Primary central nervous system lymphoma 1991-1997 - Outcome and late adverse effects after combined modality treatment

Citation
U. Herrlinger et al., Primary central nervous system lymphoma 1991-1997 - Outcome and late adverse effects after combined modality treatment, CANCER, 91(1), 2001, pp. 130-135
Citations number
18
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
CANCER
ISSN journal
0008543X → ACNP
Volume
91
Issue
1
Year of publication
2001
Pages
130 - 135
Database
ISI
SICI code
0008-543X(20010101)91:1<130:PCNSL1>2.0.ZU;2-Y
Abstract
BACKGROUND. This retrospective single-center study assesses the feasibility , therapeutic outcome, and late side effects of combined modality therapy w ith intravenous methotrexate, whole bl ain radiotherapy (WBRT), and intrave nous cytarabine in patients with primary central nervous system lymphoma (P CNSL). METHODS, All 28 consecutive patients diagnosed with PCNSL between 1991 and 1997 were scheduled to receive combined modality therapy. Seven of 28 patie nts did not receive combined modality treatment: 6 patients had WBRT alone because of poor physical condition, and 1 patient died before receiving tre atment. Of the remaining 21 patients, 5 received the complete regimen, and 16 received a modified regimen with reduced dose intensity. RESULTS. Fourteen of 21 patients (67%) treated with combined modality thera py had a complete response, 1 had a partial response. Median survival was 1 1 months in all 28 patients, 23 months in all patients with combined modali ty treatment, and II months in patients receiving the complete regimen. Of 15 examinable patients with a follow-up of 8 months or more, 10 developed s everely symptomatic and 5 mildly symptomatic or asymptomatic diffuse white matter changes. CONCLUSION, Only a small subgroup of all patients with PCNSL appeals to be eligible for receiving all parts of the combined modality regimen. Treatmen t in these patients leads to a marked prolongation of survival. The risk of late side effects is high even with modified, dose intensity-reduced versi ons of combined modality treatment (C) 2001 American Cancer Society.