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

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.

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Publication Details

Journal
ESMO Gastrointestinal Oncology
Published
2025-09-01
DOI
https://doi.org/10.1016/j.esmogo.2025.100226
Primary Topic
Colorectal Cancer Treatments and Studies
Type
article
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article

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

Stefan Kasper, Stefan Hartmann, Isabel Virchow, A.K. Trampe et al.
1 links
ESMO Gastrointestinal Oncology
Colorectal Cancer Treatments and Studies
article

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

Stefan Kasper, Stefan Hartmann, Isabel Virchow, A.K. Trampe, Josep M. Tabernero, K. Herrmann, Élena Elez, Uwe Neumann, Astrid Maria Westendorf, Cristina Dopazo, F. Salva, A. Schramm, Sven Arke Lang, M Schuler
article en

Abstract

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.

ESMO Gastrointestinal OncologyVol. 9
Hebron University (PS), National Center for Tumor Diseases (DE), Essen University Hospital (DE), Vall d'Hebron Hospital Universitari (ES), West German Heart and Vascular Center Essen (DE), Medical Research Network (US)
Openalex Percentile: Top 68%
Colorectal Cancer Treatments and Studies
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