Controversy endures regarding the optimal treatment of patients with brain metastases
(BMs). Debate persists, despite many randomized trials, perhaps because BM patients
are a heterogeneous population. The purpose of the present study was to identify significant
diagnosis-specific prognostic factors and indexes (Diagnosis-Specific Graded Prognostic
Assessment [DS-GPA]).
A retrospective database of 5,067 patients treated for BMs between 1985 and 2007 was
generated from 11 institutions. After exclusion of the patients with recurrent BMs
or incomplete data, 4,259 patients with newly diagnosed BMs remained eligible for
analysis. Univariate and multivariate analyses of the prognostic factors and outcomes
by primary site and treatment were performed. The significant prognostic factors were
determined and used to define the DS-GPA prognostic indexes. The DS-GPA scores were
calculated and correlated with the outcomes, stratified by diagnosis and treatment.
The significant prognostic factors varied by diagnosis. For non-small-cell lung cancer
and small-cell lung cancer, the significant prognostic factors were Karnofsky performance
status, age, presence of extracranial metastases, and number of BMs, confirming the
original GPA for these diagnoses. For melanoma and renal cell cancer, the significant
prognostic factors were Karnofsky performance status and the number of BMs. For breast
and gastrointestinal cancer, the only significant prognostic factor was the Karnofsky
performance status. Two new DS-GPA indexes were thus designed for breast/gastrointestinal
cancer and melanoma/renal cell carcinoma. The median survival by GPA score, diagnosis,
and treatment were determined.
The prognostic factors for BM patients varied by diagnosis. The original GPA was confirmed
for non-small-cell lung cancer and small-cell lung cancer. New DS-GPA indexes were
determined for other histologic types and correlated with the outcome, and statistical
separation between the groups was confirmed. These data should be considered in the
design of future randomized trials and in clinical decision-making.
(c) 2010 Elsevier Inc. All rights reserved.