| Literature DB >> 18564426 |
Onur Gilleard1, Andrew Goodman, Martin Cooper, Mary Davies, Julie Dunn.
Abstract
BACKGROUND: Debate regarding the benefit of radiotherapy after local excision of ductal carcinoma in situ (DCIS) continues. The Van Nuys Prognostic Index (VNPI) is thought to be a useful aid in deciding which patients are at increased risk of local recurrence and who may benefit from adjuvant radiotherapy (RT). Recently published interim data from the Sloane project has showed that the VNPI score did significantly affect the chances of getting planned radiotherapy in the UK, suggesting that British clinicians may already be using this scoring system to assist in decision making. This paper independently assesses the prognostic validity of the VNPI in a British population. PATIENTS AND METHODS: A retrospective review was conducted of all patients (n = 215) who underwent breast conserving surgery for DCIS at a single institution between 1997-2006. No patients included in the study received additional radiotherapy or hormonal treatment. Kaplan Meier survival curves were calculated, to determine disease free survival, for the total sample and a series of univariate analyses were performed to examine the value of various prognostic factors including the VNPI. The log-rank test was used to determine statistical significance of differential survival rates. Multivariate Cox regression analysis was performed to analyze the significance of the individual components of the VNPI. All analyses were conducted using SPSS software, version 14.5.Entities:
Mesh:
Year: 2008 PMID: 18564426 PMCID: PMC2459183 DOI: 10.1186/1477-7819-6-61
Source DB: PubMed Journal: World J Surg Oncol ISSN: 1477-7819 Impact factor: 2.754
Van Nuys Prognostic Index
| 1 | 2 | 3 | |
| Size of tumour (mm) | ≤ 15 | 16–40 | >40 |
| Margin width (mm) | >10 | 1–10 | <1 |
| Grade | Non high grade, no comedo necrosis | Non high grade with comedo necrosis | High grade with or without comedo necrosis |
Patient and tumour characteristics
| <60 | 104 | 48 |
| ≥ 60 | 111 | 52 |
| Comedo | 54 | 25 |
| Cribriform | 49 | 23 |
| Solid | 7 | 3 |
| Papillary | 22 | 10 |
| Mixed | 49 | 23 |
| Not specified | 34 | 16 |
| Low | 69 | 32 |
| Intermediate | 51 | 24 |
| High | 95 | 44 |
| Yes | 84 | 39 |
| No | 130 | 60 |
| Not specified | 1 | <1 |
| <5 | 46 | 21 |
| 5–10 | 63 | 29 |
| 11–20 | 55 | 26 |
| >20 | 34 | 16 |
| Not specified | 17 | 8 |
| <1 | 65 | 30 |
| 1–5 | 102 | 47 |
| >5 | 30 | 15 |
| Not specified | 18 | 8 |
| Yes | 72 | 33 |
| No | 143 | 67 |
| 3–4 | 61 | 29 |
| 5–7 | 104 | 48 |
| 8–9 | 20 | 9 |
| Not specified | 30 | 14 |
Eight-year local recurrence free survival calculated using the Kaplan-Meier method
| All recurrences | 19 | 83 |
| Invasive | 11 | 87 |
Figure 1Predicted 8 year disease free survival curve.
Predicted 8-year local recurrence free survival for selected patient and treatment characteristics
| <60 | 83.0 | 0.68 |
| ≥ 60 | 82.7 | |
| Yes | 80.4 | 0.48 |
| No | 84.7 | |
| Non high grade, no comedo necrosis | 89.9 | |
| Non high grade with comedo necrosis | 82.7 | 0.04 |
| High grade with or without comedo necrosis | 73.8 | |
| ≤ 15 | 91.0 | |
| 16–40 | 80.2 | 0.42 |
| >40 | 100 | |
| <1 | 75.8 | 0.17 |
| 1–10 | 86.5 | |
| >10 | 97.2 | |
| 3–4 | 100 | |
| 5–7 | 78.5 | 0.002 |
| 8–9 | 67.9 | |
Figure 2The influence of the VNPI on disease free survival.