Prognostic factors in brain metastases: Should patients be selected for aggressive treatment according to recursive partitioning analysis (RPA) classes?
C. Nieder et al., Prognostic factors in brain metastases: Should patients be selected for aggressive treatment according to recursive partitioning analysis (RPA) classes?, INT J RAD O, 46(2), 2000, pp. 297-302
Citations number
23
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
Purpose: To determine whether or not Radiation Therapy Oncology Group (RTOG
) recursive partitioning analysis (RPA) derived prognostic classes for pati
ents with brain metastases are generally applicable and can be recommended
as rational strategy for patient selection for future clinical trials. Incl
usion of time to non-CNS death as additional endpoint besides death from an
y cause might result in further valuable information, as survival limitatio
n due to uncontrolled extracranial disease can be explored.
Methods: We performed a retrospective analysis of prognostic factors for su
rvival and time to non-CNS death in 528 patients treated at a single instit
ution with radiotherapy or surgery plus radiotherapy for brain metastases,
For this purpose, patients were divided into groups with Karnofsky performa
nce status (KPS) <70% and KPS greater than or equal to 70%, as proposed by
the RTOG,
Results: Median overall survival was 2.9 months (2.0 months for patients wi
th KPS <70% and 3.6 months for patients with KPS greater than or equal to 7
0%,p < 0,001). We did not find other variables splitting patients with KPS
<70% in different prognostic groups. However, advanced age, multiple brain
metastases, presence of extracranial metastases, and uncontrolled primary t
umor each predicted shorter survival in patients with KPS greater than or e
qual to 70%. When grouped into the original RTOG RPA classes, our data set
split into three subgroups with different prognosis and median survival tim
es of 10,5, 3,5, and 2 months, respectively (p < 0,05), Only 3% of patients
fell into the most favorable group. Median time to non-CNS death was 4.1 m
onths (12.9 months in RPA class I, 4.9 months in RPA class II, and 3.8 mont
hs in RPA class III, respectively,p > 0.05 for RPA class II versus In). How
ever, it was 8.5 months in RPA class II patients with controlled primary tu
mor, which was found to be the only prognostic factor for time to non-CNS d
eath in patients with KPS greater than or equal to 70%. In patients with KP
S <70%, no statistically significant prognostic factors were identified for
this endpoint,
Conclusions: Despite some differences, this analysis essentially confirmed
the value of RPA-derived prognostic classes, as published by the RTOG, when
survival was chosen as endpoint, RPA class I patients seem to be most like
ly to profit from aggressive treatment strategies and should be included in
appropriate clinical trials. However, their number appears to he very limi
ted. Considering time to non-CNS death, our results suggest that certain pa
tients in RPA class II also might benefit from increased local control of b
rain metastases, (C) 2000 Elsevier Science Inc.