Background

Multi-arm multi-stage trials

Adaptive clinical trials are increasingly discussed and presented. The multi-arm, multi-stage (MAMS) design [1, 2] is one example of a flexible, seamless phase II/III randomized controlled trial. Detail on the general rationale for the MAMS design has been published elsewhere [3], but in brief, this approach allows for several research approaches to be assessed simultaneously against a common control group. Accrual resources are directed away from arms that show either insufficient activity on an intermediate primary outcome measure or unacceptable toxicity so that recruitment becomes increasingly focused towards the more promising research arms and the control arm. The MAMS design provides an efficient method for acquiring multi-agent prospective randomized data synchronously, requiring less time and needing fewer patients while simultaneously reducing the trial bureaucracy that is associated with a program of separate Phase II and Phase III trials. The MAMS approach thereby increases the likelihood of identifying one or more successful treatments in a single trial. It also decreases the likelihood of the whole trial stopping prematurely because the chance of multiple treatment approaches being insufficiently tolerated or ineffective is reduced.

The ability to add new research arms is an added advantage; initiating and conducting clinical trials remains resource-intensive and time-consuming both in terms of securing funding and gaining regulatory approval. The concept of adding new research arms within the context of an ongoing trial, thereby utilizing its existing machinery and recruitment base, is appealing. This can bring efficiencies in cost, personnel, and recruitment, leading to a reduction by many years in the time taken to initiate and recruit to the trial. This could further allow companies a longer period to generate profits within their patent.

The STAMPEDE trial

STAMPEDE (Systemic Therapies for Advancing or Metastatic Prostate cancer: Evaluation of Drug Efficacy) is a multi-center, open-label, multi-arm multi-stage randomized trial. The aim is to identify new treatments that could improve survival in men with high-risk locally advanced or metastatic prostate cancer and who are starting standard care with long-term hormone therapy (HT) with androgen deprivation. STAMPEDE assesses many research treatments, all added to standard HT: docetaxel, zoledronic acid, celecoxib and, now, abiraterone. The detailed clinical rationale of the trial has been presented elsewhere [4–6]. The trial is approved by the appropriate ethics and regulatory authorities. Figure 1 depicts the original trial and the anticipated timelines; Figure 2 shows observed accrual rates.

Figure 1
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Trial arms open to allocation and further timelines at start of trial.

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Figure 2
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Cumulative accrual of patients and activation of sites.

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Rationale for publication

The methodological details of STAMPEDE’s design and the practical issues of initiating the trial have been published elsewhere [7], but here we report on ongoing trial logistics, discussing the early stopping of two trial arms after an intermediate lack-of-sufficient-activity analysis (often referred to as a ‘lack-of-benefit’ for short) and the activation of a new research arm.

Managing early stopping following lack-of-benefit analysis

Trial design

The multi-arm multi-stage design of STAMPEDE has a series of formal intermediate analyses for each trial arm that take place at the end of each intermediate activity stage (AS); STAMPEDE has three such stages. Each research arm is compared separately to the common control arm in a pairwise fashion. However, there is no comparison of the research arms against one another at this time. The trial’s design specifies parameters for these intermediate analyses separately from the final analyses. The trial is designed to detect a clinically relevant benefit in the definitive primary outcome measure - overall survival. The assumption is that any such benefit should be preceded by a relative benefit at least as large in the intermediate primary outcome measure - failure-free survival (FFS). There is high power for each pairwise comparison throughout (≥90%) the trial and the pairwise significance level moves from permissive at the intermediate stages to strict at the final stage. Activity cut-point guidelines are derived for each intermediate analysis using the methods of Royston et al.[1] Table 1 depicts the design parameters. These are achieved using the n stage program, available in Stata [8, 9].

