Thromb Haemost 2021; 121(05): 547-551
DOI: 10.1055/a-1367-7830
Invited Editorial Focus

Safety of Apixaban for Cancer-Associated Thrombosis

Behnood Bikdeli
1  Cardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States
2  Center for Outcomes Research and Evaluation (CORE), Yale University School of Medicine, New Haven, United States
3  Cardiovascular Research Foundation (CRF), New York, United States
,
David Jiménez
4  Respiratory Department, Ramón y Cajal Hospital, IRYCIS, Madrid, Spain
5  Medicine Department, Universidad de Alcala, IRYCIS, Madrid, Spain
6  CIBER de Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain
› Author Affiliations
 

Bleeding with Apixaban and Dalteparin in Patients with Cancer-Associated Venous Thromboembolism: Results from the Caravaggio Study

Venous thromboembolism (VTE) is a common complication in patients with cancer and is associated with significant morbimortality and adverse outcomes.[1] Management of cancer-associated thrombosis poses challenges for clinicians. Compared with other patients with VTE, patients with cancer-associated VTE who receive anticoagulant therapy have a higher risk both for recurrent VTE and for bleeding complications.[2] Until recently, subcutaneous low-molecular-weight heparin (LMWH) monotherapy has been the standard of treatment for cancer-associated thrombosis.[3] [4] [5] Compared with vitamin K antagonists, LMWHs may lead to reduction in VTE events though not in bleeding or mortality.[6]

Direct oral anticoagulants (DOACs) have become the anticoagulant treatment of choice for the majority of patients with acute VTE.[3] Compared with vitamin K antagonists, in most subgroups, they are similar in efficacy but are associated with lower risk of major bleeding.[7] In addition, these drugs are given in fixed doses and do not require laboratory monitoring of the anticoagulant effect. Several trials have assessed the efficacy and safety of DOACs for patients with cancer-associated thrombosis.[8] [9] [10] [11] A recent meta-analysis included four randomized trials (2,907 patients with cancer-related VTE) that compared apixaban (two trials), edoxaban (one trial), or rivaroxaban (one trial) with dalteparin.[12] Risk for recurrent VTE was 3.5% absolute points lower in patients treated with a DOAC, but clinically relevant nonmajor bleeding (CRNMB) was 4.7% higher. Though the risk of major bleeding was nonsignificantly higher, DOACs had a 6.6% significant absolute increase in the subgroup who had gastrointestinal cancer.[12] Broadly similar observations have been noted in other meta-analyses of the DOACs for the treatment of acute VTE associated with cancer.[13]

The study by Ageno et al in this issue of Thrombosis and Haemostasis is a welcome addition to the body of evidence.[14] Using data from the multicenter, randomized, open-label, noninferiority Caravaggio trial,[11] the authors investigated sites of bleeding, clinical presentation, and course of major bleeding. Among 576 patients randomized to apixaban, major bleeding occurred in 22 (3.8%) patients, compared with 23 of 579 (4.0%) patients randomized to dalteparin. The sites of major bleeding were similar between the two treatment groups. The clinical presentation of major bleeding was severe or fatal in 6 patients on apixaban and in 5 patients on dalteparin, while the clinical course was severe in 5 patients on apixaban and in 7 patients on dalteparin. Major bleeding occurred in 9 patients with gastrointestinal cancer in each treatment group. Finally, there were 52 CRNMBs in the apixaban group and 35 in the dalteparin group. Strengths of the study include high-quality data and thorough reporting. Study limitations comprise lack of competing risk assessment, and a low number of bleeding events that precludes further phenotyping, if a true difference were to exist.

The results reported by Ageno et al come from the largest trial to date evaluating the efficacy and safety of a DOAC for patients with cancer-associated thrombosis and suggest that treatment with apixaban might be associated with a better safety profile than other DOACs. In the Hokusai VTE Cancer Trial, major bleeding occurred in 36 patients (6.9%) in the edoxaban group and in 21 patients (4.0%) in the dalteparin group (hazard ratio [HR], 1.77; 95% confidence interval [CI], 1.03–3.04)[8] ([Table 1]). There was also more CRNMB in patients receiving edoxaban (HR, 1.38; 95% CI, 0.98–1.94). In a subgroup analysis of patients with gastrointestinal cancer, major bleeding rates favored dalteparin therapy (edoxaban 13.2% vs. dalteparin 2.4%; p = 0.02). Bleeding rates were similar in the patients with nongastrointestinal cancer. There were no fatal bleeding events in the edoxaban arm and one fatal bleed in the dalteparin arm. In the SELECT-D trial, major bleeding rates were 6% for rivaroxaban and 4% for dalteparin (HR, 1.83; 95% CI, 0.68–4.96).[9] Most major bleeding events involved the gastrointestinal tract. Patients with upper gastrointestinal cancer were more likely to experience a major bleed with rivaroxaban compared with dalteparin. CRNMB was also more frequent with rivaroxaban (13% vs. 4%; HR, 3.76; 95% CI, 1.63–8.69) and primarily involved gastrointestinal or genitourinary sources.

