Kelloff G J, Boone C W, Steele V E, Crowell J A, Lubet R, Sigman C C
Chemoprevention Investigational Drug Unit, National Cancer Institute, Bethesda, Maryland 20892.
Cancer Res. 1994 Apr 1;54(7 Suppl):2015s-2024s.
The basic cancer-related chemical and biological sciences, pathology, and epidemiology have contributed to the understanding that antimutagenesis and antiproliferation are the important general mechanisms of chemoprevention and to the development of antimutagenic and anti-proliferative agents as potential chemopreventive drugs. These disciplines have also provided the biochemical and histopathological bases for identifying intermediate biomarkers that can be used as surrogate end points for cancer incidence in clinical chemoprevention trials and for selecting cohorts for these trials. Particularly important as histological biomarkers of cancer are the cytonuclear morphological and densitometric changes that define intraepithelial neoplasia (IEN). IEN changes are on the causal pathway to cancer. They may serve as target lesions in Phase II chemoprevention trials and as standards against which other earlier cellular and molecular biomarkers can be evaluated. Strategies for the clinical evaluation of chemopreventive agents have been defined for seven targets--colorectal, prostate, lung, breast, bladder, oral, and cervical cancers. Cohorts have been identified for short-term Phase II trials that investigate the effects of chemopreventive agents on IEN and on earlier biomarkers. Patients with adenomas serve as a cohort for trials in colon. One cohort for Phase II trials in prostate is patients with early stage cancers scheduled for prostatectomy; another is patients with prostatic intraepithelial neoplasia (without prostatic carcinoma). Patients treated for lung cancer are at high risk for bronchial dysplasia and second cancers; such patients are a cohort for Phase II trials in lung cancer. Presurgical breast cancer patients and patients with ductal or lobular carcinoma in situ are cohorts for studies in breast. Patients with superficial bladder cancers (Ta/T1 with or without carcinoma in situ) are cohorts for studies of chemoprevention in bladder, and patients with dysplastic oral leukoplakia are evaluated for chemoprevention of oral cancers. Cervical intraepithelial neoplasia is a prototype IEN, and patients with cervical intraepithelial neoplasia are a cohort for studies of cervical cancer.
基础癌症相关化学与生物科学、病理学及流行病学,有助于理解抗诱变和抗增殖是化学预防的重要一般机制,并推动了作为潜在化学预防药物的抗诱变剂和抗增殖剂的研发。这些学科还为识别中间生物标志物提供了生化和组织病理学基础,这些生物标志物可在临床化学预防试验中用作癌症发病率的替代终点,并为这些试验选择队列。作为癌症组织学生物标志物特别重要的是定义上皮内瘤变(IEN)的细胞核形态和密度测定变化。IEN变化处于癌症的因果途径上。它们可作为II期化学预防试验中的靶病变,以及可据此评估其他早期细胞和分子生物标志物的标准。已针对七个靶点——结直肠癌、前列腺癌、肺癌、乳腺癌、膀胱癌、口腔癌和宫颈癌,确定了化学预防剂临床评估策略。已确定用于短期II期试验的队列,这些试验研究化学预防剂对IEN和早期生物标志物的影响。腺瘤患者作为结肠癌试验的队列。前列腺II期试验的一个队列是计划进行前列腺切除术的早期癌症患者;另一个是前列腺上皮内瘤变(无前列腺癌)患者。接受肺癌治疗的患者发生支气管发育异常和二次癌症的风险很高;这类患者是肺癌II期试验的队列。术前乳腺癌患者和导管或小叶原位癌患者是乳腺癌研究的队列。浅表膀胱癌(Ta/T1期,伴或不伴原位癌)患者是膀胱癌化学预防研究的队列,发育异常的口腔白斑患者接受口腔癌化学预防评估。宫颈上皮内瘤变是IEN的一个原型,宫颈上皮内瘤变患者是宫颈癌研究的队列。