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Characteristics and Clinical Outcomes of Patients with Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Receiving Ibrutinib for ≥5 Years in the RESONATE-2 Study.
Woyach, Jennifer A; Barr, Paul M; Kipps, Thomas J; Barrientos, Jacqueline C; Ahn, Inhye E; Ghia, Paolo; Girardi, Vincent; Hsu, Emily; Jermain, Mandy; Burger, Jan A.
Affiliation
  • Woyach JA; Ohio State University Comprehensive Cancer Center, Columbus, OH 43210, USA.
  • Barr PM; Wilmot Cancer Institute, University of Rochester, Rochester, NY 14642, USA.
  • Kipps TJ; University of California San Diego Moores Cancer Center, San Diego, CA 92037, USA.
  • Barrientos JC; Mount Sinai Comprehensive Cancer Center, Miami Beach, FL 33140, USA.
  • Ahn IE; Laboratory of Lymphoid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20814, USA.
  • Ghia P; Università Vita-Salute San Raffaele and IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
  • Girardi V; Pharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
  • Hsu E; Pharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
  • Jermain M; Pharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
  • Burger JA; University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Cancers (Basel) ; 15(2)2023 Jan 13.
Article in En | MEDLINE | ID: mdl-36672456
Primary results from the phase 3 RESONATE-2 study demonstrated superior efficacy and tolerability with ibrutinib versus chlorambucil in patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). Here, we describe characteristics and outcomes of patients who received ibrutinib treatment for ≥5 years in RESONATE-2. Patients aged ≥65 years with previously untreated CLL/SLL, without del(17p), were randomly assigned 1:1 to once-daily ibrutinib 420 mg until disease progression/unacceptable toxicity (n = 136) or chlorambucil 0.5−0.8 mg/kg for ≤12 cycles (n = 133). Baseline characteristics in ibrutinib-randomized patients (n = 136) were generally similar between patients on ibrutinib treatment for ≥5 years (n = 79) versus those on treatment for <5 years (n = 57). In patients on ibrutinib treatment for ≥5 years, complete response rates improved over time, reaching 42% by 5 years. Estimated 7-year progression-free survival and overall survival rates were 82% and 94%, respectively. Adverse events (AEs) led to dose reductions in 16/79 patients (20%); these AEs were resolved for 13/16 patients (81%). AEs led to dose holds (≥7 days) in 45/79 patients (57%); these AEs were resolved for 43/45 patients (96%). More than half (58%) of ibrutinib-randomized patients benefitted from ibrutinib treatment for ≥5 years regardless of baseline characteristics. Dose modification resolved AEs for most patients, thereby facilitating continued treatment.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Cancers (Basel) Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Cancers (Basel) Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Suiza