Marta Llanos
Hospital Universitario de Canarias
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Featured researches published by Marta Llanos.
Medical Oncology | 2001
Marta Llanos; Hugo Álvarez-Argüelles; Remedios Alemán; Juana Oramas; Lucio Díaz-Flores; Norberto Batista
We analyzed 104 patients with non-Hodgkin’s lymphoma, follicular or diffuse large-B-cell-type lymphoma, in order to evaluate the correlation between clinical characteristics and immunohistochemical parameters. Immunostaining was performed by means of monoclonal antibodies against Ki-67, bcl-2, and p53 expression. Forty-nine of the patients showed follicular lymphoma. A high expression of bcl-2 was found in 93%, high expression of p53 in 57%, and low expression of Ki-67 in 96%. Follicular lymphoma grade III showed a p53 expression (p=0.07) slightly higher than follicular lymphoma grades I and II, not reaching statistical significance. Follicular lymphoma grades I and II tended to express lower Ki-67 and higher levels of bcl-2 expression than grade III (p=0.06). Fifty-five cases showed diffuse large-B-cell lymphoma. Among them, bcl-2 was absent in 39%, whereas p53 and Ki-67 expression were high in 38%. In the diffuse large-B-cell lymphomas, a high bcl-2 expression correlated with stages III and IV (p=0.03) and involvement of more than one extranodal area (p=0.03). High Ki-67 expression was also associated to extranodal involvement of more than one area (p=0.03). Overall survival of patients did not show statistically significant differences regarding Ki-67, bcl-2, and p53 tumoral expression. Prognostic factors for overall survival in the multivariate analysis were age (p=0.02) and LDH (p=0.003). Time to progression was worse among follicular lymphoma with high p53 expression than with mild/moderate p53 expression (p=0.009).
Journal of Clinical Oncology | 2004
Carlos Montalbán; Juan F. García; Víctor Abraira; Leocricia González-Camacho; Jose Luis Bello; Eulogio Conde; Miguel A. Cruz; Ramón García-Sanz; José García-Laraña; Carlos Grande; Marta Llanos; Rafael Martínez; Eduardo Flores; Miguel Méndez; Concepción Ponderós; Concepción Rayón; Pedro Sánchez-Godoy; Javier Zamora; Miguel A. Piris
PURPOSE Current therapies fail to cure a significant proportion of patients with Hodgkins lymphoma (HL). Predictive systems for stratification of the disease and selection of treatment based on sets of clinical variables, such as the international prognostic score (IPS), are of relatively small practical value. The predictive use of biologic parameters has so far provided limited and inconsistent results. Here we explore the influence of a set of molecular markers on the outcome of HL. PATIENTS AND METHODS Forty molecular markers involved in B-cell differentiation and activation, signal transduction, cell cycle, and apoptosis control were analyzed in 259 classic HL patient cases by using tissue microarrays. Univariate analysis was performed to evaluate the influence of markers on favorable outcome (complete remission of > 12 months). Significant variables were included in a multivariate logistic regression analysis, and the probability of favorable outcome was estimated. RESULTS Univariate analysis revealed four molecular markers that predicted outcome, and the multivariate analysis showed p53, Bcl-X(L), and terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate-biotin nick-end labeling (TUNEL) to have independent significance. The combination of these factors determined two groups of patients (group I, zero to one factor; group II, two to three factors) with a probability of a favorable outcome of.948 and.687, respectively. A multivariate Coxs model shows that these biologic risk groups have special predictive power in low-IPS patients. CONCLUSION The data from this exploratory study suggest that the accumulation of molecular events seems to influence the outcome of HL, particularly in the low-IPS group.
