TY - JOUR
T1 - Prognostic and predictive performance of R-ISS with SKY92 in older patients with multiple myeloma
T2 - The HOVON-87/NMSG-18 trial
AU - Kuiper, Rowan
AU - Zweegman, Sonja
AU - van Duin, Mark
AU - van Vliet, Martin H.
AU - van Beers, Erik H.
AU - Dumee, Belinda
AU - Vermeulen, Michael
AU - Koenders, Jasper
AU - van der Holt, Bronno
AU - Visser-Wisselaar, Heleen
AU - Hansson, Markus
AU - van der Velden, Annette W.G.
AU - Berna Beverloo, H.
AU - Stevens-Kroef, Marian
AU - Levin, Mark David
AU - Broijl, Annemiek
AU - Waage, Anders
AU - Sonneveld, Pieter
PY - 2020
Y1 - 2020
N2 - The standard prognostic marker for multiple myeloma (MM) patients is the revised International Staging System (R-ISS). However, there is room for improvement in guiding treatment. This applies particularly to older patients, in whom the benefit/risk ratio is reduced because of comorbidities and subsequent side effects. We hypothesized that adding gene-expression data to R-ISS would generate a stronger marker. This was tested by combining R-ISS with the SKY92 classifier (SKY-RISS). The HOVON-87/NMSG-18 trial (EudraCT: 2007-004007-34) compared melphalan-prednisone-thalidomide followed by thalidomide maintenance (MPT-T) with melphalan-prednisone-lenalidomide followed by lenalidomide maintenance (MPR-R). From this trial, 168 patients with available R-ISS status and gene-expression profiles were analyzed. R-ISS stages I, II, and III were assigned to 8%, 75%, and 7% of patients, respectively (3-year overall survival [OS] rates: 80%, 65%, 33%, P 5 8 3 1023). Using the SKY92 classifier, 13% of patients were high risk (HR) (3-year OS rates: standard risk [SR], 70%; HR, 28%; P,.001). Combining SKY92 with R-ISS resulted in 3 risk groups: SKY-RISS I (SKY-SR 1 R-ISS-I; 15%), SKY-RISS III (SKY-HR 1 R-ISS-II/III; 11%), and SKY-RISS II (all other patients; 74%). The 3-year OS rates for SKY-RISS I, II, and III are 88%, 66%, and 26%, respectively (P 5 6 3 1027). The SKY-RISS model was validated in older patients from the CoMMpass dataset. Moreover, SKY-RISS demonstrated predictive potential: HR patients appeared to benefit from MPR-R over MPT-T (median OS, 55 and 14 months, respectively). Combined, SKY92 and R-ISS classify patients more accurately. Additionally, benefit was observed for MPR-R over MPT-T in SKY92-RISS HR patients only.
AB - The standard prognostic marker for multiple myeloma (MM) patients is the revised International Staging System (R-ISS). However, there is room for improvement in guiding treatment. This applies particularly to older patients, in whom the benefit/risk ratio is reduced because of comorbidities and subsequent side effects. We hypothesized that adding gene-expression data to R-ISS would generate a stronger marker. This was tested by combining R-ISS with the SKY92 classifier (SKY-RISS). The HOVON-87/NMSG-18 trial (EudraCT: 2007-004007-34) compared melphalan-prednisone-thalidomide followed by thalidomide maintenance (MPT-T) with melphalan-prednisone-lenalidomide followed by lenalidomide maintenance (MPR-R). From this trial, 168 patients with available R-ISS status and gene-expression profiles were analyzed. R-ISS stages I, II, and III were assigned to 8%, 75%, and 7% of patients, respectively (3-year overall survival [OS] rates: 80%, 65%, 33%, P 5 8 3 1023). Using the SKY92 classifier, 13% of patients were high risk (HR) (3-year OS rates: standard risk [SR], 70%; HR, 28%; P,.001). Combining SKY92 with R-ISS resulted in 3 risk groups: SKY-RISS I (SKY-SR 1 R-ISS-I; 15%), SKY-RISS III (SKY-HR 1 R-ISS-II/III; 11%), and SKY-RISS II (all other patients; 74%). The 3-year OS rates for SKY-RISS I, II, and III are 88%, 66%, and 26%, respectively (P 5 6 3 1027). The SKY-RISS model was validated in older patients from the CoMMpass dataset. Moreover, SKY-RISS demonstrated predictive potential: HR patients appeared to benefit from MPR-R over MPT-T (median OS, 55 and 14 months, respectively). Combined, SKY92 and R-ISS classify patients more accurately. Additionally, benefit was observed for MPR-R over MPT-T in SKY92-RISS HR patients only.
U2 - 10.1182/bloodadvances.2020002838
DO - 10.1182/bloodadvances.2020002838
M3 - Article
C2 - 33351127
AN - SCOPUS:85098052619
SN - 2473-9529
VL - 4
SP - 6298
EP - 6309
JO - Blood Advances
JF - Blood Advances
IS - 24
ER -