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Bortezomib for patients with advanced-stage bronchioloalveolar carcinoma: A California cancer consortium phase II study (NCI 7003)

  • Suresh S. Ramalingam
  • , Angela Davies
  • , Jeff Longmate
  • , Martin Edelman
  • , Primo N. Lara
  • , Everett E. Vokes
  • , Miguel Villalona-Calero
  • , Barbara J. Gitlitz
  • , Karen Reckamp
  • , Ravi Salgia
  • , John J. Wright
  • , Chandra P. Belani
  • , David R. Gandara
  • Emory University
  • University of California at Davis
  • University of Pittsburgh
  • VA Medical Center
  • City of Hope National Medical Center
  • Swedish Medical Center
  • (VA) N. California Hlth. Care Syst.
  • Department of Medicine
  • U.S. Department of Veterans Affairs
  • UC Davis Comprehensive Cancer Center
  • University of Chicago
  • Fox Chase Cancer Center
  • University of Maryland Cancer Center
  • University of Texas MD Anderson Cancer Center
  • Alliance for Clinical Trials in Oncology
  • Baptist Hospital Miami
  • Ohio State University
  • Wake Forest University
  • University of Southern California
  • City of Hope Comprehensive Cancer Center
  • Vanderbilt University
  • Cedars-Sinai Medical Center
  • Dana-Farber Cancer Institute
  • Harvard University
  • National Institutes of Health
  • Pennsylvania State University
  • Drexel University
  • University of Arizona
  • University of Kansas

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Background: Bronchioloalveolar carcinoma (BAC), a subtype of non-small cell lung cancer, is a difficult disease to treat with low response rates with cytotoxic chemotherapy. Bortezomib, a proteasome inhibitor, has demonstrated objective responses in patients with BAC in early-phase clinical trials. We conducted a phase II study of bortezomib in patients with advanced-stage BAC. Methods: Patients with advanced BAC, adenocarcinoma with BAC features or BAC with adenocarcinoma features, and less than two prior regimens were eligible. Prior epidermal growth factor receptor (EGFR) inhibitor therapy was allowed. Bortezomib was administered intravenously at 1.6 mg/m on days 1 and 8 of every 21-day cycle until disease progression or unacceptable toxicity. The primary end point was response rate. The Simon two-stage design was used. Results: Forty-two patients were enrolled, and the study was halted early for slow accrual. Patient characteristics were female 55%, median age 68 years, and Eastern Cooperative Oncology Group performance status of 0 and 1 in 31 and 11 patients, respectively. Twenty-six (62%) patients had received prior therapy with an EGFR inhibitor. A median of four cycles of therapy were administered. Objective responses were noted in 5%, whereas 57% had disease stabilization. The median progression-free survival and overall survival were 5.5 and 13.6 months, respectively. Grade 3 diarrhea and fatigue were noted in three and five patients, respectively. Conclusions: Bortezomib is tolerated well and is associated with modest anticancer activity in patients with advanced BAC, including patients who progressed on EGFR inhibitor therapy.

Original languageEnglish
Pages (from-to)1741-1745
Number of pages5
JournalJournal of Thoracic Oncology
Volume6
Issue number10
DOIs
StatePublished - Oct 2011

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • BAC
  • Bortezomib
  • Bronchioloalveolar carcinoma
  • NSCLC
  • Proteasome inhibition

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