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. 2013 Jun 6;122(4):550–553. doi: 10.1182/blood-2013-03-487744

Table 1.

Survivor demographic and treatment characteristics

Participants
N = 102
Demographics N %
 Gender
  Female 56 54.9
  Male 46 45.1
 Race
  White 96 94.1
  Other 6 5.9
 Highest grade
  College graduate 32 31.4
  Noncollege graduate 70 68.6
 Current employment
  Full time 62 60.8
  Part time or unemployed 38 37.3
Mean SD Min-Max
 Current age (y) 38.4 6.2 27-55
Treatment factors
 IT MTX (mL) 103.6 88.5 0-496
 IV MTX (g/m2) 2.22 2.90 0-21.8
Age (y)
 At diagnosis 5.0 3.2 0.8-15.3
 At initial testing 11.0 3.8 4.3-23.1
 At follow-up testing 38.5 6.2 26.6-54.7
End of therapy to initial testing (y) 3.4 2.3 1.0-9.3
Diagnosis to follow-up testing (y) 33.5 5.7 18.8-46.4
Initial to follow-up testing (y) 27.6 5.6 14.0-38.4
CRT dose (Gy) N %
 18 34 33.3
 24 68 66.7
Neurocognitive assessment Mean SD
 Nonparticipants (n = 36)
  IQ at initial testing
   Verbal 92.7 14.6
   Performance 93.6 17.0
   Full Scale 92.4 15.4
 Participants (n = 102)
  IQ at initial testing
   Verbal 97.4 15.4
   Performance 95.3 16.5
   Full Scale 96.0 15.9
  IQ at follow-up testing
   Verbal 87.1 17.1
   Performance 95.7 16.8
   Full Scale 91.3 15.5
  Academic
   Reading 91.3 9.8
   Mathematics 85.8 17.48
 Attention: sustained 89.7 16.99
 Processing speed 89.5 27.45
  Memory
   Total recall 92.7 18.14
   Long-term 92.4 18.94
  Executive function
   Fluency 89.3 16.07
   Flexibility 77.6 32.01

Cumulative doses listed for intrathecal (IT) and intravenous (IV) methotrexate (MTX). Initial testing denotes first testing ≥1 year and ≤10 years after CRT. Follow-up testing denotes current testing. All neurocognitive assessment scores presented in age-adjusted standard scores with an expected mean of 100 and and SD of 15. Participants did not differ from nonparticipants in initial Verbal IQ (P = .12), Performance IQ (P = .60), or Full Scale IQ (P = .24).

IT, intrathecal; IV, intravenous; Min-Max, minimum-maximum; MTX, methotrexate.