PANAGIOTIS VELISSARIOS STAMATAKOS

PANAGIOTIS VELISSARIOS STAMATAKOS

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Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

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

Representative Publications

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29 July 2024 in World Journal of Urology
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PSPANAGIOTIS VELISSARIOS STAMATAKOS
PANAGIOTIS VELISSARIOS STAMATAKOS
CFCharalampos Fragkoulis
Charalampos Fragkoulis
IZIeronymos Zoidakis
Ieronymos Zoidakis
KNKonstantinos Ntoumas
Konstantinos Ntoumas
ZKZisis Kratiras
Zisis Kratiras
ADAthanasios Dellis
Athanasios Dellis

29 December 2024 in Current Oncology
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PAPanagiotis Angelopoulos
Panagiotis Angelopoulos
TMTitos Markopoulos
Titos Markopoulos
LLLazaros Lazarou
Lazaros Lazarou
ASAndreas Skolarikos
Andreas Skolarikos
PSPANAGIOTIS VELISSARIOS STAMATAKOS
PANAGIOTIS VELISSARIOS STAMATAKOS
DMDionysios Mitropoulos
Dionysios Mitropoulos
Background: While the clinical application of SII-ONCO-Bacillus Calmette–Guerin (BCG) for non-muscle-invasive bladder cancer (NMIBC) is well established in Greece, there is a lack of real-world data on its effectiveness and safety. This retrospective, observational, multicenter, chart-review study aims to provide real-life data on the effectiveness and safety of SII-ONCO-BCG in patients with intermediate- and high-risk NMIBC. Methods: From January 2016 to December 2023, medical records from six hospital centers were reviewed for adult patients with histologically confirmed stage Ta or T1 NMIBC (with or without carcinoma in situ [CIS]) who received at least one maintenance course of SII-ONCO-BCG after induction. Tumor recurrence and progression were monitored at scheduled time intervals. Primary outcomes included recurrence-free survival (RFS) and progression-free survival (PFS), while adverse events (AEs) constituted secondary outcomes. Results: A total of 162 patients receiving SII-ONCO-BCG were enrolled. Among all patients, 145 (89.5%) patients were men, 88 (54.3%) aged 70 years or older, 103 (63.6%) had T1, 43 (26.5%) Ta, and 21 (12.9%) concurrent CIS. The median follow-up duration was 28.9 months (range, 5–36) and the mean BCG intravesical instillation courses were 13.7 (range, 9–27). After 3-, 2-, and 1-year follow-up, RFS rates of 85.2% (95% CI, 79.7–90.7%), 85.8% (80.4–91.2%), and 87.0% (81.8–92.3%) were observed, respectively. The corresponding 3-, 2-, and 1-year PFS rates were 96.9% (94.2–99.6%), 96.9% (94.2–99.6%), and 97.5% (95.1–99.9%), respectively. During the whole follow-up period, 24 (14.8%) patients experienced at least one AE. Conclusions: This real-world study demonstrates that SII-ONCO-BCG is an effective and safe treatment for patients with intermediate- and high-risk NMIBC.

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CFCharalampos Fragkoulis
Charalampos Fragkoulis
IGIoannis Glykas
Ioannis Glykas
LTLazaros Tzelves
Lazaros Tzelves
PSPANAGIOTIS VELISSARIOS STAMATAKOS
PANAGIOTIS VELISSARIOS STAMATAKOS
GPGeorgios Papadopoulos
Georgios Papadopoulos
APAthanasios Papatsoris
Athanasios Papatsoris
Objectives: Phosphate and tensin homolog gene (PTEN) acts as a regulator of PI3-KAkt molecular pathway. ETS Related gene (ERG), an oncogene located in chromosome 21q22.2, is involved in prostate cancer (PCa) by serine 2 (TMPRSS2), a protein encoded by TMPRSS2 gene. The aim of this study is to evaluate the clinical impact of PTEN loss and ERG rearrangement in terms of oncologic results in patients diagnosed with localized PCa who underwent radical prostatectomy. Materials and methods: Prospective data were collected from a total of 74 patients who underwent open radical retropubic prostatectomy for localized PCa and immunohistochemical study was performed in tissue samples. The primary antibodies for anti-ERG antibody as well as anti-PTEN antibody were obtained from DAKO. ERG was considered positive if at least 20% of the evaluated cells were stained at least with medium intensity. PTEN protein loss was considered when the intensity of cytoplasmic and nuclear staining was mild or entirely negative across > 10% of tumor cells. Results: Homogenous loss of PTEN was associated with higher clinical International Society of Urological Pathology (ISUP) grade (p = 0.018) while no statistical significant association was present regarding the presence of ERG rearrangement with either ISUPc or ISUPp. After a median follow up of 34 months, 24 patients developed biochemical recurrence. No statistical significant correlation of ERG status with biochemical recurrence was noted while PTEN was associated with biochemical recurrence development in a statistical significant way. Lastly the combination of PTEN loss with ERG rearrangement presence was detected more often in higher ISUPc and ISUPp as well as biochemical recurrence development, although in a non statistical significant way. Conclusions: Homogenous and heterogenous PTEN loss was associated with biochemical recurrence. No association of ERG and biochemical recurrence was noted. The combination of PTEN loss and ERG rearrangement presented a trend for higher ISUPc and ISUPp as well as biochemical recurrence but not in a statistical significant way.

