Tazemetostat in the therapy of pediatric INI1-negative malignant rhabdoid tumors
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
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)
PubMed
38062114
PubMed Central
PMC10703767
DOI
10.1038/s41598-023-48774-2
PII: 10.1038/s41598-023-48774-2
Knihovny.cz E-zdroje
- MeSH
- dítě MeSH
- DNA-helikasy MeSH
- gen SMARCB1 MeSH
- jaderné proteiny MeSH
- kojenec MeSH
- lidé MeSH
- lokální recidiva nádoru farmakoterapie MeSH
- nádory centrálního nervového systému * patologie MeSH
- předškolní dítě MeSH
- rhabdoidní nádor * farmakoterapie patologie MeSH
- teratom * patologie MeSH
- transkripční faktory MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- DNA-helikasy MeSH
- gen SMARCB1 MeSH
- jaderné proteiny MeSH
- SMARCA4 protein, human MeSH Prohlížeč
- tazemetostat MeSH Prohlížeč
- transkripční faktory MeSH
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.
Department of Pharmacology and Toxicology Faculty of Pharmacy Masaryk University 62500 Brno Czechia
Department of Pharmacology Faculty of Medicine Masaryk University 62500 Brno Czechia
Zobrazit více v PubMed
Geller JI, Roth JJ, Biegel JA. Biology and treatment of rhabdoid tumor. Crit. Rev. Oncog. 2015;20:199–216. doi: 10.1615/CritRevOncog.2015013566. PubMed DOI PMC
Nesvick CL, Lafay-Cousin L, Raghunathan A, Bouffet E, Huang AA, Daniels DJ. Atypical teratoid rhabdoid tumor: Molecular insights and translation to novel therapeutics. J. Neurooncol. 2020;150:47–56. doi: 10.1007/s11060-020-03639-w. PubMed DOI PMC
Kim KH, Roberts CW. Mechanisms by which SMARCB1 loss drives rhabdoid tumor growth. Cancer Genet. 2014;207:365–372. doi: 10.1016/j.cancergen.2014.04.004. PubMed DOI PMC
Kuntz KW, et al. The importance of being me: Magic methyls, methyltransferase inhibitors, and the discovery of tazemetostat. J. Med. Chem. 2016;59:1556–1564. doi: 10.1021/acs.jmedchem.5b01501. PubMed DOI
Gounder M, et al. Tazemetostat in advanced epithelioid sarcoma with loss of INI1/SMARCB1: An international, open-label, phase 2 basket study. Lancet Oncol. 2020;21:1423–1432. doi: 10.1016/S1470-2045(20)30451-4. PubMed DOI
Morschhauser F, et al. Tazemetostat for patients with relapsed or refractory follicular lymphoma: An open-label, single-arm, multicentre, phase 2 trial. Lancet Oncol. 2020;21:1433–1442. doi: 10.1016/S1470-2045(20)30441-1. PubMed DOI PMC
Reddy AT, et al. Efficacy of high-dose chemotherapy and three-dimensional conformal radiation for atypical teratoid/rhabdoid tumor: A report from the children's oncology group trial ACNS0333. J. Clin. Oncol. 2020;38:1175–1185. doi: 10.1200/JCO.19.01776. PubMed DOI PMC
Nemes K, et al. Infants and newborns with atypical teratoid rhabdoid tumors (ATRT) and extracranial malignant rhabdoid tumors (eMRT) in the EU-RHAB Registry: A unique and challenging population. Cancers. 2022;14:2185. doi: 10.3390/cancers14092185. PubMed DOI PMC
Slavc I, et al. Improved long-term survival of patients with recurrent medulloblastoma treated with a "MEMMAT-like" metronomic antiangiogenic approach. Cancers. 2022;14:5128. doi: 10.3390/cancers14205128. PubMed DOI PMC
Ferrari A, et al. Paediatric non-rhabdomyosarcoma soft tissue sarcomas: The prospective NRSTS 2005 study by the European pediatric soft tissue sarcoma study group (EpSSG) Lancet Child Adolesc. Health. 2021;5:546–558. doi: 10.1016/S2352-4642(21)00159-0. PubMed DOI
Frühwald MC, et al. Age and DNA methylation subgroup as potential independent risk factors for treatment stratification in children with atypical teratoid/rhabdoid tumors. Neuro. Oncol. 2020;22:1006–1017. doi: 10.1093/neuonc/noz244. PubMed DOI PMC
Steinbügl M, et al. Clinical evidence for a biological effect of epigenetically active decitabine in relapsed or progressive rhabdoid tumors. Pediatr Blood Cancer. 2021;68:e29267. doi: 10.1002/pbc.29267. PubMed DOI
Witkowski L, et al. The influence of clinical and genetic factors on patient outcome in small cell carcinoma of the ovary, hypercalcemic type. Gynecol. Oncol. 2016;141:454–460. doi: 10.1016/j.ygyno.2016.03.013. PubMed DOI PMC