Table 3.

Multivariable analysis incorporating number of ctDNA mutations out of 6 significant genes, clinical factors, and plasma DNA concentration

VariableCoefficientHR95% lower CI95% upper CIP valuectRRMM-PI score
No. of ctDNA mutations, n ≥ 2 1.2 3.5 2.0 6.0 1.0 × 10−5 
Number of ctDNA mutations, n = 1 0.8 2.2 1.3 3.6 .0025 
No. of prior regimens, n ≥ 3 0.9 2.4 1.4 4.2 .0015 
No. of prior regimens, n = 2 0.4 1.5 0.8 2.8 .16 
Plasma DNA concentration: high 0.5 1.7 1.1 2.6 .020 
VariableCoefficientHR95% lower CI95% upper CIP valuectRRMM-PI score
No. of ctDNA mutations, n ≥ 2 1.2 3.5 2.0 6.0 1.0 × 10−5 
Number of ctDNA mutations, n = 1 0.8 2.2 1.3 3.6 .0025 
No. of prior regimens, n ≥ 3 0.9 2.4 1.4 4.2 .0015 
No. of prior regimens, n = 2 0.4 1.5 0.8 2.8 .16 
Plasma DNA concentration: high 0.5 1.7 1.1 2.6 .020 

HRs for PFS evaluated by Cox PH model incorporating the total number of ctDNA mutations in the 6 prognostically significant genes, clinical factors (treatment indication and number of prior therapies), and plasma DNA concentration in 161 RRMM cases analyzed by both ctDNA-seq and BMPC-seq.

High and low plasma DNA concentration by a median split. Final Cox PH model after stepwise variable selection minimizing Akaike’s information criterion are shown.

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