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Management and outcome of 500 multiple myeloma patients treated for first relapse outside clinical studies.
Avivi, Irit; Yekutiel, Naama; Shragai, Tamir; Cohen, Yael C; Grunspan, Moshe; Rivlin, Noa; Frankel, Neta; Cohen, Raanan; Weil, Clara; Chodick, Gabriel.
Afiliação
  • Avivi I; Department of Hematology, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel. iritavi@tlvmc.gov.il.
  • Yekutiel N; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel. iritavi@tlvmc.gov.il.
  • Shragai T; Maccabi Institute of Research and Innovation (Maccabitech), Maccabi Health Care Services, Tel-Aviv, Israel.
  • Cohen YC; Department of Hematology, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
  • Grunspan M; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Rivlin N; Department of Hematology, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
  • Frankel N; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Cohen R; Abbvie Inc., Hod Hasharon, Israel.
  • Weil C; Abbvie Inc., Hod Hasharon, Israel.
  • Chodick G; Abbvie Inc., Hod Hasharon, Israel.
Ann Hematol ; 102(11): 3075-3081, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37646848
ABSTRACT
Treatment options for multiple myeloma (MM) at 1st relapse are expanding. The current study compared common 2nd line regimens administered in a real-world setting. MM patients registered in Maccabi health care services and treated with second line therapy during 2014-2020 were evaluated, analyzing factors affecting time to third line therapy (TT3T). The study included 500 MM patients, previously treated with proteasome inhibitor (PI)-based induction. Median age at second line treatment was 68.5 years (IQR 61.6-76.4). Most patients received a triplet based induction composed of PI (n = 471, 94.2%), with (n = 71) or without IMID (n = 400), followed by second line treatment composed of lenalidomide-dexamethasone (RD) (n = 225, 45%) or lenalidomide-dexamethasone-daratumumab (RD-Dara (n = 104, 20.8%)). Multivariable analysis confirmed treatment type (RD-Dara vs. IMID) to be associated with a lower risk to progress to third line therapy; (HR = 0.5, 95% CI 0.3-0.86, p = 0.012). Within a median follow-up period of 22.5 months (intraquartile range 11.1-39.4 m), median TT3T was not reached in patients receiving RD-Dara vs. 32.4 months (95% CI 18.0-46.8 m) with IMID, 18 months (95% CI 10.4-25.6 m) with IMID-PI and 12.1 months (95% CI 5.6-18.7 m) with PI-based regimen. In contrast, PI vs. IMID-based therapy and increased body weight were associated with a higher likelihood of progression (HR = 2.56 (95% CI 1.49-4.42); HR = 1.43, (95% CI 0.96-2.14), p = 0.08). To conclude, second line therapy with RD-Dara was associated with a significantly longer TT3T compared with IMID-based regimen, longer than obtained with PI-IMID and PI-based regimens, in patients treated outside clinical studies and previously exposed to bortezomib.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article