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Results of a UK National Cancer Research Institute Phase II study of brentuximab vedotin using a response-adapted design in the first-line treatment of patients with classical Hodgkin lymphoma unsuitable for chemotherapy due to age, frailty or comorbidity (BREVITY)

Results of a UK National Cancer Research Institute Phase II study of brentuximab vedotin using a response-adapted design in the first-line treatment of patients with classical Hodgkin lymphoma unsuitable for chemotherapy due to age, frailty or comorbidity (BREVITY)
Results of a UK National Cancer Research Institute Phase II study of brentuximab vedotin using a response-adapted design in the first-line treatment of patients with classical Hodgkin lymphoma unsuitable for chemotherapy due to age, frailty or comorbidity (BREVITY)

Standard treatment for classical Hodgkin lymphoma (cHL) is poorly tolerated in older patients and results disappointing. We assessed safety and efficacy of brentuximab vedotin (BV), in previously untreated patients with cHL unfit for standard treatment due to age, frailty or comorbidity. The primary outcome was complete metabolic response (CMR) by positron emission tomography/computed tomography after four BV cycles (PET4). The secondary outcomes included progression-free survival (PFS), overall survival (OS), and toxicity. In all, 35 patients with a median age of 77 years and median total Cumulative Illness Rating Scale for Geriatrics (CIRS-G) score of 6 were evaluable for toxicity and 31 for response. A median of four cycles were given (range one-16). In all, 14 patients required dose reduction due to toxicity and 11 patients stopped treatment due to adverse events (AEs). A total of 716 AEs were reported, of which 626 (88%) were Grade 1/2 and 27 (77%) patients had at least one AE Grade ≥3. At PET4, CMR was 25·8% [95% confidence interval (CI) 13·7-42.2%] and objective response rate 83·9% (95% CI 63·7-90·8%). Median PFS was 7·3 months (95% CI 5·2-9·0), and OS 19·5 months. Our results suggest that BV monotherapy is tolerable but suboptimal in the front-line therapy of elderly or comorbid patients with cHL. Combining BV with other agents may be more effective. Trial Registration: Clinicaltrials.gov identifier: NCT02567851.

Hodgkin lymphoma, brentuximab Vedotin, elderly
0007-1048
Gibb, Adam
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Pirrie, Sarah J
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Linton, Kim
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Warbey, Victoria
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Paterson, Kathryn
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Davies, Andrew J
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Collins, Graham P
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Menne, Tobias
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McKay, Pamela
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Fields, Paul A
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Miall, Fiona M
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Nagy, Eszter
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Wheatley, Keith
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Reed, Rachel
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Baricevic-Jones, Ivona
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Barrington, Sally
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Radford, John
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Gibb, Adam
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Pirrie, Sarah J
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Linton, Kim
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Warbey, Victoria
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Paterson, Kathryn
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Davies, Andrew J
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Collins, Graham P
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Menne, Tobias
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McKay, Pamela
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Fields, Paul A
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Miall, Fiona M
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Nagy, Eszter
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Wheatley, Keith
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Reed, Rachel
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Baricevic-Jones, Ivona
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Barrington, Sally
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Radford, John
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Gibb, Adam, Pirrie, Sarah J, Linton, Kim, Warbey, Victoria, Paterson, Kathryn, Davies, Andrew J, Collins, Graham P, Menne, Tobias, McKay, Pamela, Fields, Paul A, Miall, Fiona M, Nagy, Eszter, Wheatley, Keith, Reed, Rachel, Baricevic-Jones, Ivona, Barrington, Sally and Radford, John (2020) Results of a UK National Cancer Research Institute Phase II study of brentuximab vedotin using a response-adapted design in the first-line treatment of patients with classical Hodgkin lymphoma unsuitable for chemotherapy due to age, frailty or comorbidity (BREVITY). British Journal of Haematology. (doi:10.1111/bjh.17073).

Record type: Article

Abstract

Standard treatment for classical Hodgkin lymphoma (cHL) is poorly tolerated in older patients and results disappointing. We assessed safety and efficacy of brentuximab vedotin (BV), in previously untreated patients with cHL unfit for standard treatment due to age, frailty or comorbidity. The primary outcome was complete metabolic response (CMR) by positron emission tomography/computed tomography after four BV cycles (PET4). The secondary outcomes included progression-free survival (PFS), overall survival (OS), and toxicity. In all, 35 patients with a median age of 77 years and median total Cumulative Illness Rating Scale for Geriatrics (CIRS-G) score of 6 were evaluable for toxicity and 31 for response. A median of four cycles were given (range one-16). In all, 14 patients required dose reduction due to toxicity and 11 patients stopped treatment due to adverse events (AEs). A total of 716 AEs were reported, of which 626 (88%) were Grade 1/2 and 27 (77%) patients had at least one AE Grade ≥3. At PET4, CMR was 25·8% [95% confidence interval (CI) 13·7-42.2%] and objective response rate 83·9% (95% CI 63·7-90·8%). Median PFS was 7·3 months (95% CI 5·2-9·0), and OS 19·5 months. Our results suggest that BV monotherapy is tolerable but suboptimal in the front-line therapy of elderly or comorbid patients with cHL. Combining BV with other agents may be more effective. Trial Registration: Clinicaltrials.gov identifier: NCT02567851.

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Accepted/In Press date: 4 August 2020
e-pub ahead of print date: 14 September 2020
Keywords: Hodgkin lymphoma, brentuximab Vedotin, elderly

Identifiers

Local EPrints ID: 444732
URI: http://eprints.soton.ac.uk/id/eprint/444732
ISSN: 0007-1048
PURE UUID: 71dbe037-103c-46e8-ae7c-880db61b9650
ORCID for Andrew J Davies: ORCID iD orcid.org/0000-0002-7517-6938

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Date deposited: 02 Nov 2020 17:32
Last modified: 17 Mar 2024 03:14

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Contributors

Author: Adam Gibb
Author: Sarah J Pirrie
Author: Kim Linton
Author: Victoria Warbey
Author: Kathryn Paterson
Author: Andrew J Davies ORCID iD
Author: Graham P Collins
Author: Tobias Menne
Author: Pamela McKay
Author: Paul A Fields
Author: Fiona M Miall
Author: Eszter Nagy
Author: Keith Wheatley
Author: Rachel Reed
Author: Ivona Baricevic-Jones
Author: Sally Barrington
Author: John Radford

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