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. 2023 Sep 21;7(22):6801–6811. doi: 10.1182/bloodadvances.2023010668

Table 1.

Summary of IRC-assessed disease responses by MZL subtypes (efficacy analysis set)

Extranodal (MALT) (n = 25) Nodal (n = 25) Splenic (n = 12) Unknown (n = 4) Total (N = 66)
ORR, % (95% CI) 64.0 (42.5-82.0) 76.0 (54.9-90.6) 66.7 (34.9-90.1) 50.0 (6.8-93.2) 68.2 (55.6-79.1)
Best overall response, n (%)
 CR 10 (40.0) 5 (20.0) 1 (8.3) 1 (25.0) 17 (25.8)
 PR 6 (24.0) 14 (56.0) 7 (58.3) 1 (25.0) 28 (42.4)
 Stable disease 4 (16.0) 5 (20.0) 3 (25.0) 1 (25.0) 13 (19.7)
 Progressive disease 3 (12.0) 1 (4.0) 1 (8.3) 1 (25.0) 6 (9.1)
Nonprogressive disease§ 1 (4.0) 0 0 0 1 (1.5)
Discontinued study before first assessment 1 (4.0) 0 0 0 1 (1.5)
Median time to response, mo (IQR) 2.8 (2.7-2.9) 2.8 (2.7-3.8) 3.6 (2.7-6.0) 2.7 (2.6-2.8) 2.8 (2.7-3.7)

MALT, mucosa-associated lymphoid tissue.

These patients presented with both nodal and extranodal lesions; therefore, the study sites were unable to classify the MZL subtype.

Two patients were excluded from the efficacy analysis set because central review determined their diagnosis as diffuse large B-cell lymphoma.

95% CIs were calculated using 2-sided Clopper-Pearson methodology.

§

One patient was classified as having “nonprogressive disease” because of a missed PET scan at cycle 3 (CT scan showed stable disease).