Obinutuzumab Pretreatment as a Novel Approach to Mitigate Formation of Anti-Drug Antibodies Against Cergutuzumab Amunaleukin in Patients with Solid Tumors

奥比努图库单抗 医学 阿替唑单抗 美罗华 肿瘤科 药效学 癌症 药理学 内科学 药代动力学 淋巴瘤 免疫疗法 彭布罗利珠单抗
作者
Solange Peters,Eric Angevin,Teresa Alonso‐Gordoa,Kristoffer Staal Rohrberg,Ignacio Melero,Begoña Mellado,Jose Luis Pérez‐Gracia,Josep Tabernero,Céline Adessi,Christophe Boetsch,Carl Watson,Joseph Dal Porto,David Dejardin,Christopher Del Nagro,Valeria Nicolini,Stefan Evers,Christian Klein,Barbara Leutgeb,Pavel Pisa,Eva Rossmann
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:30 (8): 1630-1641 被引量:6
标识
DOI:10.1158/1078-0432.ccr-23-2658
摘要

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.
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