Literature DB >> 2262369

The predictive value of cell kinetic measurements in a European trial of accelerated fractionation in advanced head and neck tumors: an interim report.

A C Begg1, I Hofland, L Moonen, H Bartelink, S Schraub, P Bontemps, R Le Fur, W Van Den Bogaert, R Caspers, M Van Glabbeke.   

Abstract

The value of cell kinetic measurements in head and neck tumors in predicting which patients will benefit from accelerated fractionation radiotherapy regimens is being tested in a multicenter European trial (EORTC trial 22851). This paper reports on the first analysis of the correlation of kinetics with outcome in this trial. A proportion of patients in both the accelerated arm (72 Gy in 5 weeks, 1.6Gy per fraction, 45 fractions) and the conventional arm (70-72 Gy in 7-8 weeks, 1.8-2.0 Gy per fraction, 35-40 fractions) were given an i.v. injection of 100 mg/m2 IUdR (iododeoxyuridine) before treatment, and a tumor biopsy was taken several hours later. The potential doubling time of the tumor (Tpot) was obtained from a flow cytometric analysis of tumor cell nuclei using an anti-IUdR antibody. From a total of 260 patients entered in the trial, 53 have undergone kinetic analysis. Adequate IUdR labeling was seen in 47 patients (88.7%), from which the mean value for Tpot was found to be 4.5 +/- 2.5 days (+/- S.D.). Of the IUdR labeled patients, 30 have now been followed up for at least 1 year, 17 with conventional and 13 with accelerated radiotherapy. These patients were split into those with fast and those with slowly growing tumors, the dividing line being the median Tpot value of 4.6 days. After conventional 7-week radiotherapy, 2 of 6 patients with "fast" growing tumors obtained local control compared with 8 of 11 with "slow" growing tumors. A small difference in local control was seen been fast and slow tumors in the accelerated arm (5/9 vs. 3/4). These preliminary data support the hypothesis that patients with fast growing tumors do poorly with conventional radiotherapy and that pretreatment kinetic measurements can select patients at risk. The predictive power of the method must await the final analysis of trial results.

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Year:  1990        PMID: 2262369     DOI: 10.1016/0360-3016(90)90357-p

Source DB:  PubMed          Journal:  Int J Radiat Oncol Biol Phys        ISSN: 0360-3016            Impact factor:   7.038


  21 in total

Review 1.  Theory and practice of predictive assays in radiation therapy.

Authors:  N E Crompton; M Ozsahin; P Schweizer; B Larsson; U M Luetolf
Journal:  Strahlenther Onkol       Date:  1997-02       Impact factor: 3.621

2.  Conventional vs accelerated fractionation in head and neck cancer.

Authors:  W Dobrowsky; E Dobrowsky; J Naudé; W Millesi; R Pavelka; M Kautzky; M Grasl; W Köhler; G D Wilson; M Reichel
Journal:  Br J Cancer Suppl       Date:  1996-07

Review 3.  Bromodeoxyuridine: a diagnostic tool in biology and medicine, Part II: Oncology, chemotherapy and carcinogenesis.

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Journal:  Histochem J       Date:  1995-12

4.  Randomized clinical trial on seven-day-per-week continuous accelerated irradiation for patients with esophageal carcinoma: preliminary report on tumor response and acute toxicity.

Authors:  Su-Ping Sun; Ya-Zhou Liu; Tao Ye; Wen Zhang; Wen-Bin Shen; Jing-Lei Shi; Hai-Ting Xu; Wei-Dong Wang
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5.  p53 negativity, CDC25B positivity, and metallothionein negativity are predictors of a response of esophageal squamous cell carcinoma to chemoradiotherapy.

Authors:  Fumiko Sunada; Masayuki Itabashi; Hisanao Ohkura; Toshiyuki Okumura
Journal:  World J Gastroenterol       Date:  2005-09-28       Impact factor: 5.742

6.  Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts.

Authors:  J Bussink; J H Kaanders; P F Rijken; C A Martindale; A J van der Kogel
Journal:  Br J Cancer       Date:  1998       Impact factor: 7.640

7.  A study on histological grading of oral squamous cell carcinoma and its co-relationship with regional metastasis.

Authors:  M Akhter; S Hossain; Quazi B Rahman; Motiur R Molla
Journal:  J Oral Maxillofac Pathol       Date:  2011-05

8.  Intra-tumoral heterogeneity of tumour potential doubling times (Tpot) in colorectal cancer.

Authors:  M S Wilson; C M West; G D Wilson; S A Roberts; R D James; P F Schofield
Journal:  Br J Cancer       Date:  1993-09       Impact factor: 7.640

9.  An assessment of the reliability and reproducibility of measurement of potential doubling times (Tpot) in human colorectal cancers.

Authors:  M S Wilson; C M West; G D Wilson; S A Roberts; R D James; P F Schofield
Journal:  Br J Cancer       Date:  1993-04       Impact factor: 7.640

10.  Intrinsic radiosensitivity and prediction of patient response to radiotherapy for carcinoma of the cervix.

Authors:  C M West; S E Davidson; S A Roberts; R D Hunter
Journal:  Br J Cancer       Date:  1993-10       Impact factor: 7.640

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