Skip to main content
. Author manuscript; available in PMC: 2021 Jun 13.
Published in final edited form as: Clin Lymphoma Myeloma Leuk. 2019 Aug 26;19(12):763–775.e2. doi: 10.1016/j.clml.2019.08.004

Table 2.

Comparison of HRU per Patient per Month Between Ibrutinib and CIT and Between Ibrutinib and BR During the Front-line Therapy Periodb, c

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.

a

Indicates P-value < .05.

b

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.

c

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.

d

RRs were calculated using generalized linear models with Poisson distribution. Models were adjusted for baseline total all-cause costs.

e

CIs and P-values were obtained from non-parametric bootstrap procedures using 500 replicates.

f

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).