Table 1

Major randomized trials of direct oral anticoagulants for the treatment of cancer-associated thrombosis

Study

Hokusai Cancer VTE[8]

SELECT-D[9]

Caravaggio[11]

Inclusion criteria

Male or female subjects with age ≥18 years

Confirmed symptomatic or unsuspected VTE

Cancer (other than basal-cell or squamous-cell carcinoma of the skin), either active or diagnosed within 2 years prior to randomization

Intention for long-term treatment with parenteral LMWH

Able to provide written informed consent

Active cancer (other than basal-cell or squamous-cell carcinoma of the skin) and confirmed VTE

Age ≥18 years

Weight ≥40 kg

ECOG ≤2

Adequate hematologic, hepatic, and renal function

Active cancer (other than basal-cell or squamous-cell carcinoma of the skin, primary brain tumor or known intracerebral metastases and acute leukemia) and confirmed VTE

Exclusion criteria

Thrombectomy, insertion of a caval filter, or use of a fibrinolytic agent to treat the current episode of VTE

More than 72 hours pretreatment with anticoagulant treatment prior to randomization to treat the current episode

Treatment with therapeutic doses of an anticoagulant other than that used for pretreatment of the current VTE episode prior to randomization

Active bleeding or any contraindication for treatment with dalteparin or edoxaban

Indication for dalteparin other than VTE

ECOG of 3 or 4

Calculated CrCl < 30 mL/min

History of HIT

Acute hepatitis, chronic active hepatitis, liver cirrhosis

Life expectancy < 3 months

Platelet count < 50,000/mL

Uncontrolled hypertension

Women of childbearing potential without proper contraceptive measures, and women who are pregnant or breast feeding

Chronic treatment with nonaspirin NSAIDs

Treatment with aspirin or dual antiplatelet therapy

Treatment with the P-gp inhibitors ritonavir, nelfinavir, indinavir, or saquinavir, ketoconazole, itraconazole, erythromycin, azithromycin, or clarithromycin at the time of randomization

Previous treatment dose of anticoagulant or > 75 mg aspirin per day

History of VTE, clinically significant liver disease, bacterial endocarditis, active bleeding or high risk of bleeding, or uncontrolled hypertension Inadequate contraceptive measures if of childbearing potential

Concomitant use of strong cytochrome P- 450 3A4 inhibitors or inducers or P-gp inhibitors or inducers

Age < 18 years

ECOG of 3 or 4

Life expectancy of less than 6 months

Administration of therapeutic doses of LMWH, fondaparinux, or UFH for more than 72 hours before randomization

3 or more doses of a VKA before randomization

Thrombectomy, vena cava filter insertion, or thrombolysis used to manage the index episode

Indication for anticoagulant treatment for a disease other than the index VTE episode

Concomitant use of strong inhibitors or inducers of both cytochrome P-450 3A4 and P-gp

Concomitant thienopyridine, aspirin, or dual antiplatelet therapy

Active bleeding or high risk of bleeding contraindicating anticoagulant treatment

Recent brain, spinal, or ophthalmic surgery

Hemoglobin level < 8 g/dL or platelet count < 75,000/mL or history of HIT

CrCl < 30 mL/min

Acute hepatitis, chronic active hepatitis, liver cirrhosis

Uncontrolled hypertension

Bacterial endocarditis

Hypersensitivity to the study drugs

Women of childbearing potential without proper contraceptive measures, and women who are pregnant or breast feeding

Definition of major bleeding

Overt bleeding that was associated with a decrease in the hemoglobin level of 2 g per deciliter or more, led to a transfusion of 2 or more units of blood, occurred in a critical site, or contributed to death

Clinically overt bleeding that was associated with a decrease in the hemoglobin level of 2 g per deciliter or more, led to a transfusion of 2 or more units of blood, occurred in a critical site, or contributed to death

Clinically overt bleeding that was associated with a decrease in the hemoglobin level of 2 g per deciliter or more, led to a transfusion of 2 or more units of blood, occurred in a critical site, necessitated surgical intervention or contributed to death

Definition of CRNMB

Overt not meeting the criteria for major bleeding, that requires medical attention or is associated with discomfort for the subject such as pain, or impairment of activities of daily life

Overt bleeding with medical intervention

Unscheduled contact with a physician

Interruption or discontinuation of a study drug

Discomfort or impairment of activities of daily life

Acute clinically overt bleeding that does not meet the criteria for major and consists of:

Any bleeding compromising hemodynamics

Spontaneous hematoma larger than 25 cm2, or 100 cm2 if there was a traumatic cause

Intramuscular hematoma documented by ultrasonography

Epistaxis or gingival bleeding requiring tamponade or other medical intervention or bleeding from venipuncture for > 5 minutes

Hematuria that was macroscopic and was spontaneous or lasted for more than 24 hours after invasive procedures

Hemoptysis, hematemesis or spontaneous rectal bleeding requiring endoscopy or other medical intervention

Any other bleeding considered to have clinical consequences for a patient such as medical intervention, the need for unscheduled contact (visit or telephone call) with a physician, or temporary cessation of a study drug, or associated with pain or impairment of activities of daily life.

