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. 2010 Jul;98(3):385-93.
doi: 10.1007/s11060-009-0090-3. Epub 2009 Dec 18.

Monotherapy with methotrexate for primary central nervous lymphoma has single agent activity in the absence of radiotherapy: a single institution cohort

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Monotherapy with methotrexate for primary central nervous lymphoma has single agent activity in the absence of radiotherapy: a single institution cohort

Julien Cobert et al. J Neurooncol. 2010 Jul.

Abstract

We have retrospectively reviewed toxicities and response of a cohort of primary central nervous system lymphoma (PCNSL) patients treated with high dose parenteral methotrexate (MTX) monotherapy without whole brain radiation. From The Massachusetts General Hospital (MGH) Cancer Registry, active since 1946, we selected all immunocompetent patients with histologic and/or radiographic PCNSL diagnosed between 1980 and 2007. We identified the recipients of MTX with leucovorin rescue as sole therapy. No patient received radiation therapy (XRT). We analyzed this cohort for toxicity, response and patterns of recurrence. The cohort of 121 patients received on average 11 cycles of intravenous MTX at a median dose of 8 g/m(2). Median interval between cycles was 10 days. After 3 months of therapy, the overall response rate was 85% (58% CR, 27% PR). The overall survival (OS) for the cohort was 7 years and progression-free survival (PFS) was 3.14 years. A trend toward a higher PFS was seen in patients who continued to receive MTX (3.48 years) every three months as compared to patients who ceased MTX after one year (2.86 years). Of 68 patients who achieved initial CR, there were 40 recurrences. Twenty-six of the 40 were re-induced with MTX as above; Sixty-nine percent again achieved CR. Eighty-one treatment-related toxicities occurred in 1316 MTX cycles. These toxicities included MRI white matter changes (N = 8) and lead to MTX cessation in 16 patients. High-dose MTX monotherapy of PCNSL is well-tolerated and provides PFS of >3 years and OS >7 years.

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Figures

Fig. 1
Fig. 1
Schematic of case ascertainment. NHL non-Hodgkin lymphoma, dx diagnosis, IOL intra-ocular lymphoma, PCNSL primary central nervous system lymphoma, CHT chemotherapy, MTX methotrexate, WBXRT whole-brain radiation therapy
Fig. 2
Fig. 2
Responses to MTX monotherapy. CR complete response, PD progressive disease, PR partial response, MR mixed response, SD stable disease
Fig. 3
Fig. 3
Overall survival of cohort (n = 121). Of 121 patients in the cohort, 53 patients died and 68 survived. The median OS was 7 years with 95% CI 4.6, 12. The 1, 5 and 10 year OS rates were 86, 58 and 44% respectively. TTP time to progression, 95% CI 95% confidence interval
Fig. 4
Fig. 4
Progression-free survival. a PFS of CR patients (n = 68)—Of 68 patients achieving CR, forty progressed, while 28 (censored) remained progression-free. The median PFS was 3.14 years with 95% CI of (2.48, 5.18). The 1, 5 and 10 years PFS rates were 87, 51 and 38%, respectively; b PFS by MTX continuation after CR—For patients who ceased MTX within two cycles of CR (dotted line), the median PFS is 2.86 years with 95% CI of (1.32, upper not reached). The 1, 2 and 5 years rate are 79, 63, and 29% respectively. For patients who continued MTX after CR (solid line), the median PFS is 5 years with 95% CI of (3, 9.2). The 1, 2 and 5 years rate are 90, 67, and 43% respectively. PFS progression-free survival; 95% CI 95% confidence interval

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