Blood | 2010
Beatriz Sanchez-Espiridion; Carlos Montalbán; Ángel López; Javier Menárguez; Pilar Sabin; Carmen Ruíz-Marcellán; Andres Lopez; Rafael Ramos; Jose Rodriguez; Araceli Cánovas; Carmen Camarero; Miguel A. Canales; Javier Alves; Reyes Arranz; Agustín Acevedo; Antonio Salar; Sergio Serrano; Águeda Bas; José María Moraleda; Pedro Sánchez-Godoy; Fernando Burgos; Concepción Rayón; Manuel F. Fresno; José García Laraña; Mónica García-Cosío; Carlos Santonja; José Luis Blanco López; Marta Llanos; Manuela Mollejo; Joaquín Gonzá Lez-Carrero
Despite improvement in the treatment of advanced classical Hodgkin lymphoma, approximately 30% of patients relapse or die as result of the disease. Current predictive systems, determined by clinical and analytical parameters, fail to identify these high-risk patients accurately. We took a multistep approach to design a quantitative reverse-transcription polymerase chain reaction assay to be applied to routine formalin-fixed paraffin-embedded samples, integrating genes expressed by the tumor cells and their microenvironment. The significance of 30 genes chosen on the basis of previously published data was evaluated in 282 samples (divided into estimation and validation sets) to build a molecular risk score to predict failure. Adequate reverse-transcription polymerase chain reaction profiles were obtained from 262 of 282 cases (92.9%). Best predictor genes were integrated into an 11-gene model, including 4 functional pathways (cell cycle, apoptosis, macrophage activation, and interferon regulatory factor 4) able to identify low- and high-risk patients with different rates of 5-year failure-free survival: 74% versus 44.1% in the estimation set (P < .001) and 67.5% versus 45.0% in the validation set (P = .022). This model can be combined with stage IV into a final predictive model able to identify a group of patients with very bad outcome (5-year failure-free survival probability, 25.2%).
Leukemia & Lymphoma | 2014
Mariano Provencio; Miguel Á. Cruz Mora; José Gómez-Codina; Cristina Quero Blanco; Marta Llanos; Francisco Ramón García-Arroyo; Luis de la Cruz; Josep Gumá Padró; Juan Ramón Delgado Pérez; Antonio Elipe Sánchez; Ruth Álvarez Cabellos; Antonio Rueda
Abstract Relapse is the main cause of therapeutic failure in follicular lymphoma (FL). We set out to evaluate the role of consolidation with Yttrium-90 ibritumomab tiuxetan in patients with intermediate- and high-risk FL after four cycles of CHOP-R (cyclophosphamide, doxorubicin, vincristine, prednisone, rituximab) and two cycles of CHOP. Thirty patients were included. The overall response rate after consolidation therapy was 93%. Of the 18 patients who presented with a partial response after induction treatment, 11 had a complete response after consolidation treatment. The complete clinical response rate was 76.6%. The most important grade 3–4 toxicity was hematological, with 46% thrombopenia and 56% neutropenia. With a median follow-up of 26 months, the means for progression-free survival and overall survival were not reached. Our data support consolidation with Yttrium-90 ibritumomab tiuxetan as an effective treatment, which provides long progression-free and overall survival, in first line after a response to induction treatment in patients with intermediate- and high-risk FL.
Leukemia & Lymphoma | 2012
Pablo Guisado-Vasco; Reyes Arranz-Sáez; Miguel Canales; Araceli Cánovas; José García-Laraña; Ramón García-Sanz; Andres Lopez; José López; Marta Llanos; José María Moraleda; Jose Rodriguez; Consuelo Rayon; Pilar Sabin; Antonio Salar; Ana Marín-Niebla; Pedro Sánchez-Godoy; José Francisco Tomás; Alfonso Muriel; Víctor Abraira; Miguel A. Piris; Juan F. García; Carlos Montalbán
Abstract The International Prognostic Score (IPS) is the most widely used system to date for identifying risk groups for the outcome of patients with advanced Hodgkin lymphoma, although important limitations have been recognized. We analyzed the value of the IPS in a series of 311 patients with advanced classical Hodgkin lymphoma (cHL) (Ann Arbor stage III, IV or stage II with B symptoms and/or bulky masses) treated with first-line chemotherapy including adriamycin (adriamycin, bleomycin, vinblastine, dacarbazine [ABVD] or equivalent variants). In univariate and multivariate analyses, stage IV disease and age ≥ 45 years were the only factors with independent predictive significance for overall survival (OS) (p = 0.002 and p < 0.001, respectively). Stage IV was still significant for freedom from progression (FFP) (p = 0.001) and age ≥ 45 years was borderline significant (p = 0.058). IPS separates prognostic groups, as in the original publication, but this is mainly due to the high statistical significance of stage IV and age ≥ 45 years. Moreover, the combination of these two factors enables a simpler system to be constructed that separates groups with different FFP and OS. In conclusion, in our series, stage IV and age ≥ 45 years are the key prognostic factors for the outcome of advanced cHL.
