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Bortezomib use and outcomes for the treatment of multiple myeloma.
Loke, Crystal; Mollee, Peter; McPherson, Ian; Walpole, Euan; Yue, Mimi; Mutsando, Howard; Wong, Phillip; Weston, Helen; Tomlinson, Ross; Hollingworth, Samantha.
Affiliation
  • Loke C; School of Pharmacy, The University of Queensland, Brisbane, Queensland, Australia.
  • Mollee P; Department of Cancer Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
  • McPherson I; Department of Cancer Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
  • Walpole E; Department of Cancer Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
  • Yue M; Department of Cancer Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
  • Mutsando H; Toowoomba Hospital, Darling Downs Hospital and Health Services, Toowoomba, Queensland, Australia.
  • Wong P; Toowoomba Hospital, Darling Downs Hospital and Health Services, Toowoomba, Queensland, Australia.
  • Weston H; Regional Cancer Care, Cancer Care Services, Sunshine Coast University Hospital, Sunshine Coast, Queensland, Australia.
  • Tomlinson R; Regional Cancer Care, Cancer Care Services, Sunshine Coast University Hospital, Sunshine Coast, Queensland, Australia.
  • Hollingworth S; School of Pharmacy, The University of Queensland, Brisbane, Queensland, Australia.
Intern Med J ; 50(9): 1059-1066, 2020 09.
Article in En | MEDLINE | ID: mdl-32369254
ABSTRACT

BACKGROUND:

The public subsidy in Australia of bortezomib (Velcade) for untreated non-transplant multiple myeloma patients was based on the VISTA trial.

AIMS:

To ascertain the health outcomes of bortezomib in 'real world' transplant-ineligible elderly patients, compared to trial data.

METHODS:

Patient and treatment data were extracted from an oncology information system, laboratory information system and medical chart audits for three Queensland public hospitals.

RESULTS:

We identified 74 patients; the median age was 75 years. Our cohort comprised 47% patients who were International Staging System stage III, 45% at stage II and 8% at stage I. Patients who had comorbidities, such as cardiac disease (41%), pulmonary disease (14%), diabetes (22%), peripheral neuropathy (14%) and other comorbidities (41%) at baseline were included. The common regimens prescribed were VMP, CVD and VD, and most patients (n = 73) received bortezomib on a once-weekly or twice-a-week basis. The overall response rate was 81%. Half (53%) of the patients did not complete their planned therapy due to toxicity (30%), suboptimal response or disease progression (15%), or death on treatment (8%). Overall survival was 40.7 months and progression free survival was 17.7 months.

CONCLUSIONS:

Our patients were older, had worse disease characteristics and more comorbidities than patients in the VISTA trial. While response rates were similar, survival outcomes appeared worse. Bortezomib-based treatment in the real world setting still carries a high risk of toxicity in the elderly population.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Multiple Myeloma Type of study: Prognostic_studies Limits: Aged / Humans Country/Region as subject: Oceania Language: En Journal: Intern Med J Journal subject: MEDICINA INTERNA Year: 2020 Document type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Multiple Myeloma Type of study: Prognostic_studies Limits: Aged / Humans Country/Region as subject: Oceania Language: En Journal: Intern Med J Journal subject: MEDICINA INTERNA Year: 2020 Document type: Article Affiliation country: Australia