Cristin-resultat-ID: 889618
Sist endret: 19. januar 2012, 21:16
Resultat
Sammendrag/abstract
2011

Associations between biomarkers and outcomes of first-line chemotherapy in advanced non-small cell lung cancer (NSCLC)

Bidragsytere:
  • Bjørn Henning Grønberg
  • Marius Lund-Iversen
  • Erik Heyerdahl Strøm
  • Odd Terje Brustugun og
  • Helge Scott

Tidsskrift

Journal of Clinical Oncology
ISSN 0732-183X
e-ISSN 1527-7755
NVI-nivå 2

Om resultatet

Sammendrag/abstract
Publiseringsår: 2011
Volum: 29
Hefte: 15
Artikkelnummer: 7535

Beskrivelse Beskrivelse

Tittel

Associations between biomarkers and outcomes of first-line chemotherapy in advanced non-small cell lung cancer (NSCLC)

Sammendrag

Background: Pemetrexed has demonstrated efficacy in the treatment of NSCLC, primarily in non-squamous cell carcinomas. One explanation may be that squamous cell carcinomas have a higher level of thymidylate synthase (TS); TS-inhibition is a key mechanism of action for pemetrexed. We conducted a phase III trial comparing pemetrexed/carboplatin (PC) with gemcitabine/carboplatin (GC) as 1st-line treatment in advanced NSCLC (Grønberg et al., JCO 2009). The aim of the present study was to investigate whether biomarkers characterize those patients who benefit the most from either regimen. Methods: Formalin-fixed, paraffin-embedded biopsies were collected. Levels of TTF1, TS, folate receptor (FR), FPGS, estrogen receptor (ER), RRM1, EGFR and PTEN were assessed using immunohistochemistry assays from Ventana Medical Systems. The percentages of positive/highly positive tumor cells and H-scores (range: 0-200) were assessed. A central pathology review was performed. Results: Biopsies from 370/436 pts enrolled onto the trial were collected - of which 239 were analyzable (PC: n=115, GC: n=124). Patient characteristics were well balanced between the treatment arms in this cohort. To date, we have assessed TTF1, TS, FR and FPGS. So far, no associations between these markers or histology (original and revised histological diagnoses) and outcomes of any of the two regimens have been revealed. TTF1 (Pos: 10.4 mo, Neg: 6.0 mo; p100: 6.3 mo; p

Bidragsytere

Aktiv cristin-person

Bjørn Henning Grønberg

  • Tilknyttet:
    Forfatter
    ved St. Olavs Hospital HF
  • Tilknyttet:
    Forfatter
    ved Institutt for klinisk og molekylær medisin ved Norges teknisk-naturvitenskapelige universitet

Marius Lund-Iversen

  • Tilknyttet:
    Forfatter
    ved Oslo universitetssykehus HF

Erik Heyerdahl Strøm

  • Tilknyttet:
    Forfatter
    ved Oslo universitetssykehus HF

Odd Terje Brustugun

  • Tilknyttet:
    Forfatter
    ved Avdeling for kreftbehandling ved Oslo universitetssykehus HF

Helge Scott

  • Tilknyttet:
    Forfatter
    ved Universitetet i Oslo
  • Tilknyttet:
    Forfatter
    ved Oslo universitetssykehus HF
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