Table 1 Design parameters by trial stage for original research arms
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The intermediate analyses are triggered when a set number of events have been observed in the control arm. Focusing on the control arm in this way enables each analysis to be monitored and anticipated without revealing data on accumulating differences (or a lack of them) from the research arms. By considering the observed accrual rate and accumulating event rate in the control arm, it is possible to anticipate the time of the next intermediate analysis with reasonable precision. This can be calculated with the ARTPEP program (also available in Stata) [10]. Therefore, the first step towards planning can easily be achieved, which facilitates the planning of when the Independent Data Monitoring Committee (IDMC) should meet to review the data.

A large proportion of agents are unsuccessful in phase III trials [11–13], so it can be reasonably anticipated that accrual to at least one research arm in a MAMS trial is likely to be stopped early. Therefore, actions can, and should be, planned in advance of any early stopping decision. The statistical design explicitly considers stopping for lack-of-benefit, but research arms can also be stopped for reasons of harm or toxicity. Plans for either contingency can therefore be developed in anticipation of either eventuality.

Advanced preparation

In the governance and oversight structure of STAMPEDE, the IDMC is advisory to a Trial Steering Committee (TSC), which has independent members (including the Chair) and representatives from the Trial Management Group (TMG), the latter being the committee responsible for the day-to-day running of the trial. The IDMC decides which accumulating data, if any, should be seen by the TSC executive when they next meet and also guides interpretation.

Before the first intermediate analysis, a joint meeting of the TSC and IDMC was held in which the design of the trial was reviewed and a number of hypothetical scenarios were considered, anticipating a number of different ‘results’ at the intermediate stages. The aim was to provoke discussion on what sort of decisions each committee might make when reviewing certain outcomes and what information the two committees could expect to see to make such recommendations and decisions.

A series of “what if…?” questions were considered months before the first intermediate activity analysis discussions were held within the trials unit and within the TMG about the actions and communications required before and after each intermediate analysis. These questions included the following: What if one arm was stopped for safety after a given review or was stopped for lack-of-benefit; what if more than one arm was halted and for the same or different reasons; and even, what if no changes were made?

Table 2 summarizes the planned actions and timelines targeted. Communicating to trial sites that changes might be forthcoming was started many weeks before each intermediate analysis. The potential for stopping recruitment to arms was built into the trial design; therefore, such activity did not require a formal protocol amendment. A letter was circulated to each clinical site from the regulatory authority confirming this fact.

Table 2 Planned actions and timelines when accrual is stopped to trial arms
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Many activities (Table 2) were planned to occur quickly after a TSC decision to stop recruitment to any arm. The planned timelines were the same for most activities, regardless whether stopping an arm for lack-of-benefit or toxicity; although the plans for notifying staff internally and turning off randomisation needed to be quicker in the instance of toxicity. The reason for this disparity in times is because it was anticipated that arms showing a lack-of-benefit could actually be showing a trend towards an advantage to the research arm, albeit an insufficiently large advantage to encourage recruitment of more patients to that comparison. For example, at the third intermediate analysis, the activity cut point is a hazard ratio of 0.89. Therefore, accrual may be stopped to an arm with a favorable hazard ratio of 0.90. In the absence of an overriding safety concern it was reasonable to allow a little more time to turn off allocation to such a treatment.

Notifications to the ethics committee(s) and the regulators were planned. Although no immediate protocol amendment would be required, it was decided that the protocol would be updated as soon as practicable after changes to study arms to simplify activities for sites. The Patient Information Sheets (PIS) would be updated immediately with removal of information that was no longer pertinent and sent to the ethics committee(s) for information.

Results

The IDMC has met at least annually to review accumulating data. The data for the first formal intermediate activity analysis were frozen on 09 February 2010 with 1,424 patients randomized and 129 control-arm FFS events. The HR guideline cut point was 1.00. The review took place on 30 March 2010 by which time 1,518 patients had been randomized. The IDMC reviewed all data on the main outcome measures and recommended no changes.

