論文

査読有り 国際誌
2020年4月

Rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone combined with high-dose methotrexate plus intrathecal chemotherapy for newly diagnosed intravascular large B-cell lymphoma (PRIMEUR-IVL): a multicentre, single-arm, phase 2 trial

The Lancet Oncology
  • Kazuyuki Shimada
  • Motoko Yamaguchi
  • Yoshiko Atsuta
  • Kosei Matsue
  • Keijiro Sato
  • Shigeru Kusumoto
  • Hirokazu Nagai
  • Jun Takizawa
  • Noriko Fukuhara
  • Koji Nagafuji
  • Kana Miyazaki
  • Eiichi Ohtsuka
  • Masataka Okamoto
  • Yasumasa Sugita
  • Toshiki Uchida
  • Satoshi Kayukawa
  • Atsushi Wake
  • Daisuke Ennishi
  • Yukio Kondo
  • Tohru Izumi
  • Yoshihiro Kin
  • Kunihiro Tsukasaki
  • Daigo Hashimoto
  • Masaaki Yuge
  • Atsumi Yanagisawa
  • Yachiyo Kuwatsuka
  • Satoko Shimada
  • Yasufumi Masaki
  • Nozomi Niitsu
  • Hitoshi Kiyoi
  • Ritsuro Suzuki
  • Takashi Tokunaga
  • Shigeo Nakamura
  • Tomohiro Kinoshita
  • 全て表示

21
4
開始ページ
593
終了ページ
602
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/s1470-2045(20)30059-0
出版者・発行元
Elsevier BV

BACKGROUND: Intravascular large B-cell lymphoma (IVLBCL) is a rare disease for which there is no available standard treatment. We aimed to ascertain the safety and activity of R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone) with high-dose methotrexate and intrathecal chemotherapy as CNS-oriented therapy for patients with previously untreated IVLBCL. METHODS: PRIMEUR-IVL is a multicentre, single-arm, phase 2 trial at 22 hospitals in Japan. Eligible patients had untreated histologically confirmed IVLBCL, were aged 20-79 years, had an Eastern Cooperative Group performance status of 0-3, and had no apparent CNS involvement at diagnosis. Patients received three cycles of R-CHOP (rituximab 375 mg/m2 intravenously on day 1 [except cycle one, which was on day 8]; cyclophosphamide 750 mg/m2, doxorubicin 50 mg/m2, and vincristine 1·4 mg/m2 [maximum 2·0 mg] intravenously on day 1 of cycle one and day 2 of cycles two and three; and prednisolone 100 mg/day orally on days 1-5 of cycle one and days 2-6 of cycles two and three) followed by two cycles of rituximab with high-dose methotrexate (3·5 g/m2 intravenously on day 2 of cycles four and five) every 2 weeks and three additional cycles of R-CHOP. Intrathecal chemotherapy (methotrexate 15 mg, cytarabine 40 mg, and prednisolone 10 mg) was administered four times during the R-CHOP phase. The primary endpoint was 2-year progression-free survival. Efficacy analyses were done in all enrolled patients; safety analyses were done in all enrolled and treated patients. The trial is registered in the UMIN Clinical Trials Registry (UMIN000005707) and the Japan Registry of Clinical Trials (jRCTs041180165); the trial is ongoing for long-term follow-up. FINDINGS: Between June 16, 2011, and July 21, 2016, 38 patients were enrolled, of whom 37 were eligible; one patient was excluded because of a history of testicular lymphoma. Median follow-up was 3·9 years (IQR 2·5-5·5). 2-year progression-free survival was 76% (95% CI 58-87). The most frequent adverse events of grade 3-4 were neutropenia and leucocytopenia, which were reported in all 38 (100%) patients. Serious adverse events were hypokalaemia, febrile neutropenia with hypotension, hypertension, and intracerebral haemorrhage (reported in one [3%] patient each). No treatment-related deaths occurred during protocol treatment. INTERPRETATION: R-CHOP combined with rituximab and high-dose methotrexate plus intrathecal chemotherapy is a safe and active treatment for patients with IVLBCL without apparent CNS involvement at diagnosis, and this regimen warrants future investigation. FUNDING: The Japan Agency for Medical Research and Development, the Center for Supporting Hematology-Oncology Trials, and the National Cancer Center.

リンク情報
DOI
https://doi.org/10.1016/s1470-2045(20)30059-0
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32171071
ID情報
  • DOI : 10.1016/s1470-2045(20)30059-0
  • ISSN : 1470-2045
  • PubMed ID : 32171071

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