Evaluation of Tumours

Site Map: Home Benign Growth Malignant Growth Progression Metastasis Dissemination Individual Effects Systematic Effects Response Diagnosis Evaluation Therapeutic Strategies Radiation Therapy Chemotherapy Other Ttherapies Prevention Causes Oncogenes Mutation Suppressor Gene DNA Repair Agents Chemicals Radiation Genetics Milestones Breast Cancer Bladder Cancer Brain Cancer Cervical Cancer Colorectal Cancer Esophageal Cancer Laryngeal Cancer Lung Cancer Liver Cancer Oral Cancer Ovarian Cancer Pancreatic Cancer Prostate Cancer Skin Cancer Stomach Cancer Uterine Cancer

A major factor governing the choice of therapy is the grade and stage of the tumour. In many cases grading and staging schemes can help to predict the behaviour of a tumour and thereby determine the most appropriate approach to treatment.

Grading schemes classify tumours according to the structure, composition, and function of tumour tissue — in clinical terms, the histological features of the tumour. The histological grade of a tumour refers to the degree of tissue differentiation or to an ensemble of tissue features that have been found to be a good predictor of the aggressiveness of the tumour. Most grading schemes classify a type of cancer into three or four levels of increasing malignancy.

Staging protocols, which are independent of grading schemes, are employed to describe the size and dissemination of the tumour, both in the organ in which it arose and beyond it. For every type of tumour, a series of tests and procedures are codified in order to assess how far the tumour has extended in the patient's body. Each tumour staging system is complemented by a grading method.

An internationally standardized classification system is the TNM staging system, put forth by the Union Internationale Contre le Cancer and the American Joint Committee on Cancer. In this system T refers to the size of the primary tumour, N to the presence and extent of lymph node metastases, and M to the presence of distant metastases.

Besides stage and grade, other prognostic factors exist for many types of cancer. Cancers can be defined not only by their appearance but also by the pattern of altered gene activity. Definition of this altered pattern by molecular tests can help to predict the rapidity of growth of the tumour, its tendency to spread, and its response to therapies.

Molecular procedures, when integrated with conventional grading and staging procedures, are likely to improve significantly the present systems of prognostication. Some are based on detecting and measuring the level of substances produced by the tumour. These substances, called tumour markers, also can aid in monitoring an individual who has received treatment for cancer to determine whether the tumour has returned. A rising level of a tumour marker in the blood will in general indicate the regrowth of the tumour. Diagnostically useful tumour markers include carcinoembryonic antigen (CEA), which is an indicator of carcinomas of the gastrointestinal tract, lung, and breast; CA 125, which is produced by ovarian cancers; CA 19-9, which indicates pancreatic or gastrointestinal cancers; and alpha-fetoprotein and chorionic gonadotropin, which can indicate testicular cancer.

Tumour markers also can be used to estimate the proportion of cells in a tumour that are actively growing. This approach has prognostic significance because tumours with a high proportion of dividing cells tend to be more aggressive.

It is often the case that the more abnormal the DNA content per cell, the more difficult the tumour will be to control. It is possible to refine the prognosis of a tumour by examining the specific genetic alterations found in the cells of the tumour. For example, neuroblastoma cells that contain amplified amounts of the N-MYC gene indicate a worse prognosis for the individual than do cells from identical tumours that have the normal genetic complement of N-MYC.

A sensitive molecular technique called the polymerase chain reaction (PCR) makes it possible to detect mutations that identify certain tumours when only a small number of cancer cells are present. For example, in individuals with leukemia who have received bone marrow transplants, a PCR assay can discover very low levels of residual malignant cells in the circulation and thus provide a sensitive indicator of the success of the therapy.