Tazemetostat in the therapy of pediatric INI1-negative malignant rhabdoid tumors

. 2023 Dec 07 ; 13 (1) : 21623. [epub] 20231207

Jazyk angličtina Země Anglie, Velká Británie Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid38062114

Grantová podpora
NU20-03-00240 Ministry of Health of the Czech Republic
NU20-03-00240 Ministry of Health of the Czech Republic
NU20-03-00240 Ministry of Health of the Czech Republic
NU20-03-00240 Ministry of Health of the Czech Republic
NU20-03-00240 Ministry of Health of the Czech Republic
NU20-03-00240 Ministry of Health of the Czech Republic
NU20-03-00240 Ministry of Health of the Czech Republic
NU20-03-00240 Ministry of Health of the Czech Republic
FNBr, 65269705 Ministry of Health of the Czech Republic - DRO
FNBr, 65269705 Ministry of Health of the Czech Republic - DRO
FNBr, 65269705 Ministry of Health of the Czech Republic - DRO
FNBr, 65269705 Ministry of Health of the Czech Republic - DRO
FNBr, 65269705 Ministry of Health of the Czech Republic - DRO
FNBr, 65269705 Ministry of Health of the Czech Republic - DRO
MUNI/A/1395/2022 Specific University Research provided by MEYS
MUNI/A/1395/2022 Specific University Research provided by MEYS
MUNI/A/1395/2022 Specific University Research provided by MEYS
MUNI/A/1395/2022 Specific University Research provided by MEYS
LX22NPO5102 National Institute for Cancer Research (Programme EXCELES)
LX22NPO5102 National Institute for Cancer Research (Programme EXCELES)
LX22NPO5102 National Institute for Cancer Research (Programme EXCELES)

Odkazy

PubMed 38062114
PubMed Central PMC10703767
DOI 10.1038/s41598-023-48774-2
PII: 10.1038/s41598-023-48774-2
Knihovny.cz E-zdroje

Rhabdoid tumors are aggressive tumors that may arise in the kidney, soft tissue, central nervous system, or other organs. They are defined by SMARCB1 (INI1) or SMARCA4 alterations. Often, very young children are affected, and the prognosis is dismal. Four patients with primary atypical teratoid rhabdoid tumor (AT/RT, a rhabdoid tumor in the central nervous system) were treated by resection and high dose chemotherapy. Tazemetostat was introduced after completion of chemotherapy. Three patients have achieved an event free survival of 32, 34, and 30 months respectively. One progressed and died. His overall survival was 20 months. One patient was treated for a relapsed atypical teratoid rhabdoid tumor. The treatment combined metronomic therapy, radiotherapy, tazemetostat and immunotherapy. This patient died of disease progression, with an overall survival of 37 months. One patient was treated for a rhabdoid tumor of the ovary. Tazemetostat was given as maintenance after resection, chemotherapy, and radiotherapy, concomitantly with immunotherapy. Her event free survival is 44 months. Only approximately 40% of patients with rhabdoid tumors achieve long-term survival. Nearly all relapses occur within two years from diagnosis. The event free survival of four of the six patients in our cohort has exceeded this timepoint. Tazemetostat has been mostly tested as a single agent in the relapsed setting. We present promising results when applied as maintenance or add on in the first line treatment.

Zobrazit více v PubMed

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