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Pomalidomide, bortezomib, and dexamethasone at first relapse in lenalidomide-pretreated myeloma: A subanalysis of OPTIMISMM by clinical characteristics.
Richardson, Paul G; Schjesvold, Fredrik; Weisel, Katja; Moreau, Philippe; Anderson, Larry D; White, Darrell; Rodriguez-Otero, Paula; Sonneveld, Pieter; Engelhardt, Monika; Jenner, Matthew; Corso, Alessandro; Dürig, Jan; Pavic, Michel; Salomo, Morten; Beksac, Meral; Oriol, Albert; Lindsay, Jindriska; Liberati, Anna Marina; Galli, Monica; Robak, Pawel; Larocca, Alessandra; Yagci, Munci; Vural, Filiz; Kanate, Abraham S; Jiang, Ruiyun; Grote, Lara; Peluso, Teresa; Dimopoulos, Meletios.
Afiliação
  • Richardson PG; Department of Medical Oncology, Jerome Lipper Multiple Myeloma Center, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA.
  • Schjesvold F; Oslo Myeloma Center at Oslo University Hospital, KG Jebsen Center for B-Cell Malignancies, University of Oslo, Oslo, Norway.
  • Weisel K; Department of Oncology, Hematology and Bone Marrow Transplantation with Section of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Moreau P; University Hospital Hôtel-Dieu, Nantes, France.
  • Anderson LD; University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • White D; Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, NS, Canada.
  • Rodriguez-Otero P; Clinica Universidad de Navarra, CIMA, IDISNA, Pamplona, Spain.
  • Sonneveld P; Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Engelhardt M; Universitätsklinikum Freiburg, Freiburg, Germany.
  • Jenner M; Southampton General Hospital, Southampton, UK.
  • Corso A; Policlinico San Matteo Universita Di Pavia, Pavia, Italy.
  • Dürig J; University Hospital Essen, Essen, Germany.
  • Pavic M; Centre Hospitalier Universitaire De Sherbrooke (CHUS), Centre de Recherche Clinique Etienne-Le Bel (CRCELB) Hopital Fleurimont, Sherbrooke, QC, Canada.
  • Salomo M; Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Beksac M; Ankara University, Ankara, Turkey.
  • Oriol A; Institut Català d'Oncologia I Institut Josep Carreras, Hospital Germans Trias i Pujol, Badalona, Spain.
  • Lindsay J; East Kent Hospitals University NHS Foundation Trust, Kent and Canterbury Hospital, Canterbury, UK.
  • Liberati AM; University of Perugia, Perugia, Italy.
  • Galli M; Ospedale Papa Giovanni XXIII, U.O. di Ematologia, Ispedali Riuniti di Bergamo, Bergamo, Italy.
  • Robak P; Medical University of Lodz, Lodz, Poland.
  • Larocca A; A.O.U. Citta della Salute e della Scienza di Torino, Torino, Italy.
  • Yagci M; Gazi University Medical Faculty, Ankara, Turkey.
  • Vural F; Ege University, Izmir, Turkey.
  • Kanate AS; West Virginia University, Morgantown, West Virginia, USA.
  • Jiang R; Bristol Myers Squibb, Princeton, New Jersey, USA.
  • Grote L; Bristol Myers Squibb, Princeton, New Jersey, USA.
  • Peluso T; Celgene International Sàrl, a Bristol-Myers Squibb Company, Boudry, Switzerland.
  • Dimopoulos M; National and Kapodistrian University of Athens, Athens, Greece.
Eur J Haematol ; 108(1): 73-83, 2022 Jan.
Article em En | MEDLINE | ID: mdl-34496096
ABSTRACT

OBJECTIVE:

We evaluated the efficacy and safety of pomalidomide, bortezomib, and dexamethasone (PVd) vs bortezomib and dexamethasone (Vd) by age, renal function, and high-risk cytogenetic abnormalities in lenalidomide-pretreated patients with multiple myeloma at first relapse.

METHODS:

OPTIMISMM was a phase 3, multicenter, open-label, randomized study (NCT01734928; N = 559). The primary endpoint was progression-free survival (PFS).

RESULTS:

Overall, 226 patients had received one prior line of therapy. PVd significantly prolonged PFS vs Vd in patients aged ≤65 years (median, 22.0 vs 13.1 months; P = .0258) and >65 years (median, 17.6 vs 9.9 months; P = .0369). Median PFS in patients with renal impairment (RI; creatinine clearance <60 mL/min) was 15.1 months with PVd vs 9.5 months with Vd (hazard ratio [HR], 0.67 [95% CI, 0.34-1.34]). In patients without RI, median PFS was 22.0 vs 13.1 months (HR, 0.45 [95% CI, 0.27-0.76]). In patients with high-risk cytogenetics, median PFS was 14.7 vs 9.9 months (HR, 0.39 [95% CI, 0.13-1.17]). PVd significantly improved overall response rate vs Vd in all subgroups. The safety profile of PVd was consistent with previous reports.

CONCLUSIONS:

These findings confirmed the benefits of PVd at first relapse, including in patients with poor prognostic factors.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Mieloma Múltiplo Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Mieloma Múltiplo Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2022 Tipo de documento: Article