Literature DB >> 25194563

Decreased ERCC1 Expression After Platinum-Based Neoadjuvant Chemotherapy in non-Small Cell Lung Cancer.

Eszter Podmaniczky1, Katalin Fábián, Judit Pápay, Rita Puskás, Márton Gyulai, József Furák, László Tiszlavicz, György Losonczy, József Tímár, Judit Moldvay.   

Abstract

We have already demonstrated in a small cohort of 17 non-small cell lung cancer patients that ERCC1 (excision repair cross-complementation group 1) protein expression decreased after platinum-based treatment, however, certain clinicopathological parameters, such as histologic subtypes, ERCC1 expression scores, chemotherapeutic combinations, response rate, gender and smoking history were not analyzed. The aim of our present study was to extend the studied cohort and analyze those parameters. ERCC1 protein expression was examined in 46 patients treated with neoadjuvant chemotherapy. 46 bronchoscopic biopsy samples (27 squamous cell carcinomas /SCC/ and 19 adenocarcinomas /ADC/) together with their corresponding surgical biopsies were studied. ERCC1 immunohistochemistry was performed on formalin-fixed, paraffin-embedded tissues. Staining scores were calculated by multiplying the percentage of positive tumor cells (0-100) by the staining intensity (0-3). 24/27 bronchoscopic SCC tissues expressed ERCC1. Thirteen of these cases became negative after neoadjuvant therapy and the expression differences between pre- and postchemotherapy samples were highly significant (p < 0.001). 11/19 bronchoscopic ADC tissues expressed ERCC1. Six of these cases became negative after neoadjuvant therapy and the expression differences were significant (p < 0.010). There was no newly expressed ERCC1 postoperatively. Comparison of staining score changes revealed more pronounced decrease in SCC (p = 0.032). We observed no correlation between initial ERCC1 level or ERCC1 decrease and overall survival, but we demonstrated correlations between decrease in ERCC1 expression and histologic subtypes of tumors and gender. We could confirm our previous data in a larger cohort that platinum-based chemotherapy affects the ERCC1 expression probably referring to an induction of tumor cell selection.

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Year:  2014        PMID: 25194563     DOI: 10.1007/s12253-014-9839-x

Source DB:  PubMed          Journal:  Pathol Oncol Res        ISSN: 1219-4956            Impact factor:   3.201


  32 in total

Review 1.  Adjuvant therapy in non-small cell lung cancer: future treatment prospects and paradigms.

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Journal:  Lung Cancer       Date:  2010-11-18       Impact factor: 5.705

4.  ERCC1-tailored chemotherapy in lung cancer: the first prospective randomized trial.

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Journal:  J Clin Oncol       Date:  2007-07-01       Impact factor: 44.544

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6.  [Relationship between ERCC1 expression and cisplatin intervention in human lung adenocarcinoma cell lines].

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7.  DNA repair by ERCC1 in non-small-cell lung cancer and cisplatin-based adjuvant chemotherapy.

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9.  The prognostic significance of ERCC1, BRCA1, XRCC1, and betaIII-tubulin expression in patients with non-small cell lung cancer treated by platinum- and taxane-based neoadjuvant chemotherapy and surgical resection.

Authors:  Chang Hyun Kang; Bo Gun Jang; Dong-Wan Kim; Doo Hyun Chung; Young Tae Kim; Sanghoon Jheon; Sook-Whan Sung; Joo Hyun Kim
Journal:  Lung Cancer       Date:  2009-08-15       Impact factor: 5.705

10.  Differences in the expression profiles of excision repair crosscomplementation group 1, x-ray repair crosscomplementation group 1, and betaIII-tubulin between primary non-small cell lung cancer and metastatic lymph nodes and the significance in mid-term survival.

Authors:  Chang Hyun Kang; Bo Gun Jang; Dong-Wan Kim; Doo Hyun Chung; Young Tae Kim; Sanghoon Jheon; Sook-Whan Sung; Joo Hyun Kim
Journal:  J Thorac Oncol       Date:  2009-11       Impact factor: 15.609

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