CHOP or THP‐COP regimens in the treatment of newly diagnosed peripheral T‐cell lymphoma,not otherwise specified: a comparison of doxorubicin and pirarubicin |
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Authors: | Yuhei Shibata Takeshi Hara Senji Kasahara Toshiki Yamada Michio Sawada Ryoko Mabuchi Takuro Matsumoto Nobuhiko Nakamura Hiroshi Nakamura Soranobu Ninomiya Junichi Kitagawa Nobuhiro Kanemura Yusuke Kito Naoe Goto Tatsuhiko Miyazaki Tsuyoshi Takami Tamotsu Takeuchi Masahito Shimizu Hisashi Tsurumi |
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Affiliation: | 1. Department of Hematology, Gifu University Graduate School of Medicine, Gifu, Japan;2. Department of Hematology, Gifu Municipal Hospital, Gifu, Japan;3. Department of Hematology, Gifu Prefectural General Medical Center, Gifu, Japan;4. Department of Hematology, Japanese Red Cross Gifu Hospital, Gifu, Japan;5. Department of Internal Medicine, Kisogawa Municipal Hospital, Gifu, Japan;6. Department of Pathology and Translational Research, Gifu University Graduate School of Medicine, Gifu, Japan;7. Pathology Division, Gifu University Hospital, Gifu, Japan |
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Abstract: | The CHOP regimen consisting of cyclophosphamide, doxorubicin (DOX), vincristine and prednisolone has been the most used regimen for peripheral T‐cell lymphoma, not otherwise specified (PTCL‐NOS). Pirarubicin [tetrahydropyranyladriamycin (THP)], a derivative of DOX, is an anthracycline with reportedly less cardiotoxicity than DOX. Here, we confirmed the efficacy of THP‐COP using THP instead of DOX in the treatment of PTCL‐NOS. The study protocol employed a retrospective, consecutive entry design. We retrospectively analysed 56 patients with PTCL‐NOS who had received THP‐COP or CHOP. These regimens were performed every 21 days. Twenty‐nine patients received THP‐COP, and 27 received CHOP. There were no significant differences in known prognostic factors, including in the International Prognostic Index (IPI) and the prognostic index for T‐cell lymphoma (PIT), between the two groups. Complete remission rates in patients with THP‐COP and CHOP were 52% in both groups; the 3‐year overall survival (OS) rates were 67% and 52% (p = 0.074), and the 3‐year progression‐free survival (PFS) rates were 51% and 29% (p = 0.070), respectively. In patients with low IPI (low or low‐intermediate), THP‐COP had significantly better 3‐year OS (100% vs. 64%; p < 0.001) and 3‐year PFS (75% vs. 33%; p < 0.05) than CHOP. Similar differences between THP‐COP and CHOP were observed in patients with a low PIT (groups 1 or 2). Our study showed that THP‐COP produced results equivalent to CHOP regarding efficacy and safety in patients with PTCL‐NOS. In patients with low IPI or PIT, THP‐COP resulted in significantly better prognosis. Copyright © 2015 John Wiley & Sons, Ltd. |
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Keywords: | peripheral T‐cell lymphoma not otherwise specified (PTCL‐NOS) non‐Hodgkin's lymphoma pirarubicin doxorubicin |
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