Table 4

Characteristics of patients with PFS greater than 12 months

Age (y)/genderHistologic subtype of HL (stage)Percent CD30+ malignant cellsBaseline SPD (cm2)Number of treatment cyclesNumber of dose delays (dose reduced to 1.2 mg/kg)Best clinical response (first observed)Reason for EOTTime off treatment (mo)PFS (mo)
71/F Mixed cellularity (IIa) 100 28.7 23 2 (cycle 10) CR (cycle 2) Investigator decision* 2.7 22.3+ 
76/F Mixed cellularity (IVb) 20 12.9 16 0 (cycle 16) CR (cycle 4) AE (PSN) 5.7 16.8+ 
64/F Classical HL NOS (IIb) 90 5.0 6 0 (no reduction) CR (EOT) AE (PSN) 12.2 16.3+ 
84/M Nodular sclerosis (IIIa) 100 37.3 15 3 (cycle 6) CR (cycle 2) AE (PSN) 1.0 14.3+ 
84/M Classical HL NOS (IIIa) 80 14.7 3 (cycle 4) CR (cycle 2) AE (PSN) 7.4 14.3 
78/M Nodular sclerosis (IIa) 90 64.4 0 (no reduction) CR (EOT) AE (orthostatic hypertension) 9.8 13.4+ 
Age (y)/genderHistologic subtype of HL (stage)Percent CD30+ malignant cellsBaseline SPD (cm2)Number of treatment cyclesNumber of dose delays (dose reduced to 1.2 mg/kg)Best clinical response (first observed)Reason for EOTTime off treatment (mo)PFS (mo)
71/F Mixed cellularity (IIa) 100 28.7 23 2 (cycle 10) CR (cycle 2) Investigator decision* 2.7 22.3+ 
76/F Mixed cellularity (IVb) 20 12.9 16 0 (cycle 16) CR (cycle 4) AE (PSN) 5.7 16.8+ 
64/F Classical HL NOS (IIb) 90 5.0 6 0 (no reduction) CR (EOT) AE (PSN) 12.2 16.3+ 
84/M Nodular sclerosis (IIIa) 100 37.3 15 3 (cycle 6) CR (cycle 2) AE (PSN) 1.0 14.3+ 
84/M Classical HL NOS (IIIa) 80 14.7 3 (cycle 4) CR (cycle 2) AE (PSN) 7.4 14.3 
78/M Nodular sclerosis (IIa) 90 64.4 0 (no reduction) CR (EOT) AE (orthostatic hypertension) 9.8 13.4+ 

EOT, end of treatment; PSN, peripheral sensory neuropathy; SPD, sum of the products of the largest diameters of up to 6 index lymph nodes or nodal masses being followed for response assessment.

*

No definite evidence of lymphoma after 23 cycles.

Consolidative radiation after EOT.

Death due to respiratory failure 8 months after the last dose of brentuximab vedotin; preexisting coronary artery disease, myelofibrosis, and macrocytic anemia.

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