Top Ten Landmark Trials Across Neuroscience - Dr Tharun Krishna

Practice parameters in clinical neuroscience have been fine-tuned in line with hard evidence to a large measure by many randomised control trials (RCT) over the years. Many RCTs have been well conceived and executed, but some have been dodged by controversies on sample size, design, and biases.

Those that have stood the test of time have come to occupy the position as ‘landmark’ trials and have left an indelible mark on our understanding on many neurological topics, and forging a consensus on contentious management issues.

We will examine ten landmark trials in Neurology and Neurosurgery briefly, with an understanding that the choice of these ten are subjective and personal, and largely heuristic.

The ten trials chosen can be categorised as those related to five in Neurosurgery, four in Neurology, and one in Psychiatry.

NEUROSURGERY

1. ISAT Trial (International Subarachnoid Aneurysm Trial)

  Lancet, 2005

The International Subarachnoid Aneurysm Trial (ISAT) had a profound influence on the management of ruptured intracranial aneurysms. As endovascular clipping started to gain more acceptance and popularity because of the lesser post-procedural pain and discomfort and hospital stay vis a vis neurosurgical clipping, a trial was needed to assess the safety and efficacy of the two procedures.

The trial enrolled 2143 patients, who were admitted to 42 centres mainly across UK and Europe, with ruptured intracranial aneurysms and who were suitable to receive either procedure. They were randomly assigned to neurosurgical clipping (n=1070) or endovascular coiling (n=1073), and the outcomes at 1 year were compared.

The primary outcome was death or dependence (defined by a modified Rankin scale of 3-6). The study reported an absolute risk reduction of 7.4% (95% CI 3.6-11.2, p=0.0001), as 326 of 1055 patients (30.9%) allocated to neurosurgery were dead or dependent at 1 year, compared to 250 of 1063 patients (23.5%) allocated to endovascular treatment,

The secondary outcomes assessed were rebleeding and risk of seizures. The risk of late rebleeding was higher in the endovascular group, whereas the risk of epilepsy was substantially lower in the same. The early survival advantage was maintained in the endovascular group for up to 7 years and was significant (log rank p=0.03).

The ISAT trial concluded that endovascular coiling is more likely to result in independent survival at 1 year than neurosurgical clipping, in patients with ruptured intracranial aneurysms suitable for both treatments.

2. NASCET (North American Symptomatic Carotid Endarterectomy Trial)

   Stroke, 1999

Efficacy and durability of Carotid Endarterectomy (CEA), the surgical treatment for symptomatic carotid stenosis, was evaluated by the North American Symptomatic Carotid Endarterectomy Trial (NASCET).

Atherosclerotic carotid artery disease may present as TIA or RIND, or as a stroke. Retinal TIA causes ipsilateral monocular blindness which may be temporary (amaurosis fugax) or permanent. Other presentations can be a hemispheric TIA, which can be contralateral motor or sensory.

The study began in 1987. A total of 1415 patients with moderate carotid stenosis (< 70 %) and severe carotid stenosis ( > 70 %) were assigned to the surgical arm of the study, and were operated on by 278 NASCET accredited surgeons (neurosurgeons and vascular surgeons). The initial surgical results reported in August 1991 showed a highly beneficial effect for CEA in patients with high-grade carotid stenosis (70-99 %), modest benefit in moderate stenosis. ( < 70 %), and no significant benefit for those with < 50 % stenosis.

The study also analysed perioperative outcome events (stroke or death), and the durability of CEA. The overall rate of perioperative stroke and death was 6.5%, but the rate of permanently disabling stroke and death was only 2.0%.

The study formed the basis for the current practice guideline recommending Carotid Endarterectomy for patients with 50% or more carotid stenosis and history of TIA or ipsilateral stroke, and that the procedure is durable.

3. International Surgical Trial in Intracerebral Haemorrhage II (STICH II) Trial

  Lancet, 2013

Surgical Trial in Intracerebral Haemorrhage II (STICH II) trial aimed to compare early surgery with initial conservative treatment for patients with intracerebral haemorrhage (ICH).

Spontaneous intracerebral haemorrhage (ICH) accounted for 20% of all strokes and has the highest morbidity and mortality, but remained elusive in having a consensus on the most effective treatment for it. The STICH trial was an important study on the role of surgical treatment for ICH.

The study compared early surgery (hematoma evacuation within 24 h of randomisation) with initial medical treatment with later evacuation if required. The surgical approach for evacuation of ICH varied from craniotomy, burr holes, endoscopy and sterotaxy, but craniotomy was the predominant choice (77%). The first STICH trial (2005) included patients with hematoma of at least 2 cm in diameter with a Glasgow Coma Scale (GCS) score of at least 5. In the STICH II trial, the criteria were revised to include only those patients having hematoma within 1 cm of the cortex surface and of between 10 and 100 mL, and a Motor score of 5 or 6 in GCS, and an Eye score of 2 or more.

