Table of Contents Purpose of This PDQ Summary General Information Cellular Classification Stage Information Treatment Option Overview Untreated Childhood Supratentorial Primitive Neuroectodermal Tumors and Pineoblastoma
Recurrent Childhood Supratentorial Primitive Neuroectodermal Tumors and Pineoblastoma Get More Information From NCI Changes to This Summary (04/09/2008) More Information
Purpose of This PDQ Summary
This PDQ cancer information summary for health professionals provides comprehensive, peer-reviewed, evidence-based information about the treatment of childhood supratentorial primitive neuroectodermal tumors and pineoblastoma. This summary is reviewed regularly and updated as necessary by the PDQ Pediatric Treatment Editorial Board.
Information about the following is included in this summary:
- Cellular classification.
- Stage information.
- Treatment options.
This summary is intended as a resource to inform and assist clinicians and other health professionals who care for pediatric cancer patients. It does not provide formal guidelines or recommendations for making health care decisions.
In the summary, treatments are described as “standard” or “conventional” and “under clinical evaluation.” These designations should not be used as a basis for reimbursement determinations.
This summary is also available in a patient version, which is written in less-technical language, and in Spanish. [Note: The PDQ childhood brain tumor treatment summaries are in the process of being substantially revised. This revision process was prompted by changes in the nomenclature and classification for pediatric central nervous system tumors. New PDQ childhood brain tumor treatment summaries will be added and some existing summaries will be replaced or their content combined with other PDQ childhood brain tumor treatment summaries in the near future.]
Back to Top General Information
This PDQ summary contains content that is also included in the new PDQ Childhood Central Nervous System Embryonal Tumors summary. In the very near future, the PDQ Childhood Supratentorial Primitive Neuroectodermal Tumors and Pineoblastoma summary will be removed from the National Cancer Institute (NCI) website and the content contained in this summary will be found in the PDQ Childhood Central Nervous System Embryonal Tumors summary.
The National Cancer Institute provides the PDQ pediatric cancer treatment information summaries as a public service to increase the availability of evidence-based cancer information to health professionals, patients, and the public.
Primary brain tumors are a diverse group of diseases that together constitute
the most common solid tumor of childhood. Brain tumors are classified
according to histology, but tumor location and extent of spread are important
factors that affect treatment and prognosis. Immunohistochemical analysis,
cytogenetic and molecular genetic findings, and measures of mitotic activity
are increasingly used in tumor diagnosis and classification.
Refer to the PDQ Childhood Brain and Spinal Cord Tumors Treatment summary for information about the general classification of childhood brain and spinal cord tumors.
Back to Top Cellular Classification
The classification of brain tumors is based on both histopathologic
characteristics and location in the brain. Undifferentiated neuroectodermal
tumors of the cerebellum have historically been referred to as
medulloblastomas, while tumors of identical histology in the pineal region are
diagnosed as pineoblastomas, and cortical lesions have been called central neuroblastomas or cortical primitive neuroectodermal tumors. Studies have suggested that the tumor cells of medulloblastomas and
supratentorial primitive neuroectodermal tumors have different molecular genetic aberrations.[1,2] This group also includes
some tumors formerly called central neuroblastomas. The nomenclature of
pediatric brain tumors is controversial and potentially confusing. Some
pathologists advocate abandoning the traditional morphologically based
classifications such as medulloblastoma in favor of a terminology that relies
more extensively on the phenotypic characteristics of the tumor. In such a
system, medulloblastoma is referred to as primitive neuroectodermal tumor and
then subdivided on the basis of cellular differentiation. The World Health Organization 2000 classification of brain tumors maintains the term
medulloblastoma for posterior fossa undifferentiated tumors.[3] It also
maintains separate categories for cerebral primitive neuroectodermal tumors and
for pineal small round cell tumors (pineoblastomas). The pathologic
classification of pediatric brain tumors is a specialized area that is
evolving; review of the diagnostic tissue by a neuropathologist who
has particular expertise in this area is strongly recommended.
References
-
Russo C, Pellarin M, Tingby O, et al.: Comparative genomic hybridization in patients with supratentorial and infratentorial primitive neuroectodermal tumors. Cancer 86 (2): 331-9, 1999.
[PUBMED Abstract]
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Nicholson JC, Ross FM, Kohler JA, et al.: Comparative genomic hybridization and histological variation in primitive neuroectodermal tumours. Br J Cancer 80 (9): 1322-31, 1999.
[PUBMED Abstract]
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Kleihues P, Cavenee WK, eds.: Pathology and Genetics of Tumours of the Nervous System. Lyon, France: International Agency for Research on Cancer, 2000.
Back to Top Stage Information
Poorly differentiated small round cell tumors of the cerebrum have been
referred to as cerebral neuroblastoma and as primitive neuroectodermal tumors.
These tumors in the pineal body have classically been called pineoblastomas.
Histologically, these tumors may be similar to cerebellar medulloblastoma with
varying proportions of features that suggest astrocytic or ependymal
differentiation. Genetic aberrations of supratentorial brain tumors appear to
be different from those of infratentorial primitive neuroectodermal tumors
(PNET, medulloblastoma).[1] Tumors may spread throughout the subarachnoid
space. Every patient with a primitive neuroectodermal tumor or with
pineoblastoma should be evaluated with diagnostic imaging of the spinal cord
and whole brain. The most sensitive method currently available for evaluating
spinal cord subarachnoid metastasis is spinal magnetic resonance imaging
performed with gadolinium. Cerebrospinal fluid should be examined
cytologically for tumor cells. There is no generally accepted staging system
for supratentorial primitive neuroectodermal tumors and for pineoblastomas, but
the staging system used for medulloblastoma is conventionally used for tumor
dissemination. Prognosis is probably related to the extent of disease both at
diagnosis and after surgery.[2-5] Patients with cystic tumors may fare better.
[Note: 2-year survival rate: 30% to 50%]
References
-
Russo C, Pellarin M, Tingby O, et al.: Comparative genomic hybridization in patients with supratentorial and infratentorial primitive neuroectodermal tumors. Cancer 86 (2): 331-9, 1999.
[PUBMED Abstract]
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Edwards MS, Hudgins RJ, Wilson CB, et al.: Pineal region tumors in children. J Neurosurg 68 (5): 689-97, 1988.
[PUBMED Abstract]
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Disclafani A, Hudgins RJ, Edwards MS, et al.: Pineocytomas. Cancer 63 (2): 302-4, 1989.
[PUBMED Abstract]
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D'Andrea AD, Packer RJ, Rorke LB, et al.: Pineocytomas of childhood. A reappraisal of natural history and response to therapy. Cancer 59 (7): 1353-7, 1987.
[PUBMED Abstract]
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Abay EO 2nd, Laws ER Jr, Grado GL, et al.: Pineal tumors in children and adolescents. Treatment by CSF shunting and radiotherapy. J Neurosurg 55 (6): 889-95, 1981.
[PUBMED Abstract]
Back to Top Treatment Option Overview
Many of the improvements in survival in childhood cancer have been made as a
result of clinical trials that have attempted to improve on the best
available, accepted therapy. Clinical trials in pediatrics are designed to compare new
therapy with therapy that is currently accepted as standard. This comparison
may be done in a randomized study of two treatment arms or by evaluating a single
new treatment and comparing the results with those that were previously obtained with
existing therapy.
Because of the relative rarity of cancer in children, all patients with brain
tumors should be considered for entry into a clinical trial. To determine and
implement optimum therapy, treatment planning by a multidisciplinary team of
cancer specialists who have experience treating childhood brain tumors is
required. Radiation therapy, if needed, is technically very demanding and
should be carried out in centers that have experience in that area to ensure
optimal results.
In the past, treatment has included surgery with radiation therapy. Evidence suggests that more extensive surgical resections are related to an
improved rate of survival for patients with medulloblastoma without
dissemination at diagnosis, primarily in children with nondisseminated
posterior fossa disease at diagnosis. This has not yet been proven for
childhood supratentorial primitive neuroectodermal and pineal (pineoblastoma)
tumors. The results of prospective, randomized trials and large
single-arm trials have suggested that adjuvant chemotherapy given during and
after radiation therapy may improve overall survival in children
with medulloblastoma. Several nonrandomized trials suggest potential benefit of postradiation chemotherapy.[1-5] Children younger than 3 years are particularly
susceptible to the adverse effects of radiation on brain development.
Debilitating effects on growth and neurologic development have frequently been
observed, especially in younger children.[6-8] For this reason, the role of
chemotherapy in allowing for a delay in the administration of radiation therapy is
under study, and preliminary results suggest that chemotherapy can be used to
delay, if not obviate, the need for radiation therapy in some children younger than 3 years with primitive neuroectodermal tumors.[9] Surveillance testing is presently a part of
all ongoing supratentorial primitive neuroectodermal studies.[10] Long-term
management of these patients is complex and requires a multidisciplinary
approach.
The designations in PDQ that treatments are “standard” or “under clinical
evaluation” are not to be used as a basis for reimbursement determinations.
References
-
Timmermann B, Kortmann RD, Kühl J, et al.: Role of radiotherapy in the treatment of supratentorial primitive neuroectodermal tumors in childhood: results of the prospective German brain tumor trials HIT 88/89 and 91. J Clin Oncol 20 (3): 842-9, 2002.
[PUBMED Abstract]
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Jakacki RI, Zeltzer PM, Boyett JM, et al.: Survival and prognostic factors following radiation and/or chemotherapy for primitive neuroectodermal tumors of the pineal region in infants and children: a report of the Childrens Cancer Group. J Clin Oncol 13 (6): 1377-83, 1995.
[PUBMED Abstract]
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Cohen BH, Zeltzer PM, Boyett JM, et al.: Prognostic factors and treatment results for supratentorial primitive neuroectodermal tumors in children using radiation and chemotherapy: a Childrens Cancer Group randomized trial. J Clin Oncol 13 (7): 1687-96, 1995.
[PUBMED Abstract]
-
Reddy AT, Janss AJ, Phillips PC, et al.: Outcome for children with supratentorial primitive neuroectodermal tumors treated with surgery, radiation, and chemotherapy. Cancer 88 (9): 2189-93, 2000.
[PUBMED Abstract]
-
Taylor RE, Bailey CC, Robinson K, et al.: Results of a randomized study of preradiation chemotherapy versus radiotherapy alone for nonmetastatic medulloblastoma: The International Society of Paediatric Oncology/United Kingdom Children's Cancer Study Group PNET-3 Study. J Clin Oncol 21 (8): 1581-91, 2003.
[PUBMED Abstract]
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Packer RJ, Sutton LN, Atkins TE, et al.: A prospective study of cognitive function in children receiving whole-brain radiotherapy and chemotherapy: 2-year results. J Neurosurg 70 (5): 707-13, 1989.
[PUBMED Abstract]
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Johnson DL, McCabe MA, Nicholson HS, et al.: Quality of long-term survival in young children with medulloblastoma. J Neurosurg 80 (6): 1004-10, 1994.
[PUBMED Abstract]
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Packer RJ, Sutton LN, Goldwein JW, et al.: Improved survival with the use of adjuvant chemotherapy in the treatment of medulloblastoma. J Neurosurg 74 (3): 433-40, 1991.
[PUBMED Abstract]
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Duffner PK, Horowitz ME, Krischer JP, et al.: Postoperative chemotherapy and delayed radiation in children less than three years of age with malignant brain tumors. N Engl J Med 328 (24): 1725-31, 1993.
[PUBMED Abstract]
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Kramer ED, Vezina LG, Packer RJ, et al.: Staging and surveillance of children with central nervous system neoplasms: recommendations of the Neurology and Tumor Imaging Committees of the Children's Cancer Group. Pediatr Neurosurg 20 (4): 254-62; discussion 262-3, 1994.
[PUBMED Abstract]
Back to Top Untreated Childhood Supratentorial Primitive Neuroectodermal Tumors and Pineoblastoma
Careful evaluation to fully determine the extent of disease must precede the
treatment of childhood supratentorial primitive neuroectodermal tumors (SPNET) and pineoblastoma. Surgery should be an attempt at maximal tumor reduction.
Postoperatively, studies should be conducted to determine if the patient has
disseminated disease.[1] Risk criteria are outlined in the stage information
section. Patients with extensive tumors should be considered at the highest
risk of relapse and should be treated on protocols specifically designed for
them.[2] Children with pineal primitive neuroectodermal tumors may have a more
favorable prognosis when treated with surgery, radiation therapy, and
chemotherapy than children with SPNETs.[2,3]
The usual postsurgical treatment is radiation therapy.[4] The suggested tumor
dose is 54 Gy to 56 Gy using conventional fractionation. Craniospinal
irradiation with 23.4 Gy to 36 Gy is also recommended because of the propensity
of this tumor to disseminate through the subarachnoid space. Given the overall
poorer prognosis for patients with extensive disease, the addition of
chemotherapy before or after radiation therapy is being explored.[5,6] The
role of chemotherapy to delay irradiation and its consequences is under
clinical evaluation; preliminary results suggest that chemotherapy can be used
to delay, modify, or, in selected cases, obviate the need for radiation
therapy.[1]
Children younger than 3 years:
Some patients younger than 3 years with newly diagnosed SPNETs and pineoblastomas will respond at least
partially to chemotherapy.[1-3,7] Some patients, especially those with
minimal residual postoperative disease, may have a long-lasting response. For
this reason, studies that use chemotherapy to delay, modify, or
possibly obviate the need for radiation therapy have been undertaken. Results of such studies for young children with SPNET and pineoblastomas have been disappointing.[1,8] Although chemotherapy is
being used to prevent neurologic damage caused by radiation therapy in very
young patients, neurologic deficits may be present in children prior to the
initiation of therapy, and progressive neurologic damage has been noted during
therapy.[9]
Current Clinical Trials
Check for U.S. clinical trials from NCI's PDQ Cancer Clinical Trials Registry that are now accepting patients with untreated childhood supratentorial primitive neuroectodermal tumor, childhood pineoblastoma and untreated childhood pineoblastoma. The list of clinical trials can be further narrowed by location, drug, intervention, and other criteria.
General information about clinical trials is also available from the NCI Web site.
References
-
Duffner PK, Horowitz ME, Krischer JP, et al.: Postoperative chemotherapy and delayed radiation in children less than three years of age with malignant brain tumors. N Engl J Med 328 (24): 1725-31, 1993.
[PUBMED Abstract]
-
Cohen BH, Zeltzer PM, Boyett JM, et al.: Prognostic factors and treatment results for supratentorial primitive neuroectodermal tumors in children using radiation and chemotherapy: a Childrens Cancer Group randomized trial. J Clin Oncol 13 (7): 1687-96, 1995.
[PUBMED Abstract]
-
Jakacki RI, Zeltzer PM, Boyett JM, et al.: Survival and prognostic factors following radiation and/or chemotherapy for primitive neuroectodermal tumors of the pineal region in infants and children: a report of the Childrens Cancer Group. J Clin Oncol 13 (6): 1377-83, 1995.
[PUBMED Abstract]
-
Disclafani A, Hudgins RJ, Edwards MS, et al.: Pineocytomas. Cancer 63 (2): 302-4, 1989.
[PUBMED Abstract]
-
Reddy AT, Janss AJ, Phillips PC, et al.: Outcome for children with supratentorial primitive neuroectodermal tumors treated with surgery, radiation, and chemotherapy. Cancer 88 (9): 2189-93, 2000.
[PUBMED Abstract]
-
Massimino M, Gandola L, Spreafico F, et al.: Supratentorial primitive neuroectodermal tumors (S-PNET) in children: A prospective experience with adjuvant intensive chemotherapy and hyperfractionated accelerated radiotherapy. Int J Radiat Oncol Biol Phys 64 (4): 1031-7, 2006.
