INTERFERON ALFA-2B VERSUS NO MAINTENANCE THERAPY DURING THE PLATEAU-PHASE IN MULTIPLE-MYELOMA - A RANDOMIZED STUDY

Citation
J. Westin et al., INTERFERON ALFA-2B VERSUS NO MAINTENANCE THERAPY DURING THE PLATEAU-PHASE IN MULTIPLE-MYELOMA - A RANDOMIZED STUDY, British Journal of Haematology, 89(3), 1995, pp. 561-568
Citations number
20
Categorie Soggetti
Hematology
ISSN journal
00071048
Volume
89
Issue
3
Year of publication
1995
Pages
561 - 568
Database
ISI
SICI code
0007-1048(1995)89:3<561:IAVNMT>2.0.ZU;2-M
Abstract
This clinical trial was designed to investigate if maintenance therapy with alfa-interferon could prolong the plateau phase in patients with multiple myeloma. In addition, the tolerability of interferon treatme nt and its effect on survival were evaluated. From September 1987 to S eptember 1989 a total of 314 patients were accrued to a multi-institut ional randomized clinical trial. All patients entered into the protoco l received standard melphalan-prednisone (MP) induction therapy. Respo nse was noted in 184 (59%) and a plateau phase achieved in 155 (49%). From the latter group, 125 eligible patients were randomized to either interferon alfa-2b or no maintenance. The patients were followed for an average of 51 months (minimum 36 months) from the time of randomiza tion. The plateau phase was significantly prolonged in the group of pa tients treated with interferon (median 13.9 v 5.7 months from the time of randomization; P < 0.0001). The interferon therapy was tolerated f airly well, moderate granulocytopenia and a chronic fatigue syndrome b eing the most frequent side-effects (22% v 18% W.H.O. grade 3 toxicity ). The median survival from randomization was almost identical in both groups (36 v 35 months). The study shows that interferon maintenance therapy given to multiple myeloma patients who have achieved a respons e to initial treatment with MP prolongs the plateau phase duration wit h tolerable toxicity. The clinical value of this finding should be int erpreted with caution, because survival was not prolonged. Further stu dies are required to clarify the role of interferon in the treatment o f multiple myeloma.