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. 2014 Jul 3;14:364. doi: 10.1186/1471-2334-14-364

Table 4.

Statistical influential variables

Variable P-value (infections vs. No infection) Odds ratio (95%CI)
Gender
0,43
0,76 (0.39-1.49)
Age (≤60,<60 years)
0,69
1.15 (0.57-2.35)
Stage
0,076
n.a
Number of prior therapies
0,015*
n.a.
Number of doses of Rituximab
0,35
n.a.
Chemotherapy in addition to Rituximab
0,006*
n.a.
Asplenia
0,45
0.56 (0.12-2.58)
Active malignancy at start of therapy §
0,007*
6.75 (1.4-32.5)*
Active malignancy at end of therapy
0,02*
3.06 (1.14-8.17)*
Application of G-CSF
0,013*#
2.38 (1.19-4.76)
Cotrimoxazole prophylaxis
0,0001*#
5.64 (2.51-12.64)
HIB/pneumococci vaccination
0,09
0.18 (0.02-1.66)
Substitution of immunoglobulins
0,45
0.56 (0.12-2.58)
Neutropenia
0,0001*
4.86 (2.37-9.99)*
Lymphopenia
0,045*
6.96 (0.79-61.26)*
Leukopenia
0,0001*
4.51 (2.09-9.74)*
Relevant comorbidities 0,63 1.16 (0.54-2.49)

*statistically significant in univariate analysis.

n.a.: not applicable.

§ as patients with maintenance therapy and nonmalignant disorders had been treated with Rituximab not all patients had active malignancy at start of therapy.

#Paradoxically, patients with infectious complications had significantly more often been treated with G-CSF and received Cotrimoxazole prophylaxis, probably as these antiinfective measures had been administered to patients receiving more intensive chemotherapeutic regimens (such as GMALL, or R-CHOEP).