Table 1.

Demographic characteristics of patients enrolled in the phase 1 study plus the expansion cohort of patients with peripheral T-cell lymphoma

CharacteristicData (N = 31)
Age, median (range), y 57 (23-79) 
Sex, n (%)  
 Male 19 (61) 
 Female 12 (39) 
Ethnicity, n (%)  
 White, non-Hispanic 19 (61) 
 White, Hispanic 6 (20) 
 Black, non-Hispanic 1 (3) 
 Black, Hispanic 4 (13) 
 Asian or Pacific Islander 1 (3) 
Lymphoma subtype, n (%)   
 Hodgkin lymphoma 12 (39) 
 Diffuse large B-cell lymphoma* 6 (20) 
 Follicular lymphoma 2 (6) 
T-cell lymphoma 11 (35) 
  Angioimmunoblastic T-cell lymphoma 3 (10) 
  Adult T-cell leukemia/lymphoma 2 (6) 
  Peripheral T-cell lymphoma-NOS (cutaneous) 1 (3) 
  Anaplastic large cell lymphoma, cutaneous 1 (3) 
  Cutaneous T-cell lymphoma 1 (3) 
  Enteropathy-associated T-cell lymphoma 1 (3) 
  Extranodal natural killer/T-cell lymphoma 1 (3) 
  T-cell lymphoblastic lymphoma 1 (3) 
Median number of prior therapies 6 (1-15) 
Prior regimens (at least 1 cycle), n (%)  
Hodgkin lymphoma (n = 12)  
 ABVD-like, BEACOPP 12 (39) 
 Platinum-based (ICE, ESHAP) 12 (39) 
 Bv-based (Bv, Bv+B, Bv+AVD) 12 (39) 
 Other alkylator-based (COPP, MOPP, B) 11 (35) 
 Lenalidomide 8 (26) 
 Gem-based (gem or GND) 7 (23) 
 Experimental drug 7 (23) 
 Other therapy 6 (20) 
B-cell lymphoma (n = 8)  
 Anthracycline-based (R-CHOP, R-EPOCH) 7 (23) 
 Platinum-based (R-ICE, R-DICE) 6 (20) 
 Nonanthracycline-based (R-CVP, R-FND, R-B, R-B-bortezomib, R-F) 4 (13) 
 Single agent anti-CD20 antibody (rituximab, ublituximab) 4 (13) 
 Idelalisib + rituximab 2 (6) 
 Experimental drug or other therapy§ 5 (16) 
T-cell lymphoma (n = 11)  
 Anthracycline-based (CHOP, CHOEP, EPOCH±bortezomib) 8 (26) 
 Gem-based (gem, p-gemox, gem+liposomal cytarabine) 4 (13) 
 HDAC inhibitor (vorinostat, ROMI) 3 (10) 
 Bv 2 (6) 
 Pralatrexate 1 (3) 
 Experimental drug or other therapy, n (%) 6 (20) 
Prior ASCT, n (%) 16 (52) 
Prior alloSCT, n (%) 5 (16) 
Radiotherapy/radioimmunotherapy, n (%) 10 (32) 
CharacteristicData (N = 31)
Age, median (range), y 57 (23-79) 
Sex, n (%)  
 Male 19 (61) 
 Female 12 (39) 
Ethnicity, n (%)  
 White, non-Hispanic 19 (61) 
 White, Hispanic 6 (20) 
 Black, non-Hispanic 1 (3) 
 Black, Hispanic 4 (13) 
 Asian or Pacific Islander 1 (3) 
Lymphoma subtype, n (%)   
 Hodgkin lymphoma 12 (39) 
 Diffuse large B-cell lymphoma* 6 (20) 
 Follicular lymphoma 2 (6) 
T-cell lymphoma 11 (35) 
  Angioimmunoblastic T-cell lymphoma 3 (10) 
  Adult T-cell leukemia/lymphoma 2 (6) 
  Peripheral T-cell lymphoma-NOS (cutaneous) 1 (3) 
  Anaplastic large cell lymphoma, cutaneous 1 (3) 
  Cutaneous T-cell lymphoma 1 (3) 
  Enteropathy-associated T-cell lymphoma 1 (3) 
  Extranodal natural killer/T-cell lymphoma 1 (3) 
  T-cell lymphoblastic lymphoma 1 (3) 
Median number of prior therapies 6 (1-15) 
Prior regimens (at least 1 cycle), n (%)  
Hodgkin lymphoma (n = 12)  
 ABVD-like, BEACOPP 12 (39) 
 Platinum-based (ICE, ESHAP) 12 (39) 
 Bv-based (Bv, Bv+B, Bv+AVD) 12 (39) 
 Other alkylator-based (COPP, MOPP, B) 11 (35) 
 Lenalidomide 8 (26) 
 Gem-based (gem or GND) 7 (23) 
 Experimental drug 7 (23) 
 Other therapy 6 (20) 
B-cell lymphoma (n = 8)  
 Anthracycline-based (R-CHOP, R-EPOCH) 7 (23) 
 Platinum-based (R-ICE, R-DICE) 6 (20) 
 Nonanthracycline-based (R-CVP, R-FND, R-B, R-B-bortezomib, R-F) 4 (13) 
 Single agent anti-CD20 antibody (rituximab, ublituximab) 4 (13) 
 Idelalisib + rituximab 2 (6) 
 Experimental drug or other therapy§ 5 (16) 
T-cell lymphoma (n = 11)  
 Anthracycline-based (CHOP, CHOEP, EPOCH±bortezomib) 8 (26) 
 Gem-based (gem, p-gemox, gem+liposomal cytarabine) 4 (13) 
 HDAC inhibitor (vorinostat, ROMI) 3 (10) 
 Bv 2 (6) 
 Pralatrexate 1 (3) 
 Experimental drug or other therapy, n (%) 6 (20) 
Prior ASCT, n (%) 16 (52) 
Prior alloSCT, n (%) 5 (16) 
Radiotherapy/radioimmunotherapy, n (%) 10 (32) 

