TY - JOUR
T1 - R-High-CHOP/CHASER/LEED with autologous stem cell transplantation in newly diagnosed mantle cell lymphoma
T2 - JCOG0406 STUDY
AU - Japan Clinical Oncology Group- Lymphoma Study Group (JCOG-LSG)
AU - Ogura, Michinori
AU - Yamamoto, Kazuhito
AU - Morishima, Yasuo
AU - Wakabayashi, Masashi
AU - Tobinai, Kensei
AU - Ando, Kiyoshi
AU - Uike, Naokuni
AU - Kurosawa, Mitsutoshi
AU - Gomyo, Hiroshi
AU - Taniwaki, Masafumi
AU - Nosaka, Kisato
AU - Tsukamoto, Norifumi
AU - Shimoyama, Tatsu
AU - Fukuhara, Noriko
AU - Yakushijin, Yoshihiro
AU - Ohnishi, Kazunori
AU - Miyazaki, Kana
AU - Sawada, Kenichi
AU - Takayama, Nobuyuki
AU - Hanamura, Ichiro
AU - Nagai, Hirokazu
AU - Kobayashi, Hirofumi
AU - Usuki, Kensuke
AU - Kobayashi, Naoki
AU - Ohyashiki, Kazuma
AU - Utsumi, Takahiko
AU - Kumagai, Kyoya
AU - Maruyama, Dai
AU - Ohmachi, Ken
AU - Matsuno, Yoshihiro
AU - Nakamura, Shigeo
AU - Hotta, Tomomitsu
AU - Tsukasaki, Kunihiro
N1 - Funding Information:
Funding information This work was supported in part by the National Cancer Center Research and Development Fund (grant numbers 23-A-16, 23-A-17, 26-A-4, 29-A-3); and by the Ministry of Health, Labour and Welfare Grants-in-Aid for Cancer Research (grant numbers 16-6, 20S-1, 20S-6), and Health and Labour Sciences Research Grants for Clinical Cancer Research (grant numbers 19-27, 22-29) The authors are grateful to the pathologists Dr Koichi Ohshima and Dr Naoya Nakamura for their support with the Central Pathology Review, to Dr Satoko Shimada for immunohistochemical analysis of SOX11 and Ki-67, and to the members of the JCOG Data Center and JCOG Operations Office for their support in preparing the manuscript (Dr Kenichi Nakamura and Dr Kenichi Miyamoto), data management (Ms Yuko Watanabe), and oversight of study management (Dr Haruhiko Fukuda).
Publisher Copyright:
© 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
PY - 2018/9
Y1 - 2018/9
N2 - 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.
AB - 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.
KW - autologous stem cell transplantation
KW - cytarabine
KW - high-dose chemotherapy
KW - mantle cell lymphoma
KW - rituximab
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U2 - 10.1111/cas.13719
DO - 10.1111/cas.13719
M3 - Article
C2 - 29957865
AN - SCOPUS:85051079444
SN - 1347-9032
VL - 109
SP - 2830
EP - 2840
JO - Cancer Science
JF - Cancer Science
IS - 9
ER -