The data for the second formal intermediate activity analysis were frozen on 01 February 2011 with 2,043 patients randomized and 209 control arm FFS events. The HR cut point was now 0.92. The IDMC meeting took place on 31 Mar 2011 by which time 2,163 patients had been randomized. The IDMC recommended that (i) the TSC see FFS data for both arms containing celecoxib and (ii) that no further patients be recruited to either celecoxib-containing arm. The detailed clinical findings are reported elsewhere [14, 15].

Practical experience

The TSC met on 06 April 2011 and approved the IDMC recommendations. They decided that (i) accrual should stop to both celecoxib-containing arms (D and F), following the lack-of-benefit guidelines; (ii) patients currently receiving celecoxib should be advised to stop celecoxib; (iii) comparative data celecoxib versus control arm (D versus A) should be shared with investigators; and (iv) data from the celecoxib plus zoledronic acid arm (F) should not be released as recruitment to the other zoledronic acid-containing arms (B and E) was to continue.

The observed HR for celecoxib versus control was 0.98, which did not meet the cut point. Although there was no clear evidence of either harm or unacceptable toxicity, no drugs are without potential for unwanted side-effects, and there was insufficient evidence of benefit to outweigh such risk.

As some patients were being advised to stop their treatment, it was decided to follow the safety rather than the lack-of-benefit timelines. By the afternoon of Day 0, (TSC meeting day) on 06 April 2011, the allocation to the celecoxib-containing arms in the randomization system had been disabled. All sites were notified by email that day and were told to re-advise patients who had consented to the trial but who had not yet been randomized. The Chief Investigator, patient representative and trials unit also agreed to a temporary revised version of the PIS. A quick response to this was facilitated by drafting many versions of the PIS before the IDMC meeting to reflect the needs following a number of hypothetical outcomes. Sites were offered a new electronic version of the revised PIS or they could manually cross out the few newly irrelevant sections of their current version. Sites were also told to advise patients to stop taking celecoxib at their next routine visit but that no urgent visits by patients to the clinic were required. A small number of patients who had been on celecoxib for many months chose to remain on treatment; only five patients are reported as still being on celecoxib at the start of July 2011.

On Day 1, phone calls were made to all site principal investigators (PIs) to ensure they were aware of and understood the actions taken. The trial team also worked with consumers to develop a summary of the results and actions to give to all patients. We thought it important for all trial patients to understand this information, not just those patients allocated to celecoxib-arms. This summary of results and actions was provided to sites for distribution to patients. Finally, industrial partners were apprised of the actions.

By Day 7, the PIS had been formally updated, submitted to the main ethics committee for information and distributed to sites. The regulatory authority was formally notified at this time. The protocol was formally amended (to version 7.0) after two months and submitted in June 2011 to the regulatory authority and ethics committee as a non-substantial amendment for information only.

These processes ran smoothly and no problems were reported from any of the governance bodies or from participating sites. The most common question from a small number of sites related to the use of new documents without apparent ‘prior’ approval. The earlier letter from the regulatory agency was sufficient to respond to these queries.

Recruitment continued to the control arm and to the remaining three research arms at good rates, with 47 patients in the 4 full weeks prior to change and 42 patients in the subsequent 4 full weeks. Importantly, follow-up continues for patients allocated to the celecoxib-containing arms.

Patients recently randomized to celecoxib-containing arms

A small number of patients randomized shortly prior to the halting of the celecoxib-containing arms had not necessarily had a chance to start their allocated treatment. It was agreed that patients allocated to arm D (HT plus celecoxib) and who still met all of the eligibility criteria for new patients joining the trial could be offered the opportunity to withdraw from STAMPEDE and to be re-randomized as a new patient. This was discussed with the relevant sites and five patients of seven meeting these criteria chose re-randomization. Since recruitment to and treatment within arm B (zoledronic acid) was continuing, patients on arm F (celecoxib plus zoledronic acid) were recommended to stop their celecoxib treatment and were not offered re-randomization. No patient will contribute more than once to any comparison. Sensitivity analyses will be considered.

