Table 2.
RRd | 95% CIe | P Valuee | |
---|---|---|---|
Ibrutinib versus CIT | |||
Monthly all-cause HRU | |||
Number of inpatient admissions | 0.74 | 0.48-1.17 | .2400 |
Number of days of inpatient stay | 0.92 | 0.49-1.83 | .8200 |
Days with outpatient services | 0.75 | 0.60-0.94 | .0200a |
Days with antineoplastic/CIT drug administration | 0.05 | 0.01-0.13 | <.0001a |
Days with outpatient services related to the antineoplastic/CIT drug administration | 0.09 | 0.03-0.19 | <.0001a |
Days with other outpatient services | 1.01 | 0.80-1.28 | .8240 |
Days with ER visits | 0.89 | 0.57-1.46 | .5360 |
Days with other services | 0.77 | 0.49-1.31 | .2520 |
Monthly cancer-related HRUf | |||
Number of inpatient admissions | 0.77 | 0.49-1.22 | .3080 |
Number of days of inpatient stay | 0.93 | 0.48-1.86 | .8640 |
Days with outpatient services | 0.64 | 0.51-0.82 | .0080a |
Days with antineoplastic/CIT drug administration | 0.05 | 0.02-0.13 | <.0001a |
Days with outpatient services related to the antineoplastic/CIT drug administration | 0.09 | 0.03-0.19 | <.0001a |
Days with other outpatient services | 0.98 | 0.79-1.30 | .8400 |
Days with ER visits | 0.78 | 0.44-1.29 | .2880 |
Days with other services | 0.70 | 0.42-1.23 | .1720 |
Ibrutinib versus BR | |||
Monthly all-cause HRU | |||
Number of inpatient admissions | 0.87 | 0.55-1.34 | .5000 |
Number of days of inpatient stay | 1.32 | 0.70-2.37 | .3960 |
Days with outpatient services | 0.74 | 0.57-0.91 | .0040a |
Days with antineoplastic/CIT drug administration | 0.04 | 0.01-0.09 | <.0001a |
Days with outpatient services related to the antineoplastic/CIT drug administration | 0.07 | 0.02-0.16 | <.0001a |
Days with other outpatient services | 1.01 | 0.78-1.25 | .9200 |
Days with ER visits | 1.01 | 0.56-1.74 | .8680 |
Days with other services | 0.94 | 0.49-1.61 | .7600 |
Monthly cancer-related HRUf | |||
Number of inpatient admissions | 0.91 | 0.56-1.44 | .7080 |
Number of days of inpatient stay | 1.36 | 0.72-2.45 | .3440 |
Days with outpatient services | 0.65 | 0.51-0.79 | <.0001a |
Days with antineoplastic/CIT drug administration | 0.04 | 0.01-0.09 | <.0001a |
Days with outpatient services related to the antineoplastic/CIT drug administration | 0.07 | 0.02-0.16 | <.0001a |
Days with other outpatient services | 1.04 | 0.82-1.30 | .6600 |
Days with ER visits | 0.91 | 0.42-1.97 | .6800 |
Days with other services | 0.88 | 0.44-1.56 | .6520 |
Abbreviations: BR = Bendamustine/rituximab; CI = confidence interval; CIT = chemoimmunotherapy; ER = emergency room; HRU = health care resource utilization; RR = rate ratio.
Indicates P-value < .05.
HRU for the weighted populations were obtained by using inverse probability of treatment weights. The inverse probability of treatment weights were estimated based on propensity score. Variables used in the propensity score calculation included the following baseline characteristics: age, gender, region, quarter and year of index date, insurance plan type, time from first chronic lymphocytic lymphoma diagnosis to index date, Charlson comorbidity index, comorbidities (hypertension, lymphoma, deficiency anemias, diabetes, coagulation deficiency, chronic pulmonary disease), and baseline use of corticosteroids.
The front-line therapy period was defined as the period from the initiation of the front-line therapy to the earliest among discontinuation of the front-line therapy (defined as a gap of more than 90 days between the last day of supply of a claim and the first day of supply of the next claim for the front-line therapy), initiation of a second-line therapy (a new antineoplastic agent not part of the front-line therapy), or end of data.
RRs were calculated using generalized linear models with Poisson distribution. Models were adjusted for baseline total all-cause costs.
CIs and P-values were obtained from non-parametric bootstrap procedures using 500 replicates.
Cancer-related HRU was defined as claims with a primary or secondary diagnosis for cancer (International Classification of Diseases, Ninth Edition Clinical Modification codes: 140-239; International Classification of Diseases, Tenth Edition Clinical Modification codes: C00-D49).