TY - JOUR
T1 - Outcome and characteristics of non-measurable myeloma
T2 - A cohort study with population-based data from the Swedish Myeloma Registry
AU - Wålinder, Göran
AU - Samuelsson, Jan
AU - Näsman, Per
AU - Hansson, Markus
AU - Juliusson, Gunnar
AU - Forsberg, Karin
AU - Svensson, Ronald
AU - Linder, Olle
AU - Carlson, Kristina
AU - Kristinsson, Sigurdur Y.
AU - Mellqvist, Ulf Henrik
AU - Hveding Blimark, Cecilie
AU - Turesson, Ingemar
AU - Nahi, Hareth
PY - 2020
Y1 - 2020
N2 - Objective: We describe survival in patients with oligo- and non-secretory multiple myeloma (MM). We refer to the whole group as non-measurable MM and compare it with secretory MM. Methods: Oligo-secretory MM was defined as M protein in serum <10 g/L and M protein in urine <200 measured as mg/day, mg/liter or mg/mmol creatinine. If patients had no M protein, they were defined as non-secretory. The groups were also subdivided by Free Light Chains (SFLC) level and ratio. Results: Out of 4325 patients with symptomatic MM in the Swedish Myeloma Registry during 2008-2016 eligible for the study, 389 patients (9%) had non-measurable MM. Out of these, 253 patients (6%) had oligo-secretory and 136 (3%) had non-secretory MM. Median survival for secretory MM was 42.7 months, non-measurable MM 40.2 months, oligo-secretory MM 38.6 months, and non-secretory MM 44.6 months. Difference in overall observed survival was non-significant for all groups when compared with secretory MM. Within non-secretory MM, stem cell transplantation (SCT), 95% being auto-SCT, was significant for superior survival in multivariate analysis (HR 0.048. P =.0015). Conclusion: In this population-based study, we found no difference in survival between oligo- or non-secretory MM when compared with secretory MM. SCT appears to be important also for patients with non-secretory disease.
AB - Objective: We describe survival in patients with oligo- and non-secretory multiple myeloma (MM). We refer to the whole group as non-measurable MM and compare it with secretory MM. Methods: Oligo-secretory MM was defined as M protein in serum <10 g/L and M protein in urine <200 measured as mg/day, mg/liter or mg/mmol creatinine. If patients had no M protein, they were defined as non-secretory. The groups were also subdivided by Free Light Chains (SFLC) level and ratio. Results: Out of 4325 patients with symptomatic MM in the Swedish Myeloma Registry during 2008-2016 eligible for the study, 389 patients (9%) had non-measurable MM. Out of these, 253 patients (6%) had oligo-secretory and 136 (3%) had non-secretory MM. Median survival for secretory MM was 42.7 months, non-measurable MM 40.2 months, oligo-secretory MM 38.6 months, and non-secretory MM 44.6 months. Difference in overall observed survival was non-significant for all groups when compared with secretory MM. Within non-secretory MM, stem cell transplantation (SCT), 95% being auto-SCT, was significant for superior survival in multivariate analysis (HR 0.048. P =.0015). Conclusion: In this population-based study, we found no difference in survival between oligo- or non-secretory MM when compared with secretory MM. SCT appears to be important also for patients with non-secretory disease.
KW - amyloidosis
KW - multiple myeloma
KW - plasma cell neoplasms
U2 - 10.1111/ejh.13351
DO - 10.1111/ejh.13351
M3 - Article
C2 - 31733147
AN - SCOPUS:85083905693
SN - 0902-4441
VL - 104
SP - 376
EP - 382
JO - European Journal of Haematology
JF - European Journal of Haematology
IS - 5
ER -