Your browser doesn't support javascript.
loading
RVD induction and autologous stem cell transplantation followed by lenalidomide maintenance in newly diagnosed multiple myeloma: a phase 2 study of the Finnish Myeloma Group.
Luoma, Sini; Anttila, Pekka; Säily, Marjaana; Lundan, Tuija; Heiskanen, Jouni; Siitonen, Timo; Kakko, Sakari; Putkonen, Mervi; Ollikainen, Hanna; Terävä, Venla; Sankelo, Marja; Partanen, Anu; Launonen, Kirsi; Räsänen, Anu; Sikiö, Anu; Suominen, Merja; Bazia, Piotr; Kananen, Kristiina; Lievonen, Juha; Selander, Tuomas; Pelliniemi, Tarja-Terttu; Ilveskero, Sorella; Huotari, Virva; Mäntymaa, Pentti; Tienhaara, Anri; Jantunen, Esa; Silvennoinen, Raija.
Afiliação
  • Luoma S; Comprehensive Cancer Center, Department of Hematology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland. sini.luoma@hus.fi.
  • Anttila P; Comprehensive Cancer Center, Department of Hematology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
  • Säily M; Hematology-Oncology Unit, Oulu University Hospital, Oulu, Finland.
  • Lundan T; Department of Clinical Chemistry and TYKSLAB, University of Turku and Turku University Hospital, Turku, Finland.
  • Heiskanen J; Comprehensive Cancer Center, Department of Hematology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
  • Siitonen T; Hematology-Oncology Unit, Oulu University Hospital, Oulu, Finland.
  • Kakko S; Hematology-Oncology Unit, Oulu University Hospital, Oulu, Finland.
  • Putkonen M; Hematology Unit, Turku University Hospital, Turku, Finland.
  • Ollikainen H; Department of Medicine, Satakunta Central Hospital, Pori, Finland.
  • Terävä V; Hematology Unit, Tampere University Hospital, Tampere, Finland.
  • Sankelo M; Hematology Unit, Tampere University Hospital, Tampere, Finland.
  • Partanen A; Department of Medicine, Kuopio University Hospital, Kuopio, Finland.
  • Launonen K; Department of Medicine, Mikkeli Central Hospital, Mikkeli, Finland.
  • Räsänen A; Hematology-Oncology Unit, Oulu University Hospital, Oulu, Finland.
  • Sikiö A; Department of Medicine, Länsi-Pohja Central Hospital, Kemi, Finland.
  • Suominen M; Department of Medicine, Kymenlaakso Central Hospital, Kotka, Finland.
  • Bazia P; Department of Medicine, Central Finland Central Hospital, Jyväskylä, Finland.
  • Kananen K; Department of Medicine, Kanta-Häme Central Hospital, Hämeenlinna, Finland.
  • Lievonen J; Department of Medicine, Kainuu Central Hospital, Kajaani, Finland.
  • Selander T; Department of Medicine, Kainuu Central Hospital, Kajaani, Finland.
  • Pelliniemi TT; Comprehensive Cancer Center, Department of Hematology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
  • Ilveskero S; Science Service Center, Kuopio University Hospital, Kuopio, Finland.
  • Huotari V; Fimlab Laboratories Ltd., Tampere, Finland.
  • Mäntymaa P; HUSLAB Helsinki University Hospital, Helsinki, Finland.
  • Tienhaara A; Fimlab Laboratories Ltd., Tampere, Finland.
  • Jantunen E; NordLab Oulu, Oulu University Hospital, Oulu, Finland.
  • Silvennoinen R; Laboratory of Eastern Finland, Kuopio University Hospital, Kuopio, Finland.
Ann Hematol ; 98(12): 2781-2792, 2019 Dec.
Article em En | MEDLINE | ID: mdl-31673775
ABSTRACT
Autologous stem cell transplantation (ASCT) combined with novel agents is the standard treatment for transplant-eligible, newly diagnosed myeloma (NDMM) patients. Lenalidomide is approved for maintenance after ASCT until progression, although the optimal duration of maintenance is unknown. In this trial, 80 patients with NDMM received three cycles of lenalidomide, bortezomib, and dexamethasone followed by ASCT and lenalidomide maintenance until progression or toxicity. The primary endpoint was the proportion of flow-negative patients. Molecular response was assessed if patients were flow-negative or in stringent complete response (sCR). By intention to treat, the overall response rate was 89%. Neither median progression-free survival nor overall survival (OS) has been reached. The OS at 3 years was 83%. Flow-negativity was reached in 53% and PCR-negativity in 28% of the patients. With a median follow-up of 27 months, 29 (36%) patients are still on lenalidomide and 66% of them have sustained flow-negativity. Lenalidomide maintenance phase was reached in 8/16 high-risk patients but seven of them have progressed after a median of only 6 months. In low- or standard-risk patients, the outcome was promising, but high-risk patients need more effective treatment approach. Flow-negativity with the conventional flow was an independent predictor for longer PFS.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco / Quimioterapia de Manutenção / Lenalidomida / Mieloma Múltiplo Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Ann Hematol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco / Quimioterapia de Manutenção / Lenalidomida / Mieloma Múltiplo Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Ann Hematol Ano de publicação: 2019 Tipo de documento: Article