Literature DB >> 15678759

VAD with or without subsequent high-dose melphalan followed by autologous stem cell support in AL amyloidosis: Japanese experience and criteria for patient selection.

Takahisa Gono1, Masayuki Matsuda, Yasuhiro Shimojima, Wataru Ishii, Jun Koyama, Kazuo Sakashita, Kenichi Koike, Yoshinobu Hoshii, Shu-ichi Ikeda.   

Abstract

Patients with AL amyloidosis were treated with VAD (vincristine, doxorubicin and dexamethasone) with or without high-dose melphalan followed by auto-PBSCT according to eligibility criteria based on disease severity, and prospectively investigated the therapeutic benefits and complications. Thirty-one patients were enrolled in this study. VAD and subsequent high-dose melphalan with auto-PBSCT were performed only in patients who met all of the eligibility criteria. Among patients ineligible for this treatment, VAD alone was performed in those with satisfactory general status. Eleven patients met the eligibility criteria, and of these, 7 were treated with VAD and subsequent high-dose melphalan with auto-PBSCT. Seven patients received VAD alone, and the remaining 17 were treated with the supportive therapy. Among the 14 patients treated with chemotherapy, 9 (5 of the 7 treated with VAD and high-dose melphalan, and 4 of the 7 treated with VAD alone) showed complete hematological response with apparent improvement of amyloidosis-related clinical symptoms. Serious complications of chemotherapy were cytomegalovirus infection and pneumocystis carinii pneumonia seen in 1 and 2 patients, respectively. These chemotherapies may be effective for reduction of M-protein and are also useful in improving of amyloidosis-induced organ dysfunction. In patients who cannot tolerate high-dose melphalan, VAD alone is a potent therapeutic option, although there are possible harmful effects on the heart and peripheral nerve.

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Year:  2004        PMID: 15678759     DOI: 10.1080/13506120412331336907

Source DB:  PubMed          Journal:  Amyloid        ISSN: 1350-6129            Impact factor:   7.141


  4 in total

1.  Bortezomib-dexamethasone versus high-dose melphalan for Japanese patients with systemic light-chain (AL) amyloidosis: a retrospective single-center study.

Authors:  Nagaaki Katoh; Akihiro Ueno; Takuhiro Yoshida; Ko-Ichi Tazawa; Yasuhiro Shimojima; Takahisa Gono; Yoshiki Sekijima; Masayuki Matsuda; Shu-Ichi Ikeda
Journal:  Int J Hematol       Date:  2016-11-10       Impact factor: 2.490

2.  AL amyloidosis with IgD-lambda monoclonal gammopathy and lambda-type Bence-Jones protein: successful treatment by autologous stem cell transplantation.

Authors:  Chanhyok Sakurai-Chin; Yoshifumi Ubara; Tatsuya Suwabe; Junichi Hoshino; Tomoki Yonaha; Eiko Hasegawa; Keiichi Sumida; Rikako Hiramatsu; Masayuki Yamanouchi; Noriko Hayami; Junji Yamauchi; Naoyuki Tominaga; Naoki Sawa; Fumi Takemoto; Kazuhiro Masuoka; Kenmei Takaichi; Kenichi Oohashi
Journal:  Clin Exp Nephrol       Date:  2010-07-15       Impact factor: 2.801

Review 3.  Targeted treatments of AL and ATTR amyloidosis.

Authors:  Pranav Chandrashekar; Anish K Desai; Barry H Trachtenberg
Journal:  Heart Fail Rev       Date:  2021-11-16       Impact factor: 4.654

4.  Successful treatment of primary AL amyloidosis by VAD therapy, high-dose melphalan, and autologous peripheral stem cell transplantation.

Authors:  Osamu Yamazaki; Yoshifumi Ubara; Tatsuya Suwabe; Shohei Nakanishi; Junichi Hoshino; Naoki Sawa; Noriko Hayami; Masayuki Yamanouchi; Fumi Takemoto; Takaichi Kenmei; Kazuhiro Masuoka; Kenichi Oohashi
Journal:  Clin Exp Nephrol       Date:  2009-06-05       Impact factor: 2.801

  4 in total

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