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Table 4 Subgroup analysis and exploration of heterogeneity in CD22 CAR-T clinical trials

From: Targeting CD22 for B-cell hematologic malignancies

Patients with available data

Overall response rate

Complete response

rate

negative Minimal residual disease

Cytokine release

syndrome

 ≥ Grade 3 cytokine release syndrome

Neurotoxicity

 ≥ Grade 3 neurotoxicity

Relapse rate

CD22 dim/negative

relapse rate

Age Group

 Children (N = 114)

76%

(68–83)

74%

(65–81)

-

87%

(80–92)

6%

(3–12)

28%

(21–37)

-

36%

(18–54)

16%

(0–32)

 Adult (N = 37)

75%

(59–87)

57%

(41–72)

-

84%

(68–93)

5%

(1–19)

11%

(4–25)

-

6%

(0–20)

3%

(0–9)

 p value

0.94

0.05*

-

0.6

0.9

0.04*

-

0.01**

0.14

Bone marrow involvement (B-ALL)

 High burden (N = 98)

74%

(65–82)

63%

(43–83)

66%

(55–75)

86%

(78–92)

7%

(3–14)

25%

(17–34)

1%

(0–7)

23%

(6–58)

8%

(1–46)

 Low burden (N = 25)

81%

(66–96)

76%

(59–93)

68%

(48–83)

88%

(69–96)

4%

(1–24)

32%

(17–52)

4%

(1–24)

40%

(23–60)

12%

(4–31)

 p value

0.22

0.54

0.82

0.81

0.6

0.46

0.32

0.37

0.73

Disease

 B-ALL (N = 133)

76%

(69–83)

72%

(65–80)

-

87%

(82–93)

4%

(1–8)

20%

(8–32)

1%

(0–3)

31%

(13–49)

11%

(0–23)

 B cell lymphoma (N = 28)

86%

(73–99)

64%

(47–82)

-

74%

(19–100)

4%

(0–12)

10%

(0–28)

0%

(0–6)

8%

(0–19)

4%

(0–12)

 p value

0.19

0.41

-

 < 0.01**

0.87

0.36

0.75

0.04*

0.35

Prior CD19 CAR-T therapy

 Yes (N = 67)

75%

(65–87)

73%

(62–86)

45%

(16–74)

76%

(62–91)

9%

(3–30)

0%

(0–6)

0%

(0–6)

19%

(0–46)

24%

(9–66)

 No (N = 15)

76%

(58–100)

79%

(58–100)

62%

(22–100)

83%

(62–100)

13%

(3–58)

0%

(0–6)

0%

(0–6)

29%

(5–52)

20%

(7–60)

 p value

0.76

0.64

0.5

0.59

0.72

1

1

0.59

0.55

  1. Data are event rate, % (95% CI), p values, or number of patients. Adults were patients aged 20 years or older; children were patients aged younger than 20 years, CAR chimeric antigen receptor