Ionut-Dimitrie Atasiei

Mr. Ionut-Dimitrie Atasiei

Carol Davila University of Medicine and Pharmacy, Bucharest, Bucureşti, Romania
orcid

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

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

Representative Publications

View All Publications
Verified
Journal Article
Open access
PDF file
Horia-Dan LiscuHoria-Dan Liscu
Horia-Dan Liscu
NVNICOLAE VERGA
NICOLAE VERGA
Ionut-Dimitrie AtasieiIonut-Dimitrie Atasiei
Ionut-Dimitrie Atasiei
CBCristinel Dumitru Badiu
Cristinel Dumitru Badiu
ADAdrian Vasile Dumitru
Adrian Vasile Dumitru
Miron Andreea IulianaMiron Andreea Iuliana
Miron Andreea Iuliana
Biomarkers in colorectal cancer (CRC) are of great interest in the current literature due to improvements in techniques such as liquid biopsy and next-generation sequencing (NGS). However, screening methods vary globally, with multi-target stool DNA (mt-sDNA) predominantly used in the USA and, more recently, the Cologuard Plus; biomarkers such as the Galectins family and septins show promise in early detection. Gut microbiome assessments, such as Fusobacterium nucleatum, are under intense exploration. Diagnostic tests, such as circulating DNA analysis via NGS, exhibit effectiveness and are being increasingly adopted. Circulating tumor cells emerge as potential alternatives to traditional methods in terms of diagnosis and prognosis. Predictive biomarkers are well established in guidelines; nonetheless, with the aid of machine learning and artificial intelligence, these biomarkers may be improved. This review critically explores the actual dynamic landscape of CRC biomarkers and future, promising biomarkers involved in screening, diagnosis, and prognosis.

16 January 2024 in Cancers
Verified
Journal Article
Open access
PDF file
Miron Andreea IulianaMiron Andreea Iuliana
Miron Andreea Iuliana
Ionut-Dimitrie AtasieiIonut-Dimitrie Atasiei
Ionut-Dimitrie Atasiei
RIRadu Tudor Ionescu
Radu Tudor Ionescu
FUFlavia Ultimescu
Flavia Ultimescu
Andrei-Alexandru BarnonschiAndrei-Alexandru Barnonschi
Andrei-Alexandru Barnonschi
FSFlorica Sandru
Florica Sandru
This review explores the interconnection between precursor lesions of breast cancer (typical ductal hyperplasia, atypical ductal/lobular hyperplasia) and the subclinical of multiple organ failure syndrome, both representing early stages marked by alterations preceding clinical symptoms, undetectable through conventional diagnostic methods. Addressing the question “Why patients with breast cancer exhibit a tendency to deteriorate”, this study investigates the biological progression from a subclinical multiple organ failure syndrome, characterized by insidious but indisputable lesions, to an acute (clinical) state resembling a cascade akin to a waterfall or domino effect, often culminating in the patient’s demise. A comprehensive literature search was conducted using PubMed, Google Scholar, and Scopus databases in October 2023, employing keywords such as “MODS”, “SIRS”, “sepsis”, “pathophysiology of MODS”, “MODS in cancer patients”, “multiple organ failure”, “risk factors”, “cancer”, “ICU”, “quality of life”, and “breast cancer”. Supplementary references were extracted from the retrieved articles. This study emphasizes the importance of early identification and prevention of the multiple organ failure cascade at the inception of the malignant state, aiming to enhance the quality of life and extend survival. This pursuit contributes to a deeper understanding of risk factors and viable therapeutic options. Despite the existence of the subclinical multiple organ failure syndrome, current diagnostic methodologies remain inadequate, prompting consideration of AI as an increasingly crucial tool for early identification in the diagnostic process.
1

29 February 2024 in Journal of Personalized Medicine
Verified
Journal Article
Open access
PDF file
Horia-Dan LiscuHoria-Dan Liscu
Horia-Dan Liscu
Ionut-Lucian Antone-IordacheIonut-Lucian Antone-Iordache
Ionut-Lucian Antone-Iordache
Ionut-Dimitrie AtasieiIonut-Dimitrie Atasiei
Ionut-Dimitrie Atasiei
AAAndreea Anghel
Andreea Anghel
AIAndreea-Teodora Ilie
Andreea-Teodora Ilie
FUFlavia Ultimescu
Flavia Ultimescu
The standard oncologic treatment of locally advanced rectal cancer is long-course radio-chemotherapy followed by surgery and adjuvant chemotherapy. This can result in a lengthy total treatment duration, sometimes up to one year from the diagnosis. Interruptions to neoadjuvant treatment can occur for a variety of reasons, forced or unforced. The main purpose of this study is to analyze the survival data of locally advanced rectal cancer patients who received neoadjuvant treatment and to find a cut-off point showing exactly how many days of interruption of neoadjuvant treatment the risk of death or disease relapse increases. We conducted a retrospective study on 299 patients with locally advanced rectal cancer using survival analysis (Kaplan–Meier curve and Cox regression) to determine survival probabilities for overall survival, local control, and disease-free survival. Patients with 0 to 3 days of neoadjuvant therapy interruption had a higher overall survival probability compared to patients with 4 or more days (90.2% compared to 57.9%, p-value < 0.001), hazard ratio 5.89 (p < 0.001). Local control and disease-free survival had a higher probability in patients with 0–2 days of interruption compared to people with 3 or more days (94% vs. 75.4%, and 82.2% vs. 50.5%, respectively, both p-values < 0.001). Patients with tumoral or nodal downstaging experienced fewer days of interruption than patients with no downstage. These findings reinforce the need for radiation oncologists to be well-organized when starting neoadjuvant treatment for rectal cancer, in order to anticipate and prevent potential treatment interruptions and achieve the best therapeutic results.