1 July 2022 in Hellenic Urology
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Journal Article
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PSPANAGIOTIS VELISSARIOS STAMATAKOS
PANAGIOTIS VELISSARIOS STAMATAKOS
EPEvangelia Papadimitriou
Evangelia Papadimitriou
TPTheodoros Paizis
Theodoros Paizis
PGPapadopoulos Georgios
Papadopoulos Georgios
KNKonstantinos Ntoumas
Konstantinos Ntoumas
Introduction and Objective: Hemorrhagic cystitis (HC) is a diffuse bladder inflammation that causes hematuria and other urinary tract complaints. Noninfectious hemorrhagic cystitis most commonly occurs in patients who have undergone pelvic radiation. In cases with refractory disease and persistent hematuria, the bladder can be irrigated with a variety of agents. Hyperbaric oxygen (HBO) therapy has been used with some success in difficult cases. In the present article, the safety and efficacy of HBO was examined as the primary treatment choice for radiation-induced HC. Evidence Acquisition: Prospective data were collected among patients with HC and previous radiotherapy. HBO was applied as a primary treatment. The primary endpoint of our study was the incidence of complete and partial response to treatment, whereas a variety of secondary endpoints were examined including the duration of response, blood transfusion rate, the avoidance of surgery, and the overall survival. Moreover, the correlation between the interval between the onset of hematuria and initiation of therapy and the success of treatment was recorded. Evidence Synthesis: A total of 20 patients participated in the study. The complete and partial response rate was 85% and 15%, respectively. All patients completed therapy while the median number of sessions needed was 31. No complications were recorded during treatment. Patients with complete response received therapy within 3 months of the hematuria onset. One patient needed cystectomy, whereas 19 patients were alive at the end of follow-up. Conclusions: HBO consists of an effective and safe treatment option in the management of radiation-induced severe HC. Further prospective studies should be undergone in order to validate its efficacy and safety profile.

31 October 2025 in BMJ Case Reports
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PSPANAGIOTIS VELISSARIOS STAMATAKOS
PANAGIOTIS VELISSARIOS STAMATAKOS
STSavvas Tsakiris
Savvas Tsakiris
ATAggelos Tzoras
Aggelos Tzoras
NFNikolaos Ferakis
Nikolaos Ferakis
Percutaneous nephrolithotomy (PCNL) is the surgical treatment of choice for large renal stones. Various complications have been reported following the PCNL technique. An infrequent yet severe surgical complication associated with PCNL is biliary peritonitis resulting from gallbladder injury during the procedure. In this article, we discuss the case of a patient who underwent PCNL. Following PCNL, the patient diagnosed with gallbladder perforation accompanied by biliary peritonitis. Furthermore, a literature review of the available evidence about clinical suspicion, diagnosis and treatment of this lethal complication is presented.

29 November 2024 in Expert Opinion on Pharmacotherapy
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PSPANAGIOTIS VELISSARIOS STAMATAKOS
PANAGIOTIS VELISSARIOS STAMATAKOS
GPGeorgios Papavasileiou
Georgios Papavasileiou
ALAggeliki Leventi
Aggeliki Leventi
APAthanasios Papatsoris
Athanasios Papatsoris
ABAristotelis Bamias
Aristotelis Bamias
CFCharalampos Fragkoulis
Charalampos Fragkoulis
IntroductionAndrogen deprivation therapy consists of the cornerstone of prostate cancer medical treatment. Until recently, castration of hypothalamus-hypophysis-gonadal axial was based on injectable medical agents. A few years ago, a novel per os administered GnRH antagonist was approved leading testosterone to castration level. Relugolix was approved by FDA in 2020, and it is the first per os administered GnRH antagonist. The present study is a literature review of the efficacy, safety and clinical perspectives of relugolix.Areas coveredA literature narrative review was conducted using PubMed/MEDLINE, Scopus, and the Cochrane library. Studies written in English language, considering efficacy, safety and cost-effectiveness of relugolix compared with other androgen deprivation therapies were included in the review.Expert opinionRecent studies have examined efficacy of relugolix revealing a testosterone suppression percentage of 78.4% after 48 weeks from treatment initiation. Moreover, relugolix has been associated with less major cardiovascular events as well as better rate of testosterone recovery after treatment completion compared with the GnRH agonists. However, there is no head-to-head trial comparing relugolix with injectable GnRH antagonists, so far. As a result, a trial comparing the methods of antagonists' administration should be performed in the future.