institutions. However, a multi-institutional series has been
reported from the German HIT group [18]. In this series of
55 patients, supratentorial tumours received 54 Gy local
RT and infratentorial tumours received CSRT 35.2 Gy in
1.6 Gy fractions with a local 20 Gy boost. All patients
received chemotherapy. Three year OS was 75.6%. The
extent of resection was significant, with a 3-year PFS of
83.3% for completely resected compared with 38.5%
for incompletely resected tumours. Overall 40 patients
had CSRT. Of 25 relapses 20 were local, 3 distant and
2 local
þ
distant. As with other studies [19,20], the
predominant pattern of relapse was local and anaplastic
EP, although associated with a worse outcome should
probably be treated according to the same guidelines as
grade II EP.
CONCLUSIONS
The data on RT dose response relationships in the
literature on the management of EP are difficult to
interpret. The majority of studies have shown a major
impact of extent of resection and histology on outcome.
There have been inadequate patient numbers to perform
reliable multivariate analyses. There is some evidence of
dose response relationship from
<
45 up to
>
50 Gy. In
most series the predominant pattern of relapse in all series
is local, even after gross total resection and post-operative
RT. There is no evidence of benefit for extended field or
craniospinal RT. The priority for future studies is to
maximise the probability of local tumour control. Mea-
sures might include increasing the proportion with
complete resection, possibly with use of chemotherapy
and ‘second look surgery’ for those with initial incomplete
resection. It may also be possible to enhance the benefit for
RT, by dose escalation with conventionally fractionated
conformal RT. This will be the subject of the planned
Children’s Oncology Group study. The role of HFRT may
justify further evaluation and results of completed studies
are awaited.
REFERENCES
1. Kleihues P, Burger PC, Scheithauer BW. The new WHO
classification of brain tumors. Brain Pathol 1993;3:255–268.
2. BloomHJG, Glees J, Bell J. The treatment and long-term prognosis
of children with intracranial tumors: A study of 610 cases, 1950–
1981. Int J Radiat Oncol Biol Phys 1991;18:723–745.
3. Nazar GB, Hoffman HJ, Becker LE, et al. Infratentorial
ependymomas in childhood: Prognostic factors and treatment.
J Neurosurg 1990;72:408–417.
4. Rousseau P, Habrand JL, Sarrazin D, et al. Treatment of intracranial
ependymomas of children: Review of a 15-year experience. Int
J Radiat Oncol Biol Phys 1994;28:381–386.
5. Pollack IF, Gerszten PC, Martinez AJ, et al. Intracranial
ependymomas of childhood: Long-term outcome and prognostic
factors. Neurosurgery 1995;37:655–666.
6. Goldwein JW, Leahy JM, Packer RJ, et al. Intracranial ependymo-
mas in children. Int J Radiat Oncol Biol Phys 1990;19:1497–1502.
7. Vanuytsel LJ, Bessell EM, Ashley SE, et al. Intracranial
ependymoma: Long-term results of a policy of surgery and
radiotherapy. Int J Radiat Oncol Biol Phys 1992;23:313–319.
8. Chiu JK, Woo SY, Ater J, et al. Intracranial ependymoma in
children: Analysis of prognostic factors. J Neurooncol 1992;13:
283–290.
9. Carrie C, Mottolese C, Bouffet E, et al. Non-metastatic childhood
ependymomas. Radiother Oncol 1995;36:101–106.
10. StubenG, StuschkeM, Kroll M, et al. Postoperative radiotherapy of
spinal and intracranial ependymomas: Analysis of prognostic
factors. Radiother Oncol 1997;45:3–10.
11. Schild SE, Nisi K, Scheithauer BW, et al. The results of
radiotherapy for ependymomas: The Mayo clinic experience. Int
J Radiat Oncol Biol Phys 1998;42:953–958.
12. McLaughlin MP, Marcus RB, Buatti JM, et al. Ependymoma:
Results, prognostic factors and treatment recommendations. Int
J Radiat Oncol Biol Phys 1998;40:845–850.
13. Paulino AC, Wen BC, Buatti JM, et al. Intracranial ependymomas:
An analysis of prognostic factors and patterns of failure. Am J Clin
Oncol 2002;25:117–122.
14. Oya N, Shibamoto Y, Nagata Y, et al. Postoperative radiotherapy
for intracranial ependymoma: Analysis of prognostic factors and
patterns of failure. J Neurooncol 2002;56:87–94.
15. Kovnar E, Curran W, Tomita T, et al. Hyperfractionated irradiation
for childhood ependymoma: Early results of a phase III Pediatric
Oncology Group study. J Neurooncol 1997;33:268.
16. Paulino AC, Wen BC. The significance of radiotherapy treatment
duration in intracranial ependymoma. Int J Radiat Oncol Biol Phys
2000;47:585–589.
17. Merchant TE, Zhu Y, Thompson SJ, et al. Preliminary results from
a Phase II trail of conformal radiation therapy for pediatric patients
with localised low-grade astrocytoma and ependymoma. Int
J Radiat Oncol Biol Phys 2002;52:325–332.
18. Timmermann B, Kortmann RD, Kuhl J, et al. Combined post-
operative irradiation and chemotherapy for anaplastic ependymo-
mas in childhood: Results of the German prospective trials HIT
88/89 and HIT 91. Int J Radiat Oncol Biol Phys 2000;46:287–
295.
19. Goldwein JW, Corn BW, Finlay JL, et al. Is craniospinal irradiation
required to cure children with malignant (anaplastic) intracranial
ependymomas? Cancer 1991;67:2766–2771.
20. Merchant TE, Jenkins JJ, Burger PC, et al. Influence of tumor grade
on time to progression after irradiation for localized ependymoma
in children. Int J Radiat Oncol Biol Phys 2002;53: 52–57.
460
Taylor