Upfront autologous stem-cell transplantation with melphalan, cyclophosphamide, etoposide, and dexamethasone (LEED) in patients with newly diagnosed primary central nervous system lymphoma

Kotaro Miyao, Reona Sakemura, Kanae Imai, Toshiyasu Sakai, Natsuko Tsushita, Tomonori Kato, Keiko Niimi, Yoshitaka Ono, Masashi Sawa

Research output: Contribution to journalArticlepeer-review

Abstract

Treatment of primary central nervous system lymphoma (PCNSL) improved in recent years. However, the high neurotoxicity and low survival rates associated with this condition remain unresolved. We report 13 consecutive patients with PCNSL for whom upfront melphalan, cyclophosphamide, etoposide, and dexamethasone (known as LEED) followed by autologous stem-cell transplantation (ASCT) was planned at the Anjo Kosei Hospital. All patients were pathologically diagnosed with diffuse large B-cell lymphoma and were negative for human immunodeficiency virus. All patients were to receive three cycles of high-dose methotrexate-based induction chemotherapy, two cycles of high-dose AraC-based chemotherapy, and LEED followed by ASCT. All 13 patients achieved a partial response, and the 3-year overall survival (OS) rate was 76.2 %. Seven of the 13 patients were alive at the last follow-up, without any adverse events, including neurotoxicity. Six of the 13 (46.2 %) patients underwent ASCT and the 3-year OS rate was 80.0 %. Although this study included only a limited number of patients, these preliminary signs of efficacy and tolerability merit further consideration. To make further improvements in survival, the rate of patients undergoing ASCT should be increased. Other prospective studies involving greater numbers of patients are required to confirm these findings.

Original languageEnglish (US)
Pages (from-to)152-158
Number of pages7
JournalInternational journal of hematology
Volume100
Issue number2
DOIs
StatePublished - Aug 2014

Keywords

  • LEED
  • PCNSL
  • Upfront autologous stem-cell transplantation

ASJC Scopus subject areas

  • Hematology

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