Abstract 648P
Background
As extended analysis of the COVID-DELAY study, we aimed to assess COVID-19 impact on diagnosis, staging and treatment outcomes of CRC patients in 2021 and 2022 compared to 2019 and 2020.
Methods
All consecutive newly diagnosed CRC patients referred to 8 Italian Oncology Departments between March and December 2019, 2020, 2021, and 2022 were evaluated. Access rate (number of patients/year), demographic characteristics, diagnostic and therapeutic temporal intervals (between date of symptoms onset, radiological and cytohistological diagnosis, treatment start, and first radiological evaluation), as well as PFS and OS were assessed and compared.
Results
Compared to 2019 (n=485), a reduction in new CRC cases was found in 2020 (n=390, -19.6%). On the other hand, a progressive increase in new CRC diagnosis was found in 2021 (n= 461, +18.2%) and 2022 (n= 509, +30.5%), compared to 2020. A higher rate of stage IV tumours was diagnosed in 2020 (31.3%) and 2021 (29.6%) compared to 2019 (20.8%), with a normalization in 2022 (22.8%) (p<0.001); a lower number of patients has been discussed in multidisciplinary tumor boards in 2020 (22.1%) compared to 2019 (34.9%), 2021 (37.0%), and 2022 (47.6%) (p<0.001). A significant difference in terms of temporal interval between histological diagnosis and first oncological examination (median of 31 vs. 38 days, respectively, p=0.004), cytohistological diagnosis and systemic treatment start (median of 52 vs. 58 day, p<0.001), first oncological appointment and systemic treatment start (median of 52 compared to 58 days, p=0.034), was found between 2020 and 2021-2022 years, respectively. At multivariate analysis, the 2021-2022 years confirmed to be associated with a reduction in the risk of disease progression compared to 2020 (HR=0.71 (0.53-0-97); p=0.031).
Conclusions
A worsening drop in CRC diagnosis in 2020, with a progressive increase in 2021 and 2022, in parallel with a higher incidence of late-stage CRC diagnosed in 2020 and 2021. This might have affected some diagnostic-therapeutic time intervals in 2021-2022 years compared to 2020.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
769P - Pharmacokinetic boosting of olaparib: An open-label, prospective, cross-over study
Presenter: Joanneke Overbeek
Session: Poster session 11
770P - Tolerability and efficacy of trabectedin plus pegylated liposomal doxorubicin (PLD) in elderly patients with ovarian cancer (OC): GEICO 105-O study
Presenter: Maria Jesus Rubio Perez
Session: Poster session 11
771P - Genomic characterization of advanced endometrial carcinosarcoma: Identification of potentially actionable targets
Presenter: Ugo De Giorgi
Session: Poster session 11
773P - Real-world results of homologous recombination deficiency testing: Comparison between two methods on 2,655 ovarian cancer patients in Spain
Presenter: Conxi Lazaro
Session: Poster session 11
774P - CCNE1 amplification defines a good prognostic subgroup among BRCAwt/HRDneg advanced high-grade ovarian cancer (HGOC)
Presenter: Felix Blanc-Durand
Session: Poster session 11
775P - A gene expression signature to predict benefit from intraperitoneal (IP) carboplatin chemotherapy in ovarian carcinoma (OC): Translational research study from the intraperitoneal therapy for ovarian cancer with carboplatin (iPocc) phase II/III trial
Presenter: David SP Tan
Session: Poster session 11
776P - Multi-omics analysis of chemo-refractory high-grade serous carcinoma patients: Insights from the DECIDER study
Presenter: Daria Afenteva
Session: Poster session 11
777P - Targeting cadherin-6 in epithelial ovarian cancer: Clinical significance of its expression and efficacy of raludotatug deruxtecan (R-DXd) in patient-derived cell models
Presenter: Daisuke Shintani
Session: Poster session 11
778P - Combined targeting poly (ADP-ribose) polymerase and receptor tyrosine kinase inhibits ovarian clear cell carcinoma progression via disrupted ribosomal biogenesis
Presenter: Chyong-Huey Lai
Session: Poster session 11
779P - Assessment of the RAD51 test to determine homologous recombination deficiency (HRD) in patients (pts) with newly diagnosed advanced high-grade epithelial ovarian cancer carcinoma (HGOC)
Presenter: Carmen Garcia Duran
Session: Poster session 11