Table 3.
Patient | Age | Sex | Lugano stage | 1st line treatment | 1st line treatment response | Salvage treatment | Relapse before HSCT | HSCT type | Clinical outcomes | Follow-up period |
---|---|---|---|---|---|---|---|---|---|---|
1 | 64 | Male | IV | 4 cycles of SMILE | CR | – | CR | Frontline auto-HSCT | Relapse → died owing to PD |
12.1 mo |
2 | 50 | Female | IV | 7 cycles of ProMACE/CytaBOM | CR | – | CR | Frontline auto-HSCT | Relapse → died owing to PD |
18.3 mo |
3 | 56 | Male | II2 | 6 cycles of DL-ICE | CR | – | CR | Frontline auto-HSCT | Relapse → died owing to PD |
13.4 mo |
4 | 60 | Male | II2 | 5 cycles of SMILE | CR | – | CR | Frontline auto-HSCT | Relapse → died owing to PD |
25.3 mo |
5 | 59 | Male | IV | 6 cycles of DL-ICE | CR | – | CR | Frontline allo-HSCT MMUD (1 antigen mismatch) |
CR, alive | 8.3 mo |
6 | 47 | Female | IV | 6 cycles of EPOCH | CR | – | CR | Frontline allo-HSCT MSD |
CR, alive | 33.2 mo |
7 | 60 | Male | I | 6 cycles of DL-ICE | CR | – | CR | Frontline allo-HSCT MUD |
CR, alive | 61.3 mo |
8 | 37 | Male | IV | 6 cycles of EPOCH | SD | 3ESHAP | CR | Salvage auto-HSCT* | CR, alive | 29.9 mo |
9 | 60 | Male | IV | 6 cycles of DL-ICE | CR→ Relapse | 4EPOCH | PR | Salvage allo-HSCT FMT (haploidentical) |
CR, died owing to septic shock |
27.6 mo |
10 | 58 | Male | IV | 3 cycles of EPOCH | PD | 5ESHAP | PR | Salvage allo-HSCT FMT (haploidentical) |
CR, died owing to septic shock |
8.5 mo |
11 | 48 | Female | IV | 4 cycles of CHOP | PD | 3ESHAP→2EPOCH | PR | Salvage allo-HSCT MSD |
Relapse → died owing to PD |
14.6 mo |
12 | 53 | Female | IV | 3 cycles of CHOP | PD | 3IVAM→3DHAP | SD | Salvage allo-HSCT MSD |
Relapse → died owing to PD |
14.5 mo |
13 | 68 | Male | II2 | 6 cycles of ProMACE/CytaBOM | PD | 6DL-ICE | CR | Salvage allo-HSCT MSD |
CR, alive | 17.2 mo |
14 | 49 | Male | IV | 4 cycles of ProMACE/CytaBOM | PD | 3DL-ICE | PR | Salvage allo-HSCT MUD |
CR, alive | 139.1 mo |
Allo-HSCT, allogeneic hematopoietic stem cell transplantation; auto-HSCT, autologous hematopoietic stem cell transplantation; CR, complete response; FMT, family-mismatched donor transplantation; MSD, matched sibling donor; MUD, matched unrelated donor; MMUD, mismatched unrelated donor; PD, progressive disease; PR, partial response; SD, stable disease
*This patient achieved CR and subsequently underwent salvage auto-HSCT with cytokine-induced killer cell infusion as a clinical trial.
CHOP consists of cyclophosphamide, doxorubicin, vincristine, and prednisone. CHOEP consists of cyclophosphamide, doxorubicin, vincristine, etoposide, and prednisone. DHAP consists of dexamethasone, high-dose cytarabine, and cisplatin. DL-ICE consists of dexamethasone, l-asparaginase, ifosfamide, carboplatin, and etoposide. EPOCH consists of etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin. ESHAP consists of etoposide, methylprednisolone, high-dose cytarabine, and cisplatin. IVAM consists of ifosfamide, etoposide, cytarabine, and methotrexate. ProMACE-CytaBOM consists of cyclophosphamide, doxorubicin, etoposide, bleomycin, vincristine, methotrexate, and prednisone. SMILE consists of dexamethasone, methotrexate, ifosfamide, l-asparaginase, and etoposide.