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R‐High‐CHOP/CHASER/LEED with autologous stem cell transplantation in newly diagnosed mantle cell lymphoma: JCOG0406 STUDY
Authors:Michinori Ogura  Kazuhito Yamamoto  Yasuo Morishima  Masashi Wakabayashi  Kensei Tobinai  Kiyoshi Ando  Naokuni Uike  Mitsutoshi Kurosawa  Hiroshi Gomyo  Masafumi Taniwaki  Kisato Nosaka  Norifumi Tsukamoto  Tatsu Shimoyama  Noriko Fukuhara  Yoshihiro Yakushijin  Kazunori Ohnishi  Kana Miyazaki  Kenichi Sawada  Nobuyuki Takayama  Ichiro Hanamura  Hirokazu Nagai  Hirofumi Kobayashi  Kensuke Usuki  Naoki Kobayashi  Kazuma Ohyashiki  Takahiko Utsumi  Kyoya Kumagai  Dai Maruyama  Ken Ohmachi  Yoshihiro Matsuno  Shigeo Nakamura  Tomomitsu Hotta  Kunihiro Tsukasaki  Japan Clinical Oncology Group‐ Lymphoma Study Group
Affiliation:1. Department of Hematology and Oncology, Kasugai Municipal Hospital, Kasugai, Japan;2. Department of Hematology and Oncology, Nagoya Daini Red Cross Hospital, Nagoya, Japan;3. Department of Hematology and Cell Therapy, Aichi Cancer Center Hospital, Nagoya, Japan;4. JCOG Data Center, National Cancer Center, Tokyo, Japan;5. Department of Hematology, National Cancer Center Hospital, Tokyo, Japan;6. Department of Hematology and Oncology, Tokai University School of Medicine, Isehara, Japan;7. Department of Hematology, National Kyushu Cancer Center, Fukuoka, Japan;8. Department of Hematology, National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan;9. Department of Hematology, Hyogo Cancer Center, Akashi, Japan;10. Center for Molecular Diagnostics and Therapeutics, Kyoto Prefectural University of Medicine, Kyoto, Japan;11. Department of Hematology, Kumamoto University Hospital, Kumamoto, Japan;12. Department of Hematology, Gunma University Hospital, Maebashi, Japan;13. Department of Medical Oncology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan;14. Department of Hematology, Tohoku University Hospital, Sendai, Japan;15. First Department of Internal Medicine, Ehime University Graduate School of Medicine, Toon, Japan;16. Department of Hematology, Hamamatsu University School of Medicine, Hamamatsu, Japan;17. Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan;18. Department of Hematology, Akita University Graduate School of Medicine and Faculty of Medicine, Akita, Japan;19. Second Department of Internal Medicine, Kyorin University School of Medicine, Tokyo, Japan;20. Division of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute, Japan;21. Department of Hematology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan;22. Department of Hematology, Saitama Cancer Center, Saitama, Japan;23. Department of Hematology, NTT Medical Center Tokyo, Shinagawa‐ku, Tokyo, Japan;24. Department of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan;25. Department of Hematology, Tokyo Medical University, Tokyo, Japan;26. Department of Hematology, Shiga General Hospital, Moriyama City, Japan;27. Department of Hematology, Chiba Cancer Center, Chiba, Japan;28. Department of Surgical Pathology, Hokkaido University Hospital, Sapporo, Japan;29. Department of Pathology, Nagoya University School of Medicine, Nagoya, Japan;30. Foundation for Promotion of Cancer Research, Tokyo, Japan;31. Department of Hematology, National Cancer Center Hospital East, Kashiwa, Japan
Abstract:Although induction immunochemotherapy including high‐dose cytarabine and rituximab followed by high‐dose chemotherapy (HDC) with autologous stem cell transplantation (ASCT) is recommended for younger patients (≤65 years old) with untreated mantle cell lymphoma (MCL), no standard induction and HDC regimen has been established. We conducted a phase II study of induction immunochemotherapy of R‐High‐CHOP/CHASER followed by HDC of LEED with ASCT in younger patients with untreated advanced MCL. Eligibility criteria included untreated MCL, stage II bulky to IV, and age 20‐65 years. Patients received 1 cycle of R‐High‐CHOP followed by 3 cycles of CHASER every 3 weeks. Peripheral blood stem cells (PBSC) were harvested during CHASER. LEED with ASCT was delivered to patients who responded to R‐High‐CHOP/CHASER. Primary endpoint was 2‐year progression‐free survival (PFS). From June 2008 to June 2012, 45 patients (median age 59 years; range 38‐65 years) were enrolled. PBSC were successfully harvested from 36 of 43 patients. Thirty‐five patients completed ASCT. Two‐year PFS was 77% (80% CI 68‐84), which met the primary endpoint. Five‐year PFS and overall survival were 52% (95% CI 34‐68%) and 71% (95% CI 51‐84%), respectively. Overall response and complete response rates after induction immunochemotherapy were 96% and 82%, respectively. The most common grade 4 toxicities were hematological. In younger patients with untreated MCL, R‐High‐CHOP/CHASER/LEED with ASCT showed high efficacy and acceptable toxicity, and it can now be considered a standard treatment option.
Keywords:autologous stem cell transplantation  cytarabine  high‐dose chemotherapy  mantle cell lymphoma  rituximab
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