Load the package hce
and check the version:
For citing the package run citation("hce")
(Samvel B. Gasparyan 2024).
Prioritized outcome composite endpoints (POCE) are a general class of endpoints combining different clinical outcomes of patients into a composite so as to preserve their different natures. A particular case of these endpoints is the hierarchical composite endpoint (HCE). It is evaluated in a fixed follow-up period and accounts for the patient’s clinically most important outcome for the analysis. HCEs are analyzed using win odds and other win statistics (Samvel B. Gasparyan et al. 2023).
Here we provide examples of HCE using in clinical trials from different therapeutic areas. General considerations for creating HCEs can be found in Samvel B. Gasparyan et al. (2022).
The DARE-19 (M. Kosiborod et al. 2021; M. N. Kosiborod et al. 2021) trial used an HCE to assess outcomes in patients hospitalized for COVID-19 and treated for 30 days. The COVID-19 HCE is presented below. It combines death, in hospital organ dysfunction events with clinical status at Day 30 for patients alive, still hospitalized but without previous organ dysfunction events, and hospital discharge as the most favorable outcome for patients discharging without organ dysfunction events and being alive at Day 30.
Below a higher category signifies a better outcome. Patients are
ranked into one and only one category based on their clinically most
severe event. For example, patients experiencing an in-hospital new or
worsening organ dysfunction event then dying will be included in the
category I
.
#> Order Category
#> 1 I Death
#> 2 II More than one new or worsened organ dysfunction events
#> 3 III One new or worsened organ dysfunction event
#> 4 IV Hospitalized at the end of follow-up (Day 30)
#> 5 V Discharged from hospital before Day 30
Patients in the category I
are compared using the timing
of the event, with an earlier event being a worse outcome (are assigned
a lower rank). Similarly, in the category III
the timing of
the event is used for ranking patients within this category. In the
category II
patients are compared using the number of
events with a higher number signifying a worse outcome. Patients in the
category IV
- hospitalized at the end of follow-up without
previous worsening events - are further ranked according to oxygen
support requirements at the hospital (IV.1
on high flow
oxygen devices, IV.2
requiring supplemental oxygen,
IV.3
not requiring supplemental oxygen, with a higher rank
being a better outcome). Patients in the category V
are
compared using the timing of the event, but, the hospital discharge
being a favorable outcome, here the earlier event signifies a better
outcome than the late event (reverse of the ranking in categories
I
and III
).
The simplest case of a COVID-19 HCE is an endpoint with ordinal scale
outcomes assessed at a given timepoint. The endpoint uses 1-8 categories
for assessing the physical limitations of hospitalized patients with
COVID-19 after 15 or 30 days of treatment. But unlike the DARE-19 HCE,
within each category it does not use the timing of events to reduce the
ties in a paiwrise comparison of patients in the active group with
patients in the control group. See, for example, COVID-19
and COVID-19b
datasest ordinal scale outcomes (Beigel et al. 2020).
table(COVID19)
#> GROUP
#> TRTP 1 2 3 4 5 6 7 8
#> Active 34 95 28 58 38 14 117 157
#> Placebo 58 121 24 60 33 8 102 115
The function hce::summaryWO()
provides the number of
wins, losses, and ties by categories. We can calculate the probability
of ties from the provided numbers.
COVID19HCE <- hce(GROUP = COVID19$GROUP, TRTP = COVID19$TRTP)
SUM <- summaryWO(COVID19HCE, ref = "Placebo")$summary
SUM$Ptie <- round(SUM$TIE/SUM$TOTAL, 2)
SUM
#> TRTP WIN LOSS TIE TOTAL WR WO Ptie
#> 1 A 135744 97143 48974 281861 1.3973627 1.3173641 0.17
#> 2 P 97143 135744 48974 281861 0.7156338 0.7590916 0.17
The kidney HCE defined in Heerspink et al. (2023) has the following ordinal outcomes (for the review of the topic see Little et al. (2023)).
#> Order Category
#> 1 I Death
#> 2 II Dialysis or kidney transplantation
#> 3 III Sustained GFR < 15 ml/min per 1.73 m2
#> 4 IV Sustained GFR decline from baseline of >= 57%
#> 5 V Sustained GFR decline from baseline of >= 50%
#> 6 VI Sustained GFR decline from baseline of >= 40%
#> 7 VII Individual GFR slope
The dataset KHCE
contains data on a kidney HCE
outcomes
dat <- KHCE
Order <- c("Death (adj)", "Chronic dialysis (adj) >=90 days",
"Sustained eGFR<15 (mL/min/1.73 m2)", "Sustained >=57% decline in eGFR",
"Sustained >=50% decline in eGFR", "Sustained >=40% decline in eGFR", "eGFR slope")
dat$GROUP <- factor(dat$GROUP, levels = Order)
table(dat$GROUP, dat$TRTP)
#>
#> A P
#> Death (adj) 40 50
#> Chronic dialysis (adj) >=90 days 17 29
#> Sustained eGFR<15 (mL/min/1.73 m2) 16 28
#> Sustained >=57% decline in eGFR 2 9
#> Sustained >=50% decline in eGFR 7 22
#> Sustained >=40% decline in eGFR 36 34
#> eGFR slope 632 578
This dataset is derived from ADSL
which contains
baseline characteristics,
ID | TRTPN | EGFRBL | STRATAN |
---|---|---|---|
1 | 1 | 44 | 1 |
2 | 1 | 31 | 3 |
3 | 1 | 28 | 4 |
4 | 1 | 61 | 4 |
5 | 1 | 37 | 4 |
6 | 2 | 35 | 1 |
ADLB
laboratory measurements of kidney function,
ID | TRTPN | AVAL | ADAY | AVISITN | PARAM | PARAMCD | PARAMN |
---|---|---|---|---|---|---|---|
1 | 1 | 40 | 357 | 7 | eGFR measurements | eGFR | 7 |
1 | 1 | 49 | 119 | 5 | eGFR measurements | eGFR | 7 |
1 | 1 | 41 | 238 | 6 | eGFR measurements | eGFR | 7 |
1 | 1 | 36 | 469 | 8 | eGFR measurements | eGFR | 7 |
1 | 1 | 40 | 721 | 10 | eGFR measurements | eGFR | 7 |
1 | 1 | 34 | 602 | 9 | eGFR measurements | eGFR | 7 |
and ADET
for the time-to-event outcomes with their
timing.
ID | AVAL | PARAM | PARAMCD | PARAMN | TRTPN |
---|---|---|---|---|---|
11 | 359 | Sustained >=50% decline in eGFR | EGFR50 | 5 | 2 |
11 | 467 | Sustained >=57% decline in eGFR | EGFR57 | 4 | 2 |
11 | 359 | Sustained >=40% decline in eGFR | EGFR40 | 6 | 2 |
11 | 841 | Sustained eGFR<15 (mL/min/1.73 m2) | EGFR15 | 3 | 2 |
15 | 962 | Death (adj) | DTHADJ | 1 | 1 |
21 | 737 | Sustained >=40% decline in eGFR | EGFR40 | 6 | 1 |
For the detailed derivation see the Technical Appendix in Heerspink et al. (2023).
In the Heart Failure population (see Kondo et al. (2023)) the following HCE was considered
#> Order Category
#> 1 I Cardiovascular death
#> 2 II Total (first and recurrent) HF hospitalizations
#> 3 III Total urgent HF visits
#> 4 IV Improvement/deterioration in KCCQ-TSS