617

ABSTRACT

OBJETIVO: Analizar la supervivencia de una serie de pacientes diagnosticados de carcinoma de células renales durante un periodo de 19 años en base a los factores pronósticos utilizados habitualmente en la práctica clínica. MÉTODOS: Estudio retrospectivo sobre 259 pacientes diagnosticados de manera consecutiva durante los años 1988 a 2006 carcinoma de células renales, que fueron tratados quirúrgicamente en nuestro servicio. A partir de los datos clínicos y patológicos y de seguimiento se ha hecho un estudio de supervivencia comparando el impacto de los factores pronósticos habituales: estadio, tamaño tumoral, grado nuclear, etc. RESULTADOS: Se realizaron 264 cirugías a los 259 pacientes de la muestra que presentaron una edad media de 61,91 años. El diagnóstico se realizó más frecuentemente por hallazgo incidental (52,12% de los casos), practicándose un 72,97% de nefrectomías radicales frente a un 26,25% de parciales. El carcinoma de células claras fue el diagnóstico histológico más frecuente (69,88%). Presentaron peor supervivencia los pacientes con carcinoma de células claras, los tumores sintomáticos, con mayor tamaño y grado nuclear de Fuhrman. A mayor estadio tumoral el pronóstico fue peor, especialmente en los tumores con estadio superior a pT3a. La presencia de ganglios linfáticos afectados o metástasis a distancia presentan una supervivencia cáncer-específica mucho más baja. La de supervivencia cáncer-específica global a los 5 años fue superior al 80%. CONCLUSIÓN: Los factores pronósticos usados clásicamente para predecir la supervivencia del cáncer renal siguen siendo útiles, en especial el estadio patológico pT. Se observa una mejor supervivencia en comparación con series más antiguas, pero este tipo de tumores sigue generando una morbimortalidad importante (AU)


OBJECTIVES: To analyze the survival rate in a series of patients with the diagnosis of renal cell carcinoma over a 19 year period based on prognostic factors usually employed in clinical practice. METHODS: Retrospective study of 259 consecutive patients with the diagnosis of renal cell carcinoma undergoing surgery in our department between 1988 and 2006. From clinical, pathological, and follow-up data we performed a survival study comparing the impact of usual prognostic factors: stage, tumor size, nuclear grade, etc. RESULTS: 264 surgical procedures were performed in 259 patients, with a mean age of 61.91 yr. The most frequent way of diagnosis was incidental finding (52.12% of the cases); radical nephrectomy was performed in 72.97% of the cases in comparison with 26.25% partial nephrectomies. Clear cell carcinoma was the most frequent histological diagnosis (69.88%). Patients with clear cell carcinoma, symptomatic tumors, bigger size, and greater Fuhrman nuclear grade presented worse survivals, mainly in tumors with stage >pT3a. The presence of involved lymph nodes or distant metas- tases is associated with a much lower cancer-specific survival. Global five-year cancer-specific survival was over 80%. CONCLUSIONS: The classical prognostic factors used to predict survival in renal cancer are still useful, mainly pathological stage pT. We observed a better survival in comparison with older series, but this kind of tumors continue generating important morbidity-mortality (AU)


Subject(s)
Humans , Male , Female , Middle Aged , Carcinoma, Renal Cell/mortality , Carcinoma, Renal Cell/pathology , Kidney Neoplasms/mortality , Kidney Neoplasms/pathology , Prognosis , Retrospective Studies , Survival Rate
5.
Arch Esp Urol ; 60(10): 1.167-1.174, 2007 Dec.
Article in Spanish | MEDLINE | ID: mdl-18273973

ABSTRACT

OBJECTIVES: To analyze the survival rate in a series of patients with the diagnosis of renal cell carcinoma over a 19 year period based on prognostic factors usually employed in clinical practice. METHODS: Retrospective study of 259 consecutive patients with the diagnosis of renal cell carcinoma undergoing surgery in our department between 1988 and 2006. From clinical, pathological, and follow-up data we performed a survival study comparing the impact of usual prognostic factors: stage, tumor size, nuclear grade, etc. RESULTS: 264 surgical procedures were performed in 259 patients, with a mean age of 6 1.91 yr. The most frequent way of diagnosis was incidental finding (52.12% of the cases); radical nephrectomy was performed in 72.97% of the cases in comparison with 26.25% partial nephrectomies. Clear cell carcinoma was the most frequent histological diagnosis (69.88%). Patients with clear cell carcinoma, symptomatic tumors, bigger size, and greater Fuhrman nuclear grade presented worse survivals, mainly in tumors with stage >pT3a. The presence of involved lymph nodes or distant metastases is associated with a much lower cancer-specific survival. Global five-year cancer-specific survival was over 80%. CONCLUSIONS: The classical prognostic factors used to predict survival in renal cancer are still useful, mainly pathological stage pT. We observed a better survival in comparison with older series, but this kind of tumors continue generating important morbidity-mortality.


Subject(s)
Carcinoma, Renal Cell/mortality , Kidney Neoplasms/mortality , Carcinoma, Renal Cell/pathology , Female , Humans , Kidney Neoplasms/pathology , Male , Middle Aged , Prognosis , Retrospective Studies , Survival Rate
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