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Table 4 Comparison of baseline characteristics and outcome measures of the recent endovascular trials [27, 194, 286]

From: Reperfusion therapy in acute ischemic stroke: dawn of a new era?

Trials

MR CLEAN [110]

ESCAPE [111]

EXTEND-IA [76]

SWIFT PRIME [112]

REVASCAT [113]

THERAPY [128]

THRACE [127]

Region

Netherlands

United States, Canada, South Korea, Ireland, United Kingdom

Australia and New Zealand

United States and Europe

Spain

United States

France

Number of centres

16

22

10

39

4

4

26

Number of patients; n (CG/IA)

500 (267/233)

315 (150/165)

70 (35/35)

196 (98/98)

206 (103/103)

108 (54/54)

412 (208/204)

BASELINE CHARACTERISTICS

Age Range

≥ 18

≥ 18

≥ 18

18–80 years

18–80 years

18–85

18–80

NIHSS Range

≥ 2

> 5

N.R.

8–29

≥ 6

≥8

10–25

Control group

Standard medical therapy (+/− IV tPA)

Standard medical therapy (+/− IV tPA)

IV-tPA only

IV-tPA only

Standard medical therapy (+/− IV tPA)

IV-tPA only

IV-tPA only

Intervention group

IAT

IAT

ET with Solitaire FR stentriever

ET with Solitaire FR stentriever

ET with Solitaire FR stentriever

ET with Penumbra aspiration system

Endovascular MT

Intervention using Stent retriever in IA arm

81.5%

86.1%

100%

100%

100%

0%

N.R.

Time window

0–6 h

0–12 h

0–6 h

0–6 h

0–8 h

0–4.5 h

0–5 h

Neurologic inclusion criteria

N.A.

Barthel Index of ≥90

mRS scores of 0–2

mRS scores of 0–1

mRS scores of 0–1

  

Neuroimaging techniques

CT/CTA

CT/CTA/CTA Multiphase (for collaterals)

CT/CTA/CTP (for mismatch)

CT/CTA/MRA/MRP/CTP (for infarct core)

CT/CTA(MRA/DSA)

CT/CTA

CT/CTA

Large artery occlusion

CTA

CTA

CTA or MRA

CTA or MRA

CTA or MRA

CTA

CTA or MRA

Affected arteries

TICA, M1, M2, A1, A2

TICA, M1

TICA, M1, M2

TICA, M1, M2

TICA, M1

MCA

ICA, M1, TB, M2

Infarct core/perfusion

N.R.

NCCT, CBV or CBF ASPECTS ≥6

CoreΨ < 70 ml (>1.2)¥

CoreΦ< 50 ml (>1.8)¥ NCCT ASPECTS ≥6

NCCT ASPECTS ≥7 DWI ASPECTS ≥6

Clot length ≥ 8 mm

N.R.

Collateral status

N.R.

Good/Moderate

N.R.

N.R.

N.R.

N.R.

N.R.

Median stroke onset to groin puncture

260 min

241 min

210 min

224 min

269 min

226 min

255 min

Baseline NIHSS [Median (IQR)]; CG vs IA

18 (14–22) vs17 (14–21)

17 (12–20) vs 16 (13–20)

13 (9–19) vs 17 (13–20)

17 (13–19) vs 17 (13–20)

17 (12–19) vs 17 (14–20)

N.R.

17 (13–20) vs 18 (15–21)

Median ASPECTS (%); CG/IA

9/9

9/9

NR/NR

9/9

8/7

N.R.

N.R.

Patients Receiving IV-rtPA (%); CG/IA

91/87

79/73

100/100

100/100

78/68

100/100

100/100

STUDY OUTCOMES

Primary Outcomes

Shift in mRS at 90 days

Shift in mRS at 90 days

Reduction in perfusion lesion volume; NIHSS reduction ≥8 pointsor mRS score of 0–1 at day 3

Distribution of mRS at 90 days; % mRS 0–2 at 90 days

Shift in mRS at 90 days

Shift in mRS at 90 days

Shift in mRS at 90 days

mRS (0–2) at 90 days %; CG vs IA

19.1 vs 32.6, P < 0.05

29.3 vs 53, P < 0.001

40 vs 70, P = 0.001

35.5 vs 60.2, P < 0.001

28.2 vs 43.7

30.4 vs 38

42.1 vs 54.2

Improvement in mRS 0–2 at 90 days

13.5%

23.7%

31.4%

24.7%

15.5%

7.6%

12.1%

sICH risk (%); CG vs IA, P

6.4 vs 7.7, P > 0.05

2.7 vs 3.6, P > 0.05

5.7 vs 0, P > 0.05

3.1 vs 0, P = 0.12

1.9 vs 1.9, P > 0.05

11.3 vs 10.9

2 vs 2, P = 0.71.

