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Phase 2 trial of ixazomib, cyclophosphamide, and dexamethasone for previously untreated light chain amyloidosis.
Muchtar, Eli; Gertz, Morie A; LaPlant, Betsy R; Buadi, Francis K; Leung, Nelson; O'Brien, Patrick; Bergsagel, P Leif; Fonder, Amie; Hwa, Yi Lisa; Hobbs, Miriam; Helgeson, Dania K; Bradt, Erin E; Gonsalves, Wilson; Lacy, Martha Q; Kapoor, Prashant; Siddiqui, Mustaqueem; Larsen, Jeremy T; Warsame, Rahma; Hayman, Suzanne R; Go, Ronald S; Dingli, David; Kourelis, Taxiarchis V; Dispenzieri, Angela; Rajkumar, S Vincent; Kumar, Shaji K.
Afiliación
  • Muchtar E; Division of Hematology.
  • Gertz MA; Division of Hematology.
  • LaPlant BR; Department of Quantitative Health Sciences, and.
  • Buadi FK; Division of Hematology.
  • Leung N; Division of Hematology.
  • O'Brien P; Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN; and.
  • Bergsagel PL; Department of Quantitative Health Sciences, and.
  • Fonder A; Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, AZ.
  • Hwa YL; Division of Hematology.
  • Hobbs M; Division of Hematology.
  • Helgeson DK; Division of Hematology.
  • Bradt EE; Division of Hematology.
  • Gonsalves W; Division of Hematology.
  • Lacy MQ; Division of Hematology.
  • Kapoor P; Division of Hematology.
  • Siddiqui M; Division of Hematology.
  • Larsen JT; Division of Hematology.
  • Warsame R; Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, AZ.
  • Hayman SR; Division of Hematology.
  • Go RS; Division of Hematology.
  • Dingli D; Division of Hematology.
  • Kourelis TV; Division of Hematology.
  • Dispenzieri A; Division of Hematology.
  • Rajkumar SV; Division of Hematology.
  • Kumar SK; Division of Hematology.
Blood Adv ; 6(18): 5429-5435, 2022 09 27.
Article en En | MEDLINE | ID: mdl-35737873
Bortezomib, a proteasome inhibitor (PI), has shown efficacy in the treatment of newly diagnosed and relapsed light chain (AL) amyloidosis, and is often used in combination with cyclophosphamide and dexamethasone. Ixazomib is the first oral PI to be approved in routine practice but has not yet been evaluated in the upfront treatment setting. Newly diagnosed AL amyloidosis patients with measurable disease and adequate organ function were enrolled. The primary objective was to determine the hematologic response rate of ixazomib in combination with cyclophosphamide and dexamethasone. Treatment was given for 12 cycles, followed by ixazomib maintenance until progression. Thirty-five patients were included; their median age was 67 years, and 69% were male. Major organ involvement included heart (66%) and kidneys (54%). A median of 4 induction cycles (range, 1-12) were administered. The overall hematologic response to induction was 63% and included complete response in 11.4% and very good partial response in 37.1% of patients. One patient was upstaged to complete response during maintenance. The most common reason for going off study was the institution of alternate therapy (61%). With a median follow-up of 29.7 months for the living patients, the 2-year progression-free survival and overall survival were 74% and 78%, respectively. The median time to alternate therapy was 7.5 months. Grade ≥3 hematologic and nonhematologic adverse events occurred in 23% and 49% of patients. Given ixazomib's favorable toxicity profile, which is an important advantage for the typically frail AL population, further evaluation of ixazomib in other combinations in the upfront setting is warranted. This trial was registered at www.clinicaltrials.gov as #NCT01864018.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Amiloidosis / Mieloma Múltiple Límite: Aged / Female / Humans / Male Idioma: En Revista: Blood Adv Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Amiloidosis / Mieloma Múltiple Límite: Aged / Female / Humans / Male Idioma: En Revista: Blood Adv Año: 2022 Tipo del documento: Article