Risk of secondary primary malignancies in multiple myeloma patients with or without autologous stem cell transplantation.


Journal

International journal of hematology
ISSN: 1865-3774
Titre abrégé: Int J Hematol
Pays: Japan
ID NLM: 9111627

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 06 08 2018
accepted: 19 09 2018
revised: 18 09 2018
pubmed: 27 9 2018
medline: 7 2 2019
entrez: 26 9 2018
Statut: ppublish

Résumé

Outcomes for patients with multiple myeloma (MM) have improved through use of novel treatments, especially lenalidomide combined with autologous stem cell transplantation. However, because of their increased life expectancy, an increased risk of secondary primary malignancies (SPMs) has been observed in MM patients, particularly after lenalidomide maintenance in both transplant-eligible (TE) and transplant-ineligible (TI) patients. To evaluate the incidence and risk factors of developing SPMs, we identified 17 TE-MM and 12 TI-MM patients with SPMs among 211 TE-MM and 280 TI-MM patients, including seven TE-MM and four TI-MM patients with hematological malignancies and ten TE-MM and eight TI-MM patients with non-hematological cancers, respectively. The median follow-up time from diagnosis was > 4 years. Multivariate analysis identified a history of high-dose cyclophosphamide use for peripheral blood stem cell harvest in TE-MM patients and > 65 years of age at diagnosis, or a history of adriamycin, lenalidomide, or thalidomide use in TI-MM patients as independent risk factors for SPMs (P < 0.001). Patients with a history of lenalidomide use had a lower risk of death among both TE-MM (P = 0.0326) and TI-MM (P < 0.001) patients. The survival benefit of receiving lenalidomide outweighed the increased risk of SPMs in both TE-and TI-MM patients.

Identifiants

pubmed: 30251131
doi: 10.1007/s12185-018-2538-8
pii: 10.1007/s12185-018-2538-8
doi:

Substances chimiques

Lenalidomide F0P408N6V4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

98-106

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Auteurs

Satoshi Yamasaki (S)

Department of Hematology and Clinical Research Institute, National Hospital Organization Kyushu Medical Center, 1-8-1 Jigyohama, Chuo-Ku, Fukuoka, 810-8563, Japan. yamas009@gmail.com.

Goichi Yoshimoto (G)

Department of Hematology/Oncology, Kyushu University Hospital, Fukuoka, Japan.

Kentaro Kohno (K)

Department of Hematology/Oncology, Japan Community Health Care Organization Kyushu Hospital, Fukuoka, Japan.

Hideho Henzan (H)

Department of Hematology, Hamanomachi Hospital, Fukuoka, Japan.

Takatoshi Aoki (T)

Department of Hematology, Harasanshin Hospital, Fukuoka, Japan.

Kazuki Tanimoto (K)

Department of Hematology, Fukuoka Red Cross Hospital, Fukuoka, Japan.

Yasuhiro Sugio (Y)

Department of Internal Medicine, Kitakyushu Municipal Medical Center, Kitakyushu, Japan.

Tsuyoshi Muta (T)

Department of Hematology, Hiroshima Red Cross Hospital and Atomic Bomb Survivors Hospital, Hiroshima, Japan.

Tomohiko Kamimura (T)

Department of Hematology, Harasanshin Hospital, Fukuoka, Japan.

Yuju Ohno (Y)

Department of Internal Medicine, Kitakyushu Municipal Medical Center, Kitakyushu, Japan.

Ryosuke Ogawa (R)

Department of Hematology/Oncology, Japan Community Health Care Organization Kyushu Hospital, Fukuoka, Japan.

Tetsuya Eto (T)

Department of Hematology, Hamanomachi Hospital, Fukuoka, Japan.

Koji Nagafuji (K)

Department of Hematology, Kurume University Hospital, Kurume, Japan.

Toshihiro Miyamoto (T)

Department of Hematology/Oncology, Kyushu University Hospital, Fukuoka, Japan.

Koichi Akashi (K)

Department of Hematology/Oncology, Kyushu University Hospital, Fukuoka, Japan.

Hiromi Iwasaki (H)

Department of Hematology and Clinical Research Institute, National Hospital Organization Kyushu Medical Center, 1-8-1 Jigyohama, Chuo-Ku, Fukuoka, 810-8563, Japan.

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