Breast Cancer Research and Treatment | 2003
Emilio Alba; N. Ribelles; Antonio Antón; R. Pérez-Carrión; J.M. López-Vega; Marta Llanos; A. Pelegri; Jesús Florián; M. Menéndez; M.J. Godes
AbstractPurpose. To evaluate the efficacy and the toxicity profile of the sequential administration of doxorubicin and docetaxel as first-line chemotherapy in metastatic breast cancer (MBC). Patients and methods. Eighty-one patients received a total of 436 cycles of chemotherapy: 236 of doxorubicin (75 mg/m2) and 200 of docetaxel (100 mg/m2 every 21 days). The first 35 patients received doxorubicin every 14 days with G-CSF support, and in the other 46 cases doxorubicin was administered every 21 days without G-CSF. Results. After entire treatment the overall response rate was 65% (18 complete responses). With a median follow-up of 19 months (range, 1–48 months), the median time to progression was 11.3 months and the median survival time was 31 months. As expected, febrile neutropenia was the most important toxicity and it appeared in 26 cycles (6%) and 19 patients (23%). In the patients that received doxorubicin every 14 days, the febrile neutropenia incidence was higher during docetaxel treatment, especially after its first administration. Conclusions. The dose and schedule of doxorubicin and docetaxel used in this trial seems to be active in first-line treatment of patients with MBC. The toxicity profile appears to be better than observed with concomitant schedules.
Clinical Lymphoma, Myeloma & Leukemia | 2017
Fernando Franco Pérez; Javier Lavernia; David Aguiar-Bujanda; José Miramón; Josep Gumá; Rut Álvarez; José Gómez-Codina; Francisco Ramon Garcia Arroyo; Marta Llanos; Miguel Marin; Jesús Alfaro; Cristina Quero; Mayte Delgado; Esteban Nogales; Francisco Menarguez; Natividad Martinez; María Torrente; Ana Royuela; Delvys Rodriguez Abreu; Mariano Provencio
Introduction Primary breast lymphoma is a rare form of localized extranodal lymphoma, which affects the mammary glands unilaterally or bilaterally, and can also affect the regional lymph nodes. Materials and Methods We reviewed 55 patients, with disease stages IE and IIE, diagnosed in 16 Spanish institutions between 1989 and 2016. A serial of clinical variables and treatment were collected, and overall survival (OS) and progression‐free survival (PFS) were calculated. Results Of the 55 patients, 96.4% were women with an average age of 69 years. A total of 53 patients corresponded to non‐Hodgkin lymphoma (NHL), of whom 36.3% had lymph node involvement upon diagnosis. Of the patients, 58.2% were stage IE, and 41.8% were stage IIE. Treatments received included radiotherapy (36.3%), chemotherapy (85.5%), and rituximab (in 38 of the 45 patients with NHL treated with chemotherapy). In all, 82.2% of complete responses were achieved. OS and progression‐free survival at 5 years in NHL patients was 76% and 73%, respectively. Conclusion Current treatments (chemotherapy, immunotherapy, and radiotherapy) achieve good control of the disease, with an OS of 5 years in 80% of the patients, although there is no consensus in treatment, given the scarce incidence of these lymphomas. Micro‐Abstract We reviewed 55 patients diagnosed with primary breast lymphoma, stages IE and IIE, in 16 Spanish institutions. Of the 55 cases, 96.4% corresponded to non‐Hodgkin lymphoma. Results of 5‐year progression‐free and overall survival were 73% and 76%, respectively. Current treatments achieve good control of the disease, with an overall survival of 5 years in 80% of the patients.
