Health-related quality of life in patients with light chain amyloidosis treated with bortezomib, cyclophosphamide, and dexamethasone ± daratumumab: results from the ANDROMEDA study

  • Vaishali Sanchorawala
  • , Giovanni Palladini
  • , Monique C Minnema
  • , Arnaud Jaccard
  • , Hans C Lee
  • , Simon Gibbs
  • , Peter Mollee
  • , Christopher Venner
  • , Jin Lu
  • , Stefan Schönland
  • , Moshe Gatt
  • , Kenshi Suzuki
  • , Kihyun Kim
  • , M Teresa Cibeira
  • , Meral Beksac
  • , Edward Libby
  • , Jason Valent
  • , Vania Hungria
  • , Sandy W Wong
  • , Michael Rosenzweig
  • Naresh Bumma, Dominique Chauveau, Katharine S Gries, John Fastenau, Nam Phuong Tran, Xiang Qin, Sandra Y Vasey, Brendan M Weiss, Jessica Vermeulen, Kai Fai Ho, Giampaolo Merlini, Raymond L Comenzo, Efstathios Kastritis, Ashutosh D Wechalekar

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

In the phase 3 ANDROMEDA trial, patients treated with daratumumab, bortezomib, cyclophosphamide, and dexamethasone (D-VCd) had significantly higher rates of organ and hematologic response compared with patients who received VCd alone. Here, we present patient-reported outcomes (PROs) from the ANDROMEDA trial. PROs were assessed through cycle 6 using three standardized questionnaires. Treatment effect through cycle 6 was measured by a repeated-measures, mixed-effects model. The magnitude of changes in PROs versus baseline was generally low, but between-group differences favored the D-VCd group. Results were generally consistent irrespective of hematologic, cardiac, or renal responses. More patients in the D-VCd group experienced meaningful improvements in PROs; median time to improvement was more rapid in the D-VCd group versus the VCd group. After cycle 6, patients in the D-VCd group received daratumumab monotherapy and their PRO assessments continued, with improvements in health-related quality of life (HRQoL) reported through cycle 19. PROs of subgroups with renal and cardiac involvement were consistent with those of the intent-to-treat population. These results demonstrate that the previously reported clinical benefits of D-VCd were achieved without decrement to patients' HRQoL and provide support of D-VCd in patients with AL amyloidosis.

Original languageEnglish
Pages (from-to)719-730
Number of pages12
JournalAmerican Journal of Hematology
Volume97
Issue number6
Early online date16 Mar 2022
DOIs
Publication statusPublished - 1 Jun 2022

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