Quantitative contribution of prognosticators to oncologic outcome after rectal cancer resection

Dis Colon Rectum. 2015 Jun;58(6):566-74. doi: 10.1097/DCR.0000000000000334.

Abstract

Background: Prognostication is an important aspect of medical practice. It relies on statistical modeling testing the correlation of variables with the outcome of interest.

Objective: In contrast with the classic approach of predictive modeling, this study aimed to estimate the unique, individual, and relative contributions. This includes the quantitative contributions of patient-, tumor-, and treatment-related factors to oncologic outcome after rectal cancer resection.

Design: This was a retrospective analysis of prospectively registered data.

Settings: The study included 65 hospitals participating on a voluntary basis in the Project on Cancer of the Rectum, a Belgian multidisciplinary improvement project of rectal cancer care.

Patients: A total of 1470 patients presenting midrectal or low-rectal adenocarcinoma without distant metastasis were included.

Intervention: The study intervention was total mesorectal excision with or without sphincter preservation.

Main outcome measures: The unique, individual, and relative contributions of a set of covariables to the statistical variability of the distant metastasis rate and overall survival have been calculated.

Results: The 5-year distant metastasis rate was 21% and overall survival 76%. A large amount of the variability of the outcomes (ie, 83.6% to 84.2%) could not be predicted by the prognostic factors. Unique contributions of the predictors ranged from 0.1% to 3.1%. The 3 risk factors with the highest unique contribution for distant metastasis were lymph node ratio, pathologic tumor stage, and total mesorectal quality; for overall survival they were age, lymph node ratio, and ASA score.

Limitations: The main weakness of this study was incomplete participation and registration in the Project on Cancer of the Rectum.

Conclusions: Several factors influence oncologic outcomes and are present in prediction models. However, the models predict relatively little of outcome variation.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / mortality
  • Adenocarcinoma / pathology
  • Adenocarcinoma / secondary
  • Adenocarcinoma / surgery*
  • Aged
  • Female
  • Humans
  • Lymphatic Metastasis
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local
  • Neoplasm Staging
  • Prognosis
  • Rectal Neoplasms / mortality
  • Rectal Neoplasms / pathology
  • Rectal Neoplasms / surgery*
  • Retrospective Studies
  • Survival Rate
  • Treatment Outcome