Literature Scan
Real-World Analysis Confirms Rivaroxaban Reduces Risk of VTE and Major Bleeding , Compared With Warfarin
Previously , a series of phase III trials from EINSTEIN investigators determined that the direct oral anticoagulant ( DOAC ) rivaroxaban is non-inferior to enoxaparin and warfarin for the prevention of recurrent venous thromboembolism ( VTE ) and was associated with a 46 percent decreased risk of major bleeding ( p = 0.002 ). To assess the safety and efficacy of rivaroxaban in a “ real-world ” population , Craig I . Coleman , PharmD , from the University of Connecticut School of Pharmacy , and co-authors analyzed a large administrative claims database , finding that , similar to what the EINSTEIN investigators reported , rivaroxaban “ appears to reduce patients ’ hazard of both recurrent VTE and major bleeding in routine practice .”
“ That our analysis ’ findings are relatively consistent with those of the EINSTEIN clinical trial program should provide an extra layer of reassurance to clinicians when prescribing rivaroxaban for acute VTE ,” the authors wrote in their report , which was published in Thrombosis and Haemostasis .
The researchers retrospectively analyzed the Truven Health MarketScan ® claims database to identify adult patients who were diagnosed with deep-vein thrombosis or pulmonary embolism ( PE ) during a hospitalization or visit to an emergency department between January 2012 and June 2015 . Patients were included in the analysis if they were newly initiated on rivaroxaban ( n = 13,609 ; 43.2 % were ≥60 years old ) or warfarin ( n = 32,244 ; 42.5 % were ≥60 years old ) within 30 days after the index event and had ≥180 days of continuous medical and prescription benefits prior to the index event ( baseline ). Patients with a VTE claim or prescription claim for an anticoagulant at baseline were excluded .
Patients were followed for a maximum of 12 months or until VTE recurrence or major bleeding , switch or discontinuation of index oral anticoagulation , or insuranceplan disenrollment . Compared with those who received warfarin , patients who received rivaroxaban tended to be younger and have fewer comorbidities , particularly hypertension , diabetes , cancer , coagulopathies , and chronic kidney disease .
Rivaroxaban was associated with a 19 percent reduction in recurrent VTE and a 21 percent reduction in major bleeding hazards , as well as decreased hazards of intracranial hemorrhage and gastrointestinal bleeding compared with patients treated with warfarin ( see TABLE 5 ). In multivariable analysis controlling for patient demographics , comorbidities , known VTE
TABLE 5 . Recurrent VTE and Major Bleeding Based on Treatment
Recurrent VTE
Major bleeding *
Rivaroxaban Cohort ( n = 13,609 )
385 ( 2.8 %)
110 ( 0.8 %)
ICH 7 ( 0.05 %)
GIB 70 ( 0.5 %)
Warfarin Cohort ( n = 32,244 )
1,132 ( 3.5 %)
335 ( 1 %)
43 ( 0.1 %)
233 ( 0.7 %)
Hazard Ratio
0.81 ( 95 % CI 0.73-0.90 )
0.79 ( 95 % CI 0.65-0.96 )
0.40 ( 95 % CI 0.21-0.78 )
0.72 ( 95 % CI 0.57-0.91 )
* Per the Cunningham definition VTE = venous thromboembolism ; ICH = intracranial hemorrhage ; GIB = gastrointestinal bleeding risk factors , and concomitant medications at baseline , these risk reductions were “ relatively consistent across subgroups ,” the authors noted , including by sex , age , obesity , presence of PE , and history of or active cancer ( see TABLE 6 ).
“ Our results were also robust to changes in study methodology ,” the researchers added . When they conducted a sensitivity analysis by removing the 12-month cap on follow-up , rivaroxaban ’ s observed effectiveness and safety were confirmed , with an 18 percent reduction in the risk of recurrent VTE ( hazard ratio [ HR ] = 0.82 ; 95 % CI 0.74-0.90 ; p value not provided ) and a 23 percent reduction in the risk of major bleeding ( HR = 0.77 ; 95 % CI 0.64- 0.93 ; p value not provided ) compared with patients treated with warfarin .
“ An interesting finding of our analysis was the relatively high proportion of cancer patients ( 15.8 %) receiving rivaroxaban for treatment of their VTE ,” the authors noted . In comparison , only 5.6 percent of patients in the EINSTEIN clinical trials received rivaroxaban . Although U . S . and European clinical guidelines do not recommend rivaroxaban and other DOACs for cancerassociated thrombosis , “ our data suggest that some patients do receive rivaroxaban in the setting of cancer-associated thrombosis , perhaps because of its convenience of administration compared to low-molecular-weight heparin .”
