Table 1.

Patient and disease characteristics

CharacteristicPart 1 (N = 12)Part 2
CLL/SLL (n = 45)R/R FL (n = 36)
Age, y    
 Median 68 68 59 
 Range 51-86 38-82 34-86 
ECOG PS    
 0 20 (44) 28 (78) 
 1 24 (53) 6 (17) 
 2 1 (2) 2 (6) 
Prior treatment status    
 TN 20 (44) 
 R/R 12 25 (56) 36 (100) 
Rituximab-refractory status for R/R FL*    
Refractory — — 14 (39) 
 Not refractory or unknown — — 22 (61) 
Refractory to most recent line of therapy*    
 Refractory — — 12 (33) 
 Not refractory or unknown — — 24 (67) 
Prior therapies for patients with R/R disease  n = 25 n = 36 
 Median 
 Range 1-9 1-4 1-9 
Bulky disease, cm    
 Node >5 — 15 (33) 17 (47) 
 Node >10 — 4 (11) 
Molecular risk factors (n = 39)    
 Unmutated IGHV — 19 (49) — 
 Del(17p)/p53 mutation — 16 (41) — 
 Del(11q) — 10 (26) — 
 Complex karyotype — 9 (23) — 
CharacteristicPart 1 (N = 12)Part 2
CLL/SLL (n = 45)R/R FL (n = 36)
Age, y    
 Median 68 68 59 
 Range 51-86 38-82 34-86 
ECOG PS    
 0 20 (44) 28 (78) 
 1 24 (53) 6 (17) 
 2 1 (2) 2 (6) 
Prior treatment status    
 TN 20 (44) 
 R/R 12 25 (56) 36 (100) 
Rituximab-refractory status for R/R FL*    
Refractory — — 14 (39) 
 Not refractory or unknown — — 22 (61) 
Refractory to most recent line of therapy*    
 Refractory — — 12 (33) 
 Not refractory or unknown — — 24 (67) 
Prior therapies for patients with R/R disease  n = 25 n = 36 
 Median 
 Range 1-9 1-4 1-9 
Bulky disease, cm    
 Node >5 — 15 (33) 17 (47) 
 Node >10 — 4 (11) 
Molecular risk factors (n = 39)    
 Unmutated IGHV — 19 (49) — 
 Del(17p)/p53 mutation — 16 (41) — 
 Del(11q) — 10 (26) — 
 Complex karyotype — 9 (23) — 

Values are n (%) except as noted.

ECOG PS, Eastern Cooperative Oncology Group performance status; PI3K, phosphoinositide 3-kinase.

*

Refractoriness was defined per protocol as less than partial response or PD within 6 mo after completion of prior rituximab-containing therapy (single agent or combination). Missing dates for some patients’ prior lines of therapy limited the number of definitely rituximab-refractory or refractory patients identified; where critical dates were missing, we classified patients conservatively as non–rituximab refractory or unknown.

Prior therapies included nucleoside analogs (fludarabine, gemcitabine, cytarabine, methotrexate), alkylating agents (cyclophosphamide, chlorambucil, bendamustine, ifosfamide, carmustine, melphalan, cisplatin, oxaliplatin, carboplatin), anthracyclines (doxorubicin, epirubicin, pirarubicin), topoisomerase inhibitors (etoposide, mitoxantrone), vinca alkyloids (vinorelbine, vincristine), anti-CD20 agents (rituximab, ofatumumab), BCL2 inhibitor (navitoclax), corticosteroids (dexamethasone, prednisone, prednisolone), histone deacetylase inhibitor (panobinostat), immunomodulators (lenalidomide), PI3K inhibitor (idelalisib), and dual-affinity retargeting antibody.

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