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Research ArticleBrain
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Diffusion-Weighted MR Imaging Derived Apparent Diffusion Coefficient Is Predictive of Clinical Outcome in Primary Central Nervous System Lymphoma

R.F. Barajas, J.L. Rubenstein, J.S. Chang, J. Hwang and S. Cha
American Journal of Neuroradiology January 2010, 31 (1) 60-66; DOI: https://doi.org/10.3174/ajnr.A1750
R.F. Barajas Jr
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J.L. Rubenstein
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J.S. Chang
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J. Hwang
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S. Cha
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    Fig 1.

    Comparison of diffusion-weighted imaging (DWI) and cellular density between high and low apparent diffusion coefficient (ADC) groups (A and F). Contrast-enhanced T1-weighted image with regions of interest surrounding enhancing regions that were pathologically diagnosed as primary central nervous system non-Hodgkin lymphoma. Arrow indicates enhancing region subjected to stereotactic biopsy. DWI (B and G), black and white ADC map (C and H), color ADC map (D and I), and biopsy specimens (E and J) from patient 2 (low ADC group) and patient 17 (high ADC group) (hematoxylin-eosin, original magnification ×100).

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    Fig 2.

    Scatterplots of cellular density measurements versus 25th percentile (ADC25%, A) and mean ADC (ADCmean, B) values within contrast-enhancing tumor regions for all 18 subjects included in this study, demonstrating statistically significant inverse correlations (ADC25%, R = −0.47, P = .05; ADCmean, R = −0.54, P = .02).

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    Fig 3.

    A and B, Patient outcome as a function of ADC25% stratification into low and high groups. Kaplan Meier analysis (A) of progression-free survival (PFS) for patients stratified into the low ADC25% group (<692, blue line) with a mean progression time of 9.4 months versus those stratified into high ADC25% group (>692, red line) with a mean progression time of 30.0 months (P = .02, logrank test). Kaplan Meier plot (B) of overall survival (OS) for patients stratified into the low ADC25% group (<692, blue line) with a mean survival of 15.8 months versus those stratified into high ADC25% group (>692, red line) with a mean survival of 30.9 months (P = .01, logrank test). C and D, Patient outcome as a function of minimum ADC value shows a statistically significant difference in PFS and OS between low and high groups (P < .05).

Tables

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    Table 1:

    Clinical, imaging, and pathologic patient population characteristicsa

    Patient No.ADC GroupAge (yr)/SexNo. Enhancing LesionsResponse to TxADC25%ADCminADCmeanOverall Cellularity
    1Low45/FMPPD534156637High
    2Low82/FSGPD541167745High
    3Low57/MMPPD646191894High
    4Low61/MMPPR528214877High
    5Low62/FMPPD589280681High
    6Low54/MMPPD638338749Low
    7Low70/MSGPR623367719High
    8Low54/FSGCR688456805High
    9Low26/MSGCR692398835High
    10High52/FMPCR693294779Low
    11High43/FSGCR725371876High
    12High81/MMPCR822411959Low
    13High53/FMPCR831414873Mixed
    14High68/MMPCR8424791016Low
    15High61/FMPCR772510781Low
    16High53/MMPCR741525891Low
    17High56/FMPCR815609893Mixed
    18High67 mol/LSGCR906614933Low
    • Note:—ADC indicates apparent diffusion coefficient; MP, multiple; SG, single; Tx, treatment; PD, progressive disease; PR, partial response; CR, complete response; ADC25%, 25th percentile ADC value; ADCmin, minimum ADC value; ADCmean, mean ADC value.

    • a Patients are stratified on the basis of the median 25th percentile value.

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    Table 2:

    Comparison of prognostic factors, cellular density, and clinical outcomea

    Age (yr)MMSEKPSDays to TxMonths to F/U MRINo. Tx to F/U MRIChange CE VolumeMonths to ProgressionMonths to Death
    Low ADC56.7 (15.6)25.2 (6.11)62.2 (6.67)13.8 (14.6)8.3 (14)2.00 (1.41)2.50 (2.88)9.4 (12.0)15.8 (9.87)
    High ADC59.3 (11.3)25.7 (4.50)66.7 (5.00)13.4 (11.7)4.0 (8.0)1.70 (0.70)3.92 (2.39)30.0 (18.0)30.9 (17.0)
    Pvalue.70.83.13.94.39.530.37<.01.03
    • Note:—MMSE indicates pretherapeutic Mini-Mental State Examination score; KPS, Karnovsky performance status; Days to Tx, mean number of days between initial diagnosis by MR imaging and initiation of methotrexate-based chemotherapy; Months to F/U MRI, mean number of months between pre- and intratherapeutic MR imaging; No. Tx to F/U MRI, mean number of methotrexate treatments between pre- and intratherapeutic MR imaging; Change CE, difference in enhancing volume between pre-and posttherapeutic imaging series; Months to Progression, mean number of months to progression based on MR imaging if event occurred; Months to Death, mean number of months to death if event occurred.

    • a All data are presented as mean (± SD). Patients are stratified based on median 25th percentile value.

    • View popup
    Table 3:

    Comparison of MR imaging findingsa

    ADCminChange ADCminADC25%Change ADC25%ADCmeanChange ADCmean
    Low ADC258 (109)−18.7 (219)608 (62)84.7 (114)771 (87.7)116 (106)
    High ADC469 (107)−120 (224)794 (67)−55.5 (84.7)889 (77.0)−42 (74)
    P value<.01.31<.01.04<.01.01
    • Note:—Change ADCmin indicates the difference between pre- and posttherapeutic ADCmin values (negative values signify net decrease in value); Change ADC25%, difference between pre- and posttherapeutic ADC25% values; Change ADCmean, difference between pre- and posttherapeutic ADCmean values.

    • a All data are presented as mean (SD). All ADC values are reported as 100 × 10−6 mm2/s.

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American Journal of Neuroradiology: 31 (1)
American Journal of Neuroradiology
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1 Jan 2010
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Diffusion-Weighted MR Imaging Derived Apparent Diffusion Coefficient Is Predictive of Clinical Outcome in Primary Central Nervous System Lymphoma
R.F. Barajas, J.L. Rubenstein, J.S. Chang, J. Hwang, S. Cha
American Journal of Neuroradiology Jan 2010, 31 (1) 60-66; DOI: 10.3174/ajnr.A1750
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R.F. Barajas, J.L. Rubenstein, J.S. Chang, J. Hwang, S. Cha
Diffusion-Weighted MR Imaging Derived Apparent Diffusion Coefficient Is Predictive of Clinical Outcome in Primary Central Nervous System Lymphoma
American Journal of Neuroradiology Jan 2010, 31 (1) 60-66; DOI: 10.3174/ajnr.A1750

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