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Changing trends in the risk factors for second primary malignancies after autologous stem cell transplantation for multiple myeloma before and after the introduction of proteasome inhibitors and immunomodulatory drugs.
Takamatsu, Hiroyuki; Matsuda, Tomohiro; Mizuno, Shohei; Takahashi, Tsutomu; Fuchida, Shin-Ichi; Hanamura, Ichiro; Kataoka, Keisuke; Tsukada, Nobuhiro; Matsumoto, Morio; Hangaishi, Akira; Doki, Noriko; Uchida, Naoyuki; Sawa, Masashi; Maruyama, Yumiko; Kurahashi, Shingo; Nagafuji, Koji; Harazaki, Yoriko; Kako, Shinichi; Iida, Shinsuke; Ichinohe, Tatsuo; Kanda, Yoshinobu; Atsuta, Yoshiko; Sunami, Kazutaka.
Afiliación
  • Takamatsu H; Department of Hematology, Kanazawa University, Kanazawa. takamaz@staff.kanazawa-u.ac.jp.
  • Matsuda T; Division of International Health Policy Research, National Cancer Center Institute for Cancer Control, Tokyo.
  • Mizuno S; Division of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute.
  • Takahashi T; Department of Hematology, Shimane University Hospital, Izumo.
  • Fuchida SI; Department of Hematology, Japan Community Health care Organization Kyoto Kuramaguchi Medical Center, Kyoto.
  • Hanamura I; Division of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute.
  • Kataoka K; Division of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan; Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo.
  • Tsukada N; Division of Hematology, Japanese Red Cross Medical Center, Tokyo.
  • Matsumoto M; Department of Hematology, National Hospital Organization Shibukawa Medical Center, Shibukawa.
  • Hangaishi A; Department of Hematology, National Center for Global Health and Medicine, Tokyo.
  • Doki N; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo.
  • Uchida N; Department of Hematology, Federation of National Public Service Personnel Mutual Aid Associations TORANOMON HOSPITAL, Tokyo.
  • Sawa M; Department of Hematology and Oncology, Anjo Kosei Hospital, Anjo.
  • Maruyama Y; Department of Hematology, University of Tsukuba Hospital, Tsukuba.
  • Kurahashi S; Division of Hematology and Oncology, Toyohashi Municipal Hospital, Toyohashi.
  • Nagafuji K; Division of Hematology and Oncology, Department of Medicine, Kurume University Hospital, Kurume.
  • Harazaki Y; Division of Hematology, Miyagi Cancer Center, Natori.
  • Kako S; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama.
  • Iida S; Division of Hematology and Oncology, Nagoya City University Hospital, Nagoya.
  • Ichinohe T; Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University.
  • Kanda Y; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan; Division of Hematology, Department of Medicine, Jichi Medical University, Shimotsuke.
  • Atsuta Y; Aichi Medical University School of Medicine / Department of Registry Science for Transplant and Cellular Therapy, Nagakute.
  • Sunami K; Department of Hematology, National Hospital Organization Okayama Medical Center, Okayama.
Haematologica ; 108(12): 3399-3408, 2023 12 01.
Article en En | MEDLINE | ID: mdl-37470160
ABSTRACT
The incidence of second primary malignancies (SPM) in long-term survivors of multiple myeloma (MM) is increasing because of increased life expectancy. We retrospectively analyzed the risk factors for SPM in patients with MM after autologous stem cell transplantation (ASCT) before and after the introduction of proteasome inhibitors and immunomodulatory drugs (IMiDs). In total, 2,340 patients newly diagnosed with MM who underwent ASCT between 1995 and 2016 were enrolled in this study. Forty-three patients developed SPM (29 solid, 12 hematological, and 2 unknown tumors), with cumulative incidence rates of 0.8% and 2.5% at 24 and 60 months, respectively. The cumulative incidence rates of hematological and solid SPM at 60 months were 0.8% and 1.8%, respectively. The overall survival (OS) rate at 60 months after ASCT was 62.9% and the OS rates after the diagnosis of SPM at 24 months were 72.2% for hematological SPM and 70.9% for solid SPM. Multivariate analysis revealed that the use of IMiDs (P=0.024) and radiation (P=0.002) were significant independent risk factors for SPM. The probabilities of developing SPM and death due to other causes (mainly MM) at 60 months were 2.5% and 36.5%, respectively, indicating that the risk of SPM was lower than that of death from MM. Furthermore, SPM between the pre-novel and novel agent eras (ASCT between 2007 and 2016) groups significantly increased (1.9% vs. 4.3% at 60 months; P=0.022). The early occurrence of SPM after ASCT should be monitored cautiously.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Primarias Secundarias / Trasplante de Células Madre Hematopoyéticas / Mieloma Múltiple Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Haematologica Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Primarias Secundarias / Trasplante de Células Madre Hematopoyéticas / Mieloma Múltiple Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Haematologica Año: 2023 Tipo del documento: Article