Anticoagulant

Edoxaban

Dalteparin

Rivaroxaban

Dalteparin

Apixaban

Dalteparin

Mean age, years

64.3

63.7

67[a]

67[a]

67.2

67.2

Weight, kg

78.8

79.1

75.7

76.1

CrCl < 50 mL/min, %

7.3

6.5

8.9

10.5

Metastatic disease, %

52.2

53.4

58

58

67.5

68.4

Anticancer treatment, %

71.6

73.1

69

70

60.8

63.4

Major bleeding, %

6.9

4.0

5.4

3.0

3.8

4.0

CRNMB, %

14.6

11.1

12.3

3.4

9.0

6.0

Major or CRNMB, %

18.6

13.9

12.2

9.7

Major GI bleeding, %

3.8

1.1

3.9

2.0

1.9

1.7

Abbreviations: CrCl, creatinine clearance; CRNMB, clinically relevant nonmajor bleeding; ECOG, Eastern Cooperative Oncology Group; GI, gastrointestinal; HIT, heparin-induced thrombocytopenia; LMWH, low-molecular-weight heparin; NSAID, nonsteroidal anti-inflammatory drug; P-gp, P-glycoprotein; UFH, unfractionated heparin; VKA, vitamin K antagonist; VTE, venous thromboembolism.


a Median values.


The potential explanations for the differences in the risks of major bleeding events remain debatable, including the differences in patient characteristics, protocol designs, distinct prespecified bleeding definitions, the anticoagulant dose or frequency (once vs. twice daily dosing), or other factors ([Table 1]). The baseline characteristics of the patients randomized in Caravaggio were comparable with those of the previous studies.[8] [9] There were similar percentages of enrolled patients with gastrointestinal cancers as well as with active and metastatic cancers in these trials. The proportion of patients who were receiving anticancer treatment or had moderate renal insufficiency were also comparable. However, the presence of active luminal tumors (i.e., luminal gastrointestinal or genitourinary tumors) was not reported in either study. In addition, there were minor differences in the definition of major bleeding across these four trials ([Table 1]). Nevertheless, similar rates of major bleeding event rates in the dalteparin arm of these trials make it unlikely that a large difference in case mix existed between them. Importantly, dabigatran, has not been specifically studied in this subgroup of patients.

What do we learn from this study for our clinical practice? DOACs provide an attractive alternative to LMWH in the treatment of VTE in cancer patients.[15] At present, due to conflicting data, the use of DOAC for patients with gastrointestinal or urological malignancies would appear risky. If they have to be used for these patients, indirect comparisons suggest that apixaban might be the safest of the DOAC medications. Since it is unlikely that different DOACs will be compared in randomized controlled trials in near future, evidence derived from routine practice can provide key insights regarding how each anticoagulant is used under routine care conditions in diverse patient populations ([Fig. 1]). For that purpose, data from large registries will complement the perspective from randomized studies.[16] [17] [18]

Zoom Image
Fig. 1 Considerations for improved knowledge generation for bleeding events in patients receiving anticoagulant therapy. DOACs, direct oral anticoagulants; RCTs, randomized controlled trials.

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Conflict of Interest

B.B. reports that he is a consulting expert, on behalf of the plaintiff, for litigation related to a specific type of IVC filters. D.J. has served as an advisor or consultant for Bayer HealthCare Pharmaceuticals, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Leo Pharma, Pfizer, ROVI, and Sanofi; served as a speaker or a member of a speakers' bureau for Bayer HealthCare Pharmaceuticals, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Leo Pharma, ROVI, and Sanofi; received grants for clinical research from Daiichi Sankyo, Sanofi, and ROVI.


Address for correspondence

David Jiménez, MD, PhD
Respiratory Department, Ramón y Cajal Hospital, IRYCIS
28034 Madrid
Spain   

Publication History

Received: 19 January 2021

Accepted: 19 January 2021

Publication Date:
20 January 2021 (online)

© 2021. Thieme. All rights reserved.

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Zoom Image
Fig. 1 Considerations for improved knowledge generation for bleeding events in patients receiving anticoagulant therapy. DOACs, direct oral anticoagulants; RCTs, randomized controlled trials.