Thalidomide maintenance therapy in Japanese myeloma patients: a multicenter, phase II clinical trial (COMET study).


Journal

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

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 16 10 2018
accepted: 23 01 2019
revised: 20 01 2019
pubmed: 1 2 2019
medline: 18 4 2019
entrez: 1 2 2019
Statut: ppublish

Résumé

A prospective, multicenter, phase II study was performed to assess the efficacy and safety of thalidomide maintenance therapy at different doses in Japanese multiple myeloma (MM) patients. This study included 34 patients (median age, 74 years) who were previously treated with not more than three prior therapies and whose response status was evaluated as at least stable disease. They were randomized into Group A (no maintenance; 12 patients), Group B (50 mg thalidomide maintenance; 12 patients), and Group C (100 mg thalidomide maintenance; 10 patients), respectively. Thalidomide maintenance therapy resulted in improved depth of response in three cases (13.6%) and sustained response after induction therapy in eight cases (36.4%). Two-year progression-free survival (PFS) was 25.0%, 33.3%, and 77.8% in Groups A, B, and C, respectively, and was significantly higher in Group C than in Group A (p = 0.005). There was no difference in the incidence of hematological or non-hematological adverse events between Groups B and C. The current study demonstrates that maintenance with daily thalidomide at 100 mg, but not 50 mg, improved depth of response and prolonged PFS, and that this treatment was feasible for use in Japanese MM patients.

Identifiants

pubmed: 30701467
doi: 10.1007/s12185-019-02607-z
pii: 10.1007/s12185-019-02607-z
doi:

Substances chimiques

Thalidomide 4Z8R6ORS6L

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

409-417

Commentaires et corrections

Type : ErratumIn

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Auteurs

Hirokazu Murakami (H)

Department of Laboratory Sciences, Gunma University Graduate School of Health Sciences, Maebashi, Japan. hmura@gunma-u.ac.jp.

Tetsuhiro Kasamatsu (T)

Department of Laboratory Sciences, Gunma University Graduate School of Health Sciences, Maebashi, Japan.

Jun Murakami (J)

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

Toru Kiguchi (T)

Department of Hematology, Chugoku Central Hospital, Fukuyama, Japan.

Takeshi Kanematsu (T)

Department of Clinical Laboratory, Nagoya University Hospital, Nagoya, Japan.

Daisuke Ogawa (D)

Department of Hematology, Nagasaki Prefectural Shimabara Hospital, Shimabara, Japan.

Hiroyuki Takamatsu (H)

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

Hiroshi Handa (H)

Department of Hematology, Gunma University, Maebashi, Japan.

Shuji Ozaki (S)

Department of Hematology, Tokushima Prefectural Central Hospital, Tokushima, Japan.

Hirokazu Miki (H)

Division of Transfusion Medicine and Cell Therapy, Tokushima University Hospital, Tokushima, Japan.

Takeshi Takahashi (T)

Department of Hematology, Gifu Municipal Hospital, Gifu, Japan.

Takaaki Takeo (T)

Department of Hematology, Yokkaichi Municipal Hospital, Yokkaichi, Japan.

Tatsuya Yamauchi (T)

Department of Hematology, Toki Municipal General Hospital, Toki, Japan.

Takanobu Morishita (T)

Department of Hematology, Japanese Red Cross Nagoya Daiichi Hospital, Nagoya, Japan.

Hiroshi Kosugi (H)

Department of Hematology, Ogaki Municipal Hospital, Ogaki, Japan.

Kazuyuki Shimizu (K)

Department of Hematology/Oncology, Higashi Nagoya National Hospital, Nagoya, Japan.

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Classifications MeSH