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NCT02362035 · OUTCOME

Overall Survival

ACP-196 (Acalabrutinib) in Combination With Pembrolizumab, for Treatment of Hematologic Malignancies · Source last updated 2026-05-13

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
MEDIAN
Unit
Months
Interval / dispersion
95% Confidence Interval
Time frame
104 weeks

What was measured

The time from the first dose date of acalabrutinib or pembrolizumab until date of death due to any cause

Analysis population: All participants in this study received both study drugs and were therefore analyzed together as a single treatment arm. Participants receiving the different regimens were not analyzed separately by regimen, as the study was designed to assess the the combination study treatment.

Groups in this outcome

Acalabrutinib + Pembrolizumab

All participants in this study received both study drugs and were therefore analysed together as a single treatment arm. Participants receiving the different regimens were not analysed separately by regimen, as the study was designed to assess the safety of the combination study treatment. The study included N=161 participants who received both acalabrutinib and pembrolizumab and are summarized together (from First stage safety lead-in and Second stage expansion). Stage 3 (additional expansion in subjects with Myelofibrosis) was planned but not conducted.

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Acalabrutinib + Pembrolizumab161

Reported measurements

Source class 1
Values in Months · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Acalabrutinib + Pembrolizumab50.4Not reported26.2NANA= not estimable. The NA of the 95% upper bound was calculated from the median. Since the upper limit of the KM curve hadn't reached 50%, there is no estimate for the upper confidence limit on the median. Therefore it's NA = not estimable.
Complete source fields
classes
  1. categories
    1. measurements
      1. comment
        NA= not estimable. The NA of the 95% upper bound was calculated from the median. Since the upper limit of the KM curve hadn't reached 50%, there is no estimate for the upper confidence limit on the median. Therefore it's NA = not estimable.
        group Id
        OG000
        lower Limit
        26.2
        upper Limit
        NA
        value
        50.4
denoms
  1. counts
    1. group Id
      OG000
      value
      161
    units
    Participants
description
The time from the first dose date of acalabrutinib or pembrolizumab until date of death due to any cause
dispersion Type
95% Confidence Interval
groups
  1. description
    All participants in this study received both study drugs and were therefore analysed together as a single treatment arm. Participants receiving the different regimens were not analysed separately by regimen, as the study was designed to assess the safety of the combination study treatment. The study included N=161 participants who received both acalabrutinib and pembrolizumab and are summarized together (from First stage safety lead-in and Second stage expansion). Stage 3 (additional expansion in subjects with Myelofibrosis) was planned but not conducted.
    id
    OG000
    title
    Acalabrutinib + Pembrolizumab
param Type
MEDIAN
population Description
All participants in this study received both study drugs and were therefore analyzed together as a single treatment arm. Participants receiving the different regimens were not analyzed separately by regimen, as the study was designed to assess the the combination study treatment.
reporting Status
POSTED
time Frame
104 weeks
title
Overall Survival
type
SECONDARY
unit Of Measure
Months

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice