Brief Article
Copyright ©2011 Baishideng Publishing Group Co.
World J Gastroenterol. Aug 14, 2011; 17(30): 3510-3517
Published online Aug 14, 2011. doi: 10.3748/wjg.v17.i30.3510
Table 1 Characteristics of 41 patients who developed nephrotoxicity induced by cisplatin combination chemotherapy
GenderM36
F5
Age58.36 ± 10.54
BSA11.677 ± 0.141
OperationNone3
RSG c BI15
RSG c BII5
RSG c R-Y7
RTG c R-Y5
Pal26
StageIA1
IB5
II5
IIIA9
IIIB2
IV19
Combination drug5-FU318
Docetaxel10
5-FU3 + MMC45
Paclitaxel3
TS-12
Irinotecan2
Capecitabine1
Table 2 Pre-acute renal failure (ARF) laboratory data1 corresponding to renal status post-ARF2
Renal status of post-ARFP value3
VariableNormal rangeUnitRecovered (n = 33)Unrecovered (n = 8)
Hb14.0–16.7g/dL10.33 ± 1.28 (n = 33)9.75 ± 0.95 (n = 8)0.238
HT14.7–50.7%29.88 ± 3.33 (n = 33)28.56 ± 2.78 (n = 8)0.307
Protein6.3–8.3g/dL6.792 ± 0.69 (n = 26)6.429 ± 0.39 (n = 7)0.191
Albumin3.5–5.0g/dL3.97 ± 0.54 (n = 26)3.87 ± 0.38 (n = 7)0.657
BUN5–23mg/dL18.07 ± 5.35 (n = 33)15.63 ± 4.03 (n = 8)0.236
SCR0.3-1.5mg/dL1.17 ± 0.20 (n = 33)1.38 ± 0.13 (n = 8)0.008
GFR120-130mL/min68.03 ± 13.31 (n = 33)59.13 ± 6.64 (n = 8)0.076
Na136–150meg/L139.24 ± 3.19 (n = 33)140.13 ± 4.09 (n = 8)0.510
Cl98–110meg/L105.31 ± 4.42 (n = 24)105.57 ± 3.65 (n = 7)0.887
K3.5–5.3meg/L4.49 ± 0.46 (n = 8)4.66 ± 0.65 (n = 8)0.284
P3.0–4.5mg/dL3.97 ± 0.81 (n = 20)3.93 ± 1.16 (n = 6)0.940
Mg1.6–2.6mg/dL2.08 ± 0.26 (n = 24)2.03 ± 0.29 (n = 7 )0.635
Ca8.0-10.0mg/dL9.15 ± 0.53 (n = 24)8.86 ± 0.30 (n = 7)0.170
Table 3 Acute renal failure (ARF) laboratory data1 corresponding to renal status post-ARF2
Renal status post-ARFP value3
VariableNormal rangeUnitRecovered (n = 33)Unrecovered (n = 8)
Hb14.0–16.7g/dL10.28 ± 1.62 (n = 31)10.238 ± 1.30 (n = 8)0.941
HT14.7–50.7%29.52 ± 4.70 (n = 32)29.93 ± 3.41 (n = 8)0.820
Protein6.3–8.3g/dL6.72 ± 0.78 (n = 24)7.00 ± 0.95 (n = 3)0.564
Albumin3.5–5.0g/dL3.95 ± 0.61 (n = 24)4.03 ± 0.65 (n = 3)0.818
BUN5–23mg/dL23.78 ± 13.60 (n = 33)23.0 ± 4.87 (n = 8)0.876
SCR0.3-1.5mg/dL1.75 ± 0.48 (n = 33)2.21 ± 0.61 (n = 8)0.026
GFR120-130mL/min43.30 ± 7.81 (n = 33)36.0 ± 8.98 (n = 8)0.026
Na136–150meg/L136.60 ± 4.36 (n = 32)137.63 ± 2.72 (n = 8)0.529
Cl98–110meg/L101.49 ± 6.59 (n = 24)99.50 ± 2.65 (n = 4)0.564
K3.5–5.3meg/L4.22 ± 0.93 (n = 32)4.46 ± 0.60 (n = 8)0.491
P3.0–4.5mg/dL4.13 ± 0.87 (n = 18)3.93 ± 0.43 (n = 4)0.659
Mg1.6–2.6mg/dL1.83 ± 0.42 (n = 22)1.833 ± 0.47 (n = 3)0.995
Ca8.0-10.0mg/dL9.06 ± 0.51 (n = 23)9.40 ± 0.80 (n = 4)0.269
Table 4 Comparison between the cycle during which nephrotoxicity occurred and the amount of accumulated cisplatin according to renal status post-acute renal failure (ARF)
Renal status post-ARFP value3
Recovered1 (n = 33)Unrecovered2 (n = 8)
The cycle nephrotoxicity occurred4.24 ± 2.096.63 ± 2.620.009
The cumulative dose of cisplatin/BSA, mg302.85 ± 152.73497.75 ± 222.610.005
Table 5 Subsequent renal status corresponding to subsequent treatment in the recovered group
Subsequent renal statusP value4
Normal1Recovered2Unrecovered3Total
Subsequent treatmentStop5207
Reduce2406
Continue58720
Total1214733
0.011
Table 6 Subsequent renal status corresponding to subsequent treatment in the unrecovered group
Subsequent renal statusP value4
Normal1Recovered2Unrecovered3Total
Subsequent treatmentStop0224
Reduce0033
Continue0011
Total0268
0.170