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Publication
Featured researches published by I. Fernandez.
Annals of Hematology | 1994
S. Pavlovsky; J. Gonzalez Llaven; M. A. Garcia Martinez; P. Sobrevilla; M. Eppinger-Helft; Ana Marin; M. López-Hernández; I. Fernandez; M. E. Rubio; S. Ibarra; M. Lluesma; G. Ruiz Arguelles; F. José de Diego
SummaryBetween May 1985 and November 1988, 143 adult patients with previously untreated acute nonlymphocytic leukemia were randomized to receive mitoxantrone and cytarabine (MTT+Ara-C) or daunomycin and cytarabine (DNM+Ara-C) in order to compare the efficacy and acute and chronic toxicities. Therapy consisted of 3 days of MTT 12 mg/m2/i.v. or DNM 45 mg/m2/i.v.; both groups received Ara-C 100 mg/m2 daily by continuous infusion (CI) for 7 days. Those who failed to achieve a complete remission after one induction course received a second induction course for 2 and 5 days at the same doses. All the patients who achieved complete remission received two consolidations of 2 days of MTT or DNM and 5 days of Ara-C in CI at the same dose as for induction. Of the 72 patients on MTT+Ara-C, 38 (53%) achieved complete remission, compared with 29 (43%) of 67 treated with DNM+Ara-C. Three and 5 patients had partial remission, 7 and 18 failed to respond, 24 and 15 died in the first 21 days of induction, of those treated with MTT+Ara-C or DNM+Ara-C, respectively (p=0.34). Median duration of complete remission and survival was 185 and 103 days or 165 and 160 days, respectively (p=0.85). More early deaths were observed with MTT+Ara-C due to greater myelosuppression, and a higher incidence of failure with DNM+Ara-C. No significant differences between treatment groups were observed in 21 categories of adverse events. The results demonstrate similar incidence of complete response, length of duration of complete remission, overall survival, and toxicity with MTT+Ara-C and DNM+Ara-C.
Fertility and Sterility | 2015
Elkin Muñoz; I. Fernandez; María Martínez; Antonia Tocino; Susana Portela; A. Pellicer; Juan A. Garcia-Velasco; Nicolás Garrido
OBJECTIVE To study reproductive outcome in patients cured of cancer who required oocyte donation (OD) owing to iatrogenic ovarian dysfunction. DESIGN Multicenter, unmatched, retrospective cohorts study. SETTING Private, university-affiliated group of clinics. PATIENT(S) Women treated and cured of cancer (n = 142) who underwent 333 cycles of OD (exposed group) and women without a previous cancer diagnosis (n = 17,844) who underwent 29,778 cycles of OD (unexposed cohort) between January 2000 and January 2012. INTERVENTION(S) Retrospective chart review. MAIN OUTCOME MEASURE(S) Pregnancy, implantation, miscarriage, and ongoing pregnancy rates. RESULT(S) There were no differences in terms of pregnancy (55.7% vs. 54.7%), implantation (39.8% vs. 38.2%), miscarriage (29.5% vs. 26.9%), or delivery rates (39.3% vs. 39.9%) between the unexposed group and the patients previously diagnosed and cured of cancer, respectively. There was no correlation between OD outcome and cancer type. CONCLUSION(S) Endometrial receptivity in women treated and cured of cancer was comparable to that of general patients without previous malignancies who had received OD, based on the largest series available in the literature.
Current Drug Targets | 2013
Elkin Muñoz; Esther Taboas; Susana Portela; J. Aguilar; I. Fernandez; Luis Muñoz; Ernesto Bosch
Abnormal luteal function is a common issue in assisted reproduction techniques associated with ovarian stimulation probably due to low levels of LH in the middle and in the late luteal phase. This defect seems to be associated with supraphysiological steroid levels at the end of follicular phase. The luteal phase insufficiency has not got a diagnostic test which has proven reliable in a clinical setting. Luteal phase after ovarian stimulation becomes shorter and insufficient, resulting in lower pregnancy rates. Luteal phase support with progesterone or hCG improves pregnancy outcomes and no differences are found among different routes of administration. However, hCG increases the risk of ovarian hyperstimulation syndrome. In relation to the length of luteal support, the day of starting it remains controversial and it does not seem necessary to continue once a pregnancy has been established. After GnRHa triggering ovulation, intensive luteal support or hCG bolus can overcome the defect in luteal phase, but more studies are needed to show the LH utility as support.
Current Pharmaceutical Biotechnology | 2012
Elkin Muñoz; Ernesto Bosch; I. Fernandez; Susana Portela; José Remohí; Antonio Pellicer
LH is a glycoprotein that plays a crucial role in folliculogenesis during the natural ovarian cycles. It has the same activity and shares receptors with hCG. However the use of LH in combination with FSH in controlled ovarian stimulation remains controversial. A practical approach concerning the usefulness of LH according to the endogenous level of LH is described herein. Specific groups of patients can benefit from ovarian stimulation with LH. New applications of LH/hCG activity are also discussed.
Fertility and Sterility | 2011
Susana Portela; I. Fernandez; T. Lopez; B. Martinez; J. Aguilar; Elkin Muñoz
Fertility and Sterility | 2013
Elkin Muñoz; L. Rodriguez; C. Martinez; J. Aguilar; Susana Portela; I. Fernandez
Fertility and Sterility | 2013
Elkin Muñoz; María Martínez; B. Martinez; J. Aguilar; Susana Portela; I. Fernandez
Fertility and Sterility | 2013
J. Aguilar; E. Taboas; M. Perez; M. Ojeda; I. Fernandez; Elkin Muñoz
Fertility and Sterility | 2012
Elkin Muñoz; E. Taboas; B. Martinez; I. Fernandez; J. Aguilar; J. Remohí
Fertility and Sterility | 2011
Elkin Muñoz; A. Carballo; I. Fernandez; D. Pabon; Susana Portela; A. Pellicer