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Table 3 Follow-up details of subjects who had further treatment after the phase Ib study

From: Combinatorial epigenetic therapy in diffuse large B cell lymphoma pre-clinical models and patients

Patient

Prior therapies

Response to prior line

Duration of response (months)

No. of AZA-vorinostat cycles

Subsequent therapies

Time between combination to subsequent therapy (days)

Response to subsequent therapies

TTP post-study (days)

OS post-study (days)

Survival status

1

RCHOP (×6)

CR

40

3

Veltuzumab with 90Y-epratuzumab

14

Significant clinical benefit

115

682

Dead

2

RCHOP (×6), VIPER (×3), BEAM, and ASCT

PD

NA

4

Oral PEP-C

16

Significant clinical benefit

408

556

Alive

3

CHOP + RT 10 years prior. De Angelis, RDICE (×3)

CR

8

2

Oral PEP-C

18

CR

220

501

Alive

4

RCHOP (×6), RDICE, RHCVAD (Bcycle)

PD

NA

2

Brentuximab + PEP-C (×4)

2

PD

79

148

Dead

5

RCHOP (×6), ESHAP (×3), lenalidomide, ibrutinib

PD

NA

4

RDICE (×3), ASCT

11

CR

436

825

Dead

6

RCHOP (×6), RDICE (×2), ibrutinib

PD

NA

1

Bendamustine (×1)

1

Significant clinical benefit

NA

45

Dead

7

RCHOP (×6), RICE (×2), R-Nav/Gem#1

PD

NA

1

Bendamustine (×1)

4

NA

NA

35

Alive

  1. Time to progression and overall survival calculated from the time the subject was taken off the study
  2. RCHOP rituximab in combination with cyclophosphamide, doxorubicin, vincristine, and prednisolone, VIPER bortezomib in combination with DICE chemotherapy plus rituximab, BEAM combination of carmustine, etoposide, cytarabine, and melphalan, ASCT autologous stem cell transplant, RT radiotherapy, RHCVAD rituximab-fractionated cyclophosphamide, vincristine, adriamycin, and dexamethasone, ESHAP etoposide, methylprednisolone, cytarabine and cisplatin, RCIE rituximab, ifosfamide, carboplatin, and etoposide, CR complete remission, PD progressive disease, NA not available, PEP-C prednisone, etoposide, procarbazine, and cyclophosphamide, TTP time to progression, OS overall survival