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
Hiroyuki Takamatsu,
Tomohiro Matsuda,
Shohei Mizuno,
Tsutomu Takahashi,
Shin-ichi Fuchida,
Ichiro Hanamura,
Keisuke Kataoka,
Nobuhiro Tsukada,
Morio Matsumoto,
Akira Hangaishi,
Noriko Doki,
Naoyuki Uchida,
Masashi Sawa,
Yumiko Maruyama,
Shingo Kurahashi,
Koji Nagafuji,
Yoriko Harazaki,
Shinichi Kako,
Shinsuke Iida,
Tatsuo Ichinohe,
Yoshinobu Kanda,
Yoshiko Atsuta,
Kazutaka Sunami,
Multiple Myeloma Working Group in the Japanese Society for Transplantation and Cellular Therapy
Affiliations
Hiroyuki Takamatsu
Department of Hematology, Kanazawa University, Kanazawa
Tomohiro Matsuda
Division of International Health Policy Research, National Cancer Center Institute for Cancer Control, Tokyo
Shohei Mizuno
Division of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute
Tsutomu Takahashi
Department of Hematology, Shimane University Hospital, Izumo
Shin-ichi Fuchida
Department of Hematology, Japan Community Health care Organization Kyoto Kuramaguchi Medical Center, Kyoto
Ichiro Hanamura
Division of Hematology, Department of Internal Medicine, Aichi Medical University, Nagakute
Keisuke Kataoka
Division of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan; Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo
Nobuhiro Tsukada
Division of Hematology, Japanese Red Cross Medical Center, Tokyo
Morio Matsumoto
Department of Hematology, National Hospital Organization Shibukawa Medical Center, Shibukawa
Akira Hangaishi
Department of Hematology, National Center for Global Health and Medicine, Tokyo
Noriko Doki
Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo
Naoyuki Uchida
Department of Hematology, Federation of National Public Service Personnel Mutual Aid Associations TORANOMON HOSPITAL, Tokyo
Masashi Sawa
Department of Hematology and Oncology, Anjo Kosei Hospital, Anjo
Yumiko Maruyama
Department of Hematology, University of Tsukuba Hospital, Tsukuba
Shingo Kurahashi
Division of Hematology and Oncology, Toyohashi Municipal Hospital, Toyohashi
Koji Nagafuji
Division of Hematology and Oncology, Department of Medicine, Kurume University Hospital, Kurume
Yoriko Harazaki
Division of Hematology, Miyagi Cancer Center, Natori
Shinichi Kako
Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama
Shinsuke Iida
Division of Hematology and Oncology, Nagoya City University Hospital, Nagoya
Tatsuo Ichinohe
Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University
Yoshinobu Kanda
Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan; Division of Hematology, Department of Medicine, Jichi Medical University, Shimotsuke
Yoshiko Atsuta
Aichi Medical University School of Medicine / Department of Registry Science for Transplant and Cellular Therapy, Nagakute
Kazutaka Sunami
Department of Hematology, National Hospital Organization Okayama Medical Center, Okayama
Multiple Myeloma Working Group in the Japanese Society for Transplantation and Cellular Therapy
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.
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.