TY - JOUR
T1 - VCAP-AMP-VECP as a preferable induction chemotherapy in transplant-eligible patients with aggressive adult T-cell leukemia-lymphoma
T2 - a propensity score analysis
AU - Fuji, Shigeo
AU - Yamaguchi, Takuhiro
AU - Inoue, Yoshitaka
AU - Utsunomiya, Atae
AU - Moriuchi, Yukiyoshi
AU - Owatari, Satsuki
AU - Miyagi, Takashi
AU - Sawayama, Yasushi
AU - Otsuka, Eiichi
AU - Yoshida, Shin ichiro
AU - Fukuda, Takahiro
N1 - Funding Information:
This research was partially supported by the Practical Research for Innovative Cancer Control from the Japan Agency for Medical Research and Development (17ck0106342h0001) and the National Cancer Research and Development Fund (29-A-14).
Funding Information:
Conflict of interest S.F. received honoraria from the Kyowa Hakko Kirin Co., Ltd.; T.Y. had ownership interests of Statcom Co., Ltd., received consulting fees from Ono Pharmaceutical Co., Ltd., honoraria from Taiho Pharmaceutical Co., Ltd., and research funding from Kyowa Hakko Kirin Co., Ltd.; and A.U. received honoraria from Kyowa Hakko Kirin, Daiichi Sankyo, Siemens, Bristol-Myers Squibb, Pfizer, Novartis Pharma, Nippon Shinyaku, Mundi Pharma, Chugai Pharma, Ono Pharmaceutical CO, Eisai, Celgene, JIMRO, and Otsuka Pharmaceutical.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - A dose-intensified multi-agent chemotherapy regimen called VCAP-AMP-VECP was investigated in Japan as front-line therapy for patients with adult T-cell leukemia-lymphoma (ATL). Although a prospective randomized controlled study showed that VCAP-AMP-VECP was superior to CHOP, the trial was rather small and no subsequent studies confirmed the benefit of VCAP-AMP-VECP over CHOP. We conducted a retrospective analysis of transplant-eligible patients with ATL who received only VCAP-AMP-VECP or CHOP, incorporating inverse probability of treatment weighting (IPTW) using propensity scoring. Overall, 947 and 513 patients were treated with VCAP-AMP-VECP and CHOP, respectively. The median follow-up of surviving patients was 1006 days. The crude probabilities of 2-year overall survival (OS) for patients in the VCAP-AMP-VECP and CHOP groups were 31.2% and 24.6%, respectively (P < 0.001). Stratified by risk group according to the modified ATL-prognostic index score at diagnosis, the crude probabilities of 2-year OS in the VCAP-AMP-VECP and CHOP groups were 39.8 and 45.0% in the low-risk group (P = 0.69), 32.2 and 21.6% in the intermediate-risk group (P < 0.001), and 17.2 and 6.2% in the high-risk group (P = 0.005). Our current analysis suggests that VCAP-AMP-VECP regimen is a preferable front-line therapy in patients with aggressive ATL in intermediate- and high-risk groups.
AB - A dose-intensified multi-agent chemotherapy regimen called VCAP-AMP-VECP was investigated in Japan as front-line therapy for patients with adult T-cell leukemia-lymphoma (ATL). Although a prospective randomized controlled study showed that VCAP-AMP-VECP was superior to CHOP, the trial was rather small and no subsequent studies confirmed the benefit of VCAP-AMP-VECP over CHOP. We conducted a retrospective analysis of transplant-eligible patients with ATL who received only VCAP-AMP-VECP or CHOP, incorporating inverse probability of treatment weighting (IPTW) using propensity scoring. Overall, 947 and 513 patients were treated with VCAP-AMP-VECP and CHOP, respectively. The median follow-up of surviving patients was 1006 days. The crude probabilities of 2-year overall survival (OS) for patients in the VCAP-AMP-VECP and CHOP groups were 31.2% and 24.6%, respectively (P < 0.001). Stratified by risk group according to the modified ATL-prognostic index score at diagnosis, the crude probabilities of 2-year OS in the VCAP-AMP-VECP and CHOP groups were 39.8 and 45.0% in the low-risk group (P = 0.69), 32.2 and 21.6% in the intermediate-risk group (P < 0.001), and 17.2 and 6.2% in the high-risk group (P = 0.005). Our current analysis suggests that VCAP-AMP-VECP regimen is a preferable front-line therapy in patients with aggressive ATL in intermediate- and high-risk groups.
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U2 - 10.1038/s41409-019-0446-z
DO - 10.1038/s41409-019-0446-z
M3 - Article
C2 - 30664725
AN - SCOPUS:85060329914
VL - 54
SP - 1399
EP - 1405
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
SN - 0268-3369
IS - 9
ER -