PLOS ONE | 2017
Mariano Provencio; Pilar Sabin; José Gómez-Codina; María Torrente; Virginia Calvo; Marta Llanos; Josep Gumá; Cristina Quero; Ana Blasco; Miguel A. Cruz; David Aguiar; Francisco Ramón García-Arroyo; Javier Lavernia; Natividad Martínez; Manuel A. Morales; Alvaro Saez-Cusi; Delvys Rodríguez; Luis de la Cruz; Jose Javier Sanchez; Antonio Rueda
Background Follicular lymphoma is the second most common non-Hodgkin lymphoma in the United States and Europe. However, most of the prospective randomized studies have very little follow-up compared to the long natural history of the disease. The primary aim of this study was to investigate the long-term survival of our series of patients with follicular lymphoma. Patients and methods A total of 1074 patients with newly diagnosed FL were enrolled. Patients diagnosed were prospectively enrolled from 1980 to 2013. Results Median follow-up was 54.9 months and median overall survival is over 20 years in our series. We analyzed the patients who are still alive beyond 10 years from diagnosis in order to fully assess the prognostic factors that condition this group. Out of 166 patients who are still alive after more than 10 years of follow-up, 118 of them (73%) are free of evident clinical disease. Variables significantly associated with survival at 10 years were stage < II (p <0.03), age < 60 years (p <0.0001), low FLIPI (p <0.002), normal β2 microglobulin (p <0.005), no B symptoms upon diagnosis (p <0.02), Performance Status 0–1 (p <0.03) and treatment with anthracyclines and rituximab (p <0.001), or rituximab (p <0.0001). Conclusions A longer follow-up and a large series demonstrated a substantial population of patients with follicular lymphoma free of disease for more than 10 years.
Leukemia & Lymphoma | 2014
Antonio Rueda; Julio Rifá; Cristina Quero; José Gómez-Codina; Adolfo Murias; Francisco Ramón García-Arroyo; Pilar Sabin; Marta Llanos; Joaquin Herrero; Francisco Lobo; Juan Ramón Delgado; Mariano Provencio
1 Á rea de Oncohematolog í a, Hospital Costa del Sol, Marbella, Spain, 2 IBIMA, Instituto de Investigaci ó n Biomedica de M á laga, Spain, 3 REDISSEC, Red de Investigaci ó n en Servicios Sanitarios en Enfermedades Cr ó nicas, 4 Servicio de Oncolog í a M é dica, Hospital Son Dureta, Palma de Mallorca, Spain, 5 Servicio de Oncolog í a M é dica, Hospital Universitario Virgen de la Victoria, M á laga, Spain, 6 Servicio de Oncolog í a M é dica, Hospital Universitario La Fe, Valencia, Spain, 7 Servicio de Oncolog í a M é dica, Hospital Insular, Las Palmas de Gran Canaria, Spain, 8 Servicio de Oncolog í a M é dica, Complejo Hospitalario de Pontevedra, Spain, 9 Servicio de Oncolog í a M é dica, Hospital Gregorio Mara ñ ó n, Madrid, Spain, 10 Servicio de Oncolog í a M é dica, Hospital Universitario de Tenerife, Spain, 11 Servicio de Oncolog í a M é dica, Hospital General Universitario de Alicante, Spain, 12 Servicio de Oncolog í a M é dica, Fundaci ó n Jim é nez D í az, Madrid, Spain, 13 Servicio de Oncolog í a M é dica, Hospital Virgen de las Nieves, Granada, Spain and 14 Servicio de Oncolog í a M é dica, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain
Cancer | 2017
Mariano Provencio; Ana Royuela; María Torrente; Marina Pollán; José Gómez-Codina; Pilar Sabin; Marta Llanos; Josep Gumá; Cristina Quero; Ana Blasco; David Aguiar; Francisco Ramón García-Arroyo; Javier Lavernia; Natividad Martínez; Manuel A. Morales; Álvaro Saenz-Cusi; Delvys Rodríguez; Virginia Calvo; Luis de la Cruz-Merino; Miguel A. Cruz; Antonio Rueda
Relatively few studies have analyzed the mortality of follicular lymphoma (FL) patients in comparison with a sex‐ and age‐matched general population. This study analyzed the overall survival (OS) of patients with FL and compared their survival with the expected survival of a general population.