The study is limited by its retrospective , claims-based
TABLE 6 . Subgroup Analysis for VTE and Major Bleeding
Subgroup Sex
Rivaroxaban Cohort
Warfarin Cohort
Hazard Ratio for VTE
Male |
7,081 |
16,220 |
0.89 ( 95 % CI 0.77-1.03 ) |
Female |
6,258 |
16,024 |
0.73 |
|
|
|
( 95 % CI 0.63-0.85 ) |
Age |
|
|
|
≥60 years |
5,081 |
14,367 |
0.61 |
|
|
|
( 95 % CI 0.50-0.75 ) |
< 60 years |
8,528 |
17,877 |
0.90 |
|
|
|
( 95 % CI 0.80-1.01 ) |
Obesity |
|
|
|
Present |
2,808 |
6,304 |
0.63 |
|
|
|
( 95 % CI 0.50-0.81 ) |
Absent |
10,801 |
25,940 |
0.87 |
|
|
|
( 95 % CI 0.78-0.98 ) |
Diagnosis |
|
|
|
PE |
5,695 |
14,712 |
0.72 |
|
|
|
( 95 % CI 0.60-0.87 ) |
No PE |
7,914 |
17,532 |
0.89 |
|
|
|
( 95 % CI 0.80-1.01 ) |
History of Cancer or Active Cancer |
Present |
1,540 |
4,080 |
1.00 |
|
|
|
( 95 % CI 0.76-1.32 ) |
Absent |
12,609 |
28,164 |
0.78 |
|
|
|
( 95 % CI 0.69-0.87 ) |
Overall |
13,609 |
32,244 |
0.81 |
|
|
|
( 95 % CI 0.73-0.90 ) |
VTE = venous thromboembolism ; PE = pulmonary embolism |
Hazard Ratio for Major Bleeding
0.65 ( 95 % CI 0.49-0.88 )
0.91 ( 95 % CI 0.70-1.18 )
0.78 ( 95 % CI 0.60-1.01 )
0.83 ( 95 % CI 0.63-1.11 )
0.60 ( 95 % CI 0.39-0.97 )
0.85 ( 95 % CI 0.69-1.05 )
0.72 ( 95 % CI 0.54-0.97 )
0.85 ( 95 % CI 0.66-1.09 )
1.00 ( 95 % CI 0.67-1.51 )
0.76 ( 95 % CI 0.61-0.95 )
0.79 ( 95 % CI 0.65-0.96 )
design ( which may introduce selection and misclassification biases ), as well confounding factors that were not identifiable .
Contributing authors report financial relationships with Bayer , Janssen , Boehringer Ingelheim , Astellas , Portola , and Takeda .
REFERENCE
Coleman CI , Bunz TJ , Turpie AGG . Effectiveness and safety of rivaroxaban versus warfarin for treatment and prevention of recurrence of venous thromboembolism . Thromb Haemost . 2017 June 22 . [ Epub ahead of print ]
Treating Financial Toxicity : Subsidies Improve Access to Oral Therapies for Medicare Beneficiaries With Myeloma
Low-income subsidies ( LIS ), which are available to Medicare beneficiaries who earn less than 150 percent of the federal poverty level , alleviate the financial burden for patients with myeloma taking immunomodulatory drugs ( IMiDs ), saving them $ 5,000 in the first year alone , according to a study published in the Journal of Clinical Oncology .
LIS also increase patients ’ access to this class of myeloma therapies , explained Adam J . Olszewski , MD , from the Rhode Island Hospital , and co-authors . In their analysis of IMiD costs , refill patterns , and health outcomes among Medicare Part D beneficiaries who were and were not eligible to receive LIS , the authors found “ an increased use of IMiDs among low-income subsidy recipients with
62 ASH Clinical News November 2017
Literature Scan
Real-World Analysis Confirms Rivaroxaban Reduces Risk of
VTE and Major Bleeding, Compared With Warfarin
Previously, a series of phase III trials from EINSTEIN
investigators determined that the direct oral anticoagulant
(DOAC) rivaroxaban is non-inferior to enoxaparin and
warfarin for the prevention of recurrent venous throm-
boembolism (VTE) and was associated with a 46 percent
decreased risk of major bleeding (p=0.002). To assess the
safety and efficacy of rivaroxaban in a “real-world” popu-
lation, Craig I. Coleman, PharmD, from the University
of Connecticut School of Pharmacy, and co-authors ana-
lyzed a large administrative claims database, finding that,
similar to what the EINSTEIN investigators reported,
rivaroxaban “appears to reduce patients’ hazard of both
recurrent VTE and major bleeding in routine practice.”
“That our analysis’ findings are relatively consistent
with those of the EINSTEIN clinical trial program should
provide an extra layer of reassurance to clinicians when
prescribing rivaroxaban for acute VTE,” the authors wrote
in their report, which was published in Thrombosis and
Haemostasis.
