Response rate and survival after conventional chemotherapy for multiple myeloma by hospitals with different inclusion rates of patients to the trials. A Finnish Leukemia Group study

Citation
T. Oivanen et al., Response rate and survival after conventional chemotherapy for multiple myeloma by hospitals with different inclusion rates of patients to the trials. A Finnish Leukemia Group study, EUR J HAEMA, 63(4), 1999, pp. 225-230
Citations number
27
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
EUROPEAN JOURNAL OF HAEMATOLOGY
ISSN journal
09024441 → ACNP
Volume
63
Issue
4
Year of publication
1999
Pages
225 - 230
Database
ISI
SICI code
0902-4441(199910)63:4<225:RRASAC>2.0.ZU;2-M
Abstract
The purpose of this study was to analyse the influence of the hospital size , measured as the number of annual patient enrolments in the Finnish Leukae mia Group trials in the period 1979-85, on response rate and survival after conventional chemotherapy for multiple myeloma. The 432 myeloma patients f or this study were derived from 4 prospective multicentre trials of the Fin nish Leukaemia Group. The comparisons of the response rate to primary chemo therapy, progression-free survival time (PFS), response rate after first re lapse and overall survival time (OS) were made between patients treated in 3 hospital categories according to annual enrolment rate. 273 of the patien ts had been treated in "large" hospitals, 120 in "intermediate" and 38 in " small" ones. The median OS of patients aged up to 70 yr was 49 months and t hat of patients older than 70 yr was 31 months. There were no significant d ifferences in response rate, PFS, response rate after first relapse and OS between the hospital categories. The most important endpoints in the treatm ent of multiple myeloma, response rate, PFS and OS are independent of the s ize of the hospital, measured as the number of annual patient entries in th e trial. This allows the decentralisation of the conventional chemotherapy of multiple myeloma, within the framework of properly organised clinical tr ials.