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Table 7 Frequency and grade of adverse events of the 12 patients

From: A phase I clinical study of immunotherapy for advanced colorectal cancers using carcinoembryonic antigen-pulsed dendritic cells mixed with tetanus toxoid and subsequent IL-2 treatment

Gradea

I

II

III

IV

V

Adverse event

Local pain

3/12b

2/12

   

Local swelling

 

1/12

   

Fever

5/12

2/12

   

Skin rash/itching/skin desquamation

3/12

2/12

   

Myalgia

1/12

    

Bilirubin

4/12

1/12

2/12

1/12

 

GPT

9/12

2/12

   

GOT

9/12

2/12

1/12

  

Hemorrhage (UGIc)

 

1/12

   

Diarrhea/Mucocitis

3/12

1/12

2/12

  

Creatinine

1/12

1/12

   

Allergy

1/12

1/12

   

Anemia

1/12

1/12

   

Short of breath

2/12

    

Sweating

1/12

    

Chillness

1/12

    

Leg edema

1/12

    
  1. aAdverse event was determined using CTCAE version 4.0
  2. b“3/12” indicates that 3 of 12 patients had at least one episode of a particular adverse event
  3. cUGI indicates upper gastrointestinal