Table 1 Safety population patient characteristics: dose escalation

From: Preclinical and first-in-human of purinostat mesylate, a novel selective HDAC I/IIb inhibitor, in relapsed/refractory multiple myeloma and lymphoma

Baseline Demographics & Disposition

N = 29

sex, n (%)

Male

18 (62)

Female

11 (38)

Age, median years (range)

53 (22–72)

Histology, n (%)

MM

11 (37.9)

Lymphoma

18 (62)

Subtype, n (%)

DLBCL

11 (37.9)

FL

3 (10.3)

Large B-cell lymphoma

1 (3.4)

cHL

1 (3.4)

PTCL-NOS

1 (3.4)

AITL

1 (3.4)

Stage of MM, n (%)

II

1 (9.1)

III

10 (90.9)

Stage of DLBCL, n (%)

I–II

1 (9.1)

III–IV

10 (90.9)

No. prior regimens, median (range)

MM

3 (1–7)

Lymphoma

2 (1–4)

Prior therapy of MM, n (%)

Lenalidomide, Bortezomib, Dexamethasone

11 (100)

Daratumumab

3 (27.3)

Autologous Stem Cell Transplantation

2 (18.2)

BCMA-CAR-T

1 (9.1)

Prior therapy of DLBCL, n (%)

Chidamide+RCHOP

2 (18.2)

Autologous stem cell transplantation

2 (18.2)

  1. MM multiple myeloma, DLBCL diffuse large B-cell lymphoma, FL follicular lymphoma, cHL classic hodgkin lymphoma, peripheral T cell lymphoma-not otherwise specified, AITL angioimmunoblastic T-cell lymphoma. RCHOP Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisone