Abstract 2146P
Background
Venous thromboembolism (VTE) in cancer patients is a common complication that requires a multidisciplinary management. In April 2021 we established in the Medical Oncology Department of our hospital a “Cancer-associated thrombosis (CAT) clinic” in order to provide immediate support in prevention and management of VTE to physicians involved in cancer patients’ treatment. The aim of this analysis is to describe the characteristics of patients evaluated, the decisions taken and their results.
Methods
Between May 2021 and April 2023, 124 patients have been evaluated in the “CAT clinic” of the Medical Oncology Department of the Hospital General Universitario Gregorio Marañón (Madrid, Spain) with a mean follow-up of 4.25 months (standard deviation +/- 5.47 months).
Results
The main reason for referral to clinic was VTE treatment (n=120; 96.8%) and the most frequent thrombotic event was pulmonary thromboembolism (n=56; 46.7%). The most common tumors were breast (n=29; 23.4%), lung (n=21; 16.9%) and colon cancer (n=16; 12.9%). Most patients had metastatic disease (n=85; 72.0%), active cancer (n=101; 81.5%) or are receiving antineoplastic therapies (n=95; 76.6%). A modification of anticoagulation therapy was conducted in 99 patients (80.5%): change of anticoagulant drug in 77 patients (most of them from low molecular weight heparins to direct-acting oral anticoagulants [n=51;66.2%]) or change of anticoagulant dose in 49 patients (most of them from therapeutic dose to prophylactic dose in patients with low risk of recurrence and/or high risk of bleeding [n=27;55.1%]). Recurrence of VTE was observed in 8 patients (6.7%) and major bleeding (MB) in 4 patients (3.3%). In particular, 63 patients (52.5%) have received or are receiving apixaban for VTE treatment. No differences were observed between patients receiving apixaban and general population in tumor type, stage, antineoplastic treatment, or thrombotic event. VTE recurrence was seen in 2 patients (3.2%) and MB in 1 patient (1.6%) during apixaban treatment.
Conclusions
The “CAT clinic” has allowed us to adapt the anticoagulant treatment in most of patients, obtaining low complication rates (recurrence/bleeding).
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
L. Ortega Morán: Financial Interests, Personal, Invited Speaker: Leo Pharma, Rovi, Menarini, Servier. J. Soto Alsar: Financial Interests, Personal, Invited Speaker: Merck, Ipsen, Pfizer, Leo Pharma; Financial Interests, Personal, Training: MSD, Angelini, Vifor Pharma, Rovi, Amgen, Pfizer, Roche, Janssen, Sanofi; Non-Financial Interests, Personal, Other: Pfizer, Sanofi. R. Jiménez Rodríguez: Financial Interests, Personal, Invited Speaker: Amgen, Kyowa Kyrin; Financial Interests, Personal, Training: Mylan. C. López Jiménez: Financial Interests, Personal, Invited Speaker: Servier; Financial Interests, Personal, Training: Rovi. R. Martín Lozano: Financial Interests, Personal, Training: Sanofi. G. Torres Perez-Solero: Financial Interests, Personal, Invited Speaker: Adacap, Ipsen, Amgen, Roche, Merck, Servier; Financial Interests, Personal, Advisory Role: Adacap; Financial Interests, Personal, Training: Amgen, Roche, Merck, Lilly, Ipsen, Pfizer, Servier, Sanofi, Rovi, Adacap. M. Martin Jimenez: Financial Interests, Research Grant: Roche, Puma, Novartis; Financial Interests, Advisory Board: AstraZeneca, Amgen, Taiho Oncology, Roche/Genentech, Novartis, PharmaMar, Eli Lilly, Puma, Daiichi Sankyo, Menarini/Stemline, Pfizer; Financial Interests, Invited Speaker: AstraZeneca, Lilly, Amgen, Roche/Genentech, Novartis, Pfizer. A.J. Munoz Martin: Financial Interests, Personal, Advisory Role: Sanofi, Pfizer, BMS, AstraZeneca, MSD, Roche, GSK, Taiho Oncology, Servier, Leo Pharma; Financial Interests, Personal, Speaker’s Bureau: Rovi, Stada, Menarini, Amgen, Merck; Financial Interests, Personal, Research Funding: Rovi, Celgene, Leo Pharma; Financial Interests, Personal, Training: AstraZeneca, Amgen, Merck, Roche. All other authors have declared no conflicts of interest.
Resources from the same session
2173P - Exploring the complex needs of older patients receiving targeted therapies and immune checkpoint inhibitors for renal and skin cancers at the Royal Marsden Hospital
Presenter: Niamh Cunningham
Session: Poster session 07
2174P - The impact of exposure to antibiotic (ATB) and proton pump inhibitor (PPI) therapy on immune checkpoint inhibitor (ICI) treatment on overall survival (OS): A population-based study
Presenter: Lawson Eng
Session: Poster session 07
2175P - Sex and age-related differences in immunotherapy-induced toxicities
Presenter: Mafalda Teixeira da Costa
Session: Poster session 07
2176P - Rechallenge of immune checkpoint inhibitors after immune-related adverse events: A systematic review
Presenter: Jin Young Kim
Session: Poster session 07
2177P - Immunotherapy adverse events association with inflammation scores: A real-world data analysis from a Portuguese hospital
Presenter: Catarina Fernandes
Session: Poster session 07
2179P - Prospective monitoring of autoimmune events in cancer immunotherapy patients: A report on the first 658 patients in the PRAISE study
Presenter: Eden Sebbag
Session: Poster session 07
2180P - Detrimental effect of an early exposure to antibiotics on the outcomes of immunotherapy in a multi-tumor cohort of patients
Presenter: Víctor Albarrán
Session: Poster session 07
2181P - Effect of different corticosteroid treatment strategies on checkpoint inhibitors pneumonitis outcomes
Presenter: Hui Guo
Session: Poster session 07
2182P - Patient involvement to improve prospective follow-up: Quality of life data after cancer immunotherapy from the PRAISE study
Presenter: Eden Sebbag
Session: Poster session 07
2183P - The relevance of HFpEF in immunotherapy-induced myocarditis: An analysis of 65 patients
Presenter: Adam Chapman
Session: Poster session 07