N. Thomakos
National and Kapodistrian University of Athens
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Publication
Featured researches published by N. Thomakos.
European Journal of Cancer | 2012
Aristotle Bamias; Maria Sotiropoulou; Flora Zagouri; P. Trachana; K. Sakellariou; Efthimios Kostouros; K. Kakoyianni; Alexandros Rodolakis; G. Vlahos; Dimitrios Haidopoulos; N. Thomakos; A. Antsaklis; M. A. Dimopoulos
AIM Ovarian carcinomas have been classified into types I and II according to the hypothesised mode of carcinogenesis and molecular characteristics. The prognostic significance of this classification has not been studied. PATIENTS AND METHODS Five hundred and sixty-eight patients with histologically confirmed, ovarian, fallopian tube or peritoneal carcinomas, international federation of gynecology and obstetrics (FIGO) stages IIC-IV, treated with paclitaxel/platinum following cytoreductive surgery, were included in this analysis. Type I included low-grade serous, mucinous, endometrioid and clear-cell and type II high-grade serous, unspecified adenocarcinomas and undifferentiated carcinomas. RESULTS Median overall survival (OS) was 49 months for type I versus 45 for type II (p=0.576). In contrast to type II, there was considerable prognostic heterogeneity among the subtypes included in type I. Cox regression analysis showed that cell-type classification: low-grade serous, mucinous, endometrioid, clear-cell, type II (high-grade serous, unspecified adenocarcinomas, undifferentiated carcinoma) was an independent predictor of survival (respective median OS 121 versus 15 versus 64 versus 29 versus 45 months, p=0.003). On the contrary, histopathological subtype or tumour type (I versus II) did not offer additional prognostic information. CONCLUSION The proposed model of ovarian tumourigenesis does not reflect tumour behaviour in advanced disease. Tumour-cell type is the most relevant histopathological prognostic factor in advanced ovarian cancer treated with platinum/paclitaxel.
Journal of Obstetrics and Gynaecology | 2012
Ioannis Biliatis; N. Thomakos; Alexandros Rodolakis; Nikolaos Akrivos; Dimitrios Zacharakis; A. Antsaklis
Therapy for endometrial, ovarian and cervical cancer in young women can cause sudden onset of intense menopausal symptoms, such as hot flushes, emotional disorders and sexual dysfunction. In order to overcome these unpleasant and sometimes severe symptoms, hormone replacement therapy (HRT) has proven to be very effective. However, its safety remains controversial. We reviewed English literature and examined whether administration of HRT in this specific population is related with more recurrences and worse prognosis. Current scientific data, comprising mainly retrospective studies, suggest that recurrence rates and survival are comparable between HRT users and non-users. However, large randomised trials are missing and definitive conclusions cannot be drawn. Gynaecological cancer survivors using HRT, although they seem to have little if any risk for recurrence, should be correctly informed about the lack of strong evidence.
Gynecologic Oncology | 2011
Aristotle Bamias; A. Karadimou; Nikolaos Soupos; Maria Sotiropoulou; Flora Zagouri; Dimitrios Haidopoulos; N. Thomakos; Alexandros Rodolakis; A. Antsaklis; M. A. Dimopoulos
OBJECTIVE Early-stage epithelial ovarian cancer represents a prognostically heterogenous group. We studied prognostic factors in patients treated with adjuvant paclitaxel/carboplatin chemotherapy. METHODS Data was extracted from 147 patients with FIGO stage IA/IB, grade 2/3 or stage IC/IIA (any grade) who underwent primary surgery followed by paclitaxel/carboplatin chemotherapy. RESULTS Median follow-up was 88 months. Ten-year relapse-free (RFS) and disease-specific survival (DSS) were: 81% (95% confidence interval [CI]: 73-89) and 81% (95% CI: 73-89). On multivariate analysis, non serous histology was associated with reduced risk for RFS (0.294, 95% CI: 0.112-0.577, p=0.001) and DSS (0.194, 95% CI: 0.075-0.504, p=0.001), while high-risk category (stage IC/IIA and grade 2/3) with increased risk for RFS (3.989, 95% CI: 1.189-13.389, p=0.009) and DSS (3.989, 95% CI: 1.064-16.386, p=0.038). The combination of histology and grade identified 3 groups with distinctly different 10-year RFS and DSS rates (p<0.001): grade 1 (100% and 100%), non-serous grade 2/3 (83% and 86%) and serous grade 2/3 (60% and 60%). CONCLUSIONS Serous histology is an adverse prognostic factor in early-stage ovarian cancer treated with adjuvant paclitaxel/carboplatin. Risk stratification according to histology and grade is a useful discriminator of prognosis and can be used in the design of future studies.
