72 research outputs found

    Ovarian Cancer Biomarkers: A Focus on Genomic and Proteomic Findings

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    Among the gynaecological malignancies, ovarian cancer is one of the neoplastic forms with the poorest prognosis and with the bad overall and disease-free survival rates than other gynaecological cancers; several studies, analyzing clinical data and pathological features on ovarian cancers, have focused on the identification of both diagnostic and prognostic markers for applications in clinical practice. High-throughput technologies have accelerated the process of biomarker discovery, but their validity should be still demonstrated by extensive researches on sensibility and sensitivity of ovarian cancer novel biomarkers, determining whether gene profiling and proteomics could help differentiate between patients with metastatic ovarian cancer and primary ovarian carcinomas, and their potential impact on management

    Management challenges of deep infiltrating endometriosis.

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    Deep infiltrating endometriosis (DIE) is considered the most aggressive form among the three phenotypes that constitute endometriosis. It can affect the whole pelvis, subverting the anatomy and functionality of vital organs, with an important negative impact on the patient’s quality of life. The diagnosis of DIE is based on clinical and physical examination, instrumental examination, and, if surgery is needed, the identification and biopsy of lesions. The choice of the best therapeutic approach for women with DIE is often challenging. Therapeutic options include medical and surgical treatment, and the decision should be dictated by the patient’s medical history, disease stage, symptoms severity, and personal choice. Medical therapy can control the symptoms and stop the development of pathology, keeping in mind the side effects derived from a long-term treatment and the risk of recurrence once suspended. Surgical treatment should be proposed only when it is strictly necessary (failed hormone therapy, contraindications to hormone treatment, severity of symptoms, infertility), preferring, whenever possible, a conservative approach performed by a multidisciplinary team. All therapeutic possibilities have to be explained by the physicians in order to help the patients to make the right choice and minimize the impact of the disease on their lives

    Cesarean scar pregnancy treated by artery embolisation combined with diode laser: a novel approach for a rare disease

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    Cesarean scar pregnancy (CSP) is a rare form of ectopic pregnancy which represents a consequence of a previous cesarean section. It is associated with major maternal morbidity and mortality and has potential implications on future fertility. Because of possible serious complications, CSP should be swiftly diagnosed and treated. There is no management protocol for this rare, life-threatening condition, and each patient should be evaluated individually. Several types of conservative treatment have been used to treat cesarean scar pregnancy: dilation and curettage (D&C), excision of trophoblastic tissues, local or systemic administration of methotrexate, bilateral hypogastric artery ligation, and selective uterine artery embolization with curettage and/or methotrexate administration. In our study we present a cesarean scar pregnancy of a 40-year-old woman who was treated with angiographic uterine artery embolization (UAE) followed by hysteroscopic diode laser resection. Our combined UAE-hysteroscopic laser surgery appears to offer an effective, safe, and minimally invasive surgical treatment

    Development of a Nomogram Predicting the Risk of Persistence/Recurrence of Cervical Dysplasia

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    Background: Cervical dysplasia persistence/recurrence has a great impact on women's health and quality of life. In this study, we investigated whether a prognostic nomogram may improve risk assessment after primary conization. Methods: This is a retrospective multi-institutional study based on charts of consecutive patients undergoing conization between 1 January 2010 and 31 December 2014. A nomogram assessing the importance of different variables was built. A cohort of patients treated between 1 January 2015 and 30 June 2016 was used to validate the nomogram. Results: A total of 2966 patients undergoing primary conization were analyzed. The median (range) patient age was 40 (18-89) years. At 5-year of follow-up, 6% of patients (175/2966) had developed a persistent/recurrent cervical dysplasia. Median (range) recurrence-free survival was 18 (5-52) months. Diagnosis of CIN3, presence of HR-HPV types, positive endocervical margins, HPV persistence, and the omission of HPV vaccination after conization increased significantly and independently of the risk of developing cervical dysplasia persistence/recurrence. A nomogram weighting the impact of all variables was built with a C-Index of 0.809. A dataset of 549 patients was used to validate the nomogram, with a C-index of 0.809. Conclusions: The present nomogram represents a useful tool for counseling women about their risk of persistence/recurrence after primary conization. HPV vaccination after conization is associated with a reduced risk of CIN2+

    Characteristics and patterns of care of endometrial cancer before and during COVID-19 pandemic

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    Objective: Coronavirus disease 2019 (COVID-19) outbreak has correlated with the disruption of screening activities and diagnostic assessments. Endometrial cancer (EC) is one of the most common gynecological malignancies and it is often detected at an early stage, because it frequently produces symptoms. Here, we aim to investigate the impact of COVID-19 outbreak on patterns of presentation and treatment of EC patients. Methods: This is a retrospective study involving 54 centers in Italy. We evaluated patterns of presentation and treatment of EC patients before (period 1: March 1, 2019 to February 29, 2020) and during (period 2: April 1, 2020 to March 31, 2021) the COVID-19 outbreak. Results: Medical records of 5,164 EC patients have been retrieved: 2,718 and 2,446 women treated in period 1 and period 2, respectively. Surgery was the mainstay of treatment in both periods (p=0.356). Nodal assessment was omitted in 689 (27.3%) and 484 (21.2%) patients treated in period 1 and 2, respectively (p<0.001). While, the prevalence of patients undergoing sentinel node mapping (with or without backup lymphadenectomy) has increased during the COVID-19 pandemic (46.7% in period 1 vs. 52.8% in period 2; p<0.001). Overall, 1,280 (50.4%) and 1,021 (44.7%) patients had no adjuvant therapy in period 1 and 2, respectively (p<0.001). Adjuvant therapy use has increased during COVID-19 pandemic (p<0.001). Conclusion: Our data suggest that the COVID-19 pandemic had a significant impact on the characteristics and patterns of care of EC patients. These findings highlight the need to implement healthcare services during the pandemic

