High-Dose Melphalan versus Melphalan plus Dexamethasone for AL Amyloidosis

Arnaud Jaccard(Centre Hospitalier Universitaire de Limoges), Philippe Moreau(Centre Hospitalier Universitaire de Nantes), Véronique Leblond(Sorbonne Université), Xavier Leleu(Centre Hospitalier Universitaire de Lille), Lotfi Benboubker(Centre Hospitalier Universitaire de Tours), Olivier Hermine(Assistance Publique – Hôpitaux de Paris), Christian Récher(Hôpital Purpan), Bouchra Asli(Assistance Publique – Hôpitaux de Paris), Bruno Lioure(Hôpitaux Universitaires de Strasbourg), Bruno Royer(Centre Hospitalier Universitaire Amiens-Picardie), Fabrice Jardin(Centre Henri Becquerel), Frank Bridoux(Centre Hospitalier Universitaire de Poitiers), B. Grosbois(Centre Hospitalier Universitaire de Rennes), J. Jaubert(Institute Cancer De La Loire Lucien Neuwirth), Jean‐Charles Piette(Assistance Publique – Hôpitaux de Paris), Pierre Ronco(Sorbonne Université), Fabrice Quet(Centre Hospitalier Universitaire de Limoges), Michel Cogné(Centre National pour la Recherche Scientifique et Technique (CNRST)), Jean‐Paul Fermand(Assistance Publique – Hôpitaux de Paris)
New England Journal of Medicine
September 12, 2007
Cited by 516

Abstract

BACKGROUND: High-dose chemotherapy followed by autologous hematopoietic stem-cell transplantation has been reported to provide higher response rates and better overall survival than standard chemotherapy in immunoglobulin-light-chain (AL) amyloidosis, but these two strategies have not been compared in a randomized study. METHODS: We conducted a randomized trial comparing high-dose intravenous melphalan followed by autologous hematopoietic stem-cell rescue with standard-dose melphalan plus high-dose dexamethasone in patients with AL amyloidosis. Patients (age range, 18 to 70 years) with newly diagnosed AL amyloidosis were randomly assigned to receive intravenous high-dose melphalan plus autologous stem cells or oral melphalan plus oral high-dose dexamethasone. RESULTS: Fifty patients were enrolled in each group. The results were analyzed on an intention-to-treat basis, with overall survival as the primary end point. After a median follow-up of 3 years, the estimated median overall survival was 22.2 months in the group assigned to receive high-dose melphalan and 56.9 months in the group assigned to receive melphalan plus high-dose dexamethasone (P=0.04). Among patients with high-risk disease, overall survival was similar in the two groups. Among patients with low-risk disease, there was a nonsignificant difference between the two groups in overall survival at 3 years (58% in the group assigned to receive high-dose melphalan vs. 80% in the group assigned to receive melphalan plus high-dose dexamethasone; P=0.13). CONCLUSIONS: The outcome of treatment of AL amyloidosis with high-dose melphalan plus autologous stem-cell rescue was not superior to the outcome with standard-dose melphalan plus dexamethasone. (ClinicalTrials.gov number, NCT00344526 [ClinicalTrials.gov].).


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