Table 1 Main characteristics and clinical data of HIV+ and HIV− patients with non-Hodgkin lymphoma receiving HDC and ASCT.
HIV+ patients (#=11)a | HIV− patients (#=9) | |
---|---|---|
number (%)b | number (%) | |
Sex (males) | 11 (100%) | 5 (56%)* |
Age: median years (range) | 46 (29–54) | 51 (27–70) |
Detectable HIV-viral load at enrolment | 1 (9%)c | na |
Hepatitis B surface antigen positive | 0 (0%) | 1 (11%) |
Hepatitis C virus positive | 3 (27%) | 0 (0%) |
Epstein Barr virus positive | 4d | 1 |
Histology | ||
DLBCL | 5 (45%) | 8 (89%) |
Plasmablastic lymphoma | 4 (36%) | 0 (0%) |
Anaplastic large cell lymphoma ALK-negative | 1 (9%) | 0 (0%) |
Intermediate BL/DLBCL | 1 (9%) | 0 (0%) |
High grade B-cell lymphoma, unclassified | 0 (0%) | 1 (11%) |
Ann-Arbor classification | ||
Stage I–II | 1 (9%) | 2 (22%) |
Stage III–IV | 10 (91%) | 7 (78%) |
Disease status | ||
1st complete remission | 3 (27%) | 4 (44%) |
2nd complete remission | 1 (9%) | 1 (11%) |
1st partial remission | 6 (55%) | 4 (44%) |
chemosensitive relapse | 1 (9%) | 0 (0%) |
Previous lines of therapies: | ||
1 | 7 (64%) | 7 (78%) |
2 | 3 (27%) | 2 (22%) |
3 | 1 (9%) | 0 (0%) |
Rituximab treatment before ASCT | 5 (45%) | 9 (100%)* |
Conditioning regimen: | ||
BEAMe | 10 (91%) | 9 (100%) |
Carmustine-thiotepaf | 1 (9%) | 0 (0%) |
T0g versus the last day of induction chemotherapy: median days (range) | 55 (40–212) | 50 (36–132) |
T0g versus the last rituximab administration: median days (range) | 98 (43–107) | 73 (43–139) |
Mobilized CD34+cells: median × 106 (range) | 5.8 (2.65–12.9) | 16.3 (6.4–20.7)* |
Infused CD34+cells: median × 106/Kg of body weight (range) | 5.8 (2.65–9.5) | 6.9 (4.4–9.4) |
Neutrophil engraftment: median days (range) | 10 (9–12) | 9 (8–11) |
Late onset neutropenia | 2 (18%) | 2 (22%) |
Platelet engraftment: median days (range) | 13 (10–16) | 12 (10–16) |
Radiotherapy after ASCT | 6 (55%) | 3 (33%) |