Venetoclax plus cyclophosphamide and topotecan in heavily pre-treated relapsed metastatic neuroblastoma: a single center case series

The prognosis of relapsed/refractory (R/R) neuroblastoma (NB) is dismal, calling for new therapeutic strategies. Venetoclax (VEN) is a highly selective, potent, orally bioavailable, BCL-2 inhibitor small-molecule that showed a synergistic effect with cyclophosphamide and topotecan (Cy-Topo) in murin...

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Veröffentlicht in:Scientific reports 2023-11, Vol.13 (1), p.19295-19295, Article 19295
Hauptverfasser: De Ioris, Maria Antonietta, Fabozzi, Francesco, Del Bufalo, Francesca, Del Baldo, Giada, Villani, Maria Felicia, Cefalo, Maria Giuseppina, Garganese, Maria Carmen, Stracuzzi, Alessandra, Tangari, Federica, Greco, Arturo Maria, Giovannoni, Isabella, Carta, Roberto, D’Andrea, Maria Luisa, Mastronuzzi, Angela, Locatelli, Franco
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Sprache:eng
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Zusammenfassung:The prognosis of relapsed/refractory (R/R) neuroblastoma (NB) is dismal, calling for new therapeutic strategies. Venetoclax (VEN) is a highly selective, potent, orally bioavailable, BCL-2 inhibitor small-molecule that showed a synergistic effect with cyclophosphamide and topotecan (Cy-Topo) in murine NB models. Our aim was to evaluate the feasibility of VEN plus Cy-Topo in children with R/R NB. Four patients, who had previously failed > 3 lines of treatment, were treated with VEN plus Cy-Topo based on a 28-day schedule in an outpatient setting. BCL-2 expression in immunochemistry on tumor samples at relapse and the BCL2 gene status was evaluated in all patients. The main toxicity was hematological, with grade 4 neutropenia and thrombocytopenia occurring in all courses and leading to transient VEN discontinuation. Grade 3 oral mucositis was observed in 1/8 courses. No other grade 2–4 toxicities were observed. BCL-2 was expressed in all tumors, while no molecular abnormalities in the BCL-2 genes were detected. A stable disease was observed in all patients, without any progression during the study period. VEN plus Cy-Topo is well tolerated, with encouraging results that may be improved by testing the schedule in less advanced patients.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-023-44993-9