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PD-L1 blockade in combination with carboplatin as immune induction in metastatic lobular breast cancer: the GELATO trial.
Voorwerk, Leonie; Isaeva, Olga I; Horlings, Hugo M; Balduzzi, Sara; Chelushkin, Maksim; Bakker, Noor A M; Champanhet, Elisa; Garner, Hannah; Sikorska, Karolina; Loo, Claudette E; Kemper, Inge; Mandjes, Ingrid A M; de Maaker, Michiel; van Geel, Jasper J L; Boers, Jorianne; de Boer, Maaike; Salgado, Roberto; van Dongen, Marloes G J; Sonke, Gabe S; de Visser, Karin E; Schumacher, Ton N; Blank, Christian U; Wessels, Lodewyk F A; Jager, Agnes; Tjan-Heijnen, Vivianne C G; Schröder, Carolien P; Linn, Sabine C; Kok, Marleen.
Affiliation
  • Voorwerk L; Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Isaeva OI; Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Horlings HM; Department of Pathology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Balduzzi S; Department of Biometrics, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Chelushkin M; Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Bakker NAM; Division of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Champanhet E; Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Garner H; Oncode Institute, Utrecht, the Netherlands.
  • Sikorska K; Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Loo CE; Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Kemper I; Oncode Institute, Utrecht, the Netherlands.
  • Mandjes IAM; Department of Biometrics, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • de Maaker M; Department of Radiology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • van Geel JJL; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Boers J; Department of Biometrics, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • de Boer M; Division of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Salgado R; Department of Medical Oncology, University Medical Center Groningen, Groningen, the Netherlands.
  • van Dongen MGJ; Department of Medical Oncology, University Medical Center Groningen, Groningen, the Netherlands.
  • Sonke GS; Department of Medical Oncology, GROW, Maastricht University Medical Center, Maastricht, the Netherlands.
  • de Visser KE; Department of Pathology, GZA-ZNA hospitals, Antwerp, Belgium.
  • Schumacher TN; Division of Research, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Blank CU; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Wessels LFA; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Jager A; Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
  • Tjan-Heijnen VCG; Oncode Institute, Utrecht, the Netherlands.
  • Schröder CP; Department of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
  • Linn SC; Oncode Institute, Utrecht, the Netherlands.
  • Kok M; Division of Molecular Oncology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Nat Cancer ; 4(4): 535-549, 2023 04.
Article in En | MEDLINE | ID: mdl-37038006
ABSTRACT
Invasive lobular breast cancer (ILC) is the second most common histological breast cancer subtype, but ILC-specific trials are lacking. Translational research revealed an immune-related ILC subset, and in mouse ILC models, synergy between immune checkpoint blockade and platinum was observed. In the phase II GELATO trial ( NCT03147040 ), patients with metastatic ILC were treated with weekly carboplatin (area under the curve 1.5 mg ml-1 min-1) as immune induction for 12 weeks and atezolizumab (PD-L1 blockade; triweekly) from the third week until progression. Four of 23 evaluable patients had a partial response (17%), and 2 had stable disease, resulting in a clinical benefit rate of 26%. From these six patients, four had triple-negative ILC (TN-ILC). We observed higher CD8+ T cell infiltration, immune checkpoint expression and exhausted T cells after treatment. With this GELATO trial, we show that ILC-specific clinical trials are feasible and demonstrate promising antitumor activity of atezolizumab with carboplatin, particularly for TN-ILC, and provide insights for the design of highly needed ILC-specific trials.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Lobular / Triple Negative Breast Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: Nat Cancer Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Lobular / Triple Negative Breast Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: Nat Cancer Year: 2023 Document type: Article Affiliation country: