4.4 Article

Southwestern Oncology Group Phase II Trial (S0526) of Pemetrexed in Bronchioloalveolar Carcinoma Subtypes of Advanced Adenocarcinoma

Journal

CLINICAL LUNG CANCER
Volume 14, Issue 4, Pages 351-355

Publisher

CIG MEDIA GROUP, LP
DOI: 10.1016/j.cllc.2012.12.004

Keywords

Lung adenocarcinoma; Bronchioloalveolar carcinoma (BAC); Pemetrexed

Categories

Funding

  1. Public Health Services Cooperative Agreement
  2. National Cancer Institute, National Institutes of Health, Department of Health and Human Services [CA32102, CA38926, CA45377, CA45560, CA58882, CA35090, CA20319, CA46441, CA63844, CA11083, CA67663, CA42777, CA37981, CA12644]
  3. Eli Lilly and Company
  4. Response Genetics
  5. National Cancer Institute/National Institutes of Health
  6. lung cancer tumor specimen bank

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Bronchioloalveolar carcinoma (BAC) subtypes of lung adenocarcinoma represent approximately 10% to 15% of new non-small-cell lung cancer cases (NSCLC). Based on preclinical data supporting the relevance of alpha-folate receptors in BAC, this trial was designed to assess pemetrexed in patients with this pathologic subtype of lung adenocarcinoma. This trial demonstrated that single-agent pemetrexed is active against this histologic subset. Background: Pemetrexed, a multitargeted antifolate drug, is an active agent in non-small-cell lung cancer (NSCLC), especially adenocarcinomas. Based on preclinical data supporting the relevance of alpha-folate receptors in adenocarcinoma of the bronchioloalveolar carcinoma (BAC) subtype, this trial was designed to assess pemetrexed in patients with this pathologic subtype of lung adenocarcinoma. Patients and Methods: Patients with histologically confirmed stage IIIB (with malignant pleural effusion) or stage IV adenocarcinoma with BAC features or pure BAC were eligible. Treatment consisted of pemetrexed, 500 mg/m(2), administered intravenously every 21 days. Results: Of 27 patients enrolled, 24 were eligible and assessable for adverse events: Toxicity was primarily hematologic, consisting of leukopenia/neutropenia, thrombocytopenia, and anemia. The median follow-up among patients still alive (n = 8) was 35 months (range, 26-47 months). Among 17 patients with measurable disease, the response rate was 23% (all partial responses; 95% confidence interval [CI], 10%-56%). The median progression-free survival (PFS) and overall survival (OS) were 6 and 25 months, respectively. Conclusion: Pemetrexed is active and well tolerated and, in patients with adenocarcinoma BAC subtypes, likely related to its underlying mechanism of action as a multitargeted antifolate drug.

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