Evidence map›Paper›PMID 41647992›Full record

ArticleESMO gastrointestinal oncology2025

Preoperative immunotherapy with atezolizumab and tiragolumab in patients with colorectal liver metastases-the PURPLE trial.

S Kasper, E Elez, U Neumann, S Lang, A-K Trampe, F Salva, C Dopazo, I Virchow, S Hartmann, K Herrmann and 4 more

Abstract read
In one paragraph

Article in ESMO gastrointestinal oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

14 authors.

S KasperDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, a member of the imCORE network, Essen, Germany.
E ElezDepartment of HPB Surgery and Transplants, Barcelona Hospital Campus, a member of the imCORE network, Barcelona, Spain.
U NeumannNational Center for Tumor Diseases (NCT), NCT West, Essen, Germany.
S LangDepartment of General, Visceral and Transplantation Surgery, West German Cancer Center, University Hospital Essen, a member of the imCORE network, Essen, Germany.
A-K TrampeDepartment of General, Visceral and Transplantation Surgery, West German Cancer Center, University Hospital Essen, a member of the imCORE network, Essen, Germany.
F SalvaVall d'Hebron Institute of Oncology, Medical Oncology, Vall d'Hebron Barcelona Hospital Campus, a member of the imCORE network, Barcelona, Spain.
C DopazoDepartment of HPB Surgery and Transplants, Barcelona Hospital Campus, a member of the imCORE network, Barcelona, Spain.
I VirchowDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, a member of the imCORE network, Essen, Germany.
S HartmannNational Center for Tumor Diseases (NCT), NCT West, Essen, Germany.
K HerrmannNational Center for Tumor Diseases (NCT), NCT West, Essen, Germany.
J TaberneroDepartment of HPB Surgery and Transplants, Barcelona Hospital Campus, a member of the imCORE network, Barcelona, Spain.
A WestendorfInstitute of Medical Microbiology, University Hospital Essen, a member of the imCORE network, Essen, Germany.
M SchulerDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, a member of the imCORE network, Essen, Germany.
A SchrammDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, a member of the imCORE network, Essen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In colorectal cancer (CRC), the liver is the most common site of metastasis, which is the leading cause of CRC-related mortality. Hepatic resection offers long-term survival in some patients with CRC liver metastases (CRLM), but recurrence rates remain high (50%-75% within 2 years). Preoperative immunotherapy may induce tumor regression and improve long-term surgical outcomes. The PURPLE trial evaluates the feasibility, safety, and efficacy of short-term preoperative immunotherapy with the anti-programmed death-ligand 1 (PD-L1) antibody atezolizumab and the anti-T cell immunoreceptor with Ig and ITIM domains (TIGIT) antibody tiragolumab in patients with resectable CRLM. Study design: PURPLE is an international, open-label, multicenter, randomized phase II 'window of opportunity' trial. Patients with resectable CRLM are randomized 2 : 1 to receive two cycles of atezolizumab (840 mg) plus tiragolumab (420 mg) before surgery (experimental arm) or immediate surgery (control arm). The primary endpoint is the percentage of patients with complete or major pathological regression of the resected metastases (tumor regression grade 1/2, Rubbia-Brandt criteria). The statistical design follows Simon's two-stage approach with interim and final analyses comparing pathological response rates using descriptive and exploratory methods. Secondary endpoints include feasibility, safety, post-operative complications, and metabolic response by positron emission tomography. Exploratory studies characterize immune cell infiltration, tumor mutational burden, and circulating tumor DNA dynamics.

Indexed as

atezolizumabclinical trialcolorectal liver metastasespreoperative immunotherapytiragolumab

Identifiers

PMID41647992
PMCPMC12836742

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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.