[PUBMED Abstract]
-
Duffner PK, Cohen ME, Sanford RA, et al.: Lack of efficacy of postoperative chemotherapy and delayed radiation in very young children with pineoblastoma. Pediatric Oncology Group. Med Pediatr Oncol 25 (1): 38-44, 1995.
[PUBMED Abstract]
-
Timmermann B, Kortmann RD, Kühl J, et al.: Role of radiotherapy in supratentorial primitive neuroectodermal tumor in young children: results of the German HIT-SKK87 and HIT-SKK92 trials. J Clin Oncol 24 (10): 1554-60, 2006.
[PUBMED Abstract]
-
Mulhern RK, Horowitz ME, Kovnar EH, et al.: Neurodevelopmental status of infants and young children treated for brain tumors with preirradiation chemotherapy. J Clin Oncol 7 (11): 1660-6, 1989.
[PUBMED Abstract]
Back to Top Recurrent Childhood Supratentorial Primitive Neuroectodermal Tumors and Pineoblastoma
Recurrence is not uncommon in both benign and malignant childhood brain tumors
and may develop many years after initial treatment.[1] Disease can be at the
primary tumor site or, especially in malignant tumors, at noncontiguous central
nervous system sites. Systemic relapse is rare but may occur. At time of
relapse, a complete evaluation for extent of recurrence is indicated for all
malignant tumors and, at times, for benign lesions. Biopsy or surgical
resection may be necessary for confirmation of relapse because other entities,
such as secondary tumor and treatment-related brain necrosis, may be clinically
indistinguishable from tumor recurrence. The need for surgical intervention
must be individualized on the basis of the initial tumor type, the length of
time between initial treatment and the reappearance of the lesion, and the
clinical picture. Patients with supratentorial primitive neuroectodermal
tumors or pineoblastomas that recur after radiation therapy alone should be
considered for treatment with known active agents, which include vincristine,
cyclophosphamide, cisplatin, carboplatin, and etoposide; response is seen in
more than 50% of patients.[2,3] Entry into studies of novel therapeutic
approaches at the time of relapse after radiation therapy alone or radiation
therapy and chemotherapy should be considered.[4,5] Information about ongoing clinical trials is available from the NCI Web site.
Current Clinical Trials
Check for U.S. clinical trials from NCI's PDQ Cancer Clinical Trials Registry that are now accepting patients with recurrent childhood supratentorial primitive neuroectodermal tumor, recurrent childhood pineoblastoma and childhood pineoblastoma. The list of clinical trials can be further narrowed by location, drug, intervention, and other criteria.
General information about clinical trials is also available from the NCI Web site.
References
-
Jenkin D, Greenberg M, Hoffman H, et al.: Brain tumors in children: long-term survival after radiation treatment. Int J Radiat Oncol Biol Phys 31 (3): 445-51, 1995.
[PUBMED Abstract]
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Cangir A, van Eys J, Berry DH, et al.: Combination chemotherapy with MOPP in children with recurrent brain tumors. Med Pediatr Oncol 4 (3): 253-61, 1978.
[PUBMED Abstract]
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Needle MN, Molloy PT, Geyer JR, et al.: Phase II study of daily oral etoposide in children with recurrent brain tumors and other solid tumors. Med Pediatr Oncol 29 (1): 28-32, 1997.
[PUBMED Abstract]
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Gaynon PS, Ettinger LJ, Baum ES, et al.: Carboplatin in childhood brain tumors. A Children's Cancer Study Group Phase II trial. Cancer 66 (12): 2465-9, 1990.
[PUBMED Abstract]
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Gentet JC, Doz F, Bouffet E, et al.: Carboplatin and VP 16 in medulloblastoma: a phase II Study of the French Society of Pediatric Oncology (SFOP). Med Pediatr Oncol 23 (5): 422-7, 1994.
[PUBMED Abstract]
Back to Top Get More Information From NCI
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Back to Top Changes to This Summary (04/09/2008)
The PDQ cancer information summaries are reviewed regularly and updated as
new information becomes available. This section describes the latest
changes made to this summary as of the date above.
Editorial changes were made to this summary.
Back to Top More Information
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