The primary outcome was measured on a 8-point Glasgow Outcome Scale obtained through postal questionnaires from patients at 6 months follow-up. Patients were grouped based on their clinical status at randomisation.into good and poor prognosis groups. Favourable outcome was defined as good recovery or moderate disability on the Glasgow Outcome Scale for the good prognosis group, and was inclusive of severe disability for the poor prognosis group.

The trial randomised 1033 patients from 83 centres in 27 countries to early surgery (503) versus initial conservative treatment (530). At 6 months follow-up, 26% patients (122 out of 468) randomised to early surgery had a favourable outcome, compared to 24% (118 out of 496) randomised to initial conservative treatment (odds ratio 0.89, p=0.414, absolute benefit 2.3% (-3.2 to 7.7), relative benefit 10% (-13 to 33)).

The STICH trial showed no overall benefit for patients with spontaneous ICH from early surgery compared to initial conservative treatment.

4. National Acute Spinal Cord Injury Study (NASCIS III) Trial

  JAMA 1997

Traumatic acute spinal cord injury (SCI) has devastating sequelae if not attended to urgently. National Acute Spinal Cord Injury Study III (NASCIS III) was formulated to devise a framework for optimal timing and dosing of methylprednisolone that was identified earlier a potential agent that could forestall free-radical mediated neuronal destruction in acute SCI.

The study compared the efficacy of methylprednisolone when administered for 24 hours and 48 hours respectively, and that of tirilazad mesylate administered for 48 hours, at 16 centres across North America.

A total of 499 patients with acute spinal cord injury sustained within 8 hours of injury were included in the trial. All patients initially received an intravenous bolus of methylprednisolone (30 mg/kg) and were then randomised to two groups - 24-hour (n=166) and 48-hour (n=167) groups.

Patients then received a methylprednisolone infusion of 5.4 mg/kg per hour for 24 hours or 48 hours accordingly. The tirilazad group (n=166) was administered 2.5 mg/kg bolus infusion of tirilazad mesylate every 6 hours for 48 hours.

The outcomes measured were motor function at the time of initial presentation, at 6 weeks and at 6 months, and change in Functional Independence Measure (FIM) measured at 6 weeks and 6 months.

Patients treated with methylprednisolone for 24 hours showed improved motor recovery at 6 weeks (P=.09) and 6 months (P=.07) compared to those treated for 48 hours after injury. Patients treated with tirilazad for 48 hours showed motor recovery rates equivalent to patients who received methylprednisolone for 24 hours.

The study recommended that patients with acute SCI who receive methylprednisolone within 3 hours of injury should be maintained on the treatment regimen for 24 hours, and those who were initiated on methylprednisolone 3 to 8 hours after injury should be maintained for 48 hours.

5. Corticosteroids Randomization After Significant Head injury (CRASH) Trial

  Lancet, 2004

Corticosteroids were in use for a long time for the treatment of head trauma on the assumption that it reduced risk of death.

Medical Research Council of UK initiated the Corticosteroids Randomization After Significant Head injury (CRASH) study to examine the validity of the assertion by recruiting 20000 patients, but the recruitment was stopped after 10008 adult patients by the steering committee after the data monitoring committee disclosed the results.

Adults with head injury and a Glasgow Coma Score (GCS) of 14 or less were randomly allocated 48 h infusion of corticosteroids (methylprednisolone) or placebo, within 8 h of injury. Primary outcomes assessed were death within 2 weeks of injury, and death or disability at 6 months.

The risk of death from all causes within 2 weeks was higher in the corticosteroids group (21.1%, 1052 patients) compared to 17.9% (893 patients) of the placebo group (relative risk 1.18 [95% CI 1.09-1.27]; p=0.0001).

CRASH trial revealed that there is no reduction in mortality with methylprednisolone in the 2 weeks after head injury.

NEUROLOGY

6. National Institute of Neurological Disorders and Stroke (NINDS) rt-PA Stroke Traial

  NEJM, 1995

Cerebral angiography performed soon after strokes have detected arterial occlusions in 80 percent of acute infarctions. Thrombolytic recanalization of occluded arteries may mitigate the extent and severity of the brain if done before the process of infarction sets in.

NINDS recombinant human tissue Plasminogen Activator (rt-PA) Stroke study was carried out for a critical assessment of the risks and the potential benefit of thrombolytic therapy as its inherent risk to precipitate an intracerebral haemorrhage is high.

The trial was conducted in two parts. Part 1 (291 patients) examined clinical efficacy of rt-PA as indicated by an improvement of 4 points over base-line values in the score of the National Institutes of Health Stroke Scale (NIHSS) or the resolution of the neurologic deficit within 24 hours of the onset of stroke.

Part 2 (333 patients) used a global test statistic to assess clinical outcome at three months, based on the Barthel index, modified Rankin scale, Glasgow Outcome Scale, and NIHSS.

In part I, there was no significant difference between the t-PA group and the placebo group in terms of neurologic improvement at 24 hours. In part 2, patients treated with t-PA were shown to be at least 30 percent more likely to have minimal or no disability at three months when compared to the placebo-group.

Symptomatic intracerebral haemorrhage within 36 hours after the onset of stroke occurred in 6.4 percent of patients given t-PA but only in 0.6 percent of patients given placebo (P<0.001). The rt-PA group had a mortality of 17% at three months, whereas it was 21% in the placebo group (P = 0.30).

NINDS rt-PA Stroke study concluded that intravenous t-PA within three hours of the onset of ischemic stroke improved clinical outcome at three months, despite an increased incidence of symptomatic intracerebral haemorrhage.

7. DAWN Study (Thrombectomy 6 to 24 Hours after Stroke)

  NEJM, 2018

The DAWN (DWI or CTP Assessment with Clinical Mismatch in the Triage of Wake-Up and Late Presenting Strokes Undergoing Neurointervention with Trevo) study compared endovascular thrombectomy plus standard medical care with standard medical care alone for the treatment of patients with acute stroke who had a mismatch between clinical deficit and infarct.within a period of 6 to 24 hours.

The study enrolled patients with occlusion of the intracranial internal carotid artery or proximal middle cerebral artery who had last been known to be well 6 to 24 hours earlier and who had a mismatch between the severity of the clinical deficit and the infarct volume.

The patients were randomly assigned to two groups: thrombectomy plus standard care (thrombectomy group) and standard care alone (control group). The primary endpoints were the mean score for disability and the rate of functional independence.

The conclusion of the DAWN study was that patients with acute stroke who had last been known to be well 6 to 24 hours earlier and who had a mismatch between clinical deficit and infarct fared better with thrombectomy plus standard care than with standard care alone, in terms of outcomes for disability at 90 days.

8. International Stroke Trial (IST)

    Lancet, 1997

International Stroke Trial (IST) was aimed at assessing the safety and efficacy of antithrombotic therapy (antiplatelet or anticoagulant agents) versus control in acute ischaemic stroke.

The study enrolled 19435 patients with suspected acute ischaemic stroke at 467 hospitals in 36 countries, and were randomised to two groups within 48 hours of symptom onset.

Half the patients were allocated to Aspirin group (300 mg of aspirin daily v/s no aspirin) and the other half to Heparin group (5000 or 12500 IU bd of unfractionated heparin v/s no heparin). The primary outcomes were death within 14 days, and death or dependency at 6 months.

The IST study suggested a small but worthwhile improvement at 6 months.for the aspirin group, but no clinical advantage for the heparin group. Aspirin produced a small but real reduction of deaths or recurrent strokes during the first few weeks, and therefore the study recommended that aspirin be started as soon as possible after the onset of ischaemic stroke.

9. Controlled High Risk Avonex Multiple Sclerosis (CHAMPS) Trial

  NEJM 2000

The Controlled High Risk Avonex Multiple Sclerosis Prevention Study (CHAMPS) was meant for assessing the effect of Interferon beta-1a (Avonex) on the rate of development of clinically definite multiple sclerosis.

The study enrolled 383 patients after the onset of a first demyelinating event, with brain MRI evidence of subclinical demyelination. Patients were treated with corticosteroids and were randomly assigned to receive weekly intramuscular injections of 30 microg interferon beta-1a or placebo.

The outcome was development of clinically definite multiple sclerosis or >1 new or enlarging T2 lesions on brain magnetic resonance imaging.

The study reported that Interferon beta-1a was beneficial when initiated at the first clinical demyelinating event in those patients with brain magnetic resonance imaging evidence of subclinical demyelination, and that the beneficial effect was present for optic neuritis, brainstem-cerebellar syndromes, and spinal cord syndromes.

PSYCHIATRY

10. Sequenced Treatment Alternatives to Relieve Depression (STAR*D) Trial

STAR*D trial was the largest (4000 adult patients in the age group 18-75) prospective clinical trial of treatment of major depressive disorder ever conducted. The study evaluated various treatment strategies to improve clinical outcomes for real-world patients with treatment-resistant depression. Depression accounts for nearly 10% of all primary care visits and are seen by primary care physicians.

The study compared various treatment options for those who do not attain a satisfactory response with citalopram, a selective serotonin reuptake inhibitor antidepressant, and provided guidance on how to initiate therapy and how to proceed if the initial treatment fails.

STAR*D trial was designed with a four-step protocol wherein there are four treatment levels, each lasting up to 14 weeks. All patients started at level 1 and moved up to the next level if they had not entered remission by 14 weeks.

Those who achieved remission stayed at the same level and were followed for up to 1 year. Citalopram was administered at level 1. Those patients without sufficient symptomatic benefit were randomised to level 2 treatments (4 switch options -sertraline, bupropion, venlafaxine, cognitive therapy; and 3 augment options - bupropion, buspirone, cognitive therapy).

The drugs available for switch options at level 3 are venlafaxine, bupropion, venlafaxine or bupropion and those for augment options are lithium or thyroid hormone. The level 4 randomization included tranylcypromine, or the combination of mirtazapine and venlafaxine.

Though the study did not identify therapies of choice for each level, its algorithmic approach was easy to integrate into both primary care or speciality care practice in the community for major depressive illness.