3.

预处理相关不良反应

Adverse events associated with the conditioning regimens

Adverse events* > grade 2	IEAC group (n=43)	CEAC group (n=63)	P
*: Hematological adverse events were not included.
Infection	6 (14.0%)	12(19.0%)	0.493
Oral mucositis	3 (7.0%)	3(4.8%)	0.955
Nausea and Vomiting	3 (7.0%)	1(1.6%)	0.301
Liver damage	0 (0.0%)	4(6.3%)	0.145
Cardiotoxicity	0 (0.0%)	3(4.8%)	0.270
Hypokalemia	1 (2.3%)	1(1.6%)	1.000
Diarrhea	1 (2.3%)	0(0.0%)	0.406
Treatment-related death	0 (0.0%)	2(3.2%)	0.513