Parenchymal Hematoma Risk (%); CG/IA

6 vs 6

2.0 vs 4.8

8.6 vs 11.4

N.R. vs N.R.

5.8 vs 5.8

N.A.

9.45 vs 13.8, P = 0.53

Mortality (%); CG vs IA, P

22.1 vs 21, P > 0.05

19 vs10.4, P = 0.04

20 vs 8.6, P > 0.05

12.4 vs 9.2, P > 0.05

15.5 vs 18.4, P = 0.06

23.9 vs 12

13 vs 12; P = 0.70

Decrease in mortality at 90 days

1.1%

8.6%

11.4%

3.2%

−2.9%

11.9%

1%

Complete recanalization rates

mTICI Score 2b/3

58.7%

72.4%

86.2%

88.0%

65.7%

N.R.

N.R.

Complete recanalization based on neuroimaging 24–27 h later; CG vs IA

68/207 (33%)a vs 141/187 (75%)a

N.A. vs N.A.

15/35 (43%)a vs 33/35 (94%)a

21/52 (40%)b vs 53/64 (83%)b

N.A. vs N.A.

N.A.

N.A.

Brain infarction volume at 24 hc (mean, 95% CI); CG vs IA, P

79 mL (34–125) vs 49 mL (22–96), P < 0.01

N.A. vs N.A.

N.A. vs N.A.

35 mL (0–407) vs 32 mL (0–503), P = 0.09

39 mL (12–87) vs 16 mL (8–59), P = 0.02

N.A.

N.A.

NNT

7.1

4.2

3.2

4.0

6.3

13.2

8.3

  1. IQR Interquartile range; TICA Terminal internal carotid artery (Carotid T/L); M1 and M2 Branches of the MCA; A1 and A2 Branches of the ACA; mTICI Modified Thrombolysis in Cerebral Infarction; mRS Modified Rankin Scale; N.R. Not required; N.S. Not significant; N.A. Not available; CTA Computed tomography angiography; NCCT Non-contract computed tomography; CBV Cerebral blood volume; CBF Cerebral blood flow; MRA Magnetic resonance angiography; ASPECTS Alberta Stroke Program Early CT score; CG Control group; IA Intervention arm; IAT Intra-arterial therapy; TB Upper third of the basilar artery; MCA Middle cerebral artery; M2 Insular portion of the MCA; M1 Proximal portion of the MCA; ET Endovascular Thrombectomy; MT Mechanical thrombectomy; ESCAPE Endovascular Treatment for Small Core and Anterior Circulation Proximal Occlusion With Emphasis on Minimizing CT to Recanalization Times; EXTEND-IA Extending the Time for Thrombolysis in Emergency Neurological Deficits—Intra-Arterial; MR CLEAN Multicentre Randomized Clinical Trial of Endovascular Treatment for Acute Ischemic Stroke in the Netherlands; NIHSS National Institutes of Health Stroke Scale; REVASCAT Randomized Trial of Revascularization with Solitaire FR Device Versus Best Medical Therapy in the Treatment of Acute Stroke Due to Anterior Circulation LVO Presenting within 8 h of Symptom Onset; SWIFT PRIME Solitaire with the Intention for Thrombectomy as Primary Endovascular Treatment; NNT Number needed to treat for benefit (mRS score 0–2); THRACE Mechanical thrombectomy after intravenous alteplase versus alteplase alone after stroke
  2. ¥Target mismatch ratio; λ Sum of median of parameters; ΦThe ischemic core was assessed by MRI or CT; ΨThe ischemic core was defined by regional cerebral blood flow on CT perfusion or diffusion-weighted imaging; aRecanalization shown in brain CTA/MRA at 24 h; bReperfusion shown in brain CT perfusion/MR perfusion at 27 h; cBrain infarction volume at 24 h after treatment measured with CT in MR CLEAN trial and with CT or MRI in SWIFT PRIME and REVASCAT trials