論文

査読有り 国際誌
2018年9月

Final analysis of the JALSG Ph+ALL202 study: tyrosine kinase inhibitor-combined chemotherapy for Ph+ALL.

Annals of hematology
  • Yoshihiro Hatta
  • Shuichi Mizuta
  • Keitaro Matsuo
  • Shigeki Ohtake
  • Masako Iwanaga
  • Isamu Sugiura
  • Noriko Doki
  • Heiwa Kanamori
  • Yasunori Ueda
  • Chikamasa Yoshida
  • Nobuaki Dobashi
  • Tomoya Maeda
  • Toshiaki Yujiri
  • Fumihiko Monma
  • Yoshikazu Ito
  • Fumihiko Hayakawa
  • Jin Takeuchi
  • Hitoshi Kiyoi
  • Yasushi Miyazaki
  • Tomoki Naoe
  • 全て表示

97
9
開始ページ
1535
終了ページ
1545
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1007/s00277-018-3323-8

The Japan Adult Leukemia Study Group (JALSG) Ph+ALL202 study reported a high complete remission (CR) rate for Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL) patients treated with imatinib-combined chemotherapy. However, the long-term treatment efficacy remains uncertain. Here, we report a final analysis of the JALSG Ph+ALL202 study. The outcomes were compared with those of the JALSG ALL93 and ALL97 studies, which were conducted in the pre-imatinib era. Ninety-nine newly diagnosed Ph+ALL patients were enrolled in Ph+ALL202 (median age, 45 years; median follow-up, 4.5 years). CR was achieved in 96/99 (97%) patients. Fifty-nine of these 96 patients (61%) underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT) in their first CR (CR1). The 5-year overall and disease-free survival (DFS) rates were 50 and 43%, respectively, which were significantly higher compared to those in the pre-imatinib era (15 and 19%, respectively). Multivariate analysis revealed that imatinib administration, allo-HSCT in CR1, and a white blood cell count < 30 × 109/L were favorable independent prognostic factors for long-term DFS. Improved odds of receiving allo-HSCT and a lower relapse rate leaded to good long-term outcomes. The 3-year DFS tended to be higher in PCR-negative than that in PCR-positive patients (29 vs. 14%) in the non-HSCT patients, and this tendency was also seen in the allo-HSCT patients (59 vs. 50%). The higher rate of CR upon imatinib use may have contributed to these improvements.

リンク情報
DOI
https://doi.org/10.1007/s00277-018-3323-8
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/29694642
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097750
ID情報
  • DOI : 10.1007/s00277-018-3323-8
  • PubMed ID : 29694642
  • PubMed Central 記事ID : PMC6097750

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