Andrada Loghin

Dr. Andrada Loghin


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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1 January 2014
Verified
Journal Article
Closed access
ANAdela Nechifor-Boila
Adela Nechifor-Boila
RCRamona Catana
Ramona Catana
ALAndrada Loghin
Andrada Loghin
TRTatiana Georgiana Radu
Tatiana Georgiana Radu
ABAngela Borda
Angela Borda

Verified
Journal Article
Open access
PDF file
ALAndrada Loghin
Andrada Loghin
MPMaria Catalina Popelea
Maria Catalina Popelea
TCTodea-Moga Ciprian-Doru
Todea-Moga Ciprian-Doru
ICIuliu Gabriel Cocuz
Iuliu Gabriel Cocuz
ABAngela Borda
Angela Borda
Eosinophilic solid and cystic renal cell carcinoma (ESC-RCC) is a novel and uncommon type of renal cell carcinoma, which has been recently recognized and introduced as a distinct entity in the WHO 2022 kidney tumor classification. Previously known as “unclassified RCC”, followed by “tuberous sclerosis complex (TSC)-associated RCC”, ESC-RCC is now a distinct category of kidney tumor, with its own name, with specific clinical manifestations, and a unique morphological, immunohistochemical and molecular profile. Due to its recent introduction and the limited available data, the diagnosis of ESC-RCC is still a complex challenge, and it is probably frequently misdiagnosed. The secret of diagnosing this tumor lies in the pathologists’ knowledge, and keeping it up to date through research, thereby limiting the use of outdated nomenclature. The aim of our case-based review is to provide a better understanding of this pathology and to enrich the literature with a new case report, which has some particularities compared to the existing cases.

28 April 2021 in Life
Verified
Journal Article
Open access
PDF file
INIoan Alin Nechifor-Boila
Ioan Alin Nechifor-Boila
ALAndrada Loghin
Andrada Loghin
ANAdela-Corina Nechifor-Boilă
Adela-Corina Nechifor-Boilă
MDMyriam Decaussin-Petrucci
Myriam Decaussin-Petrucci
SVSeptimiu Voidăzan
Septimiu Voidăzan
ABAngela Borda
Angela Borda
In the present study, we analyzed Programmed Death Ligand-1 (PD-L1) expression in radical cystectomy (RC) specimens from patients with muscle-invasive urothelial carcinoma (UC), in order to assess any correlations with specific clinicopathological features and its potential prognostic value. A multi-institutional study was performed within the departments of urology and pathology at the Mureș County Hospital, Romania, and Centre Hospitalier Lyon Sud, France. Sixty-nine patients with MIBC were included, for whom tumor histology (conventional versus histological variant/differentiation), tumor extension (T), lymph node involvement (N), and distant metastases (M) were recorded. PD-L1 immunostaining was performed using the 22C3 clone and was interpreted using the combined positive score (CPS) as recommended (Dako Agilent, Santa Clara, CA, USA). Positive PD-L1 immunostaining was more prevalent among UCs with squamous differentiation compared to conventional UCs and trended towards an improved OS (p = 0.366). We found the T stage to be a risk factor for poor survival in PD-L1-positive patients (HR 2.9, p = 0.021), along with the N stage in PD-L1-negative patients (HR 1.98, p = 0.007). No other clinicopathological factor was found to be significantly associated with PD-L1 positivity. Thus, we confirm the need for PD-L1 immunostaining prior to initiating immune checkpoint inhibitor therapy for a more accurate assessment of the patients’ chances of responding to treatment.

1 January 2015
Verified
Journal Article
Closed access
ANAdela Corina Nechifor-Boilă
Adela Corina Nechifor-Boilă
ALAndrada Loghin
Andrada Loghin
VVVictor Vacariu
Victor Vacariu
VHVasile Bogdan Halaţiu
Vasile Bogdan Halaţiu
ABAngela Borda
Angela Borda


28 February 2025 in Cancers
Verified
Journal Article
Open access
PDF file
Andrada-Claudia TătarAndrada-Claudia Tătar
Andrada-Claudia Tătar
ALAndrada Loghin
Andrada Loghin
ANAdela-Corina Nechifor-Boilă
Adela-Corina Nechifor-Boilă
ARAndrada Raicea
Andrada Raicea
MPMaria-Cătălina Popelea
Maria-Cătălina Popelea
ABAngela Borda
Angela Borda
Background/Objectives: UBC demonstrates a relatively low prevalence in patients under 50 years old. Our study aimed to compare the pathological characteristics of UBC in young and elderly patients and to assess the age-related variations in these characteristics. Methods: This retrospective study from January 2018 to December 2022 encompassed 762 patients with an initial diagnosis of UBC. To evaluate the pathological characteristics of UBC in young patients, compared to elderly patients, we divided our cohort using a cut-off age of 50 years. Additionally, to evaluate the age-dependent variations in these characteristics, we further stratified our patients into three age groups (≤50, 51–70, and >70 years old). Results: Of the 762 patients included in our study, 37 (4.86%) were young (≤50 years old), with a median age of 44 and a M:F ratio of 3.11:1. Conventional UC was the most common histology (86.5%). Regarding tumour grade, we noticed a higher prevalence of PUNLMP (10.8% versus 2.3%) and LGPUC (45.9% versus 37.1%) and a lower prevalence of HGPUC (43.2% versus 60%) and CIS (0% versus 0.6%) in young patients (p = 0.008). In this group, the pTa stage revealed a higher prevalence (64.9% versus 46.8%), while pT1 and pT2 showed a lower prevalence (32.1% versus 18.9% and 20.6% versus 16.2%) (p = 0.179). All results remained consistent when the cohort was stratified into three age groups, showing age-related variations (p = 0.001 and p = 0.089, respectively). Conclusions: In young patients, UBC tends to be of a lower grade and stage compared to elderly patients, and these characteristics demonstrate a gradual age-related stratification.