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Ruxolitinib and methylprednisolone for treatment of patients with relapsed/refractory multiple myeloma.
Berenson, James R; Martinez, Daisy; Safaie, Tahmineh; Boccia, Ralph; Yang, Honghao; Moezi, Mehdi; Lim, Stephen; Schwartz, Gary; Eshaghian, Shahrooz; Swift, Regina; Eades, Benjamin M; Bujarski, Sean; Regidor, Bernard; Kim, Clara; Kim, Susanna; Vescio, Robert.
  • Berenson JR; Institute for Myeloma and Bone Cancer Research, West Hollywood, California, USA.
  • Martinez D; Oncotherapeutics, West Hollywood, California, USA.
  • Safaie T; Berenson Cancer Center, West Hollywood, California, USA.
  • Boccia R; Oncotherapeutics, West Hollywood, California, USA.
  • Yang H; Oncotherapeutics, West Hollywood, California, USA.
  • Moezi M; Center for Cancer and Blood Disorders, Bethesda, Maryland, USA.
  • Lim S; Global Oncology, Alhambra, California, USA.
  • Schwartz G; Cancer Specialists of North Florida, Fleming Island, Florida, USA.
  • Eshaghian S; Cedars-Sinai Samuel Oschin Cancer Center, Los Angeles, California, USA.
  • Swift R; Berenson Cancer Center, West Hollywood, California, USA.
  • Eades BM; Compassionate Oncology Medical Group, Los Angeles, California, USA.
  • Bujarski S; Berenson Cancer Center, West Hollywood, California, USA.
  • Regidor B; Berenson Cancer Center, West Hollywood, California, USA.
  • Kim C; Berenson Cancer Center, West Hollywood, California, USA.
  • Kim S; Berenson Cancer Center, West Hollywood, California, USA.
  • Vescio R; Oncotherapeutics, West Hollywood, California, USA.
Br J Haematol ; 200(6): 722-730, 2023 03.
Article in English | MEDLINE | ID: covidwho-2251898
ABSTRACT
Although Janus kinase (JAK) inhibitors have demonstrated efficacy for treating autoimmune disorders and myeloproliferative neoplasms, their efficacy in treating other types of cancer has not been clearly demonstrated. We evaluated oral ruxolitinib (15 mg twice daily) with oral methylprednisolone (40 mg every other day) for multiple myeloma (MM) patients with progressive disease who had received a proteasome inhibitor, lenalidomide, glucocorticosteroids and three or more prior regimens. All of the planned 29 patients had been enrolled with follow-up until 28 April 2022. Median lines of prior therapy were 6 (range 3-12). Cytogenetics and fluorescent in situ hybridization were evaluable in 28 patients; 9 (32%) and 17 (70%) patients showed high-risk cytogenetics and/or 1q+, respectively. The overall response rate was 31%. The median duration of response was 13.1 (range 2.8-22.0) months. Median progression-free survival rate was 3.4 (range 0.5-24.6) months, Overall, the treatment was well tolerated. The combination of ruxolitinib and methylprednisolone demonstrated significant clinical activity among previously heavily-treated MM patients, and responses were achieved among patients who had high-risk cytogenetics. This is the first clinical study to show activity of JAK inhibitors in combination with steroids for MM patients and expands the potential use of these drugs to those with cancers other than myeloproliferative neoplasms.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Multiple Myeloma Type of study: Cohort study / Experimental Studies / Prognostic study Limits: Humans Language: English Journal: Br J Haematol Year: 2023 Document Type: Article Affiliation country: Bjh.18593

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Multiple Myeloma Type of study: Cohort study / Experimental Studies / Prognostic study Limits: Humans Language: English Journal: Br J Haematol Year: 2023 Document Type: Article Affiliation country: Bjh.18593