A(B)VD, Adriamycin, bleomycin, vinblastine, dacarbazine; B bendamustine; BAC, bendamustine, cytarabine; BEACOPP, bleomycin, etoposide, Adriamycin, cyclophosphamide, vincristine, procarbazine, prednisone; Bv, brentuximab vedotin; COPP, cyclophosphamide, vincristine, procarbazine, prednisone/Adriamycin; CVP, cyclophosphamide, vincristin, prednisone; (D)ICE, (dexamethasone) ifosphamide, carboplatin, etoposide; EPOCH, etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin; ESHAP, etoposide, methylprednisolone, high-dose cytarabine, cisplatin; FND, fludarabine, mitoxanthrone, dexamethasone; Gem, gemcitabine; gemox, gemcitabine+oxaliplatin; GND, gemcitabine, navelbine, liposomal doxorubicin; IVAC, etoposide, ifosfamide, cytarabine, methotrexate; MOPP, mechlorethamine, vincristine, procarbazine, prednisone; (R)-CHO(E)P, rituximab, cyclophosphamide, doxorubicin, vincristine (etoposide) prednisone; (p)GemOx, (peg-asparaginase) gemcitabine, oxaliplatin; SMILE, dexamethasone, methotrexate, ifosfamide, l-asparaginase, etoposide.

*

3 nodal, 2 transformed from follicular lymphoma, 1 cutaneous.

ACY1215, umbralisib, PI3K inhibitor+JAK inhibitor, pralatrexate+ROMI, vorinostat+niacinamide, Nedd8-activating enzyme inhibitor MLN4924, CUDC907, belinostat, CPI-0610, SB743921, MDX-060.

EPOCH, IVAC, vinblastine+bleomycin+methotrexate, vinblastine, pembrolizumab (compassionate use), EBV-specific cytotoxic T-lymphocytes, alternative medicine.

§

Anti-CD37, vorinostat-niacinamide±etoposide, ibrutinib, umbralisib, pralatrexate, brentuximab vedotin, R-lenalidomide.

Pralatrexate+ROMI, bortezomib, Nelarabine, mogamulizumab, bexarotene, photopheresis±interferon, total skin electron beam therapy, pembrolizumab, bendamustine, ICE, SMILE, BAC.

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