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A BCMA/CD16A bispecific innate cell engager for the treatment of multiple myeloma.
Kakiuchi-Kiyota, Satoko; Ross, Thorsten; Wallweber, Heidi Ackerly; Kiefer, James R; Schutten, Melissa M; Adedeji, Adeyemi O; Cai, Hao; Hendricks, Robert; Cohen, Sivan; Myneni, Srividya; Liu, Luna; Fullerton, Aaron; Corr, Nicholas; Yu, Lanlan; de Almeida Nagata, Denise; Zhong, Shelly; Leong, Steven R; Li, Ji; Nakamura, Rin; Sumiyoshi, Teiko; Li, Jinze; Ovacik, Ayse Meric; Zheng, Bing; Dillon, Mike; Spiess, Christoph; Wingert, Susanne; Rajkovic, Erich; Ellwanger, Kristina; Reusch, Uwe; Polson, Andrew G.
Afiliación
  • Kakiuchi-Kiyota S; Genentech Research and Early Development, San Francisco, CA, USA.
  • Ross T; Affimed GmbH, Heidelberg, Germany.
  • Wallweber HA; Genentech Research and Early Development, San Francisco, CA, USA.
  • Kiefer JR; Genentech Research and Early Development, San Francisco, CA, USA.
  • Schutten MM; Genentech Research and Early Development, San Francisco, CA, USA.
  • Adedeji AO; Genentech Research and Early Development, San Francisco, CA, USA.
  • Cai H; Genentech Research and Early Development, San Francisco, CA, USA.
  • Hendricks R; Genentech Research and Early Development, San Francisco, CA, USA.
  • Cohen S; Genentech Research and Early Development, San Francisco, CA, USA.
  • Myneni S; Genentech Research and Early Development, San Francisco, CA, USA.
  • Liu L; Genentech Research and Early Development, San Francisco, CA, USA.
  • Fullerton A; Genentech Research and Early Development, San Francisco, CA, USA.
  • Corr N; Genentech Research and Early Development, San Francisco, CA, USA.
  • Yu L; Genentech Research and Early Development, San Francisco, CA, USA.
  • de Almeida Nagata D; Genentech Research and Early Development, San Francisco, CA, USA.
  • Zhong S; Genentech Research and Early Development, San Francisco, CA, USA.
  • Leong SR; Genentech Research and Early Development, San Francisco, CA, USA.
  • Li J; Genentech Research and Early Development, San Francisco, CA, USA.
  • Nakamura R; Genentech Research and Early Development, San Francisco, CA, USA.
  • Sumiyoshi T; Genentech Research and Early Development, San Francisco, CA, USA.
  • Li J; Genentech Research and Early Development, San Francisco, CA, USA.
  • Ovacik AM; Genentech Research and Early Development, San Francisco, CA, USA.
  • Zheng B; Genentech Research and Early Development, San Francisco, CA, USA.
  • Dillon M; Genentech Research and Early Development, San Francisco, CA, USA.
  • Spiess C; Genentech Research and Early Development, San Francisco, CA, USA.
  • Wingert S; Affimed GmbH, Heidelberg, Germany.
  • Rajkovic E; Affimed GmbH, Heidelberg, Germany.
  • Ellwanger K; Affimed GmbH, Heidelberg, Germany.
  • Reusch U; Affimed GmbH, Heidelberg, Germany.
  • Polson AG; Genentech Research and Early Development, San Francisco, CA, USA. polson@gene.com.
Leukemia ; 36(4): 1006-1014, 2022 04.
Article en En | MEDLINE | ID: mdl-35001074
ABSTRACT
Despite the recent progress, multiple myeloma (MM) is still essentially incurable and there is a need for additional effective treatments with good tolerability. RO7297089 is a novel bispecific BCMA/CD16A-directed innate cell engager (ICE®) designed to induce BCMA+ MM cell lysis through high affinity binding of CD16A and retargeting of NK cell cytotoxicity and macrophage phagocytosis. Unlike conventional antibodies approved in MM, RO7297089 selectively targets CD16A with no binding of other Fcγ receptors, including CD16B on neutrophils, and irrespective of 158V/F polymorphism, and its activity is less affected by competing IgG suggesting activity in the presence of M-protein. Structural analysis revealed this is due to selective interaction with a single residue (Y140) uniquely present in CD16A opposite the Fc binding site. RO7297089 induced tumor cell killing more potently than conventional antibodies (wild-type and Fc-enhanced) and induced lysis of BCMA+ cells at very low effector-to-target ratios. Preclinical toxicology data suggested a favorable safety profile as in vitro cytokine release was minimal and no RO7297089-related mortalities or adverse events were observed in cynomolgus monkeys. These data suggest good tolerability and the potential of RO7297089 to be a novel effective treatment of MM patients.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Anticuerpos Biespecíficos / Mieloma Múltiple Límite: Humans Idioma: En Revista: Leukemia Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Anticuerpos Biespecíficos / Mieloma Múltiple Límite: Humans Idioma: En Revista: Leukemia Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos