The aim of this retrospective study is to review and describe the safety and the efficacy of recombinant human interleukin-11 (I) i (Baijieyi), using information already recorded in 20 medical records, The time periods include May 8th of 2008 to december 31st of 2016.
Study Type
OBSERVATIONAL
Enrollment
2,000
Cancer Hospital Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China
Days that platelet count firstly rebound to 75×10^9/L, 100×10^9/L, respectively, from the first time below 75×10^9/L at the chemotherapy cycle and the last chemotherapy cycle
For prevention
Time frame: 56 days
Days that platelet count firstly rebound to 75×10^9/L, 100×10^9/L
For treatment
Time frame: 28 days after the administration of Baijieyi
the maximum and minimum platelet count at the chemotherapy cycle and the last chemotherapy cycle
For prevention
Time frame: 56 days
the lasting days of platelet count below 50×10^9/L at the chemotherapy cycle and the last chemotherapy cycle
For prevention
Time frame: 56 days
The number of platelet transfusions at the chemotherapy cycle and the last chemotherapy cycle
For prevention
Time frame: 56 days
the percentage of patients whose platelet count firstly recovered above 75×10^9/L and 100×10^9/L
For treatment
Time frame: 28 days after the administration of Baijieyi
the maximum and minimum platelet count, the lasting days of platelet count below 50×10^9/L
For treatment
Time frame: 28 days after the administration of Baijieyi
The number of platelet transfusions
For treatment
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Time frame: 28 days after the administration of Baijieyi