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HITM-SURE: Hepatic immunotherapy for metastases phase Ib anti-CEA CAR-T study utilizing pressure enabled drug delivery.
Katz, Steven C; Moody, Ashley E; Guha, Prajna; Hardaway, John C; Prince, Ethan; LaPorte, Jason; Stancu, Mirela; Slansky, Jill E; Jordan, Kimberly R; Schulick, Richard D; Knight, Robert; Saied, Abdul; Armenio, Vincent; Junghans, Richard P.
Afiliación
  • Katz SC; Surgery, Roger Williams Medical Center, Providence, Rhode Island, USA skatz@chartercare.org.
  • Moody AE; Medicine, Roger Williams Medical Center, Providence, Rhode Island, USA.
  • Guha P; Surgery, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Hardaway JC; Surgery, Roger Williams Medical Center, Providence, Rhode Island, USA.
  • Prince E; Surgery, Roger Williams Medical Center, Providence, Rhode Island, USA.
  • LaPorte J; Surgery, Roger Williams Medical Center, Providence, Rhode Island, USA.
  • Stancu M; Radiology, Roger Williams Medical Center, Providence, Rhode Island, USA.
  • Slansky JE; Surgery, Roger Williams Medical Center, Providence, Rhode Island, USA.
  • Jordan KR; Pathology, Roger Williams Medical Center, Providence, Rhode Island, USA.
  • Schulick RD; Research, University of Colorado Denver School of Medicine, Aurora, Colorado, USA.
  • Knight R; Research, University of Colorado Denver School of Medicine, Aurora, Colorado, USA.
  • Saied A; Research, University of Colorado Denver School of Medicine, Aurora, Colorado, USA.
  • Armenio V; Sorrento Therapeutics Inc, San Diego, California, USA.
  • Junghans RP; Surgery, Roger Williams Medical Center, Providence, Rhode Island, USA.
J Immunother Cancer ; 8(2)2020 08.
Article en En | MEDLINE | ID: mdl-32843493
In recent years, cell therapy technologies have resulted in impressive results in hematologic malignancies. Treatment of solid tumors with chimeric antigen receptor T-cells (CAR-T) has been less successful. Solid tumors present challenges not encountered with hematologic cancers, including high intra-tumoral pressure and ineffective CAR-T trafficking to the site of disease. Novel delivery methods may enable CAR-T therapies for solid tumor malignancies. A patient with liver metastases secondary to pancreatic adenocarcinoma received CAR-T targeting carcinoembryonic antigen (CEA). Previously we reported that Pressure-Enabled Drug Delivery (PEDD) enhanced CAR-T delivery to liver metastases 5.2-fold. Three doses of anti-CEA CAR-T were regionally delivered via hepatic artery infusion (HAI) using PEDD technology to optimize the therapeutic index. Interleukin-2 was systemically delivered by continuous intravenous infusion to support CAR-T in vivo. HAI of anti-CEA CAR-T was not associated with any serious adverse events (SAEs) above grade 3 and there were no on-target/off-tumor SAEs. Following CAR-T treatment, positron emission tomography-CT demonstrated a complete metabolic response within the liver, which was durable and sustained for 13 months. The response was accompanied by normalization of serum tumor markers and an abundance of CAR+ cells found within post-treatment tumor specimens. The findings from this report exhibit biologic activity and safety of regionally infused CAR-T for an indication with limited immune-oncology success to date. Further studies will determine how HAI of CAR-T may be included in multidisciplinary treatment plans for patients with liver metastases. ClinicalTrials.gov number, NCT02850536.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Hepáticas Límite: Humans / Male / Middle aged Idioma: En Revista: J Immunother Cancer Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Hepáticas Límite: Humans / Male / Middle aged Idioma: En Revista: J Immunother Cancer Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido