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A phase II trial of the BCL-2 homolog domain 3 mimetic AT-101 in combination with docetaxel for recurrent, locally advanced, or metastatic head and neck cancer

  • Paul L. Swiecicki
  • , Emily Bellile
  • , Assuntina G. Sacco
  • , Alexander T. Pearson
  • , Jeremy M.G. Taylor
  • , Trachette L. Jackson
  • , Douglas B. Chepeha
  • , Matthew E. Spector
  • , Andrew Shuman
  • , Kelly Malloy
  • , Jeffrey Moyer
  • , Erin McKean
  • , Scott McLean
  • , Ammar Sukari
  • , Gregory T. Wolf
  • , Avraham Eisbruch
  • , Mark Prince
  • , Carol Bradford
  • , Thomas E. Carey
  • , Shaomeng Wang
  • Jacques E. Nör, Francis P. Worden

Research output: Contribution to journalArticlepeer-review

Abstract

Background: AT-101 is a BCL-2 Homolog domain 3 mimetic previously demonstrated to have tumoricidal effects in advanced solid organ malignancies. Given the evidence of activity in xenograft models, treatment with AT-101 in combination with docetaxel is a therapeutic doublet of interest in metastatic head and neck squamous cell carcinoma. Patients and Methods: Patients included in this trial had unresectable, recurrent, or distantly metastatic head and neck squamous cell carcinoma (R/M HNSCC) not amenable to curative radiation or surgery. This was an open label randomized, phase II trial in which patients were administered AT-101 in addition to docetaxel. The three treatment arms were docetaxel, docetaxel plus pulse dose AT-101, and docetaxel plus metronomic dose AT-101. The primary endpoint of this trial was overall response rate. Results: Thirty-five patients were registered and 32 were evaluable for treatment response. Doublet therapy with AT-101 and docetaxel was well tolerated with only 2 patients discontinuing therapy due to treatment related toxicities. The overall response rate was 11 % (4 partial responses) with a clinical benefit rate of 74 %. Median progression free survival was 4.3 months (range: 0.7–13.7) and overall survival was 5.5 months (range: 0.4–24). No significant differences were noted between dosing strategies. Conclusion: Although met with a favorable toxicity profile, the addition of AT-101 to docetaxel in R/M HNSCC does not appear to demonstrate evidence of efficacy.

Original languageEnglish (US)
Pages (from-to)481-489
Number of pages9
JournalInvestigational New Drugs
Volume34
Issue number4
DOIs
StatePublished - Aug 1 2016
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2016, Springer Science+Business Media New York.

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

  • AT-101
  • BH3 mimetic
  • Docetaxel
  • Gossypol
  • Head and neck neoplasms
  • Metronomic dosing

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