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Titlebook: Chemotherapy and Radiotherapy of Gastrointestinal Tumors; Hans Otto Klein Book 1981 Springer-Verlag Berlin Heidelberg 1981 Chemotherapy.Ra

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On a Change of SU(3) into Three SU(2),U(1)espective of whether they were cured by surgery (Duke’s A), had advanced cancer (Duke’s D), or took no razoxane when randomized to take it, then as might be expected any differences there may be between the razoxane-treated and control patients with minimal residual disease (Duke’s B and C) are so d
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A Controlled Prospective Trial of Adjuvant Razoxane in Resectable Colorectal Cancer,espective of whether they were cured by surgery (Duke’s A), had advanced cancer (Duke’s D), or took no razoxane when randomized to take it, then as might be expected any differences there may be between the razoxane-treated and control patients with minimal residual disease (Duke’s B and C) are so d
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Chemotherapy and Radiotherapy of Gastrointestinal Tumors
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0080-0015 e tumours induce [6, 8, 11]. The drug is not cytotoxic in the usual sense, does not affect non-dividing cells, and only blocks cell division during a brief peri978-3-642-81683-3978-3-642-81681-9Series ISSN 0080-0015 Series E-ISSN 2197-6767
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Book 1981nt prognostic groups [4] and the paucity of drugs that have shown activity in the advanced disease [10]. Of the few drugs which are active in the advanced disease, only 5-fluorouracil (5-FU) and razoxane «±1,2-bis(3,4-dioxopiperazin-1-yl)propane) are suitable for long-term adjuvant treatment [2, 9].
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On a Change of SU(3) into Three SU(2),U(1)half-life may offer the advantage of maintaining a higher level of cytocidal activity over a longer period of time without the problem of serious side effects, especially in the nervous system, as can be observed after a single high-dose injection of ftorafur [27].
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