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A081105

(An ALCHEMIST sub-study) Randomized Double Blind Placebo Controlled Study of Erlotinib or Placebo in Patients with Completely Resected Epidermal Growth Factor Receptor (EGFR) Mutant Non-Small Lung Cancer (NSCLC) 

Inclusion Criteria

  • Previously registered to A151216, with the result of lung cancer harboring an EGFR exon 19 deletion or L858R mutation. The testing must have been performed by one of the following criteria:
    • Patient registered to A151216 and the assessment performed centrally by the protocol specified laboratory.
    • By a local CLIA certified laboratory. The report must indicate the result as well as the CLIA number of the laboratory that performed the assay. These patients will also have been registered to A151216, but can be enrolled on A081105 regardless of the central lab results.
  • Patients with known resistant mutations in the EGFR TK domain (T790M) are not eligible. Patients that are both EGFR mutant and ALK rearrangements will be registered to A081105.
  • Completely resected stage IB (≥4 cm), II or IIIA non-squamous NSCLC with negative margins.
  • Patients may not have received neoadjuvant therapy (chemo or radiotherapy) for this lung cancer.
  • Complete recovery from surgery and standard post-operative therapy (if required). Patients must be completely recovered from surgery at the time of randomization; the minimum time requirement between date of surgery and randomization must be at least 28 days, the maximum time requirement between surgery and randomization must be 90 days if no adjuvant chemotherapy was administered, 240 days if adjuvant chemotherapy was administered, and 300 days if adjuvant chemotherapy and radiation therapy was administered.
  • No history of cornea abnormalities.
  • Age ≥18 years.
  • ECOG Performance Status 0-1.
  • No locally advanced or metastatic cancer requiring systemic therapy within 5 years prior to registration.  No secondary primary lung cancer diagnosed concurrently or within 2 years prior to registration.
  • Non-pregnant and non-lactating.
  • Required Initial Laboratory Values
    • Granulocytes ≥ 1,500/µl
    • Platelets ≥ 100,000/µl
    • Total bilirubin ≤1.5 x ULN
    • SGOT ≤ 1.5 x ULN
    • Serum Creatinine ≤ 1.5 x ULN

Treatment Plan

Eligible patients will be randomized 1:1 to receive either erlotinib p.o. once daily or observation for up to 2 years or until disease progression or excessive toxicity. 

All investigational study drugs will be provided free of charge for this study.


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