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Intratumorale Thymidylatsynthasespiegel können ein längeres tumorfreies Überleben unter adjuvanter 5-Fluorouraciltherapie bei Patienten mit kolorektalen Karzinomen vorhersagen

Intratumoral thymidylate synthase levels can predict disease-free survival in patients with colorectal cancer receiving adjuvant 5-FU chemotherapy

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Chirurgisches Forum 2001 für experimentelle und klinische Forschung

Part of the book series: Deutsche Gesellschaft für Chirurgie ((FORUMBAND,volume 30))

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Abstract

Patients with stage II and III colorectal cancer may receive adjuvant 5-fluorouracil (5- FU) after Ro resection of their primary tumor. In spite of this adjuvant treatment 30 – 40% of the patients develop local or distant recurrences. Owing to the fact that 30% of the patients will never develop a recurrence, even without adjuvant therapy, only 30% really profit from the adjuvant treatment. Presently it is not possible to identify responded and non-responders. However, several in vitro and in vivo studies have shown that high intratumoral thymidylate synthase (TS) levels are associated with 5-FU resistance. TS is a key enzyme of DNA synthesis and is irreversibly blocked by the active metabolite of 5-FU. The aim of this retrospective study was to investigate the value of intratumoral TS quantitation as a predictive marker for disease-free survival and recurrence in patients with colorectal cancer receiving adjuvant 5-FU chemotherapy. Therefore, we investigated patients from two adjuvant prospective-randomized multicenter studies (FOGT 1 — colon cancer, FOGT 2 — rectal cancer). Independently of the study arm, all patients received weekly 5-FU (450 mg/m2 i.v. in 90 min) in combination with levamisol (3x50 mg/day for 3 days every 14 days) until postoperative week 52. Patient monitoring was independent of this data evaluation. TS mRNA quantitation was performed from paraffin-embedded primary tumor sections using polymerase chain reaction after RNA isolation and reverse transcription. TS quantitation was successfully performed in 194 patients. Based on other studies (Salonga et al. 2000), patients were stratified according to their high (n = 88) and low (n = 106) TS level. Patients with high and low TS did not show a difference in recurrence rate, with 36 and 35%, respectively. The median diseasefree survival of patients with low TS (38 of 106) was 644 days (389 – 770 days). In contrast, the median disease-free survival of patients with high TS (31 of 88) was only 364 days. Patients with low TS levels had a 1.8-fold longer disease-free survival than patients with high TS (p = 0.0156 log-rank test). We conclude from the results of this retrospective study that patients with low TS profit more from adjuvant 5-FU chemotherapy than patients with high TS levels. In order to improve adjuvant treatment of colorectal cancer, in the future, patients with low TS should receive low dose 5-FU and leucovorin, whereas patients with high TS should receive other 5-FU regimens or other agents for adjuvant treatment.

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Literatur

  • Kornmann M, Danenberg KD, Arber N, Beger HG, Danenberg PV, Korc M (1999) Inhibition of cyclin D1 expression in human pancreatic cancer cells is associated with increased chemosensitivity and decreased expression of multiple chemoresistance genes. Cancer Res 59: 3505–3511

    PubMed  CAS  Google Scholar 

  • Link KH, Staib L, Bernhart H, Kreuser ED, Suhr P, Röttinger E, Beger HG (1997) Acceptannce and toxicity of postoperative adjuvant therapy in colon and rectal cancers. Onkologie 20: 235–238

    Article  Google Scholar 

  • Masuda N, Ohnishi T, Kawamoto S, Monden M, Okubo K (1999) Analysis of chemical modification of RNA from formalin-fixed samples and optimization of molecular biology applications for such samples. Nucl Acids Res 27: 4436–4443

    Article  PubMed  CAS  Google Scholar 

  • Salonga D, Danenberg KD, Johnson M, Metzger R, Groshen S, Tsao-Wei DD, Lenz HJ, Leichman CG, Leichman L, Diasio RB, Danenberg PV (2000) Colorectal tumors responding to 5-fluorouracil have low gene expression levels of dihydropyrimidine dehydrogenase, thymidylate synthase, and thymidine phosphorylase. Clin Cancer Res 6: 1322–1327

    PubMed  CAS  Google Scholar 

  • Van Triest B, Pinedo HM, Giaccone G, Peters GJ (2000) Downstream molecular determinants of response to 5-fluorouracil and antifolate thymidylate synthase inhibitors. Ann Oncol 11: 385–391

    Google Scholar 

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Correspondence to M. Kornmann .

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© 2001 Springer-Verlag Berlin Heidelberg

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Kornmann, M. et al. (2001). Intratumorale Thymidylatsynthasespiegel können ein längeres tumorfreies Überleben unter adjuvanter 5-Fluorouraciltherapie bei Patienten mit kolorektalen Karzinomen vorhersagen. In: Schönleben, K., Neugebauer, E., Hartel, W., Menger, M.D. (eds) Chirurgisches Forum 2001 für experimentelle und klinische Forschung. Deutsche Gesellschaft für Chirurgie, vol 30. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-56698-1_29

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  • DOI: https://doi.org/10.1007/978-3-642-56698-1_29

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-41718-7

  • Online ISBN: 978-3-642-56698-1

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