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Dive into the research topics where Alicia Olarte is active.

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Featured researches published by Alicia Olarte.


Brachytherapy | 2014

Volume of high-dose regions and likelihood of locoregional control after perioperative high-dose-rate brachytherapy: do hotter implants work better?

Rafael Martínez-Monge; Mauricio Cambeiro; Luis Ramos; Alicia Olarte; G. Valtueña; Mikel San-Julian; Juan Alcalde; Luis Naval-Gías; M. Jurado

PURPOSE To determine whether perioperative high-dose-rate brachytherapy (PHDRB) implants with larger high-dose regions produce increased locoregional control. METHODS AND MATERIALS Patients (n=166) enrolled in several PHDRB prospective studies conducted at the University of Navarre were analyzed. The PHDRB was given to total doses of 16Gy/4 b.i.d. or 24Gy/6 b.i.d. treatments for negative or close/positive margins along with 45Gy/25 Rx of external beam radiation therapy. The histogram-based generalized equivalent uniform dose (EUD) formulism was used to quantify and standardize the dose-volume histogram into 2-Gy equivalents. The region of interest analyzed included: tissue volume encompassed by the prescription isodose of 4Gy (TV100). Routine dose reporting parameters such as physical dose and single-point 2-Gy equivalent dose were used for reference. RESULTS After a median followup of 7.4 years (range, 3-12+), 50 patients have failed, and 116 remain controlled at last followup. Overall, EUD was not different in the patients who failed compared with controls (89.1Gy vs. 86.5Gy; p=not significant). When patients were stratified by risk using the University of Navarre Predictive Model, very high-risk patients (i.e., tumors ≥3cm resected with close <1mm/positive margins) had an improved locoregional control with higher EUD values (p=0.028). This effect was not observed in low-, intermediate-, and high-risk University of Navarre Predictive Model categories. CONCLUSIONS In very high-risk patients, enlarged high-dose regions can produce a dose-response effect. Routine dose reporting methods such as physical dose and single-point 2-Gy equivalent dose may not show this effect, but it can be revealed by histogram-based EUD assessment.


Clinical & Translational Oncology | 2016

Stereotactic body radiotherapy (SBRT) for the treatment of inoperable stage I non-small cell lung cancer patients

Lucia Ceniceros; J. Aristu; Eduardo Castanon; Christian Rolfo; Jairo Legaspi; Alicia Olarte; G. Valtueña; Marta Moreno; Ignacio Gil-Bazo

IntroductionLung cancer is the most frequent neoplasm in humans. Surgery is considered the best therapeutic approach for stage I non-small lung cell cancer (NSCLC). However, a remarkable amount of patients are considered as inoperable. Stereotactic body radiotherapy (SBRT) has risen as an option for those patients, rendering excellent results in quality of life and survival.Materials and methodsWe analyzed clinical studies published between 2002 and 2015 which included SBRT as a treatment modality. Our own clinical series was analyzed as well. The patterns of failure following SBRT were investigated, together with the outcomes and the toxicity observed.ResultsSBRT has proven to maintain an excellent local control. The analysis showed the tumor size and the histology as determinant factors for the response to treatment.ConclusionAccording to the published evidence as well as our own experience, SBRT is a safe and feasible approach for early NSCLC. Its results may be comparable with surgery treatment.


Brachytherapy | 2016

Dose escalation with external beam radiation therapy and high-dose-rate brachytherapy combined with long-term androgen deprivation therapy in high and very high risk prostate cancer: Comparison of two consecutive high-dose-rate schemes

Alicia Olarte; Mauricio Cambeiro; Marta Moreno-Jiménez; Leire Arbea; Jose Luis Perez-Gracia; Ignacio Gil-Bazo; Ignacio Pascual; Javier Aristu; Rafael Martínez-Monge

PURPOSE To compare rectal toxicity, urinary toxicity, and nadir+2 PSA relapse-free survival (bRFS) in two consecutive Phase II protocols of high-dose-rate (HDR) brachytherapy used at the authors institution from 2001 to 2012. METHODS AND MATERIALS Patients with National Comprehensive Cancer Network high risk and very high risk prostate cancer enrolled in studies HDR4 (2001-2007, n = 183) and HDR2 (2007-2012, n = 56) were analyzed. Patients received minipelvis external beam radiation therapy/intensity-modulated external radiotherapy to 54 Gy and 2 years of androgen blockade along with HDR brachytherapy. HDR4 protocol consisted of four 4.75 Gy fractions delivered in 48 hours; the HDR2 protocol delivered two 9.5 Gy fractions in 24 hours. Average 2-Gy equivalent dose (α/β = 1.2) prostate D90 doses for the HDR4 and HDR2 groups were 89.8 Gy and 110.5 Gy, respectively (p = 0.0001). Both groups were well balanced regarding risk factors. Prior transurethral resection of the prostate was more frequent in the HDR2 group (p = 0.001). RESULTS After a median followup of 7.4 years (range, 2-11.2), there was no difference in adverse grade ≥ 2 rectal events (HDR4 = 10.4% vs. HDR2 = 12.5%; p = ns) or grade ≥3 (HDR4 = 2.2% vs. HDR2 = 3.6%; p = ns). No differences in urinary grade ≥2 adverse events (HDR4 = 23% vs. HDR2 = 26.8%; p = ns) or grade ≥3 (HDR4 = 7.7% vs. HDR2 = 8.9%; p = ns) were detected. The 7-year bRFS for HDR4 and HDR2 protocols was 88.7% and 87.8%, respectively (p = ns). CONCLUSIONS HDR4 and HDR2 protocols produce similar results in terms of toxicity and bRFS at the intermediate time point of 7 years.


