Evidence map›Paper›PMID 36947985›Full record

Trial reportESMO open2023

Safety and efficacy of cobimetinib plus atezolizumab in patients with solid tumors: a phase II, open-label, multicenter, multicohort study.

E Sherman, J L Lee, P R Debruyne, B Keam, S J Shin, A Gramza, I Caro, R Amin, K Shah, Y Yan and 2 more

Open access · goldAbstract readMulticenter StudyClinical Trial, Phase II
In one paragraph

Trial report in ESMO open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 8 institutions in 4 countries.

E ShermanMemorial Sloan Kettering Cancer Center, Head and Neck Oncology Service, New York, USA. Electronic address: shermane@mskcc.org.
J L LeeUniversity of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea.
P R DebruyneKortrijk Cancer Centre, AZ Groeninge, Kortrijk, Belgium; Anglia Ruskin University, School of Life Sciences, Cambridge, UK.
B KeamSeoul National University Hospital, Department of Internal Medicine, Seoul.
S J ShinYonsei Cancer Center, Department of Internal Medicine, Seoul, South Korea.
A GramzaGeorgetown University Medical Center, Division of Hematology and Oncology, Washington DC.
I CaroGenentech, Inc, South San Francisco, USA.
R AminGenentech, Inc, South San Francisco, USA.
K ShahGenentech, Inc, South San Francisco, USA.
Y YanGenentech, Inc, South San Francisco, USA.
R HuddartThe Royal Marsden, Royal Marsden Hospital Fulham, Urology Unit, Chelsea, London. Electronic address: https://twitter.com/robert_huddart.
T PowlesBarts & London School of Medicine, Garrod Building, London, UK. Electronic address: https://twitter.com/tompowles1.
AZ Groeninge · BEGeorgetown University · USMemorial Sloan Kettering Cancer Center · USRoyal Marsden NHS Foundation Trust · GBSeoul National University Hospital · KRTwitter (United States) · USUlsan College · KRYonsei University · KR

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundAlthough introduction of immune checkpoint inhibitors has revolutionized the treatment of cancer, their response rates are generally low. Preclinical and early phase clinical data suggest that MEK inhibition may sensitize tumors to immune checkpoint inhibitors by upregulating tumor antigen expression, programmed death-ligand 1 (PD-L1) expression, and tumor T-cell infiltration. We evaluated the efficacy and safety of cobimetinib plus atezolizumab in patients with advanced solid tumors in the open-label, multicohort phase II COTEST study. PATIENTS AND

methodsThis analysis of the COTEST trial included patients from cohorts 1-4 [1-3: anti-programmed cell death protein 1 (PD-1)/PD-L1 treatment-naive patients; 4: patients with disease progression on anti-PD-1/anti-PD-L1 treatment] who received cobimetinib 60 mg once daily for the first 21 days and intravenous infusions of atezolizumab 840 mg on days 1 and 15 of each 28-day cycle. Efficacy endpoints included objective response rate, overall survival, progression-free survival (PFS), and disease control rate.

resultsOverall, 77 patients were enrolled in cohorts 1-4 (78% male; median age 62.8 years). Objective response rate was 20% in cohort 1 [squamous cell carcinoma of the head and neck (SCCHN)], 30% in cohort 2 (urothelial carcinoma), and 18% in cohort 3 (renal cell carcinoma); there were no responders among 20 patients in cohort 4 (SCCHN). The disease control rates in cohorts 1-4 were 50%, 40%, 24%, and 25%, respectively. The median PFS was 5.5, 3.4, 3.4, and 3.6 months in cohorts 1-4, respectively, and the median overall survival was 16.8, 18.7, 21.7, and 7.7 months, respectively. Most adverse events were of grade 1/2 and were manageable.

conclusionsCobimetinib plus atezolizumab had moderate activity in patients with anti-PD-1/PD-L1 treatment-naive SCCHN and urothelial carcinoma, and weak activity in anti-PD-1/PD-L1 treatment-naive renal cell carcinoma, and no activity in checkpoint inhibitor-treated patients.

Indexed as

Carcinoma, Renal CellCarcinoma, Transitional CellKidney NeoplasmsUrinary Bladder NeoplasmsAntibodies, Monoclonal, HumanizedAzetidinesFemaleHumansImmune Checkpoint InhibitorsMaleMiddle AgedPiperidinesAntibodies, Monoclonal, HumanizedatezolizumabAzetidinescobimetinibImmune Checkpoint InhibitorsPiperidinesatezolizumabcobimetinibCOTESTphase II trialsolid tumors

Identifiers

PMID36947985
PMCPMC10163002
OpenAlexW4328112747

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.