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Abstract CT301: A phase Ib study to evaluate RO7198457, an individualized Neoantigen Specific immunoTherapy (iNeST), in combination with atezolizumab in patients with locally advanced or metastatic solid tumors

Authors :
Charles G. Drake
Jingbin Zhang
Brian S. Henick
Guy Jerusalem
Rachel Sabado
Christian H. Ottensmeier
Scott A. Laurie
Jack Huang
Lawrence Fong
Lars Mueller
Fadi Braiteh
Thomas Powles
George A. Fisher
Ignacio Melero
Patricia LoRusso
Patrick Twomey
Ani Sarkis Balmanoukian
Raid Aljumaily
Jeffery Yachnin
Achim Rittmeyer
Michael S. Gordon
Eelke Gort
Rom Leidner
Aglaia Schiza
R. Camidge
Ryan J. Sullivan
Marcus Schmidt
Manesh Yadav
Sylvie Rottey
Marco A. J. Iafolla
Martin Schuler
Matthew D. Hellmann
Juanita Lopez
Johanna C. Bendell
Felicitas Mueller
Özlem Türeci
Luc Dirix
Laura Molenaar-Kuijsten
Ugur Sahin
Kit Wong
Patrick A. Ott
Evelyna Derhovanessian
Source :
Cancer Research. 80:CT301-CT301
Publication Year :
2020
Publisher :
American Association for Cancer Research (AACR), 2020.

Abstract

Background: Neoantigens arising from somatic mutations are attractive targets for cancer immunotherapy as they may be recognized as foreign by the immune system. RO7198457, a systemically administered RNA-Lipoplex iNeST was designed to stimulate T cell responses against neoantigens. A first-in-human Phase Ib study of RO7198457, in combination with the aPD-L1 antibody atezolizumab is being conducted in patients with locally advanced or metastatic solid tumors. Methods: RO7198457 is manufactured on a per-patient basis and contains up to 20 tumor-specific neoepitopes. Nine doses of RO7198457 were administered i.v. in weekly and bi-weekly intervals during the 12-week induction stage and every 24 weeks during the maintenance stage. Atezolizumab 1200 mg was administered on Day 1 of each 21-day cycle. Results: In total, 132 patients enrolled in cohorts with doses ranging from 15-50 μg RO7198457 in combination with atezolizumab. Most common tumor types were NSCLC, TNBC, melanoma and CRC. The median number of prior therapies was 3 (range 1-11). 39% of patients received prior immunotherapy. Most patients had low levels of PD-L1 expression (93% patients with Citation Format: Juanita S. Lopez, Ross Camidge, Marco Iafolla, Sylvie Rottey, Martin Schuler, Matthew Hellmann, Ani Balmanoukian, Luc Dirix, Michael Gordon, Ryan Sullivan, Brian S. Henick, Charles Drake, Kit Wong, Patricia LoRusso, Patrick Ott, Lawrence Fong, Aglaia Schiza, Jeffery Yachnin, Christian Ottensmeier, Fadi Braiteh, Johanna Bendell, Rom Leidner, George Fisher, Guy Jerusalem, Laura Molenaar-Kuijsten, Marcus Schmidt, Scott A. Laurie, Raid Aljumaily, Achim Rittmeyer, Eelke Gort, Ignacio Melero, Lars Mueller, Rachel Sabado, Patrick Twomey, Jack Huang, Manesh Yadav, Jingbin Zhang, Felicitas Mueller, Evelyna Derhovanessian, Ugur Sahin, Özlem Türeci, Thomas Powles. A phase Ib study to evaluate RO7198457, an individualized Neoantigen Specific immunoTherapy (iNeST), in combination with atezolizumab in patients with locally advanced or metastatic solid tumors [abstract]. In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr CT301.

Details

ISSN :
15387445 and 00085472
Volume :
80
Database :
OpenAIRE
Journal :
Cancer Research
Accession number :
edsair.doi.dedup.....e8287ff8d15d9e75073283982355f7f9
Full Text :
https://doi.org/10.1158/1538-7445.am2020-ct301