Thiotepa-based high-dose therapy for autologous stem cell transplantation in lymphoma: a retrospective study from the EBMT
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie, práce podpořená grantem
PubMed
26569093
DOI
10.1038/bmt.2015.273
PII: bmt2015273
Knihovny.cz E-zdroje
- MeSH
- autologní štěp MeSH
- cytarabin aplikace a dávkování MeSH
- dospělí MeSH
- karmustin aplikace a dávkování MeSH
- lidé středního věku MeSH
- lidé MeSH
- lymfom mortalita terapie MeSH
- melfalan aplikace a dávkování MeSH
- míra přežití MeSH
- mladiství MeSH
- podofylotoxin aplikace a dávkování MeSH
- přežití bez známek nemoci MeSH
- protokoly protinádorové kombinované chemoterapie aplikace a dávkování MeSH
- registrace * MeSH
- retrospektivní studie MeSH
- senioři MeSH
- thiotepa aplikace a dávkování MeSH
- transplantace kmenových buněk * MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cytarabin MeSH
- karmustin MeSH
- melfalan MeSH
- podofylotoxin MeSH
- thiotepa MeSH
Clinical information about thiotepa-based autologous stem cell transplantation (auto-SCT) outside the primary central nervous system lymphoma (PCNSL) field is sparse. In this registry-based retrospective study, we evaluated potential risks and benefits of thiotepa-based preparative regimens compared with BEAM (carmustine, etoposide, cytarabine, melphalan) in auto-SCT for diffuse large B-cell lymphoma (DLBCL, excluding PCNSL), follicular lymphoma (FL) or Hodgkin lymphoma (HL). A total of 14 544 patients (589 thiotepa and 13 955 BEAM) met the eligibility criteria, and 535 thiotepa- and 1031 BEAM-treated patients were matched in a 1:2 ratio for final comparison. No significant differences between thiotepa and BEAM groups for any survival end point were identified in the whole sample or disease entity subsets. For a more detailed analysis, 47 TEAM (thiotepa, etoposide, cytarabine, melphalan)-treated patients were compared with 75 matched BEAM patients with additional collection of toxicity data. Again, there were no significant differences between the two groups for any survival end point. In addition, the frequency of common infectious and non-infectious complications including secondary malignancies was comparable between TEAM and BEAM. These results indicate that thiotepa-based high-dose therapy might be a valuable alternative to BEAM in DLBCL, HL and FL. Further evaluation by prospective clinical trials is warranted.
APHP Hopital Saint louis Hemato Oncology Paris Diderot University Sorbonne Paris Cité Paris France
Cardarelli Hospital Napoli Italy
Department of Hematology and Oncology Helios Hospital Erfurt Erfurt Germany
Department of Hematology Azienda Ospedali Riuniti Villa Sofia Cervello Palermo Italy
Department of Hematology Freiburg University Medical Center Freiburg Germany
Department of Hematology Pitié Salpêtrière Hospital Paris France
Department of Medicine 5 University Hospital Heidelberg Heidelberg Germany
Hematologie Hospices Civils de Lyon and Université Claude Bernard Lyon 1 Pierre Bénite France
Hematology Department Centre Leon Berard Lyon France
Hematology Department Paoli Calmettes Institute Marseille Aix Marseille University Marseille France
Hematology Unit Arcispedale S Maria Nuova IRCCS Reggio Emilia Italy
Hematology Unit Ospedale Civile Piacenza Italy
Hematology Unit S Maria delle Croci Hospital Ravenna Italy
Institut Català d'Oncologia Hospital Duran i Reynals Barcelona Spain
Lymphoma Working Party European Society for Blood and Marrow Transplantation Paris France
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