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

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...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2020-08, Vol.80 (16_Supplement), p.CT301-CT301
Hauptverfasser: Lopez, Juanita S., Camidge, Ross, Iafolla, Marco, Rottey, Sylvie, Schuler, Martin, Hellmann, Matthew, Balmanoukian, Ani, Dirix, Luc, Gordon, Michael, Sullivan, Ryan, Henick, Brian S., Drake, Charles, Wong, Kit, LoRusso, Patricia, Ott, Patrick, Fong, Lawrence, Schiza, Aglaia, Yachnin, Jeffery, Ottensmeier, Christian, Braiteh, Fadi, Bendell, Johanna, Leidner, Rom, Fisher, George, Jerusalem, Guy, Molenaar-Kuijsten, Laura, Schmidt, Marcus, Laurie, Scott A., Aljumaily, Raid, Rittmeyer, Achim, Gort, Eelke, Melero, Ignacio, Mueller, Lars, Sabado, Rachel, Twomey, Patrick, Huang, Jack, Yadav, Manesh, Zhang, Jingbin, Mueller, Felicitas, Derhovanessian, Evelyna, Sahin, Ugur, Türeci, Özlem, Powles, Thomas
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Sprache:eng
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Zusammenfassung: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
ISSN:0008-5472
1538-7445
DOI:10.1158/1538-7445.AM2020-CT301