This is a multicenter, observational, retrospective and prospective study conducted within the REMO (Reggio Emilia - Modena) network in the Emilia-Romagna region (Italy), promoted by AUSL-IRCCS of Reggio Emilia. The study aims to evaluate the impact of surgical centralization and treatment strategies adopted during the COVID-19 pandemic on oncologic outcomes in patients diagnosed with the epithelial ovarian cancer (EOC) from 2018 to 2023. The retrospective component includes patients treated between 2018 and 2023, while the prospective component consists of clinical follow-up of those patients over the next five years.
Epithelial ovarian cancer (EOC) is a highly aggressive malignancy, frequently diagnosed at an advanced stage and requiring a combined approach of surgery and systemic therapy. Complete cytoreductive surgery remains the most important prognostic factor, as residual disease ≥1 cm significantly worsens survival. In November 2019, a regional decree in Emilia-Romagna (Italy) introduced the centralization of EOC treatment to high-volume centers to improve care quality and clinical outcomes. Shortly thereafter, the onset of the COVID-19 pandemic led to a severe reduction in healthcare resources, including surgical capacity, ICU beds, and staff availability. This situation resulted in a higher proportion of patients being referred for neoadjuvant chemotherapy, with surgery performed mainly in selected patients with better performance status and higher chances of complete resection. During this period, an increase in centralized treatments, multidisciplinary evaluations, BRCA testing, and use of interval debulking surgery (IDS) was observed. This observational, retrospective study is designed to evaluate whether centralization and pandemic-related treatment modifications influenced oncological outcomes. The primary objective is to compare progression-free survival (PFS) and overall survival (OS) among patients treated during three different timeframes: pre-centralization/pre-pandemic (2018-2019), peak pandemic phase (2020-2021), and pandemic control phase (2022-2023). Secondary objectives include describing treatment strategies after initial diagnosis (type of surgery, chemotherapy, maintenance therapies), tumor characteristics (histology, BRCA/HRD status), recurrence patterns (site, symptoms, treatment), and the proportion of patients receiving secondary surgery, radiotherapy, Bevacizumab, and/or PARP inhibitors. No experimental interventions are included, and all patients received treatment according to routine clinical practice.
Study Type
OBSERVATIONAL
Enrollment
200
Observational data collection only
Azienda Unità - Sanitaria locale di Modena - Ospedale Razzini Carpi
Carpi, Modena, Italy
Azienda Unità - Sanitaria locale di Modena - Ospedale di Mirandola
Mirandola, Modena, Italy
Azienda Unità - Sanitaria locale di Modena - Ospedale Pavullo nel Frignano
Pavullo nel Frignano, Modena, Italy
Azienda Unità - Sanitaria locale di Modena - Ospedale Civile Sassuolo
Sassuolo, Modena, Italy
Azienda Unità - Sanitaria locale di Modena - Ospedale di Vignola
Vignola, Modena, Italy
Azienda USL IRCCS di Reggio Emilia
Reggio Emilia, RE, Italy
Azienda Ospedaliero - Universitario di Modena
Modena, Italy
Progression-Free Survival (PFS)
Time from initial diagnosis of epithelial ovarian cancer to the date of first documented disease progression or death from any cause, whichever occurs first.
Time frame: Up to 5 years from diagnosis
Overall Survival (OS)
Time from initial diagnosis to death from any cause. Patients still alive will be censored at the date of last follow-up.
Time frame: Up to 5 years from diagnosis
Type of treatment received after initial diagnosis
Classification of treatment pathways including type of surgery (primary or interval debulking), type of chemotherapy (neoadjuvant, adjuvant, or palliative), and use of maintenance therapies.
Time frame: Within 12 months from diagnosis
Use of targeted therapies (Bevacizumab and/or PARP inhibitors)
Percentage of patients treated with Bevacizumab, PARP inhibitors, or both, in adjuvant or maintenance settings.
Time frame: Within 12 months from completion of first-line chemotherapy
Rate and characteristics of recurrence
Frequency, site, and symptoms of disease recurrence, and rate of patients undergoing secondary surgery or radiotherapy.
Time frame: Up to 5 years from diagnosis
Rate of radiotherapy use in recurrent disease
Proportion of patients with recurrence treated with radiotherapy, including treatment site, dose, and clinical response.
Time frame: Up to 5 years from diagnosis
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