Evidence map›Paper›PMID 41511400›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2026

TAPISTRY: A Phase II Study of Atezolizumab in Patients with Tumor Mutational Burden-High Tumors.

David M Thomas, Jeong Eun Kim, Fabrice Barlesi, Uwe M Martens, Maciej Krzakowski, Rafal Dziadziuszko, Jae Ho Jeong, Gennaro Daniele, Timothy R Wilson, Felice Wu and 5 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Trial
  2. Article
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

15 authors.

David M ThomasCentre for Molecular Oncology, University of New South Wales, Sydney, Australia.ORCID 0000-0002-2527-5428
Jeong Eun KimDepartment of Oncology, Asan Medical Centre, University of Ulsan College of Medicine, Seoul, Republic of Korea.ORCID 0000-0001-9766-1531
Fabrice BarlesiDepartment of Medical Oncology, International Centre for Thoracic Cancers (CICT), Gustave Roussy, Villejuif, France.ORCID 0000-0001-5793-3539
Uwe M MartensFaculty of Medicine, Paris Saclay University, Kremlin-Bicêtre, France.ORCID 0000-0001-7999-4359
Maciej KrzakowskiDepartment of Lung Cancer and Thoracic Tumors, Maria Sklodowska-Curie Memorial, National Research Institute of Oncology, Warsaw, Poland.ORCID 0000-0003-3324-0900
Rafal DziadziuszkoDepartment of Oncology & Radiotherapy and Early Phase Clinical Trials Centre, Medical University of Gdańsk, Gdańsk, Poland.ORCID 0000-0001-8080-9843
Jae Ho JeongDepartment of Oncology, Asan Medical Centre, University of Ulsan College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-8749-2612
Gennaro DanielePhase 1 Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0001-5360-1895
Timothy R WilsonGenentech, Inc., South San Francisco, California.ORCID 0009-0009-5421-1755
Felice WuGenentech, Inc., South San Francisco, California.ORCID 0009-0001-6159-8398
Brian P SimmonsGenentech, Inc., South San Francisco, California.ORCID 0000-0003-1613-5308
Sid PatelGenentech, Inc., South San Francisco, California.ORCID 0009-0000-1831-9819
Maria SbirnacRoche, Mississauga, Canada.ORCID 0009-0006-8790-0870
Monika KaulGenentech, Inc., South San Francisco, California.ORCID 0009-0002-8039-5665
Shirish M GadgeelDepartment of Internal Medicine, Henry Ford Cancer Institute/Henry Ford Health System, Detroit, Michigan.ORCID 0000-0001-5240-3811

Funding

Genentech (Genentech USA)
6 · The paper itself

Abstract

purposePatients with tumor mutational burden (TMB)-high tumors can derive benefit from atezolizumab, though previous studies have used inconsistent TMB cutoffs. We report data for atezolizumab in patients with TMB-high solid tumors from the phase II TAPISTRY multicohort trial, using TMB cutoffs of ≥13 and ≥16 mutations per megabase (mut/Mb). PATIENTS AND

methodsPatients with PD-L1 inhibitor-naïve, TMB-high (≥13 mut/Mb), advanced/metastatic solid tumors received atezolizumab every 21 days [1,200 mg for adults, 15 mg/kg (up to 1,200 mg/kg) for children]. The primary endpoint was independent review committee (IRC)-assessed objective response rate (ORR) for TMB ≥16 mut/Mb. Secondary endpoints (using TMB ≥13 mut/Mb) included IRC-assessed ORR, duration of response (DOR), progression-free survival (PFS), and safety.

resultsAs of November 9, 2023 (median survival follow-up: 9.8 months), 148 patients received treatment. Median age was 63 years, 31.8% of patients had >2 prior therapy lines, and the most common tumor types were colorectal (29.1%), breast (8.8%), and gastroesophageal (8.8%). IRC-assessed ORR was 22.3% [95% confidence interval (CI), 15-31.2] with TMB ≥16 mut/Mb (n = 112), and 20.2% (95% CI, 13.6-28.1) with TMB ≥13 mut/Mb (n = 129). Median IRC-assessed DOR was not estimable. Median IRC-assessed PFS was 2.8 (95% CI, 1.7-5.4) and 2.7 (95% CI, 1.5-4.2) months using TMB ≥16 and ≥13 mut/Mb, respectively. Adverse events were reported in 93.2% of patients, of which 53.4% were treatment-related (no grade 5) and 40.5% were grade ≥3.

conclusionsAtezolizumab led to moderate antitumor activity in various TMB-high solid tumors. Safety was consistent with previous reports.

Indexed as

Antibodies, Monoclonal, HumanizedBiomarkers, TumorMutationNeoplasmsAdultAgedAged, 80 and overChildFemaleHumansMaleMiddle AgedTumor BurdenYoung AdultAntibodies, Monoclonal, HumanizedatezolizumabBiomarkers, Tumor

Identifiers

PMID41511400
PMCPMC13012244

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.