Treatment in newly diagnosed elderly/frail cHL
Regimen . | Phase . | n . | Stage . | Median age, y . | CRR, % . | PFS . | Frail . | Reference . |
---|---|---|---|---|---|---|---|---|
BV and anti PD-1 therapies in elderly/frail patients | ||||||||
BV | 2 | 27 | I-IV | 78 | 73 | Median, 10.5 mo | 81% were impaired in ≥1 aspect of GA | 84 |
BV (BREVITY) | 2 | 38 | II-IV | 76 | 26 | Median, 7.3 mo | Median CIRS-G score was 6 in evaluable patients | 85 |
BV (1.2 mg/m2) +bendamustine (HALO) | 1/2 | 59 | II-IV | 70 | 63 | 54% at 2 y | 79% | 87 |
BV+DTIC | 2 | 19 | I-IV | 69 | 68 | Median PFS, 46.8 mo | 50% | 86,88 |
BV (1.8 mg/m2) +bendamustine (70 mg/m2) | 2 | 20 | I-IV | 75 | 88 | Median PFS, 40.3 mo | 45% | 86,88 |
BV+nivo (≤16 cycles) | 2 | 21 | II-IV | 72 | 79 | Median PFS not reached | GA not reported* | 88 |
BV+nivo (8 cycles) | 2 | 46 | II-IV | 71 | 68 | Median PFS, 21.8 mo | GA not assessed† | 89 |
Sequential BV→AVD‡ | 2 | 48 | II-IV | 69 | 81 | 85% at 2 y | Median CIRS-G score was 7 | 90 |
Standard chemotherapies in elderly/frail patients | ||||||||
ABVD×6-8§ | 3§ | 23 | II-IV | 66 | 65 | 64% at 5 y | — | 83 |
Stanford V§ | 3§ | 21 | II-IV | 64 | 62 | 51% at 5 y | — | 83 |
ABVD×2+IFRT‖ | 3‖ | 70 | I-II | 64 | 96 | 70% at 5 y | — | 94 |
AVD×2+IFRT¶ | 3¶ | 82 | I-II | 66 | 98 | 70% at 5 y | — | 94 |
PVAG×6-8 | 2 | 59 | II-IV | 68 | 78 | 58% at 3y | — | 96 |
Regimen . | Phase . | n . | Stage . | Median age, y . | CRR, % . | PFS . | Frail . | Reference . |
---|---|---|---|---|---|---|---|---|
BV and anti PD-1 therapies in elderly/frail patients | ||||||||
BV | 2 | 27 | I-IV | 78 | 73 | Median, 10.5 mo | 81% were impaired in ≥1 aspect of GA | 84 |
BV (BREVITY) | 2 | 38 | II-IV | 76 | 26 | Median, 7.3 mo | Median CIRS-G score was 6 in evaluable patients | 85 |
BV (1.2 mg/m2) +bendamustine (HALO) | 1/2 | 59 | II-IV | 70 | 63 | 54% at 2 y | 79% | 87 |
BV+DTIC | 2 | 19 | I-IV | 69 | 68 | Median PFS, 46.8 mo | 50% | 86,88 |
BV (1.8 mg/m2) +bendamustine (70 mg/m2) | 2 | 20 | I-IV | 75 | 88 | Median PFS, 40.3 mo | 45% | 86,88 |
BV+nivo (≤16 cycles) | 2 | 21 | II-IV | 72 | 79 | Median PFS not reached | GA not reported* | 88 |
BV+nivo (8 cycles) | 2 | 46 | II-IV | 71 | 68 | Median PFS, 21.8 mo | GA not assessed† | 89 |
Sequential BV→AVD‡ | 2 | 48 | II-IV | 69 | 81 | 85% at 2 y | Median CIRS-G score was 7 | 90 |
Standard chemotherapies in elderly/frail patients | ||||||||
ABVD×6-8§ | 3§ | 23 | II-IV | 66 | 65 | 64% at 5 y | — | 83 |
Stanford V§ | 3§ | 21 | II-IV | 64 | 62 | 51% at 5 y | — | 83 |
ABVD×2+IFRT‖ | 3‖ | 70 | I-II | 64 | 96 | 70% at 5 y | — | 94 |
AVD×2+IFRT¶ | 3¶ | 82 | I-II | 66 | 98 | 70% at 5 y | — | 94 |
PVAG×6-8 | 2 | 59 | II-IV | 68 | 78 | 58% at 3y | — | 96 |
CIRS-G, Cumulative Illness Rating Scale-Geriatric comorbidity score; DTIC, dacarbazine; GA, geriatric assessment; IFRT, involved field radiation therapy.
Patients ≥60 year of age who were considered unfit for conventional chemotherapy were included in the study.
Patients were selected based on abnormal organ function that would render them poor candidates for standard chemotherapy.
Patients received 2 cycles of BV followed by 6 cycles of AVD and then 4 cycles of BV consolidation in those who responded.
Secondary analysis of E2496 data.
Secondary analysis of GHSG HD10 study data.
Secondary analysis of GHSG HD13 study data.