Successful Treatment of Primary Central Nervous System Lymphoma without Irradiation in Children: Single Center Experience.
10.3346/jkms.2012.27.11.1378
- Author:
Jong Hyung YOON
1
;
Hyoung Jin KANG
;
Hyery KIM
;
Ji Won LEE
;
June Dong PARK
;
Kyung Duk PARK
;
Hee Young SHIN
;
Hyo Seop AHN
Author Information
1. Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea. hyshin@snu.ac.kr
- Publication Type:Case Reports ; Research Support, Non-U.S. Gov't
- Keywords:
Primary CNS Lymphoma;
Children;
Irradiation
- MeSH:
Adolescent;
Antineoplastic Combined Chemotherapy Protocols/*therapeutic use;
Central Nervous System Neoplasms/diagnosis/*drug therapy;
Child;
Child, Preschool;
Cyclophosphamide/therapeutic use;
Cytarabine/therapeutic use;
Disease-Free Survival;
Doxorubicin/therapeutic use;
Etoposide/therapeutic use;
Female;
Humans;
Hydrocortisone/therapeutic use;
Infant;
Leucovorin/therapeutic use;
Lymphoma, Non-Hodgkin/diagnosis/*drug therapy;
Male;
Methotrexate/therapeutic use;
Prednisone/therapeutic use;
Recurrence;
Retrospective Studies;
Tomography, X-Ray Computed;
Treatment Outcome;
Vincristine/therapeutic use
- From:Journal of Korean Medical Science
2012;27(11):1378-1384
- CountryRepublic of Korea
- Language:English
-
Abstract:
Primary CNS lymphoma (PCNSL) is a very uncommon disease in children, and usually treated by chemotherapy, combined with focal or craniospinal radiotherapy (RT). However, adverse effects of RT are a concern. We evaluated the outcomes of childhood PCNSL, treated with systemic and intrathecal chemotherapy, but without RT. For fifteen years, six patients among 175 of non-Hodgkin lymphoma were diagnosed as PCNSL in Seoul National University Children's Hospital and we analyzed their medical records retrospectively. Their male:female ratio was 5:1, and median age was 10.1 yr. The primary sites were the sellar area in three patients, parietal area in one, cerebellum in one, and multiple areas in one. Their pathologic diagnoses were diffuse large B-cell lymphoma in three patients, Burkitt lymphoma in two, and undifferentiated B-cell lymphoma in one. Five were treated with the LMB96 treatment protocol, and one was treated with the CCG-106B protocol. None had RT as a first-line treatment. One patient had a local relapse and received RT and salvage chemotherapy, without success. No patient had treatment-related mortality. Their estimated 5-yr event-free and overall survival rates were both 83.3%. In conclusion, PCNSL is a rare disease in childhood, but successfully treated by chemotherapy without RT.