Oncology | 2011
Aristotle Bamias; Christina Bamia; Alexandra Karadimou; Nikolaos Soupos; Flora Zagouri; Alexandros Rodolakis; Dimitrios Haidopoulos; George Vlahos; N. Thomakos; A. Antsaklis; Meletios A. Dimopoulos
Objective: We investigated the efficacy of risk-adapted adjuvant paclitaxel/carboplatin chemotherapy in early-stage ovarian carcinoma. Methods: Fifty-three patients were treated according to the risk of relapse: patients with stages IA or IB or with grade 1 (low risk) received 4 cycles of paclitaxel and carboplatin; patients with IC/IIA and grade 2 or 3 (high risk) received 6 cycles of chemotherapy. The outcome was compared with that of 95 patients who were all treated with 4 cycles. Results: Median follow-up was 88, 113 and 42 months for the whole cohort, non-risk-adapted and risk-adapted treatment, respectively. Five-year relapse-free and disease-specific survival was 86 and 93% for the whole population, 96 and 97% for low-risk and 81 and 91% for high-risk patients. Risk classification was the only significant prognostic factor for relapse-free (p = 0.011) and disease-specific survival (p = 0.039). Among high-risk patients, the administration of 6 cycles was associated with a significantly lower relapse rate after censoring events, which occurred beyond 2 years (3 vs. 18%; p = 0.013), but this difference was diminished at 5 years (23 vs. 25%; p = 0.797). Conclusions: Six cycles of chemotherapy reduced the risk of relapse within 2 years, but the benefit from two additional cycles beyond this time is questionable.
Gynecologic Oncology | 2012
Alexandros Rodolakis; N. Thomakos; G. Vlachos; Dimitrios Haidopoulos; K. Sarris; M. Sotiropoulou; I. Papaspyrou; A. Antsaklis
Gynecologic Oncology | 2013
N. Thomakos; Dimitrios Zacharakis; D. Louradou; Alexandros Rodolakis; N. Skampardonis; Maria Sotiropoulou; Dimitrios Haidopoulos; G. Vlachos; A. Antsaklis
Gynecologic Oncology | 2018
S. Dimopoulou; N. Thomakos; M. Sotiropoulou; K. Ntzeros; D.E. Vlachos; Dimitrios Haidopoulos; Michalis Liontos; Aristotle Bamias; Alexandros Rodolakis
Gynecologic Oncology | 2017
Sofia-Paraskevi Trachana; N. Thomakos; Dimitrios Haidopoulos; M. Sotiropoulou; D.E. Vlachos; G. Vlachos; Alexandros Rodolakis
Gynecologic Oncology | 2017
I. Anastasakis; N. Thomakos; Michalis Liontos; M. Sotiropoulou; Dimitrios Haidopoulos; D.E. Vlachos; Aristotle Bamias; G. Vlachos; Alexandros Rodolakis
Gynecologic Oncology | 2016
I. Koutroumpa; N. Thomakos; M. Sotiropoulou; Dimitrios Haidopoulos; D.C. Papatheodorou; M. Davidovic-Grigoraki; Aristotle Bamias; G. Vlachos; Alexandros Rodolakis