Anticoagulation management and outcomes in cancer-associated ovarian and renal vein thrombosis: A multicenter retrospective cohort study
Notice bibliographique
Résumé
Abstract Background: Ovarian and renal vein thromboses (OVT, RVT) are rare in the general population but occur more frequently in patients with cancer. Their optimal management and outcomes remain undefined. Aim: To investigate anticoagulation (AC) management and clinical outcomes in patients with active cancer and OVT or RVT. Methods: We conducted a retrospective cohort study at two tertiary centers (Ottawa, Canada; Rome, Italy), including adult patients (≥ 18 years) with a diagnosis of OVT or RVT and active cancer between June 2019 and December 2023. Patients with tumor thrombus were excluded. All patients were followed for 12 months or until death, whichever occurred earlier. The primary outcome was the 6-month cumulative incidence of recurrent venous thromboembolism (VTE). The primary safety outcome was 6-month cumulative incidence of major bleeding events (defined by ISTH criteria). Secondary outcomes included incidences of clinically relevant non-major bleeding (CRNMB) at 6 months, and recurrent VTE, major bleeding, CRNMB, and mortality at 12 months. Descriptive analyses were performed for the overall cohort and stratified by AC use. Continuous variables were summarized using mean (standard deviation, SD) or median (interquartile range, IQR) as appropriate, and categorical variables as counts and percentages. The 6-and 12-month cumulative incidences were analyzed using the Kaplan-Meier method with 95% confidence intervals (CI), considering death as a competing risk. Results: We included 82 patients with cancer-associated OVT (n=67) and/or RVT (n=25, 10 had concurrent OVT and RVT). The mean (SD) age was 63.4 (11.8), with the majority (n=78, 95%) being female. The most common cancer type was gynecological (n=44, 53.7%), with the majority having advanced stage (III or IV) (n=68, 82.9%). Over 84% of patients received anticancer therapy within 3 months and 83% continued cancer therapy following the index VTE. Most VTE (n=80, 97.6%) were incidental. AC was initiated in 82% of patients (n=67), among whom 80% were given therapeutic doses. The most common type of AC was low-molecular-weight heparin (LMWH, 64.2%), followed by direct oral anticoagulant (31.3%). The median (IQR) time to start AC after diagnosis was 1 (0-11) day, with the median (IQR) duration of AC of 10.8 (5.9-12) months. Three patients had recurrent VTE (two new proximal lower extremity deep vein thromboses and one extension to the inferior vena cava), all occurring within 6 months, resulting in the same overall 6- and 12-month cumulative incidences of recurrent VTE of 3.8% (95% CI, 1.0–9.7). The incidences of recurrent VTE in patients started on AC and no AC were 1.5% (95% CI, 0.1–7.2) (n=1) and 14.3% (95% CI, 2.1–37.7) (n=2), respectively. Similarly, all major bleeding events (n=2) occurred within the first 6 months, with the same overall 6- and 12-month cumulative incidences of major bleeding of 2.5% (95% CI, 0.5-7.9). All major bleeding occurred in anticoagulated patients and on therapeutic doses of LMWH. The 6-month incidence of CRNMB was 3.8% (95% CI, 1.0–9.8) and that of 12 month was 6.6% (95% CI, 2.4-13.7). The 12-month incidence of mortality was 25.2% (95% CI, 16.2–35.2). Interpretation: In this cohort of cancer-associated OVT or RVT, 97.6% were incidental VTE. Most patients were treated with therapeutic AC. The overall incidences of recurrent VTE and major bleeding events were relatively low, and all occurred within the first 6 months. Anticoagulation appeared to be effective but was associated with a modest risk of bleeding complications. Although this study was limited by its retrospective cohort design, small sample size, and wide CIs, it provided valuable data to the limited literature on managing these types of unusual site VTE.
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Comment cette classification a été obtenuedéplier
Prédiction machine sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.
Scores du classifieur distillé par catégorie (deux têtes)
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,001 | 0,004 |
| Méta-épidémiologie (sens strict) | 0,000 | 0,000 |
| Méta-épidémiologie (sens large) | 0,001 | 0,001 |
| Bibliométrie | 0,001 | 0,002 |
| Études des sciences et des technologies | 0,001 | 0,000 |
| Communication savante | 0,001 | 0,001 |
| Science ouverte | 0,001 | 0,001 |
| Intégrité de la recherche | 0,001 | 0,001 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,001 | 0,000 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».