Protocol and guidance
The meta-analysis conducted adheres to the PRISMA statement (Preferred Reporting Items for Systematic Reviews and Meta-Analyses)[12]. We included randomized controlled trials (RCTs) with a parallel design that randomized participants to BMT and MT versus BMT alone.
Literature search and data extraction
We conducted a systematic review using Embase, Medline and the Cochrane Central Register of Controlled Trials (CENTRAL) from inception to July 2022. Appendix A contains the predefined search strategy.
We also searched the following trial registers, the US National Institutes of Health Ongoing Trials Register: ClinicalTrials.gov[13] , the World Health Organization International Clinical Trials Registry Platform[14] and reviewed the reference list of key papers. In an effort to identify further published, unpublished, and ongoing trials, we conducted a search of various gray literature sources, dissertation and theses databases, and databases of conference abstracts. No time limits or language restrictions were used.
Eligibility of the studies for the quantitative analysis was rated by four independent readers (AM, BD, BL, and IB). We collated multiple reports of the same study so that each study, not each reference, was the unit of interest in the review. Randomized, single blinded studies were included into the quantitative synopsis if the study followed patients up for at least 90 days using the modified Rankin Score (mRS)[15] and reported on adverse events and mortality.
Patients must have been included within 24 hours of stroke onset and have a clinical syndrome in keeping with a posterior circulation stroke. We defined BMT as thrombolysis, antiplatelet or antithrombotic treatment. Data inconsistencies in the papers selected for inclusion were discussed and resolved by mutual consensus.
Statistical analysis
For the dichotomous outcomes we combined the pooled individual study RRs and 95% confidence intervals (CIs) for each outcome using a random-effects Mantel-Haenszel model given the potential for methodological heterogeneity (see Discussion). In included studies we treated the participant as the unit of analysis. We used both a visual inspection of CIs and the I2 statistic to calculate the degree of statistical heterogeneity; where we took an I2 value of 50% as an indicator of moderate heterogeneity, and an I2 of ≥75% as an indicator of substantial heterogeneity.
Results of the search
Our database searches retrieved a total of 687 articles, following the review process we identified four randomized trials (see Figure 1). Two from the initial search strategy and two following the presentation of two randomized trials (ATTENTION[7] and BAOCHE[9]) at the European Stroke Conference[11]. Although the full texts were not available for these articles, we found sufficient information from the presented data in order to conduct a meta-analysis.
Included studies
Four randomized, single blinded studies were included in the quantitative analysis[5, 6, 8, 10]. The trials included participants aged greater than 18 who had a clinical posterior circulation stroke syndrome with confirmed basilar occlusion on CT angiogram or MR angiogram imaging. The trials included participants thrombolysed if presenting with no contraindications. We defined sICH as per the individual trials’ primary analysis.
Characteristics of included trials
All four randomized controlled trials have similar study designs (randomized, prospective, open-label trials with blinded outcome assessment) with a primary outcome of a modified Rankin Score of 0-3 at 90 days (See Table 1: Key characteristics).
BASICS (Basilar Artery International Cooperation Study)
BASICS took place over eight years with 300 participants enrolled and a low crossover rate of 3.33%. The slow recruitment rate of BASICS does call into question the presence of bias in the enrolled population. Trial centers involved in BASICS had high rates of treatment of eligible patients outside the trial (29.2%) of which a high percentage of patients went on to receive endovascular therapy (79%). Furthermore, over the course of the study, there were amendments to the methodology to facilitate recruitment. This led to the inclusion of more mild strokes (NIHSS <10) which could lead to an undervaluing of the effect of endovascular therapy.
There was no significant difference between the primary outcome measure in the endovascular therapy arm (44.2%) vs best medical therapy (37.7%). Mortality rates were not significantly different (38.3% with intervention and 43.2% with best medical therapy). However, symptomatic ICH rates were higher as expected with endovascular therapy. Whilst not powered, the subgroup analysis of mild strokes does suggest that patients with mild strokes did better with best medical therapy (a high rate of use of intravenous thrombolysis in BASICS, near 80% in both arms) whereas those with larger strokes (NIHSS >10) did better with endovascular therapy.
BEST (Basilar Artery Occlusion Endovascular Intervention vs Standard Medical Treatment)
BEST was a multi-center Chinese trial (28 centers) which took place over 3 years and intended to recruit 288 participants. However, the trial was terminated early with only 131 patients enrolled due to a high crossover rate of 13% (much higher than the other 3 RCTs discussed in this paper, which all had <5% crossover rate). When looking at the baseline demographics of the patients recruited, the patients of BEST had a noticeably higher admission NIHSS (32 in intervention and 26 in control) vs other trials which tended to a median NIHSS of 19-22.
With the intention to treat analysis, there was no statistically significant difference between the trial arms. However, a second look accounting for the effect of crossovers (majority of crossovers in this trial were patients who were randomized to best medical therapy alone and went on to have endovascular therapy) showed that more patients achieved the primary outcome with endovascular therapy compared to best medical therapy alone in both per-protocol (44% vs 25%) and as treated populations (47% vs 24%). Unlike ATTENTION and BAOCHE, mortality figures were not different between trial arms despite a higher rate of symptomatic ICH in patients who received endovascular therapy.
