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. 2021 Oct 22;5(20):4185–4197. doi: 10.1182/bloodadvances.2021004939

Table 4.

Univariable competing risk regression models for LP

Characteristic No. HR 95% CI P
Age at VLDRT (y) 299 1.01 0.99-1.02 .5
Sex 299
 Male
 Female 0.89 0.57-1.37 .6
Histology at VLDRT 299
 FL
 MZL 0.65 0.39-1.11 .12
 Low-grade indolent 0.80 0.32-1.97 .6
Best overall response* 235
 CR
 PR, SD, or PD 2.75 1.48-5.10 .001
Maximum SUV before VLDRT 251
 0-5
 5-7.5 0.82 0.36-1.84 .6
 7.5-10 0.68 0.27-1.73 .4
 10-15 1.59 0.78-3.24 .2
 ≥15 1.30 0.36-4.74 .7
 Unspecified but less than liver background 0.73 0.28-1.88 .5
Stage at VLDRT 299
 Early
 Advanced 1.20 0.77-1.87 .4
Nodal status 299
 Nodal
 Extranodal 0.59 0.38-0.94 .024
 Both 1.36 0.57-3.26 .5
Site category 299
 Cutaneous
 Non-cutaneous 1.29 0.69-2.40 .4
Pre-VLDRT lesion size (cm) 264
 0-6
 ≥6 5.53 3.23-9.48 <.001
Intent of VLDRT 299
 Non-curable
 Potentially curable 0.30 0.12-0.73 .008
Previous No. of lines of systemic therapy 299
 0
 1 1.95 1.06-3.57 .031
 2-4 2.23 1.29-3.84 .004
 > 4 3.73 1.47-9.47 .006
Previous rituximab 299 1.71 1.10-2.65 .017
*

Given the variability in time of best response assessment, this factor was assessed using a landmark analysis with landmark time at 6 months after VLDRT.