Evidence map›Paper›PMID 28950298›Full record

Trial reportAnnals of oncology : official journal of the European Society for Medical Oncology2017

Atezolizumab in platinum-treated locally advanced or metastatic urothelial carcinoma: post-progression outcomes from the phase II IMvigor210 study.

A Necchi, R W Joseph, Y Loriot, J Hoffman-Censits, J L Perez-Gracia, D P Petrylak, C L Derleth, D Tayama, Q Zhu, B Ding and 2 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Annals of oncology : official journal of the European Society for Medical Oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02108652 (A Phase II, Multicenter, Single-Arm Study of Atezolizumab in Patients With Locally Advanced or Metastatic Urothelial Bladder Cancer), which is not on this map. Cited by 183 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
183citing papers in PubMed, 5 pooled it
15.4field-weighted citation impact, top 1% 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.

NCT02108652 phase2completednot on this map

A Phase II, Multicenter, Single-Arm Study of Atezolizumab in Patients With Locally Advanced or Metastatic Urothelial Bladder Cancer

TypeinterventionalSponsorHoffmann-La RocheRan2014 to 2023Enrolled310ConditionsBladder CancerArmsAtezolizumab
3 · Its place in the literature

Who cites it

183 citing papers in PubMed, 5 syntheses or guidelines pooled it, 317 citations in OpenAlex.

  1. Immunotherapy for advanced or metastatic urothelial carcinoma.The Cochrane database of systematic reviews · 2023
    Pooled it
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  7. Identification of a distinct cluster of LY6EBritish journal of cancer · 2026
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  13. Medea: An omics AI agent for therapeutic discovery.bioRxiv : the preprint server for biology · 2026
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123 more citing papers are in PubMed but not listed here.

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 7 institutions in 4 countries.

A NecchiDepartment of Medical Oncology, Fondazione IRCCS, Istituto Nazionale dei Tumori, Milan, Italy.
R W JosephDepartment of Hematology/Oncology, Mayo Clinic, Jacksonville, USA.
Y LoriotDepartment of Oncology, Gustave Roussy, Villejuif, France.
J Hoffman-CensitsSidney Kimmel Cancer Center at Jefferson, Thomas Jefferson University, Philadelphia, USA.
J L Perez-GraciaDepartment of Medical Oncology, Clínica Universidad de Navarra, Pamplona, Spain.
D P PetrylakSmilow Cancer Center, Yale University, New Haven, USA.
C L DerlethDepartment of Oncology, Genentech, Inc., South San Francisco, USA.
D TayamaDepartment of Oncology, Genentech, Inc., South San Francisco, USA.
Q ZhuDepartment of Oncology, Genentech, Inc., South San Francisco, USA.
B DingDepartment of Oncology, Genentech, Inc., South San Francisco, USA.
C KaiserDepartment of Oncology, Genentech, Inc., South San Francisco, USA.
J E RosenbergMemorial Sloan Kettering Cancer Center, New York, USA.
Clinica Universidad de Navarra · ESFondazione IRCCS Istituto Nazionale dei Tumori · ITInstitut Gustave Roussy · FRMemorial Sloan Kettering Cancer Center · USSidney Kimmel Cancer Center · USSmilow Cancer Hospital · USWinnMed · US

Funding

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

Abstract

backgroundConventional criteria for tumor progression may not fully reflect the clinical benefit of immunotherapy or appropriately guide treatment decisions. The phase II IMvigor210 study demonstrated the efficacy and safety of atezolizumab, a programmed death-ligand 1-directed antibody, in patients with platinum-treated locally advanced or metastatic urothelial carcinoma. Patients could continue atezolizumab beyond Response Evaluation Criteria In Solid Tumors (RECIST) v1.1 progression at the investigator's discretion: this analysis assessed post-progression outcomes in these patients. PATIENTS AND

methodsPatients were treated with atezolizumab 1200 mg i.v. every 3 weeks until loss of clinical benefit. Efficacy and safety outcomes in patients who experienced RECIST v1.1 progression and did, or did not, continue atezolizumab were analyzed descriptively.

resultsIn total, 220 patients who experienced progression from the overall cohort (n = 310) were analyzed: 137 continued atezolizumab for ≥ 1 dose after progression, 19 received other systemic therapy, and 64 received no further systemic therapy. Compared with those who discontinued, patients continuing atezolizumab beyond progression were more likely to have had a baseline Eastern Cooperative Oncology Group performance status of 0 (43.1% versus 31.3%), less likely to have had baseline liver metastases (27.0% versus 41.0%), and more likely to have had an initial response to atezolizumab (responses in 11.7% versus 1.2%). Five patients (3.6%) continuing atezolizumab after progression had subsequent responses compared with baseline measurements. Median post-progression overall survival was 8.6 months in patients continuing atezolizumab, 6.8 months in those receiving another treatment, and 1.2 months in those receiving no further treatment. Atezolizumab exposure-adjusted adverse event frequencies were generally similar before and following progression.

conclusionIn this single-arm study, patients who continued atezolizumab beyond RECIST v1.1 progression derived prolonged clinical benefit without additional safety signals. Identification of patients most likely to benefit from atezolizumab beyond progression remains an important challenge in the management of metastatic urothelial carcinoma. CLINICALTRIALS.GOV ID: NCT02108652.

Indexed as

AdultAgedAged, 80 and overAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsCohort StudiesFemaleHumansMaleMiddle AgedNeoplasm GradingUrinary Bladder NeoplasmsUrologic NeoplasmsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsatezolizumabatezolizumabimmunotherapyPD-L1post-progression outcomesprogrammed death-ligand 1urothelial cancer

Identifiers

PMID28950298
PMCPMC5834063
OpenAlexW2752793362

What OpenQuestion holds

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Registered trials

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.