TY - JOUR
T1 - Efficacy of upfront high-dose chemotherapy plus rituximab followed by autologous peripheral blood stem cell transplantation for untreated high-intermediate-, and high-risk diffuse large B-cell lymphoma
T2 - a multicenter prospective phase II study (JSCT-NHL04)
AU - Murayama, Tohru
AU - Fukuda, Takahiro
AU - Okumura, Hirokazu
AU - Sunami, Kazutaka
AU - Sawazaki, Aiko
AU - Maeda, Yoshinobu
AU - Tsurumi, Hisashi
AU - Uike, Naokuni
AU - Hidaka, Tomonori
AU - Takatsuka, Yoshifusa
AU - Eto, Tetsuya
AU - Tsuda, Hiroyuki
AU - Fujisaki, Tomoaki
AU - Miyamoto, Toshihiro
AU - Tsuneyoshi, Naoko
AU - Iyama, Satoshi
AU - Nagafuji, Koji
AU - Harada, Mine
N1 - Funding Information:
This work was supported by a Grant from the Regional Medicine Research Foundation (Tochigi, Japan).
Publisher Copyright:
© 2016, The Japanese Society of Hematology.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - To evaluate the efficacy and feasibility of upfront high-dose chemotherapy (HDCT) and rituximab (R) followed by autologous peripheral blood stem cell transplantation (auto-PBSCT) in patients with newly diagnosed high-intermediate(HI)-, and high(H)-risk diffuse large B-cell lymphoma (DLBCL), we conducted a multicenter prospective phase II trial. In 15–60-year-old patients with H- or HI-risk DLBCL, after three courses of (R-)CHOP14, high-dose etoposide was given prior to peripheral blood stem cell harvesting. After an additional three courses of (R-)CHOP14, auto-PBSCT was performed following HDCT. The primary endpoint of the study is progression-free survival (PFS) at 2 years after registration in eligible patients. The expected PFS and the threshold PFS were estimated to be 70 and 50 %, respectively. Among 40 eligible patients registered, 30 patients completed treatment. With a median observation period in surviving eligible patients of 63 months, the 2- and 4-year PFS after registration were 79.9 and 72.0 %, respectively. The 2- and 4-year overall survival (OS) were 92.5 and 84.6 %, respectively. In 30 patients who completed treatment, the 4-year PFS and OS after auto-PBSCT were 79.2 and 85.9 %, respectively. In conclusion, the results of our study suggest that upfront HDCT and auto-PBSCT combined with rituximab is highly effective as an initial treatment for HI-, and H-risk DLBCL.
AB - To evaluate the efficacy and feasibility of upfront high-dose chemotherapy (HDCT) and rituximab (R) followed by autologous peripheral blood stem cell transplantation (auto-PBSCT) in patients with newly diagnosed high-intermediate(HI)-, and high(H)-risk diffuse large B-cell lymphoma (DLBCL), we conducted a multicenter prospective phase II trial. In 15–60-year-old patients with H- or HI-risk DLBCL, after three courses of (R-)CHOP14, high-dose etoposide was given prior to peripheral blood stem cell harvesting. After an additional three courses of (R-)CHOP14, auto-PBSCT was performed following HDCT. The primary endpoint of the study is progression-free survival (PFS) at 2 years after registration in eligible patients. The expected PFS and the threshold PFS were estimated to be 70 and 50 %, respectively. Among 40 eligible patients registered, 30 patients completed treatment. With a median observation period in surviving eligible patients of 63 months, the 2- and 4-year PFS after registration were 79.9 and 72.0 %, respectively. The 2- and 4-year overall survival (OS) were 92.5 and 84.6 %, respectively. In 30 patients who completed treatment, the 4-year PFS and OS after auto-PBSCT were 79.2 and 85.9 %, respectively. In conclusion, the results of our study suggest that upfront HDCT and auto-PBSCT combined with rituximab is highly effective as an initial treatment for HI-, and H-risk DLBCL.
KW - Autologous peripheral blood stem cell transplantation
KW - CHOP14
KW - Diffuse large B-cell lymphoma
KW - High-dose chemotherapy
KW - Rituximab
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U2 - 10.1007/s12185-016-1976-4
DO - 10.1007/s12185-016-1976-4
M3 - Article
C2 - 27084252
AN - SCOPUS:84963766464
SN - 0925-5710
VL - 103
SP - 676
EP - 685
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 6
ER -