Abstract CT042: Atezolizumab (atezo) + platinum/gemcitabine (plt/gem) vs placebo + plt/gem in patients (pts) with previously untreated locally advanced or metastatic urothelial carcinoma (mUC): Updated overall survival (OS) from the randomized phase III study IMvigor130
Background: The IMvigor130 primary analysis demonstrated a statistically significant progression-free survival (PFS) benefit and encouraging OS with atezo + plt/gem (Arm A) vs placebo + plt/gem (Arm C) as first-line mUC treatment, although interim OS results did not cross the pre-specified threshold...
Gespeichert in:
Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 2021-07, Vol.81 (13_Supplement), p.CT042-CT042 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Background: The IMvigor130 primary analysis demonstrated a statistically significant progression-free survival (PFS) benefit and encouraging OS with atezo + plt/gem (Arm A) vs placebo + plt/gem (Arm C) as first-line mUC treatment, although interim OS results did not cross the pre-specified threshold for significance (Galsky Lancet 2020). Here we report the 2nd interim OS for Arm A vs C, including efficacy by type of chemotherapy (chemo) given.
Methods: Pts were randomized 1:1:1 to Arm A, B (atezo monotherapy) or C. Investigators pre-specified the type of chemo pts would receive if assigned to Arms A or C (gem + either cisplatin or carboplatin). Co-primary endpoints (EPs) were RECIST 1.1 PFS and OS (Arm A vs C; ITT) and OS (Arm B vs C; ITT, IC2/3) tested using a hierarchical approach. Safety and secondary efficacy EPs (objective response rate and duration of response) are reported. Exploratory OS analyses by type of chemo were pre-specified.
Results: As of data cutoff, June 14, 2020 (median follow-up, 13.3 mo), OS event rates were 67% in Arm A and 70% in Arm C. Efficacy data are shown (Table). Subsequent non-protocol immunotherapy use was 7% in Arm A vs 24% in Arm C. Of pts in the safety population (Arm A: 454; Arm C: 389), 81% and 80%, respectively, had a Gr 3/4 treatment-related AE (TRAE). No new Gr 5 TRAEs occurred since the 1st analysis (Gr 5 TRAEs: 2% in Arm A vs 1% in Arm C). Gr 3/4 AEs of special interest occurred in 9% in Arm A and 4% in Arm C.
Conclusions: OS with atezo + plt/gem vs placebo + plt/gem in this updated analysis of IMvigor130 was consistent with the 1st interim analysis (not yet statistically significant). The impact of atezo plus chemo on outcomes may differ based on the specific platinum regimen; these exploratory findings warrant further investigation. OS follow-up is ongoing. Safety profile of atezo + plt/gem was consistent with each agent.
IMvigor130 efficacy (second interim OS analysis)Arm A:Arm C:atezo + plt/gemplacebo + plt/gem(n=451)(n=400)OS HR (95% CI)aITT0.84 (0.71, 1.00); P=0.026bCisplatin (n=273)0.73 (0.54, 0.98)PD-L1 IC2/3 (n=69)c0.66 (0.32, 1.36)PD-L1 IC0/1 (n=204)c0.72 (0.52, 1.01)Carboplatin (n=578)0.91 (0.74, 1.10)PD-L1 IC2/3 (n=130)c0.80 (0.52, 1.23)PD-L1 IC0/1 (n=448)c0.94 (0.75, 1.18)Median OS (95% CI), moITT16.1 (14.2, 18.8)13.4 (11.9, 15.2)Cisplatin21.6 (17.5, 25.4)14.6 (11.7, 18.4)Carboplatin14.3 (12.0, 16.5)13.0 (10.6, 15.2)Objective response rate (95% CI), %ITT (n=844)d48 (43, 53)45 (40, 50)Cisplatin (n=271)d |
---|---|
ISSN: | 0008-5472 1538-7445 |
DOI: | 10.1158/1538-7445.AM2021-CT042 |