Association of miR-141 and miR-200c with time to recurrence (TTR) and overall survival (OS) in resected non-small-cell lung cancer (NSCLC) adenocarcinoma (ADC) patients (p).

Authors

null

Marc Campayo

Department of Medical Oncology, Hospital Clinic de Barcelona, Barcelona, Spain

Marc Campayo , Alfons Navarro , Rut Tejero , Maria L Cabanas , Laureano Molins , Ramon M Marrades , Jose Ramirez , Mariano Monzo , Nuria Vinolas

Organizations

Department of Medical Oncology, Hospital Clinic de Barcelona, Barcelona, Spain, School of Medicine, University of Barcelona, IDIBAPS, Barcelona, Spain, Department of Pathology, CDB, IDIBPAS, Hospital Clinic de Barcelona, Barcelona, Spain, Thoracic Surgery, ICT, IDIBAPS, Hospital Clinic de Barcelona, Barcelona, Spain, Department of Pneumology. ICT. IDIBAPS. Hospital Clinic de Barcelona, Barcelona, Spain, Department of Pathology, CDB, IDIBAPS, Hospital Clinic de Barcelona, Barcelona, Spain, Hospital Clinic de Barcelona, Barcelona, Spain

Research Funding

No funding sources reported

Background: Surgical resection remains the standard curative treatment for early-stage NSCLC, but nearly 50% of p experience recurrence, highlighting the need for novel diagnostic and therapeutic strategies. Moreover, treatments in NSCLC are often histology-dependent, underlining the need for histology-related markers. MicroRNAs (miRNAs) are promising molecular markers in cancer, with marked differences in expression according to histology. miR-200 family members have been associated in vitro with the regulation of epithelial-mesenchymal transition. We have examined their impact on outcome in resected NSCLC p. Methods: We analyzed miRNA expression using TaqMan assays in 160 tumor samples from NSCLC p who had undergone surgical resection and correlated our findings with TTR and OS. Results: p characteristics: age, 67 (51-83); 140 male; 96 (60%) stage I, 34 (21.3%) stage II, 30 (18.7%) stage III; 77(48.1%) ADC, 71(44.4%) squamous cell carcinoma (SCC); 16 (9.1%) received adjuvant treatment. With a median follow-up of 28 months (m), 64 p (40%) had relapsed. TTR for the 107 p with high miR-200c was 26.7 m vs 100.2 m for the 52 p with low miR-200c (P=0.032). OS for p with high miR-200c was 71.2 m vs. 125 m for p with low miR-200c (P=0.01). TTR for 112 p with high miR-141 was 26.7 m vs. 100.2 m for 46 p with low miR-141 (P=0.06). OS for p with high miR-141 was 72 m vs. 118 m for p with low miR-141 (P=0.02). Interestingly, neither miR-200c nor miR-141 correlated with TTR or OS in SCC p. In contrast, in ADC p, the prognostic value of both miRNAs increased: miR-200c (TTR, P=0.01; OS, P<0.0001) and miR-141 (TTR, P=0.003; OS, P<0.0001). This prognostic value was maintained in the subgroup of stage I p: miR-200c (TTR, P=0.011; OS, P<0.001) and miR-141 (TTR, P=0.018; OS, P<0.001). In the multivariate analysis, miR-200c and miR-141 emerged as an independent prognostic factor for OS (OR: 3.2, P=0.006; OR:2.5, P=0.02, respectively) together with age>65 (OR: 3.3, P=0.001) and stage I (OR: 0.3, P=0.004). Conclusions: miR-200c and miR-141 expression is associated with TTR and OS in resected ADC but not in SCC NSCLC p.

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Abstract Details

Meeting

2013 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Lung Cancer - Non-small Cell Local-regional/Small Cell/Other Thoracic Cancers

Track

Lung Cancer

Sub Track

Local-Regional Non–Small Cell Lung Cancer

Citation

J Clin Oncol 31, 2013 (suppl; abstr 7547)

DOI

10.1200/jco.2013.31.15_suppl.7547

Abstract #

7547

Poster Bd #

21A

Abstract Disclosures