Ana C Oliveira

Prof. Dr. Ana C Oliveira

orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 November 2023 in Journal of Clinical Oncology
Verified
Journal Article
Closed access
PZPier Luigi Zinzani
Pier Luigi Zinzani
JMJiří Mayer
Jiří Mayer
CFChristopher R. Flowers
Christopher R. Flowers
FBFontanet Bijou
Fontanet Bijou
AOAna C Oliveira
Ana C Oliveira
JTJudith Trotman
Judith Trotman
Deep and durable responses with zanubrutinib plus obinutuzumab in patients with R/R FL.

18 December 2023 in Cancers
Verified
Journal Article
Open access
PDF file
APAlexandra Pons-Riverola
Alexandra Pons-Riverola
HCHerminio Morillas Climent Climent
Herminio Morillas Climent Climent
JBJavier Berdejo
Javier Berdejo
SPSonia Pernas
Sonia Pernas
HPHelena Pomares
Helena Pomares
PMPedro Moliner
Pedro Moliner
Cardiovascular disease is a common problem in cancer patients that is becoming more widely recognized. This may be a consequence of prior cardiovascular risk factors but could also be secondary to the anticancer treatments. With the goal of offering a multidisciplinary approach to guaranteeing optimal cancer therapy and the early detection of related cardiac diseases, and in light of the recent ESC Cardio-Oncology Guideline recommendations, we developed a Cardio-Oncology unit devoted to the prevention and management of these specific complications. This document brings together important aspects to consider for the development and organization of a Cardio-Oncology program through our own experience and the current evidence.

5 December 2014 in Annals of Hematology
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Journal Article
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AOAna C Oliveira
Ana C Oliveira
ASA. Fernández de Sevilla
A. Fernández de Sevilla
ADA. Domingo
A. Domingo
EBE. De La Banda
E. De La Banda
EDEva Domingo-Domenech
Eva Domingo-Domenech
EGE. González-Barca
E. González-Barca

30 November 2022 in International Journal of Hematology
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Journal Article
Closed access
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AOAna C Oliveira
Ana C Oliveira
JRJosep Maria Roncero
Josep Maria Roncero
CFChristelle Ferrá
Christelle Ferrá
JNJanilson Do Nascimento
Janilson Do Nascimento
MRMarta Rodriguez-Luaces
Marta Rodriguez-Luaces
EGEva González-Barca
Eva González-Barca

16 February 2011 in Leukemia & Lymphoma
Verified
Journal Article
Closed access
AOAna C Oliveira
Ana C Oliveira
EBEsmeralda de la Banda
Esmeralda de la Banda
EDEva Domingo-Domenech
Eva Domingo-Domenech
MEMaite Encuentra
Maite Encuentra
SMSantiago Mercadal
Santiago Mercadal
EBEVA MARIA GONZALEZ BARCA
EVA MARIA GONZALEZ BARCA
Retrospective series have reported many clinical and biological significant prognostic factors in chronic lymphocytic leukemia (CLL). We describe a prospective cohort of 135 patients with CLL homogeneously studied at diagnosis for prognostic factors. Biological variables analyzed were CD38 and ZAP-70 expression, fluorescence in situ hybridization (FISH) for 13q-, +12, 11q-, and 17p-, and conventional cytogenetics. Univariate and multivariate analysis for progression-free survival (PFS) were performed in patients with early stage (Rai 0-1) CLL. CD38 was positive in 42 (31.6%) patients and ZAP-70 in 47 (35.9%). The most frequent FISH finding was isolated 13q- in 50 (38.5%) patients, and 17p- -was found in 11 (8.4%). Among 135 patients, 114 (84.4%) were Rai 0-1 at diagnosis and 39 (28.9%) presented adenopathies. With a median follow-up of 39 months, the presence of lymphadenopathy in patients with Rai 0-1 stage CLL was the only significant variable for predicting PFS in multivariate analysis (odds ratio [OR] 7, 95% confidence interval [CI] 2.2-22, p = 0.001). When only biological factors were analyzed, CD38 expression (OR 3.2, 95% CI 1.1-9.3, p = 0.03) and 17p- (OR 3.5, 95% CI 0.95-13.1, p = 0.05) correlated with worse PFS. A longer follow-up is necessary to analyze the prognostic value of these variables regarding overall survival.

21 March 2025 in Cancers
Verified
Journal Article
Open access
PDF file
MPMaria Poza
Maria Poza
AMAlejandro Martín-Muñoz
Alejandro Martín-Muñoz
PPPATRICIA LÓPEZ PEREIRA
PATRICIA LÓPEZ PEREIRA
GFGloria Figaredo
Gloria Figaredo
IZIrene Zamanillo
Irene Zamanillo
AUAna 1 Jiménez Ubieto
Ana 1 Jiménez Ubieto
Background/Objectives: This study aimed to determine whether interim PET/CT (iPET) scans could identify follicular lymphoma (FL) patients at high risk of relapse following first-line therapy. Methods: A total of 117 FL patients who underwent iPET scans were included, with responses interpreted using the Deauville score (DS). Progression-free survival (PFS) was evaluated over a median follow-up of 34 months. Results: Overall, 34% of patients were classified as iPET (+), with significantly worse estimated 5-year PFS compared to iPET (−) patients (34% vs. 76%, hazard ratio 4.3, p < 0.001). Multivariate analysis confirmed iPET (+) as an independent predictor of PFS. Conclusions: Interim PET results are significant predictors of PFS in FL first-line therapy and could inform response-adapted treatment strategies.