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Obinutuzumab Pretreatment as a Novel Approach to Mitigate Formation of Anti-Drug Antibodies Against Cergutuzumab Amunaleukin in Patients with Solid Tumors.
Peters, Solange; Angevin, Eric; Alonso-Gordoa, Teresa; Rohrberg, Kristoffer; Melero, Ignacio; Mellado, Begoña; Perez-Gracia, Jose-Luis; Tabernero, Josep; Adessi, Celine; Boetsch, Christophe; Watson, Carl; Dal Porto, Joseph; Dejardin, David; Del Nagro, Christopher; Nicolini, Valeria; Evers, Stefan; Klein, Christian; Leutgeb, Barbara; Pisa, Pavel; Rossmann, Eva; Saro, José; Umana, Pablo; Charo, Jehad; Teichgräber, Volker; Steeghs, Neeltje.
Affiliation
  • Peters S; Department of Oncology, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne University, Lausanne, Switzerland.
  • Angevin E; Drug Development Department (DITEP), Institut Gustave Roussy, Villejuif, France.
  • Alonso-Gordoa T; Medical Oncology Department, Ramon y Cajal University Hospital, Madrid, Spain.
  • Rohrberg K; Phase 1 Unit, Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Melero I; Oncology and Immunology Department, Clinica Universidad de Navarra and CIBERONC, Pamplona, Spain.
  • Mellado B; Department of Medical Oncology, Hospital Clinic, Barcelona, Spain.
  • Perez-Gracia JL; Translational Genomics and Targeted Therapies in Solid Tumors, IDIBAPS, Barcelona, Spain.
  • Tabernero J; Department of Medicine, University of Barcelona, Barcelona, Spain.
  • Adessi C; Oncology and Immunology Department, Clinica Universidad de Navarra and CIBERONC, Pamplona, Spain.
  • Boetsch C; Medical Oncology Department, Vall d'Hebron Hospital Campus and Institute of Oncology (VHIO), UVic-UCC, IOB-Quiron, Barcelona, Spain.
  • Watson C; F. Hoffmann-La Roche Ltd, Research & Early Development Oncology, Basel, Switzerland.
  • Dal Porto J; F. Hoffmann-La Roche Ltd, Research & Early Development Oncology, Basel, Switzerland.
  • Dejardin D; A4P Consulting Ltd, Sandwich, United Kingdom.
  • Del Nagro C; Discovery, Genentech, Inc., South San Francisco, California.
  • Nicolini V; Product Development, Data Science, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Evers S; Research & Early Development Oncology, F. Hoffmann-La Roche Ltd, Zurich, Switzerland.
  • Klein C; F. Hoffmann-La Roche Ltd, Research & Early Development Oncology, Basel, Switzerland.
  • Leutgeb B; F. Hoffmann-La Roche Ltd, Research & Early Development Oncology, Basel, Switzerland.
  • Pisa P; Research & Early Development Oncology, F. Hoffmann-La Roche Ltd, Zurich, Switzerland.
  • Rossmann E; Product Development Oncology F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Saro J; Research & Early Development Oncology, F. Hoffmann-La Roche Ltd, Zurich, Switzerland.
  • Umana P; Product Development, Safety Science, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Charo J; Research & Early Development Oncology, F. Hoffmann-La Roche Ltd, Zurich, Switzerland.
  • Teichgräber V; Research & Early Development Oncology, F. Hoffmann-La Roche Ltd, Zurich, Switzerland.
  • Steeghs N; Research & Early Development Oncology, F. Hoffmann-La Roche Ltd, Zurich, Switzerland.
Clin Cancer Res ; 30(8): 1630-1641, 2024 Apr 15.
Article de En | MEDLINE | ID: mdl-38319672
ABSTRACT

PURPOSE:

The immunocytokine cergutuzumab amunaleukin (CEA-IL2v) showed manageable safety and favorable pharmacodynamics in phase I/Ib trials in patients with advanced/metastatic carcinoembryonic antigen-positive (CEA+) solid tumors, but this was accompanied by a high incidence of anti-drug antibodies (ADA). We examined B-cell depletion with obinutuzumab as a potential mitigation strategy. EXPERIMENTAL

DESIGN:

Preclinical data comparing B-cell depletion with rituximab versus obinutuzumab are summarized. Substudies of phase I/Ib trials investigated the effect of obinutuzumab pretreatment on ADA development, safety, pharmacodynamics, and antitumor activity of CEA-IL2v ± atezolizumab in patients with advanced/metastatic or unresectable CEA+ solid tumors who had progressed on standard of care.

RESULTS:

Preclinical data showed superior B-cell depletion with obinutuzumab versus rituximab. In clinical studies, patients received CEA-IL2v monotherapy with (n = 16) or without (n = 6) obinutuzumab pretreatment (monotherapy study), or CEA-IL2v + atezolizumab + obinutuzumab pretreatment (n = 5; combination study). In the monotherapy study, after four cycles (every 2 weeks treatment), 0/15 evaluable patients administered obinutuzumab pretreatment had ADAs versus 4/6 patients without obinutuzumab. Obinutuzumab pretreatment with CEA-IL2v monotherapy showed no new safety signals and pharmacodynamic data suggested minimal impact on T cells and natural killer cells. Conversely, increased liver toxicity was observed in the combination study (CEA-IL2v + atezolizumab + obinutuzumab pretreatment).

CONCLUSIONS:

These preliminary findings suggest that obinutuzumab pretreatment before CEA-IL2v administration in patients with CEA+ solid tumors may be a feasible and potent ADA mitigation strategy, with an acceptable safety profile, supporting broader investigation of obinutuzumab pretreatment for ADA mitigation in other settings.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Antigène carcinoembryonnaire / Anticorps monoclonaux humanisés / Tumeurs Limites: Humans Langue: En Journal: Clin Cancer Res Sujet du journal: NEOPLASIAS Année: 2024 Type de document: Article Pays d'affiliation: Suisse

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Antigène carcinoembryonnaire / Anticorps monoclonaux humanisés / Tumeurs Limites: Humans Langue: En Journal: Clin Cancer Res Sujet du journal: NEOPLASIAS Année: 2024 Type de document: Article Pays d'affiliation: Suisse