    Insight from an Italian Delphi Consensus on EVAR feasibility outside the instruction for use: the SAFE EVAR Study

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    BACKGROUND: The SAfety and FEasibility of standard EVAR outside the instruction for use (SAFE-EVAR) Study was designed to define the attitude of Italian vascular surgeons towards the use of standard endovascular repair (EVAR) for infrarenal abdominal aortic aneurysm (AAA) outside the instruction for use (IFU) through a Delphi consensus endorsed by the Italian Society of Vascular and Endovascular Surgery (Societa Italiana di Chirurgia Vascolare ed Endovascolare - SICVE). METHODS: A questionnaire consisting of 26 statements was developed, validated by an 18 -member Advisory Board, and then sent to 600 Italian vascular surgeons. The Delphi process was structured in three subsequent rounds which took place between April and June 2023. In the first two rounds, respondents could indicate one of the following five degrees of agreement: 1) strongly agree; 2) partially agree; 3) neither agree nor disagree; 4) partially disagree; 5) strongly disagree; while in the third round only three different choices were proposed: 1) agree; 2) neither agree nor disagree; 3) disagree. We considered the consensus reached when >70% of respondents agreed on one of the options. After the conclusion of each round, a report describing the percentage distribution of the answers was sent to all the participants. RESULTS: Two -hundred -forty-four (40.6%) Italian Vascular Surgeons agreed to participate the first round of the Delphi Consensus; the second and the third rounds of the Delphi collected 230 responders (94.3% of the first -round responders). Four statements (15.4%) reached a consensus in the first rounds. Among the 22 remaining statements, one more consensus (3.8%) was achieved in the second round. Finally, seven more statements (26.9%) reached a consensus in the simplified last round. Globally, a consensus was reached for almost half of the proposed statements (46.1%). CONCLUSIONS: The relatively low consensus rate obtained in this Delphi seems to confirm the discrepancy between Guideline recommendations and daily clinical practice. The data collected could represent the source for a possible guidelines' revision and the proposal of specific Good Practice Points in all those aspects with only little evidence available

    Practice patterns and 90-day treatment-related morbidity in early-stage cervical cancer

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    To evaluate the impact of the Laparoscopic Approach to Cervical Cancer (LACC) Trial on patterns of care and surgery-related morbidity in early-stage cervical cancer

    Isterectomia Radicale Robotica versus Laparoscopica con Linfadenectomia in pazienti con Carcinoma Cervicale in fase iniziale: uno studio multicentrico.

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    Abstract Scopo dello studio è stato quello di confrontare retrospettivamente in una serie di 99 donne la sicurezza, efficacia, morbidità ed il tasso di recidive dopo isterectomia radicale laparoscopica (TLRH) con linfadenectomia versus isterectomia radicale robotica con linfadenectomia (RRH) nel trattamento del carcinoma cervicale in fase iniziale. Sono state consecutivamente arruolate nel nostro studio 99 pazienti allo stadio FIGO Ia1 con invasione degli spazi linfovascolari (LVSI), Ia2, Ib1, Ib2 and IIa di carcinoma cervicale, 76 delle quali sono state sottoposte ad Isterectomia Radicale totalmente Laparoscopica con linfadenectomia e 23 ad Isterectomia Radicale Robotica con linfadenectomia. La linfadenectomia para-aortica fino all’arteria mesenterica inferiore è stata eseguita in tutti i casi con linfonodi pelvici positivi all’esame istologico estemporaneo. Le perdite ematiche sono state di 157 ml nel gruppo RRH (95% CI 50-400) e 95 ml nel gruppo TLRH (95% CI 30-500) (p>0.05). La durata media dell’ospedalizzazione è stata di 3 giorni nel gruppo RRH (95% CI 2-7) e 4 giorni nel gruppo TLRH (95% CI 3-7) (N.S.). La durata media dell’intervento è stata di 255±25 nel gruppo TLRH (182-415) e di 323±30 nel gruppo RRH (161-433) (p<0.01). Non è stata osservata nessuna differenza significativa tra i due gruppi nel tasso di recidive post-intervento. In conclusione, la nostra esperienza conferma che la chirurgia robotica fornisce una visione tridimensionale, notevole precisione chirurgica con riduzione del tremore, una notevole riduzione della fatica e maggiore libertà dei movimenti rispetto alla laparoscopia convenzionale che richiede un training più lungo con una più lunga curva di crescita. Nonostante i maggiori costi legati all’utilizzo della tecnologia robotica, l’isterectomia radicale robotica può essere considerata una sicura ed efficace opzione chirurgica nel trattamento del carcinoma cervicale in fase iniziale con una morbidità simile a quella riportata nell’approccio laparoscopico. Il tempo operatorio è risultato più lungo nel gruppo robotico, ma il tasso di recidive ed il tasso di complicanze intra e postoperatorie appaiono simili in entrambi i gruppi, sebbene trials clinici multicentrici randomizzati ed un più lungo follow-up saranno necessari per valutare i risultati a lungo termine di entrambe queste procedure
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