Table of Contents Table of Contents
Previous Page  1572 / 1708 Next Page
Information
Show Menu
Previous Page 1572 / 1708 Next Page
Page Background

METHODS AND MATERIALS

Study group

Between 1963 and 1994, 80 patients with ependymomas

were identified from the Radiation Oncology Tumor Reg-

istry. The outcome of therapy was retrospectively analyzed.

Included in the study were 33 females and 47 males ranging

in age from 1 to 69 years, with a median age of 33.5 years.

Statistical methods

Survival and local control rates were the principle end-

points of the analysis. Local failure was defined as progres-

sion of local symptoms or as tumor growth documented on

neuroimaging studies. Survival and local control rates were

determined with the Kaplan-Meier product limit method.

The statistical significance of differences between the

curves was determined by the log-rank test. Multivariate

analysis was performed with the Cox proportional hazards

model. Follow-up ranged from 5 to 30 years, with a median

follow-up of 10.4 years.

Surgery and pathologic features

Primary sites included the supratentorial brain in 13 pa-

tients, infratentorial brain in 32 patients, and spinal cord in

35 patients. Seventy patients were found to have low-grade

(1 and 2) tumors and 10 had high-grade (3 and 4) tumors.

The distribution of tumor grade, sub-type, and site of origin

are found in Tables 1 and 2. Myxopapillary tumors were

uniformally grade 1 tumors found in the lumbar spine

region. The following studies were performed to assess for

seeding of the central nervous system (CNS): myelography

in 40 patients, MRI in 21 patients, CT scans in 25 patients,

and CSF cytology in 24 patients. Based on the findings of

clinical studies (myelography, MRI, CT, or CSF cytology),

4 patients (6%) were found to have seeding of the CNS at

the time of diagnosis, including 2 of 70 (3%) with low-grade

tumors and 2 of 10 (20%) with high-grade tumors.

The extent of tumor resection was determined by a care-

ful review of operative reports. Gross total resections were

performed in 17 (21%) patients, subtotal resections in 57

(71%) patients, and biopsy alone in the remaining 6 (8%)

patients (Table 3). Of the 45 patients with tumors arising in

the brain, gross total resections were performed in 7 (16%),

subtotal resections in 36 (80%), and biopsies in 2 (4%). Of

the 35 patients with tumors arising in the brain, gross total

resections were performed in 10 (29%), subtotal resections

in 21 (67%), and biopsies in 4 (11%).

Tumors were graded on a 4 grade scale: grade 1 lesions

lacked mitotic activity; grade 2 lesions exhibited occasional

mitoses; grade 3 lesions showed brisk mitotic activity, and

often some endothelial proliferation; grade 4 tumors showed

high mitotic indices and prominent endothelial prolifera-

tion. As a rule, high-grade (3 and 4) were markedly cellular

and often showed nucleolar prominence. Palisading necro-

sis was most often seen in grade 4 lesions. Cellular pleo-

morphism and simple non-palisading necrosis were not

considered useful grading parameters.

Post-operative therapy

All 80 patients underwent radiation therapy as a portion

of their initial treatment sequence (Table 3). The most

common indication for radiotherapy was the presence of

residual tumor in 63 patients. The remaining 17 patients

received adjuvant therapy following gross total resection,

78 of whom received treatment at Mayo Clinic and 2 at

other institutions. Treatment was delivered with 4, 6, or 10

MV photons. Radiotherapy was delivered to the craniospi-

nal axis in 20 patients, to the whole brain in 3 patients, to the

total spine in 6 patients, and to the primary tumor bed (brain

or spine) alone in the remaining 51 cases. Doses adminis-

tered to the primary tumor bed and to areas of gross disease

ranged from 24 to 59.4 Gy (median 49.7 Gy) in 1.8–2.0 Gy

fractions. Twenty-five (31%) of the 80 patients received

doses less than 45 Gy to the primary tumor bed. Prophy-

lactic doses administered to uninvolved regions ranged from

28.5 to 40.0 Gy. The doses delivered and the field arrange-

ments used were based on the treating physician’s prefer-

ences.

Table 2. Tumor type and site of origin

Tumor type Brain Upper spine Lumbar spine Total

Myxopapillary

0

0

12

12

Other types

45

16

7

68

Total

45

16

19

80

Table 1. Tumor grade and site of origin

Tumor grade

Brain

Spine

Total

1–2

36

34

70

3–4

9

1

10

Total

45

35

80

Table 3. Summary of therapy

Tumor grade

Surgery

Radiotherapy

Biopsy

STR GTR Local field

WBRT/WSRT

CSRT

Adjuvant chemotherapy

1–2

6

49

15

49

8

13

1

3–4

0

8

2

2

1

7

0

STR

5

subtotal resection; GTR

5

gross total resection; WBRT

5

whole brain radiotherapy; WSRT

5

whole spine radiotherapy;

CSRT

5

craniospinal radiotherapy.

954

I. J. Radiation Oncology

Biology

Physics

Volume 42, Number 5, 1998