ATTENTION (Endovascular Treatment of Acute Basilar Artery Occlusion)
In comparison to BEST and BASICS, ATTENTION randomized patients with an extended window of 0-12 hours. In contrast to the other studies discussed in this paper, ATTENTION had a randomization rate of 2:1 for intervention to control arms and the trial took place across 36 high volume Chinese thrombectomy centers. One third of patients in both arms received intravenous thrombolysis.
The most statistically significant finding was that 46% of the endovascular therapy group achieved the primary outcome of mRS 0-3 at 90 days compared to only 22.8% in the best medical therapy arm (with an adjusted risk ratio of 2.1, p <0.001). ATTENTION was also positive in its secondary outcomes with patients who received endovascular therapy fairing better in terms of overall disability (odds radio 2.8 (1.8 – 4.4 CI) and more independent functional outcomes (33.2% compared to 10.5% in best medical therapy (adjusted risk ratio 3.2, 1.8 – 5.4). Similar to BAOCHE, there were more symptomatic intracranial hemorrhagic events. Despite this, mortality was significantly reduced following endovascular therapy (36.7% vs 55.3% with best medical therapy).
BAOCHE (Basilar Artery Occlusion Chinese Endovascular Trial)
BAOCHE is the first randomized trial which investigated the outcomes in late presenters with BAO. Patients were only randomized within the 6 – 24 hour window from symptom onset where they were ineligible for intravenous thrombolysis or had not achieved recanalization after IVT.
Although the trial aimed to recruit 318 patients, the trial was terminated at the planned interim analysis after 217 patients were enrolled due to the statistically significant difference in primary outcome. 46.4% of patients who received endovascular therapy compared to 24.3% of patients who received best medical therapy along achieved the primary outcome with an adjusted odds ratio of 2.92 (1.56 – 5.47, p = 0.001). In terms of safety, whilst the intervention arm had a higher rate of symptomatic intracranial hemorrhages (as per ECASS-II criteria), the overall 90 day mortality was less in the intervention arm (30.9% compared to 42.1% in the control arm).
Table 1: Key characteristics
|
BASICS
|
BEST
|
ATTENTION
|
BAOCHE
|
Date
|
2011-2019
|
2015-2017
|
2021-2022
|
2016-2022
|
Symptom onset to inclusion (hours)
|
0-6
|
0-8
|
0-12
|
6-24
|
Number screened
|
424
|
288
|
507
|
Data not available
|
Number of participants
|
300
|
131
|
340
|
217
|
Crossover (percentage)
|
3/154 (1.9) to BMT
7/146 (4.7) to MT
|
3/66 (4.5) to BMT
14/65 (21.5) to MT
|
3/226 (1.3) to BMT
3/114 (2.6) to MT
|
1/110 (0.9) to BMT
4/107 (3.7) to MT
|
Median NIHSS at presentation (IQR)
|
Intervention: 21.9
Control:
22.1
(IQR not available)
|
Intervention:
32 (18-38)
Control:
26 (13-37)
|
Intervention:
24 (15-35)
Control:
24 (14-35)
|
Intervention:
20 (14.5-29)
Control:
19 (12-30)
|
Intravenous thrombolysis (%)
|
Intervention: 121/154 (78.6)
Control: 116/146 (79.5)
|
Intervention:
18/66 (27)
Control:
21/65 (32)
|
Intervention:
69/226 (30.5)
Control:
39/114 (34.2)
|
Intervention: 15/110(13.6)
Control:
23/107 (21.5)
|
Blinding
|
Open-label, blinded outcome assessment
|
Open-label, blinded outcome assessment
|
Open-label, blinded outcome assessment
|
Open-label, blinded outcome assessment
|
mRS (≤3)
(percentage)
|
Intervention:
68/154 (44.1)
Control:
55/146 (37.6)
|
Intervention:
28/66 (42.4)
Control:
21/65 (32.3)
|
Intervention:
104/226 (46)
Control:
26/114 (22.8)
|
Intervention: 51/110 (46.3)
Control:
26/107 (24.2)
|
Mortality at day 90 (percentage)
|
Intervention:
59 (38.3)
Control:
63 (43.2)
|
Intervention:
22 (33.3)
Control:
25 (38.4)
|
Intervention:
83 (36.7)
Control:
63 (55.2)
|
Intervention:
34 (30.9)
Control:
45 (42.1)
|
sICH
(percentage)
|
Intervention:
6 (4.5)
Control:
1 (0.7)
|
Intervention:
5 (8)
Control:
0
|
Intervention:
12 (5)
Control:
0
|
Intervention:
6 (8.8)
Control:
1 (2.3)
|
Follow up:
|
24hrs, 90 days
|
24hrs, 90 days
|
24hrs, 90 days
|
24hrs, 90 days, 6 months, 1 year
|