A meta-analysis of prognostic roles of molecular markers in papillary thyroid carcinoma

Author:

Vuong Huy Gia1,Duong Uyen N P2,Altibi Ahmed M A3,Ngo Hanh T T4,Pham Thong Quang1,Tran Hung Minh5,Gandolfi Greta6,Hassell Lewis7

Affiliation:

1. 1Department of PathologyCho Ray Hospital, Ho Chi Minh City, Vietnam

2. 2Pham Ngoc Thach University of MedicineHo Chi Minh City, Vietnam

3. 3Faculty of MedicineUniversity of Jordan, Amman, Jordan

4. 4Department of PathologyUniversity of Medicine and Pharmacy, Ho Chi Minh City, Vietnam

5. 5Faculty of MedicineUniversity of Medicine and Pharmacy, Ho Chi Minh City, Vietnam

6. 6Laboratory of Translational ResearchArcispedale S. Maria Nuova-IRCCS, Reggio Emilia, Italy

7. 7Department of PathologyUniversity of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA

Abstract

The prognostic role of molecular markers in papillary thyroid carcinoma (PTC) is a matter of ongoing debate. The aim of our study is to investigate the impact of RAS, BRAF, TERT promoter mutations and RET/PTC rearrangements on the prognosis of PTC patients. We performed a search in four electronic databases: PubMed, Scopus, Web of Science and Virtual Health Library (VHL). Data of hazard ratio (HR) and its 95% confidence interval (CI) for disease-specific survival (DSS) and disease-free survival (DFS) were directly obtained from original papers or indirectly estimated from Kaplan–Meier curve (KMC). Pooled HRs were calculated using random-effect model weighted by inverse variance method. Publication bias was assessed by using Egger’s regression test and visual inspection of funnel plots. From 2630 studies, we finally included 35 studies with 17,732 patients for meta-analyses. TERT promoter mutation was significantly associated with unfavorable DSS (HR = 7.64; 95% CI = 4.00–14.61) and DFS (HR = 2.98; 95% CI = 2.27–3.92). BRAF mutations significantly increased the risk for recurrence (HR = 1.63; 95% CI = 1.27–2.10) but not for cancer mortality (HR = 1.41; 95% CI = 0.90–2.23). In subgroup analyses, BRAF mutation only showed its prognostic value in short-/medium-term follow-up. Data regarding RAS mutations and RET/PTC fusions were insufficient for meta-analyses. TERT promoter mutation can be used as an independent and reliable marker for risk stratification and predicting patient’s outcomes. The use of BRAF mutation to assess patient prognosis should be carefully considered.

Publisher

Bioscientifica

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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