| Literature DB >> 24527431 |
E Chatzimichail1, D Matthaios2, D Bouros3, P Karakitsos4, K Romanidis5, S Kakolyris2, G Papashinopoulos1, A Rigas1.
Abstract
Cancer is a leading cause of death worldwide and the prognostic evaluation of cancer patients is of great importance in medical care. The use of artificial neural networks in prediction problems is well established in human medical literature. The aim of the current study was to assess the prognostic value of a series of clinical and molecular variables with the addition of γ -H2AX-a new DNA damage response marker-for the prediction of prognosis in patients with early operable non-small cell lung cancer by comparing the γ -H2AX-based artificial network prediction model with the corresponding LR one. Two prognostic models of 96 patients with 27 input variables were constructed by using the parameter-increasing method in order to compare the predictive accuracy of neural network and logistic regression models. The quality of the models was evaluated by an independent validation data set of 11 patients. Neural networks outperformed logistic regression in predicting the patient's outcome according to the experimental results. To assess the importance of the two factors p53 and γ -H2AX, models without these two variables were also constructed. JR and accuracy of these models were lower than those of the models using all input variables, suggesting that these biological markers are very important for optimal performance of the models. This study indicates that neural networks may represent a potentially more useful decision support tool than conventional statistical methods for predicting the outcome of patients with non-small cell lung cancer and that some molecular markers, such as γ -H2AX, enhance their predictive ability.Entities:
Year: 2014 PMID: 24527431 PMCID: PMC3910456 DOI: 10.1155/2014/160236
Source DB: PubMed Journal: Int J Genomics ISSN: 2314-436X Impact factor: 2.326
Characteristics of the prediction variables.
| Variables | No. of patients | Percentage (%) |
|---|---|---|
| Total number of patients | 96 | |
| Age (years) | ||
| Mean ± SD | 65.64 ± 7.23 | |
| <65 | 36 | 37.5 |
| ≥65 | 60 | 62.5 |
| Gender | ||
| Male | 77 | 80.2 |
| Female | 19 | 19.8 |
| Histology | ||
| Adenocarcinoma | 42 | 43.8 |
| Squamous cell carcinoma | 42 | 43.8 |
| Large cell carcinoma | 8 | 8.3 |
| Undifferentiated carcinoma | 4 | 4.1 |
| T status | ||
| T1 | 13 | 13.5 |
| T2 | 65 | 67.7 |
| T3 | 18 | 18.8 |
| Regional lymph node status (N) | ||
| N0 | 50 | 52.1 |
| N1 | 27 | 28.1 |
| N2 | 19 | 19.8 |
| Stage | ||
| I | 41 | 42.7 |
| II | 22 | 22.9 |
| III | 31 | 32.3 |
| IV | 2 | 2.1 |
| Grade | ||
| Low | 25 | 26 |
| Medium/high | 71 | 74 |
| Border of bronchus | ||
| Positive | 12 | 12.5 |
| Negative | 84 | 87.5 |
|
| ||
| FEV1 < 70% | 17 | 17.7 |
| Positive vessel infiltration | 41 | 42.7 |
| Positive lymphatic infiltration | 21 | 21.9 |
| Positive pleural infiltration | 46 | 47.9 |
| Chemotherapy adjuvant | 72 | 75.0 |
| Radiotherapy adjuvant | 41 | 42.7 |
| High expression of P53 | 55 | 57.3 |
| High expression of caspase 3 | 24 | 25.0 |
| High expression of | 25 | 26.0 |
| High expression of Ki67 | 29 | 30.2 |
Selected input variables by the parameter-increasing method.
| Order of | 1-year survival | 3-year survival | 4-year survival | |||
|---|---|---|---|---|---|---|
| ANN | LR | ANN | LR | ANN | LR | |
| 1 | High expression of | High expression | High expression of | High expression of Ki67 | Age | N2 number |
| 2 | High expression of | Chemotherapy adjuvant | High expression of | Histology | Histology | |
| 3 | First metastasis | Radiotherapy adjuvant | N1 number | Grade | Border of | |
| 4 | High expression of P53 | Grade | N | |||
| 5 | Gender | High expression of P53 | Radiotherapy adjuvant | |||
| 6 | High expression of | |||||
| 7 | High expression of | |||||
| 8 | Fev1 < 70% | |||||
| 9 | High expression of P53 | |||||
Comparison of predictive models for 1-, 3-, and 4-year using ANN and LR.
| 1-year prediction | 3-year prediction | 4-year prediction | ||||
|---|---|---|---|---|---|---|
| ANN | LR | ANN | LR | ANN | LR | |
| JR (%) | 87.1 | 88.2 | 88.2 | 87.1 | 88.2 | 87.1 |
| No. of patients | 74/85 | 75/85 | 75/85 | 74/85 | 75/85 | 74/85 |
| Accuracy (%) | 93.3 | 90.7 | 78.7 | 74.3 | 92 | 91.9 |
| No. of patients | 69/74 | 68/75 | 59/75 | 55/74 | 69/75 | 68/74 |
Selected input variables by the parameter-increasing method.
| Order of selection | 1-year prediction | 1-year prediction without |
|---|---|---|
| 1 | High expression | High expression of caspase 3 |
| 2 | High expression | Stage |
| 3 | First metastasis site | First |
| 4 | High expression | Border of |
| 5 | Gender | Fev1 < 70% |
Comparison of predictive models for 1-year prediction.
| 1-year | 1-year prediction without | |
|---|---|---|
| JR (%) | 87.1 | 72.3 |
| No. of patients | 74/85 | 62/85 |
| Accuracy | 93.3 | 85.4 |
| No. of patients | 69/74 | 53/62 |
Estimation of 3- and 4-year outcome prediction for unlearned data set.
| 3-year prediction | 4-year prediction | |||
|---|---|---|---|---|
| Learning | Validation | Learning | Validation | |
| JR (%) | 88.2 | 72.7 | 88.2 | 81.8 |
| No. of patients | 75/85 | 8/11 | 75/85 | 9/11 |
| Accuracy (%) | 78.7 | 75 | 92 | 88.9 |
| No. of patients | 59/75 | 6/8 | 69/75 | 8/9 |