PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
August 11, 2021Haematologica33 citationsOpen Access

Renal function and clinical outcome of patients with cancer-associated venous thromboembolism randomized to receive apixaban or dalteparin. Results from the Caravaggio trial

CBCecilia BecattiniRBRupert BauersachsGMGiorgio Maraziti

Structured PICO

Does oral apixaban reduce major bleeding and recurrent VTE in adult patients with cancer-associated VTE and renal impairment compared to subcutaneous dalteparin?

P
Population
1,142 adult patients with cancer who had symptomatic or incidental acute proximal deep vein thrombosis (DVT) or pulmonary embolism (PE), with baseline creatinine assessment at randomization (creatinine clearance ≥30 mL/min). Includes 275 patients with moderate renal impairment (30-59 mL/min) and 444 patients with mild renal impairment (60-89 mL/min).
I
Intervention
Oral apixaban 10 mg twice daily for the first 7 days, followed by 5 mg twice daily for 6 months
C
Comparator
Subcutaneous dalteparin 200 IU per kilogram of body weight once daily for the first month, followed by 150 IU per kilogram once daily for 6 months
O
Outcome
Co-primary outcomes: major bleeding and recurrent VTE defined according to Caravaggio criteria and occurring from randomization to day 180hard clinical

In cancer patients with VTE and moderate renal impairment, apixaban is a safe and potentially more effective alternative to dalteparin for preventing recurrent VTE without increasing major bleeding.

Limitations

  • 13 patients excluded due to lack of baseline creatinine value or violation of inclusion requirement (CrCl >30 mL/min)
  • Open-label randomized study design
  • Subgroup analysis with limited numbers of events, making findings hypothesis-generating
  • Cannot provide information on the efficacy and safety of apixaban and dalteparin in severe renal impairment

Abstract

The effect of renal impairment (RI) on risk of bleeding and recurrent thrombosis in cancer patients treated with direct oral anticoagulants for venous thromboembolism (VTE) is undefined. We ran a prespecified analysis of the randomized Caravaggio study to evaluate the role of RI as a risk factor for bleeding or recurrence in patients treated with dalteparin or apixaban for cancerassociated VTE. RI was graded as moderate (creatinine clearance between 30-59 mL/minute; 275 patients) and mild (between 60- 89 mL/minute; 444 patients). In the 1142 patients included in this analysis, the incidence of major bleeding was similar in patients with moderate vs. no or mild RI (HR 1.06-95% CI: 0.53-2.11), with no difference in the relative safety of apixaban and dalteparin. Recurrent VTE was not different in moderate vs. no or mild RI (HR=0.67, 95% CI: 0.38-1.20); in moderate RI, apixaban reduced recurrent VTE compared to dalteparin (HR=0.27, 95% CI: 0.08-0.96; P for interaction 0.1085). At multivariate analysis, no association was found between variation of renal function over time and major bleeding or recurrent VTE. Advanced or metastatic cancer was the only independent predictor of major bleeding (HR=2.84, 95% CI: 1.20-6.71), with no effect of treatment with apixaban or dalteparin. In our study, in cancer patients treated with apixaban or dalteparin, moderate RI was not associated with major bleeding or recurrent VTE. In patients with moderate renal failure, the safety profile of apixaban was confirmed with the potential for improved efficacy in comparison to dalteparin. ClinicalTrials.gov identifier: NCT03045406.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Becattini et al. (2021) studied this question.

synapsesocial.com/papers/6a20949ce9ae715d2b0c8f9dhttps://doi.org/10.3324/haematol.2021.279072
Ask AI
Helpful
Bookmark
Share
View Full Paper