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Phase 2 study of pemetrexed plus carboplatin, or pemetrexed plus cisplatin with concurrent radiation therapy followed by pemetrexed consolidation in patients with favorable-prognosis inoperable stage IIIA/B non-small-cell lung cancer

  • Hak Choy
  • , Lee S. Schwartzberg
  • , Shaker R. Dakhil
  • , Edward B. Garon
  • , David E. Gerber
  • , Janak K. Choksi
  • , Ramaswamy Govindan
  • , Guangbin Peng
  • , Andrew Koustenis
  • , Joseph Treat
  • , Coleman Obasaju
  • University of Texas Southwestern Medical Center
  • West Clinic
  • Cancer Center of Kansas
  • University of California at Los Angeles
  • Alamance Cancer Center
  • Washington University St. Louis
  • Lilly USA, LLC

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

Introduction: There is no consensus chemotherapy regimen with concurrent radiotherapy (RT) for inoperable stage IIIA/B non-small-cell lung cancer. This trial evaluated pemetrexed with carboplatin (PCb) or cisplatin (PC) with concurrent RT followed by consolidation pemetrexed. Methods: In this open-label, noncomparative phase II trial, patients with inoperable stage IIIA/B non-small-cell lung cancer (initially all histologies, later restricted to nonsquamous) were randomized (1:1) to PCb or PC with concurrent RT (64-68 Gy over days 1-45). Consolidation pemetrexed monotherapy was administered every 21 days for three cycles. Primary endpoint was 2-year overall survival (OS) rate. Results: From June 2007 to November 2009, 98 patients were enrolled (PCb: 46; PC: 52). The 2-year OS rate was PCb: 45.4% (95% confidence interval [CI], 29.5-60.0%); PC: 58.4% (95% CI, 42.6-71.3%), and in nonsquamous patients was PCb: 48.0% (95% CI, 29.0-64.8%); PC: 55.8% (95% CI, 38.0-70.3%). Median time to disease progression was PCb: 8.8 months (95% CI, 6.0-12.6 months); PC: 13.1 months (95% CI, 8.3-not evaluable [NE]). Median OS (months) was PCb: 18.7 (95% CI, 12.9-NE); PC: 27.0 (95% CI, 23.2-NE). The objective response rates (ORRs) were PCb: 52.2%; PC: 46.2%. Grade 4 treatment-related toxicities (% PCb/% PC) were: anemia, 0/1.9; neutropenia, 6.5/3.8; thrombocytopenia, 4.3/1.9; and esophagitis, 0/1.9. Most patients completed scheduled chemotherapy and RT during induction and consolidation phases. No drug-related deaths were reported during chemoradiotherapy. Conclusions: Because of study design, efficacy comparisons cannot be made. However, both combinations with concurrent RT were active and well tolerated.

Original languageEnglish
Pages (from-to)1308-1316
Number of pages9
JournalJournal of Thoracic Oncology
Volume8
Issue number10
DOIs
StatePublished - 2013
Externally publishedYes

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

  • Adenocarcinoma/mortality
  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols/therapeutic use
  • Carboplatin/administration & dosage
  • Carcinoma, Large Cell/mortality
  • Carcinoma, Non-Small-Cell Lung/mortality
  • Carcinoma, Squamous Cell/mortality
  • Chemoradiotherapy
  • Cisplatin/administration & dosage
  • Female
  • Follow-Up Studies
  • Glutamates/administration & dosage
  • Guanine/administration & dosage
  • Humans
  • Lung Neoplasms/mortality
  • Male
  • Middle Aged
  • Neoplasm Staging
  • Pemetrexed
  • Prognosis
  • Survival Rate

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