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预测放射可治愈性。

Predicting radiocurability.

作者信息

Peters L J, Brock W, Johnson T

出版信息

Cancer. 1985 May 1;55(9 Suppl):2118-22. doi: 10.1002/1097-0142(19850501)55:9+<2118::aid-cncr2820551414>3.0.co;2-d.

DOI:10.1002/1097-0142(19850501)55:9+<2118::aid-cncr2820551414>3.0.co;2-d
PMID:3919926
Abstract

Several predictors of tumor radiocurability are already integrated into clinical practice, e.g., tumor size, gross morphologic features (i.e., infiltrative or exophytic), histologic type, and grade. These are relatively imprecise, however, and none is specific. The aim of research into predictive assays is not only to refine the discrimination of existing predictors but also to suggest specific experimental approaches for overcoming tumor radioresistance in individual patients. Two broad categories of predictive assays can be defined: direct and indirect measurements of tumor cell survival and/or repair capability following irradiation and measurement of cellular and extracellular parameters affecting radiosensitivity. Examples from ongoing research at the University of Texas M. D. Anderson Hospital using one technique from each category (the micronucleus assay and flow cytometric analysis of tumor cell proliferation kinetics and ploidy) are used to illustrate potential methods of selecting patients for fast neutron radiotherapy.

摘要

几种肿瘤放射可治愈性的预测指标已被纳入临床实践,例如肿瘤大小、大体形态特征(即浸润性或外生性)、组织学类型和分级。然而,这些指标相对不够精确,且无一具有特异性。预测分析研究的目的不仅是优化现有预测指标的辨别能力,还在于提出针对个体患者克服肿瘤放射抗性的具体实验方法。可定义两类广泛的预测分析:照射后对肿瘤细胞存活和/或修复能力的直接和间接测量,以及对影响放射敏感性的细胞和细胞外参数的测量。德克萨斯大学MD安德森医院正在进行的研究中,分别使用每类中的一种技术(微核试验以及肿瘤细胞增殖动力学和倍性的流式细胞术分析)的实例,用于说明为快中子放射治疗选择患者的潜在方法。

相似文献

1
Predicting radiocurability.预测放射可治愈性。
Cancer. 1985 May 1;55(9 Suppl):2118-22. doi: 10.1002/1097-0142(19850501)55:9+<2118::aid-cncr2820551414>3.0.co;2-d.
2
Potential methods for predicting tumor radiocurability.预测肿瘤放射可治愈性的潜在方法。
Int J Radiat Oncol Biol Phys. 1986 Apr;12(4):459-67. doi: 10.1016/0360-3016(86)90053-2.
3
Experience with fast neutron radiotherapy at the M.D. Anderson Hospital with emphasis on the randomized head and neck trial.
Strahlentherapie Sonderb. 1981;77:11-6.
4
Fast neutron radiation therapy.快中子放射治疗
Annu Rev Biophys Bioeng. 1982;11:359-90. doi: 10.1146/annurev.bb.11.060182.002043.
5
Early changes in flow cytometric DNA profiles induced by californium-252 neutron brachytherapy in squamocellular carcinomas of the uterine cervix.锎-252中子近距离治疗引起的子宫颈鳞状细胞癌流式细胞术DNA图谱的早期变化。
Neoplasma. 1998;45(2):96-101.
6
Correlation of radiation-induced micronucleus frequency with clonogenic survival in cells of one diploid and two tetraploid murine tumor cell lines of the same origin.同一来源的一个二倍体和两个四倍体小鼠肿瘤细胞系中,辐射诱导的微核频率与克隆形成存活率的相关性。
Radiat Res. 1997 Jan;147(1):29-34.
7
Preliminary clinical results from U.S. fast neutron teletherapy studies.美国快中子远距放射疗法研究的初步临床结果。
Cancer. 1977 Oct;40(4):1434-8. doi: 10.1002/1097-0142(197710)40:4<1434::aid-cncr2820400412>3.0.co;2-p.
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Preliminary report of the M. D. Anderson Hospital/Texas A & M variable energy cyclotron fast-neutron therapy pilot study.MD安德森医院/德克萨斯农工大学可变能量回旋加速器快中子治疗试点研究的初步报告。
AJR Am J Roentgenol. 1979 Apr;132(4):637-42. doi: 10.2214/ajr.132.4.637.
9
Comparison of the effects of neutron and/or photon irradiation on spontaneous squamous-cell carcinoma in mice.中子和/或光子辐照对小鼠自发性鳞状细胞癌影响的比较。
Radiology. 1980 Jan;134(1):219-25. doi: 10.1148/radiology.134.1.6444252.
10
[Clinical significations of G2-M stage partial synchronization on radiation therapies of uterine cervical carcinomas (author's transl)].G2-M期部分同步化在子宫颈癌放射治疗中的临床意义(作者译)
Nihon Gan Chiryo Gakkai Shi. 1981 Dec 20;16(7):1456-67.

引用本文的文献

1
Oxygen distributions partly explain the radiation response of human squamous cell carcinomas.氧分布部分解释了人类鳞状细胞癌的辐射反应。
Br J Cancer Suppl. 1996 Jul;27:S185-90.
2
Radiation-resistant and repair-proficient human tumor cells may be associated with radiotherapy failure in head- and neck-cancer patients.
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2684-8. doi: 10.1073/pnas.83.8.2684.
3
Radiation responses of subrenally transplanted syngeneic and allogeneic mouse fibrosarcomas.肾下移植的同基因和异基因小鼠纤维肉瘤的辐射反应
Jpn J Cancer Res. 1988 Jun;79(6):766-71. doi: 10.1111/j.1349-7006.1988.tb02234.x.