Literature DB >> 27127763

Predictive value of BRCA1 expression on the efficacy of chemotherapy based on anti-microtubule agents: a pooled analysis across different malignancies and agents.

Qihua He1, Mingzhe Zhang1, Jianrong Zhang1, Shengyi Zhong1, Yang Liu1, Jianfei Shen1, Jiaxi He1, Long Jiang1, Chenglin Yang1, Yuan Zeng1, Minzhang Guo1, Xuewei Chen1, Jianxing He1, Wenhua Liang1.   

Abstract

BACKGROUND: Breast cancer susceptibility gene 1 (BRCA1) expression has been suggested as a predictor in anti-neoplastic treatment with anti-microtubule agents. However, the existing evidence is conflicting. Consulting the literature, we sought to examine the true impact of BRCA1 expression on the efficacy of anti-microtubule agents.
METHODS: Medline by PubMed and Embase databases were searched for eligible studies. The primary endpoints were objective response rate (ORR) and progression free survival (PFS). Additional subgroup analyses stratified for detection methods, regimen, and patient origin were also performed.
RESULTS: A total of 13 relevant studies involving a total of 1,490 cases were enrolled. Involved agents included paclitaxel, docetaxel and vinorelbine; Malignancies included non-small cell lung cancer, gastric cancer, esophageal carcinoma, ovarian carcinoma, malignant pleural mesothelioma, breast cancer, and small cell lung cancer. Through meta-analyses, we observed a potentially greater ORR in the population with high BRCA1 expression vs. low BRCA1 expression (OR 1.63, 95% CI: 0.92 to 2.88, P=0.09) but the heterogeneity is severe (P=0.01; I(2)=61%). Similar results were observed in PFS (high vs. low expression, HR 0.93, 95% CI: 0.75 to 1.15, P=0.49; heterogeneity, P<0.01, I(2)=75%). After stratification by testing methods, a significantly higher ORR in the population with high BRCA1 expression was shown in the subgroup using mRNA as a quantitative method (OR 2.90, 95% CI: 1.92 to 4.39, P<0.01; I(2)=0) whereas the difference in the subgroup using immunohistochemistry (IHC) was not significant (OR 0.60, 95% CI: 0.33 to 1.10, P=0.10; I(2)=0). Stratification by regimen (platinum-based vs. non platinum-based) and patient origin (Asian vs. Caucasian) did not reduce the heterogeneity.
CONCLUSIONS: Although the predictive value of BRCA1 expression on the anti-microtubule chemotherapy remained uncertain based on overall results, our exploratory analyses suggested that detection using mRNA might be a preferred technique, however, further validation is required to substantiate our findings.

Entities:  

Keywords:  Breast cancer susceptibility gene 1 (BRCA1); anti-microtubule agents; meta-analysis

Year:  2016        PMID: 27127763      PMCID: PMC4828752          DOI: 10.21037/atm.2016.03.27

Source DB:  PubMed          Journal:  Ann Transl Med        ISSN: 2305-5839


  28 in total

1.  Mechanism of inhibition of cell proliferation by Vinca alkaloids.

Authors:  M A Jordan; D Thrower; L Wilson
Journal:  Cancer Res       Date:  1991-04-15       Impact factor: 12.701

2.  Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints.

Authors:  M K Parmar; V Torri; L Stewart
Journal:  Stat Med       Date:  1998-12-30       Impact factor: 2.373

3.  ERCC1 and BRAC1 mRNA expression levels in the primary tumor could predict the effectiveness of the second-line cisplatin-based chemotherapy in pretreated patients with metastatic non-small cell lung cancer.

Authors:  Chara Papadaki; Maria Sfakianaki; Georgios Ioannidis; Eleni Lagoudaki; Maria Trypaki; Kostas Tryfonidis; Dimitris Mavroudis; Efstathios Stathopoulos; Vassilis Georgoulias; John Souglakos
Journal:  J Thorac Oncol       Date:  2012-04       Impact factor: 15.609

4.  Meta-analysis in clinical trials.

Authors:  R DerSimonian; N Laird
Journal:  Control Clin Trials       Date:  1986-09

5.  Operating characteristics of a rank correlation test for publication bias.

Authors:  C B Begg; M Mazumdar
Journal:  Biometrics       Date:  1994-12       Impact factor: 2.571

6.  BRCA1 expression and improved survival in ovarian cancer patients treated with intraperitoneal cisplatin and paclitaxel: a Gynecologic Oncology Group Study.

Authors:  J L Lesnock; K M Darcy; C Tian; J A Deloia; M M Thrall; C Zahn; D K Armstrong; M J Birrer; T C Krivak
Journal:  Br J Cancer       Date:  2013-03-05       Impact factor: 7.640

7.  Correlation of BRCA1, TXR1 and TSP1 mRNA expression with treatment outcome to docetaxel-based first-line chemotherapy in patients with advanced/metastatic non-small-cell lung cancer.

Authors:  C Papadaki; E Tsaroucha; L Kaklamanis; E Lagoudaki; M Trypaki; K Tryfonidis; D Mavroudis; E Stathopoulos; V Georgoulias; J Souglakos
Journal:  Br J Cancer       Date:  2010-12-14       Impact factor: 7.640

Review 8.  Breast cancer susceptibility gene 1 (BRCA1) predict clinical outcome in platinum- and toxal-based chemotherapy in non-small-cell lung cancer (NSCLC) patients: a system review and meta-analysis.

Authors:  Yanlong Yang; Yuanliang Xie; Lei Xian
Journal:  J Exp Clin Cancer Res       Date:  2013-03-15

9.  Tumor BRCA1, RRM1 and RRM2 mRNA expression levels and clinical response to first-line gemcitabine plus docetaxel in non-small-cell lung cancer patients.

Authors:  Ioannis Boukovinas; Chara Papadaki; Pedro Mendez; Miquel Taron; Dimitris Mavroudis; Anastasios Koutsopoulos; Maria Sanchez-Ronco; Jose Javier Sanchez; Maria Trypaki; Eustathios Staphopoulos; Vassilis Georgoulias; Rafael Rosell; John Souglakos
Journal:  PLoS One       Date:  2008-11-11       Impact factor: 3.240

Review 10.  The role of BRCA1 in the cellular response to chemotherapy.

Authors:  Richard D Kennedy; Jennifer E Quinn; Paul B Mullan; Patrick G Johnston; D Paul Harkin
Journal:  J Natl Cancer Inst       Date:  2004-11-17       Impact factor: 13.506

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