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
759P - Nimotuzumab combined with concurrent chemo-radiotherapy in patients with locally advanced cervical squamous cell carcinoma: A randomized, controlled, open-label, multicenter study
Presenter: Junjie Wang
Session: Poster session 11
760P - Efficacy and safety of nimotuzumab plus radiotherapy for elderly patients with locally advanced cervical squamous cell carcinoma
Presenter: Ang Qu
Session: Poster session 11
761P - A phase II trial of avelumab in combination with pegylated liposomal doxorubicin in recurrent/metastatic endometrial cancer (GEICO 70-E): analysis according to molecular classification
Presenter: Josep M. Piulats
Session: Poster session 11
764P - Tislelizumab (Anti-PD-1) combined with definitive chemoradiotherapy in recurrent and/or metastatic cervical cancer (PILOT-2020-511): A single-arm, phase II trial
Presenter: JUN ZHU
Session: Poster session 11
765P - SABRINA study: A phase II study of senaparib monotherapy for patients (pts) with BRCA1/2 mutated recurrent platinum-sensitive ovarian cancer (PSOC)
Presenter: Xiaohua Wu
Session: Poster session 11
766P - A comparative study of sequential and interdigitated brachytherapy with chemoradiation in patients of locally advanced carcinoma cervix
Presenter: Shreya Singh
Session: Poster session 11
767P - Phase I/II study of toripalimab with cisplatin-based concurrent IMRT for local advanced cervical cancer
Presenter: Ping Jiang
Session: Poster session 11
768P - Preliminary results of an open-label, multicentric, phase Ib/II study to assess the safety and efficacy of AsiDNA, a DNA repair inhibitor, in addition to PARP inhibitor in patients with relapsed platinum sensitive ovarian cancer already treated with PARPi for at least 6 months (RevoCAN)
Presenter: Patricia Pautier
Session: Poster session 11