The researchers retrospectively analyzed the Truven
Health MarketScan® claims database to identify adult
patients who were diagnosed with deep-vein thrombosis
or pulmonary embolism (PE) during a hospitalization or
visit to an emergency department between January 2012
and June 2015. Patients were included in the analysis
if they were newly initiated on rivaroxaban (n=13,609;
43.2% were ≥60 years old) or warfarin (n=32,244; 42.5%
were ≥60 years old) within 30 days after the index event
and had ≥180 days of continuous medical and prescrip-
tion benefits prior to the index event (baseline). Patients
with a VTE claim or prescription claim for an anticoagu-
lant at baseline were excluded.
Patients were followed for a maximum of 12 months
or until VTE recurrence or major bleeding, switch or dis-
continuation of index oral anticoagulation, or insurance-
plan disenrollment. Compared with those who received
warfarin, patients who received rivaroxaban tended to
be younger and have fewer comorbidities, particularly
hypertension, diabetes, cancer, coagulopathies, and chronic
kidney disease.
Rivaroxaban was associated with a 19 percent reduc-
tion in recurrent VTE and a 21 percent reduction in
major bleeding hazards, as well as decreased hazards of
intracranial hemorrhage and gastrointestinal bleeding
compared with patients treated with warfarin (see
TABLE 5 ). In multivariable analysis controlling for
patient demographics, comorbidities, known VTE
Recurrent VTE and Major
Bleeding Based on Treatment
TABLE 5.
Rivaroxaban
Cohort
(n=13,609) Warfarin
Cohort
(n=32,244) Hazard
Ratio
Recurrent
VTE 385
(2.8%) 1,132
(3.5%) 0.81
(95% CI 0.73-0.90)
Major
bleeding* 110
(0.8%) 335
(1%) 0.79
(95% CI 0.65-0.96)
ICH 7
(0.05%) 43
(0.1%) 0.40
(95% CI 0.21-0.78)
GIB 70
(0.5%) 233
(0.7%) 0.72
(95% CI 0.57-0.91)
*Per the Cunningham definition
VTE = venous thromboembolism; ICH = intracranial hemorrhage;
GIB = gastrointestinal bleeding
62
ASH Clinical News
TABLE 6.
Subgroup Analysis for VTE and Major Bleeding
risk factors, and concomi-
Rivaroxaban
Warfarin
Hazard Ratio
Hazard Ratio for Major
tant medications at base-
Subgroup
Cohort
Cohort
for VTE
Bleeding
line, these risk reductions
Sex
were “relatively consistent
Male
7,081
16,220
0.89
0.65
across subgroups,” the au-
(95% CI 0.77-1.03)
(95% CI 0.49-0.88)
thors noted, including by
Female
6,258
16,024
0.73
0.91
sex, age, obesity, presence
(95% CI 0.63-0.85)
(95% CI 0.70-1.18)
of PE, and history of or ac-
Age
tive cancer (see TABLE 6 ).
≥60 years
5,081
14,367
0.61
0.78
“Our results were also
(95% CI 0.50-0.75)
(95% CI 0.60-1.01)
robust to changes in study
<60 years
8,528
17,877
0.90
0.83
methodology,” the research-
(95% CI 0.80-1.01)
(95% CI 0.63-1.11)
ers added. When they con-
Obesity
ducted a sensitivity analysis
Present
2,808
6,304
0.63
0.60
by removing the 12-month
(95% CI 0.50-0.81)
(95% CI 0.39-0.97)
cap on follow-up, rivaroxa-
Absent
10,801
25,940
0.87
0.85
ban’s observed effectiveness
(95% CI 0.78-0.98)
(95% CI 0.69-1.05)
and safety were confirmed,
Diagnosis
with an 18 percent reduc-
tion in the risk of recurrent
PE
5,695
14,712
0.72
0.72
(95% CI 0.60-0.87)
(95% CI 0.54-0.97)
VTE (hazard ratio [HR]
= 0.82; 95% CI 0.74-0.90;
No PE
7,914
17,532
0.89
0.85
(95% CI 0.80-1.01)
(95% CI 0.66-1.09)
p value not provided) and
History of Cancer or Active Cancer
a 23 percent reduction in
the risk of major bleeding
Present
1,540
4,080
1.00
1.00
(95% CI 0.76-1.32)
(95% CI 0.67-1.51)
(HR=0.77; 95% CI 0.64-
0.93; p value not provided)
Absent
12,609
28,164
0.78
0.76
(95% CI 0.69-0.87)
(95% CI 0.61-0.95)
compared with patients
treated with warfarin.
Overall
13,609
32,244
0.81
0.79
(95% CI 0.73-0.90)
(95% CI 0.65-0.96)
“An interesting finding
VTE = venous thromboembolism; PE = pulmonary embolism
of our analysis was the
relatively high proportion
of cancer patients (15.8%)
receiving rivaroxaban for treatment of their VTE,” the
design (which may introduce selection and misclassifi-
authors noted. In comparison, only 5.6 percent of patients cation biases), as well confounding factors that were not
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