Literature DB >> 16550603

Prediction of treatment outcome by cisplatin-DNA adduct formation in patients with stage III/IV head and neck squamous cell carcinoma, treated by concurrent cisplatin-radiation (RADPLAT).

Frank J P Hoebers1, Dick Pluim, Marcel Verheij, Alfons J M Balm, Harry Bartelink, Jan H M Schellens, Adrian C Begg.   

Abstract

The purpose of our study was to test the predictive value of cisplatin-DNA adduct levels in head and neck squamous cell carcinoma (HNSCC) patients treated with cisplatin-radiation. Patients with advanced-stage HNSCC were treated within a randomized trial, investigating the optimal route of cisplatin administration, concurrently with radiation. Cisplatin was administered intra-arterially (IA, 150 mg/m2, with systemic rescue by sodium thiosulfate) or intravenously (IV, 100 mg/m2). In a subgroup, adducts were quantified in normal tissue and tumor. 32P-postlabeling was used to quantify intrastrand guanosine-guanosine adducts (GG-adducts) and adenosine-guanosine adducts (AG-adducts). Adduct levels were correlated with treatment outcome. Thirty-five patients were included (21 IV and 14 IA). At median follow-up of 27 months, locoregional (LR) control was 75% at 1 and 70% at 2 years. Adduct levels in tumor were 4-5-fold higher than in white blood cells (WBC) for both IA and IV treatment (p = 0.01). Adduct formation in WBC and buccal cells was higher in IV treated patients compared with IA infusion (p = 0.049 and 0.005 for GG-adducts in WBC and buccal cells, respectively). Adducts in tumors after IA infusion were not statistically different from those after IV. A strong correlation was observed between GG- and AG-adduct formation (r = 0.86, p < 0.001). Patients with higher GG adduct levels (>median) in primary tumor had significantly better disease free survival (DFS) than patients with lower (< or = median) adduct levels (p = 0.02). For overall survival (OS), a nonsignificant trend was observed, again in favor of patients with higher adduct levels (p = 0.06). In conclusion, cisplatin-DNA adduct formation in primary tumor appears to be predictive for DFS in HNSCC. No differences were observed in intratumoral adduct levels between IA and IV treatments, despite selective infusion of high-dose cisplatin with the IA procedure. However, systemic adduct levels (WBC and buccal cells) from IV patients were higher than in IA patients, consistent with less systemic exposure after IA administration. Copyright 2006 Wiley-Liss, Inc.

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Year:  2006        PMID: 16550603     DOI: 10.1002/ijc.21919

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  15 in total

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Authors:  Ti Zhang; Shuang Cai; Chad Groer; Wai Chee Forrest; Qiuhong Yang; Eva Mohr; Justin Douglas; Daniel Aires; Sandra M Axiak-Bechtel; Kimberly A Selting; Jeffrey A Swarz; Deborah J Tate; Jeffrey N Bryan; M Laird Forrest
Journal:  J Pharm Sci       Date:  2016-05-04       Impact factor: 3.534

2.  Microdose-Induced Drug-DNA Adducts as Biomarkers of Chemotherapy Resistance in Humans and Mice.

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Journal:  Mol Cancer Ther       Date:  2016-11-30       Impact factor: 6.261

Review 3.  Use of Accelerator Mass Spectrometry in Human Health and Molecular Toxicology.

Authors:  Heather A Enright; Michael A Malfatti; Maike Zimmermann; Ted Ognibene; Paul Henderson; Kenneth W Turteltaub
Journal:  Chem Res Toxicol       Date:  2016-10-11       Impact factor: 3.739

4.  Combined treatment with lexatumumab and irradiation leads to strongly increased long term tumour control under normoxic and hypoxic conditions.

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Journal:  Radiat Oncol       Date:  2009-10-27       Impact factor: 3.481

Review 5.  Personalized medicine for targeted and platinum-based chemotherapy of lung and bladder cancer.

Authors:  George D Cimino; Chong-xian Pan; Paul T Henderson
Journal:  Bioanalysis       Date:  2013-02       Impact factor: 2.681

6.  DNA alkylation products formed by 1-(2-chloroethyl)-1-nitrosourea as molecular dosimeters of therapeutic response.

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7.  Sensitive CometChip assay for screening potentially carcinogenic DNA adducts by trapping DNA repair intermediates.

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Journal:  Nucleic Acids Res       Date:  2020-02-20       Impact factor: 16.971

8.  Sodium Thiosulfate for Protection from Cisplatin-Induced Hearing Loss.

Authors:  Penelope R Brock; Rudolf Maibach; Margaret Childs; Kaukab Rajput; Derek Roebuck; Michael J Sullivan; Véronique Laithier; Milind Ronghe; Patrizia Dall'Igna; Eiso Hiyama; Bénédicte Brichard; Jane Skeen; M Elena Mateos; Michael Capra; Arun A Rangaswami; Marc Ansari; Catherine Rechnitzer; Gareth J Veal; Anna Covezzoli; Laurence Brugières; Giorgio Perilongo; Piotr Czauderna; Bruce Morland; Edward A Neuwelt
Journal:  N Engl J Med       Date:  2018-06-21       Impact factor: 91.245

9.  DNA-bound platinum is the major determinant of cisplatin sensitivity in head and neck squamous carcinoma cells.

Authors:  Sanne R Martens-de Kemp; Simone U Dalm; Fiona M J Wijnolts; Arjen Brink; Richard J Honeywell; Godefridus J Peters; Boudewijn J M Braakhuis; Ruud H Brakenhoff
Journal:  PLoS One       Date:  2013-04-17       Impact factor: 3.240

10.  Oxaliplatin-DNA adduct formation in white blood cells of cancer patients.

Authors:  A C Pieck; A Drescher; K G Wiesmann; J Messerschmidt; G Weber; D Strumberg; R A Hilger; M E Scheulen; U Jaehde
Journal:  Br J Cancer       Date:  2008-05-27       Impact factor: 7.640

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