Brachytherapy | 2015

Time to loading and locoregional control in perioperative high-dose-rate brachytherapy: The tumor bed effect revisited.

Rafael Martínez-Monge; G. Valtueña; Marta Santisteban; Mauricio Cambeiro; L. Arbea; Luis Ramos; Alicia Olarte; Mikel San-Julian; Juan Alcalde; Luis Naval-Gías; M. Jurado

PURPOSE To determine whether the time to loading (TTL) affects locoregional control. METHODS AND MATERIALS Locoregional control status was determined in 301 patients enrolled in several perioperative high-dose-rate brachytherapy (PHDRB) prospective studies conducted at the University of Navarre. The impact of the time elapsed from catheter implantation to the first PHDRB treatment (TTL) was analyzed. Patients treated with PHDRB alone (n = 113), mainly because of prior irradiation, received 32 Gy in eight twice-a-day treatments or 40 Gy in 10 twice-a-day treatments for negative or close/positive margins, respectively. Patients treated with PHDRB + external beam radiation therapy (EBRT) (n = 188) received 16 Gy in four twice-a-day treatments or 24 Gy in six twice-a-day treatments for negative or close/positive margins followed by 45 Gy of EBRT in 25 treatments. RESULTS After a median followup of 6.5 years (range, 2-13.6+), 113 patients have failed (37.5%), 65 in the PHDRB-alone group (57.5%) and 48 in the combined PHDRB + EBRT group (25.5%). Patients who started PHDRB before Postoperative Day 5 had a 10-year locoregional control rate of 66.7% and patients who started PHDRB on Postoperative Day 5 or longer had a 10-year locoregional control rate of 51.8% (p = 0.009). Subgroup analysis detected that this difference was only observed in the recurrent cases treated with PHDRB alone (Subset 2; n = 99; p = 0.004). No correlation could be detected between locoregional control rate and TTL in the other patient subsets although a trend toward a decreased locoregional control rate after a longer TTL was observed when they were grouped together (p = 0.089). CONCLUSIONS Patients should start PHDRB as soon as possible to maximize locoregional control especially in those recurrent cases treated with PHDRB alone. The time effect in other disease scenarios is less clear.


Brachytherapy | 2014

Phase II trial of image-based high-dose-rate interstitial brachytherapy for previously irradiated gynecologic cancer

Rafael Martínez-Monge; Mauricio Cambeiro; Maria E. Rodriguez-Ruiz; Alicia Olarte; Luis Ramos; E. Villafranca; Natividad Bascón; M. Jurado


The Journal of Nuclear Medicine | 2014

Prediction of recurrence and survival analysis after radiotherapy of glioblastoma using 11C-Methionine PET/CT and MR

Carmen Vigil; Elena Prieto; Maria Ribelles; Alicia Olarte; Miguel Hernandez; G. Valtueña; Gemma Quincoces; José A. Richter; Javier Aristu; Javier Arbizu


Gaceta Médica de Bilbao | 2018

Radioterapia estereotáxica (SBRT) de las oligometástasis pulmonares

Pedro Ensunza; Clara Eíto; Alicia Olarte; G. Valtueña; Patricia Gago; Brais Rodríguez


Gaceta Médica de Bilbao | 2018

Radioterapia estereotáxica (SRS) de las metástasis cerebrales

Pedro Ensunza; Clara Eíto; Alicia Olarte; G. Valtueña; Patricia Gago; Brais Rodríguez


Journal of Clinical Oncology | 2017

Thymidylate synthase (TS) polymorphisms (Pol) in buffy coat-derived genomic DNA as a clinical outcome predictor in non-Asian stage III/IV non-small cell lung cancer (NSCLC) patients (pts) receiving pemetrexed (Pem).

Estefanía Arévalo; Inés López; Maria Antonia Fotuño; Eduardo Castanon; Víctor Collado; Maria Alma Rodriguez; Alicia Olarte; Maria Pilar Andueza; Jose Luis Perez Gracia; Ana Patiño-García; Ignacio Gil-Bazo


Journal of Clinical Oncology | 2017

Bevacizumab plus irinotecan in patients with recurrent high grade malignant gliomas.

Jairo Legaspi; Lucia Ceniceros; Jaime Espinós; G. Valtueña; Patricia Martin; Eduardo Castanon Alvarez; Javier Aristu; Iosune Baraibar; Diego Salas; Pablo Sala; Itziar Gardeazabal; Leyre Zubiri Oteiza; Alicia Olarte; Ignacio Gil-Bazo; Pablo Dominguez; Juan Pablo Fusco; María Isabel Velayos Martínez; José Manuel Aramendía; Oscar Fernández-Hidalgo; Marta Santisteban

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M. Jurado

University of Navarra

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