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R-THP-COP versus R-CHOP in patients younger than 70 years with untreated diffuse large B cell lymphoma: A randomized, open-label, noninferiority phase 3 trial.
Hara, Takeshi; Yoshikawa, Takeshi; Goto, Hideko; Sawada, Michio; Yamada, Toshiki; Fukuno, Kenji; Kasahara, Senji; Shibata, Yuhei; Matsumoto, Takuro; Mabuchi, Ryoko; Nakamura, Nobuhiko; Nakamura, Hiroshi; Ninomiya, Soranobu; Kitagawa, Junichi; Kanemura, Nobuhiro; Nannya, Yasuhito; Katsumura, Naoki; Takahashi, Takeshi; Kito, Yusuke; Takami, Tsuyoshi; Miyazaki, Tatsuhiko; Takeuchi, Tamotsu; Shimizu, Masahito; Tsurumi, Hisashi.
  • Hara T; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Yoshikawa T; Department of Hematology, Matsunami General Hospital, Kasamatsu, Japan.
  • Goto H; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Sawada M; Division of Hematology, Gifu Municipal Hospital, Gifu, Japan.
  • Yamada T; Department of Hematology, Gifu Red-Cross Hospital, Gifu, Japan.
  • Fukuno K; Department of Hematology, Gifu Prefectural General Medical Center, Gifu, Japan.
  • Kasahara S; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Shibata Y; Division of Hematology, Gifu Municipal Hospital, Gifu, Japan.
  • Matsumoto T; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Mabuchi R; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Nakamura N; Department of Internal Medicine, Kisogawa Municipal Hospital, Kisogawa, Japan.
  • Nakamura H; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Ninomiya S; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Kitagawa J; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Kanemura N; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Nannya Y; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Katsumura N; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Takahashi T; Department of Internal Medicine, Chuno Kosei Hospital, Seki, Japan.
  • Kito Y; Department of Hematology, Matsunami General Hospital, Kasamatsu, Japan.
  • Takami T; Department of Pathology and Translational Research, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Miyazaki T; Department of Pathology and Translational Research, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Takeuchi T; Pathology Division, Gifu University Hospital, Gifu, Japan.
  • Shimizu M; Department of Pathology and Translational Research, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Tsurumi H; First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Hematol Oncol ; 36(4): 638-644, 2018 Oct.
Article en En | MEDLINE | ID: mdl-29882279
ABSTRACT
Pirarubicin (tetrahydropyranyl adriamycin [THP]) is an anthracyclin with less cardiotoxicity than doxorubicin (DOX). We previously reported the efficacy and safety of R-THP-COP consisting of rituximab (R), THP, cyclophosphamide (CPA), vincristine (VCR), and prednisolone (PSL) for diffuse large B cell lymphoma (DLBCL) in phase 2 studies. Here, we prospectively compared the efficacy and safety of the R-THP-COP and standard R-CHOP regimen (consisting of R, CPA, DOX, VCR, and PSL) in a noninferiority phase 3 trial. This prospective, randomized phase 3 study included patients younger than 70 years of age with previously untreated DLBCL. The regimen consisted of R (day 1), DOX, or THP (day 3), CPA (day 3), VCR (day 3), and PSL for 5 days every 3 weeks for 6 to 8 cycles. Between July 5, 2006 and June 11, 2013, 81 patients were randomly assigned to the treatment groups (R-CHOP group, 40 patients; R-THP-COP group, 41 patients). R-THP-COP was noninferior to R-CHOP, as assessed by the primary endpoint of complete response rate (85% vs 85% respectively). With a median follow-up of 75.2 months, the 5-year overall survival was 87% in the R-CHOP group and 82% in the R-THP-COP group (hazard ratio [HR] 0.89, 95% confidence interval [CI] 0.31-2.49; P = .82). The 5-year progression-free survival was 74% in the R-CHOP group and 79% in the R-THP-COP group (HR 1.37, 95% CI 0.56-3.55; P = .49). No grade 3 cardiac side effects were observed in either group. No serious late adverse reactions were observed in either group, with the exception of therapy-related acute myeloid leukemia in the R-THP-COP group. These data indicate that R-THP-COP is noninferior to R-CHOP with regard to clinical response, and has an acceptable safety profile. Thus, this regimen may be an alternative therapy to R-CHOP.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma de Células B Grandes Difuso Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma de Células B Grandes Difuso Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article