Your browser doesn't support javascript.
loading
Oncogenic and immunological targets for matched therapy of pediatric blood cancer patients: Dutch iTHER study experience.
Boer, Judith M; Ilan, Uri; Boeree, Aurélie; Langenberg, Karin P S; Koster, Jan; Koudijs, Marco J; Hehir-Kwa, Jayne Y; Nierkens, Stefan; Rossi, Corinne; Molenaar, Jan J; Goemans, Bianca F; den Boer, Monique L; Zwaan, C Michel.
Afiliação
  • Boer JM; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
  • Ilan U; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
  • Boeree A; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
  • Langenberg KPS; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
  • Koster J; Amsterdam UMC University of Amsterdam, Center for Experimental and Molecular Medicine, Laboratory of Experimental Oncology and Radiobiology Amsterdam The Netherlands.
  • Koudijs MJ; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
  • Hehir-Kwa JY; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
  • Nierkens S; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
  • Rossi C; Center for Translational Immunology UMC Utrecht Utrecht The Netherlands.
  • Molenaar JJ; Department of Pediatric Oncology, Hematology, and Immunology Heidelberg University Hospital Heidelberg Germany.
  • Goemans BF; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
  • den Boer ML; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
  • Zwaan CM; Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Hemasphere ; 8(7): e122, 2024 Jul.
Article em En | MEDLINE | ID: mdl-39011126
ABSTRACT
Over the past 10 years, institutional and national molecular tumor boards have been implemented for relapsed or refractory pediatric cancer to prioritize targeted drugs for individualized treatment based on actionable oncogenic lesions, including the Dutch iTHER platform. Hematological malignancies form a minority in precision medicine studies. Here, we report on 56 iTHER leukemia/lymphoma patients for which we considered cell surface markers and oncogenic aberrations as actionable events, supplemented with ex vivo drug sensitivity for six patients. Prior to iTHER registration, 34% of the patients had received allogeneic hematopoietic cell transplantation (HCT) and 18% CAR-T therapy. For 51 patients (91%), a sample with sufficient tumor percentage (≥20%) required for comprehensive diagnostic testing was obtained. Up to 10 oncogenic actionable events were prioritized in 49/51 patients, and immunotherapy targets were identified in all profiled patients. Targeted treatment(s) based on the iTHER advice was given to 24 of 51 patients (47%), including immunotherapy in 17 patients, a targeted drug matching an oncogenic aberration in 12 patients, and a drug based on ex vivo drug sensitivity in one patient, resulting in objective responses and a bridge to HCT in the majority of the patients. In conclusion, comprehensive profiling of relapsed/refractory hematological malignancies showed multiple oncogenic and immunotherapy targets for a precision medicine approach, which requires multidisciplinary expertise to prioritize the best treatment options for this rare, heavily pretreated pediatric population.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Hemasphere Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Hemasphere Ano de publicação: 2024 Tipo de documento: Article