30 January 2025 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
Horia-Dan LiscuHoria-Dan Liscu
Horia-Dan Liscu
NVNICOLAE VERGA
NICOLAE VERGA
Ionut-Dimitrie AtasieiIonut-Dimitrie Atasiei
Ionut-Dimitrie Atasiei
AIAndreea-Teodora Ilie
Andreea-Teodora Ilie
MVMaria Vrabie
Maria Vrabie
Miron Andreea IulianaMiron Andreea Iuliana
Miron Andreea Iuliana
Rectal cancer (RC) presents significant challenges in diagnosis and treatment, with increasing incidence among younger populations. Treatment approaches, particularly for locally advanced rectal cancer (LARC), have evolved, notably with the introduction of total neoadjuvant therapy (TNT). TNT combines neoadjuvant chemotherapy and chemoradiotherapy before surgery, improving overall survival and reducing both metastasis and local recurrence rates compared to traditional methods, while enabling more patients to complete the full oncological treatment. Clinical trials, such as RAPIDO, OPRA, and PRODIGE 23, have demonstrated the effectiveness of TNT in tumor downstaging and complete pathological responses, offering better outcomes for patients; however, debates persist regarding the role of neoadjuvant radiotherapy, with novel strategies exploring its omission in specific cases to reduce toxicity and enhance quality of life. In addition, organ preservation strategies, such as the watch-and-wait (WW) approach, have emerged as viable options for patients with a complete response to neoadjuvant therapy. Future directions point towards personalized treatment plans incorporating radiogenomics and the integration of artificial intelligence into diagnostics to optimize patient outcomes. This review aims to synthesize current treatment strategies and ongoing advancements in rectal cancer management, providing insights into potential future innovations.

16 February 2024 in Journal of Personalized Medicine
Verified
Journal Article
Open access
PDF file
Miron Andreea IulianaMiron Andreea Iuliana
Miron Andreea Iuliana
AAAlexandra Valentina Anghel
Alexandra Valentina Anghel
Ionut-Lucian Antone-IordacheIonut-Lucian Antone-Iordache
Ionut-Lucian Antone-Iordache
Ionut-Dimitrie AtasieiIonut-Dimitrie Atasiei
Ionut-Dimitrie Atasiei
Cătălin Alexandru AnghelCătălin Alexandru Anghel
Cătălin Alexandru Anghel
Horia-Dan LiscuHoria-Dan Liscu
Horia-Dan Liscu
Breast cancer (BC) significantly impacts the quality of life (QoL) of affected individuals. This study, conducted at Colțea Clinical Hospital, Bucharest, aimed to assess the impact of organ failures and metastases on QoL in breast cancer patients using EORTC QLQ-C30 and EORTC QLQ-BR45 questionnaires and the survival rate to understand the clinical journey and the quality of life status in breast cancer patients. From January 2019 to October 2022, a prospective, observational study surveyed 874 patients, revealing 201 fatalities, 66 refusals, and 607 eligible participants. Results indicated statistically significant differences in various QoL aspects for patients experiencing heart failure, including physical functioning, pain, insomnia, global health status, and overall summary score. Kidney failure exhibited significance in physical functioning for QLQ-C30 and body image, sexual functioning, and endocrine sexual symptoms for QLQ-BR45. Respiratory failure demonstrated significant differences across multiple QoL domains. Patients with bone metastases reported lower physical functioning (p = 0.006) and increased pain (p = 0.002). This study has revealed an overall 5-year life expectancy of 68.8%, with survival rates of 93.8% for Stage I, 86.3% for Stage II, and 77.2% for Stage III breast cancer. Metastatic cancer patients have shown a 35.6% survival rate over 45 months, with a median survival duration of 36 months. A significant limitation of our study was the administration of the questionnaire only once, preventing us from quantifying the impact of specific treatment types on quality of life. This study emphasizes the necessity of using standardized QoL assessments in clinical practice from the initial presentation to ongoing follow-up.
1

15 January 2025 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
IPIuliana Pantelimon
Iuliana Pantelimon
ASAndra Maria Stancu
Andra Maria Stancu
SCSimona Coniac
Simona Coniac
Miron Andreea IulianaMiron Andreea Iuliana
Miron Andreea Iuliana
Ionut-Dimitrie AtasieiIonut-Dimitrie Atasiei
Ionut-Dimitrie Atasiei
LGLaurentia Nicoleta Gales
Laurentia Nicoleta Gales
Background/Objectives: In Romania, breast cancer is the second most common cancer, the third leading cause of cancer death, and the most prevalent cancer overall. De novo advanced-stage breast cancer often presents in clinical practice, and treatment decisions are best made in a multidisciplinary tumor board (MTD) involving surgeons, radiotherapists, and medical oncologists. Significant advances in systemic therapies, particularly in progression-free survival (PFS) and overall survival (OS), have surpassed traditional palliative mastectomy and radiotherapy for local control. Therefore, the purpose of this study is to emphasize the importance of the initial choice of treatment for patient prognosis. Methods: We expose two cases of patients with de novo severe, advanced-stage, hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer and their management and outcome using cyclin-dependent kinase (CDK) 4/6 inhibitor and radiotherapy. An extensive review of the literature from the past five years was also conducted. Results: The role of palliative mastectomy is diminishing, as many patients are opting for novel therapies, including cyclin-dependent kinase (CDK) 4/6 inhibitors, which may improve quality of life. Conclusions: First-line therapy for locally advanced breast cancer has suffered changes due to the implementation of systemic targeted therapy. However, drug resistance—either de novo or acquired—remains a critical consideration. MTD discussions and informed patient decisions are essential to achieving a personalized, evidence-based treatment outcome.