Handling investigator assumptions

Investigators will no doubt make implicit assumptions about any research arms that continue accrual beyond each intermediate analysis. However, community uncertainty should not be affected by unreleased data from these intermediate comparisons. The knowledge that there are likely encouraging data on an early outcome measure at the intermediate analyses just reinforces the need to continue randomization to gain stronger evidence for the definitive primary outcome measure. If any of the arms showed early results for the definitive primary outcome measure that would be sufficiently convincing to influence clinical practice, the IDMC could recommend early release of the data. The strengths and weaknesses of that data would be discussed.

Designing new comparisons

Rationale for including new research arms

The practical reasons for choosing the five research arms at the outset of STAMPEDE has been discussed previously [7]. The STAMPEDE TMG has now successful activated one further research arm (G, abiraterone) and further arms are being considered.

The motivations for including a new research arm are many. The philosophy at the outset was to evaluate multiple agents from different classes but as new agents emerge and potential synergies from agents within the same class become a possibility, it is important that consideration is given to testing these alone, and possibly in combination, within the framework of a MAMS trial design. Agents and approaches should only be considered for addition when there are robust and convincing scientific hypotheses.

There is huge interest in new ‘hormone therapies’ for prostate cancer with the first such agent, abiraterone, an androgen biosynthesis inhibitor, licensed in 2011. Drugs approved in patients with late stage disease will generally go on to be tested in earlier settings. The efficiencies available in MAMS trials [3] are as relevant to new agents as they are in the original arms. These efficiencies include the following: (i) using one protocol to allow for new comparisons to be introduced by amendment; (ii) quicker recruitment to the new comparison by activating participating sites for the new comparison more quickly than is possible in any new, separate study; (iii) the increased chance of allocation of a research arm, which may appeal to many patients, thereby boosting accrual; (iv) the contemporaneous accrual to comparisons which overlap in time means no gaps between, and no competition between, trials; (v) phase II assessments of activity are incorporated; and (vi) together, the duration and cost of such a setting up a new comparison in this way would be considerably shorter and lower than any separate, new trial.

The rationale for considering any new research arm would need to be clear. The STAMPEDE TMG set forward a number of criteria summarized in Table 3.

Table 3 Criteria for potential new research arms
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When to add new arms

Many new agents are being developed in prostate cancer, often with differing mechanisms of action and demonstrable survival advantages in the later, castrate-refractory stages of the disease. These include approaches based on cytotoxic chemotherapy (cabazitaxel) [16], immunotherapy (sipuleucel-T) [17], radionuclides (radium-223) [18], novel androgen blockade (MDV3100) [19–21], and cellular pathway targeting drugs (cabozantinib) [22]. However, ahead of all of these in the development process has been abiraterone acetate (Zytiga: Janssen Pharmaceuticals). HT eventually fails for most men, even though they have castrate levels of circulating androgens. This is called castration-refractory prostate cancer (CRPC). Recent evidence suggests the failure is due to persistent activity of the androgen receptor, occurring because of intracellular conversion of steroids precursors to androgenic steroids by prostate cancer cells. A key enzyme in this process is CYP17, an enzyme which represents a logical target for therapy in later stages of prostate cancer [23]. Abiraterone is a selective inhibitor of CYP17 and is highly active in patients developing resistance to standard androgen ablation therapies [24–26]. First results of a phase III study comparing abiraterone to placebo in CRPC patients following chemotherapy with docetaxel reported an absolute improvement in overall survival of more than 4 months, hazard ratio 0.65 (95% CI, 0.54 to −0.77) [27]. The drug received marketing authorization in European Union from September 2011 and there is a robust biological hypothesis [28]. The TMG hypothesized that abiraterone could have a greater absolute effect when given to men with high-risk disease starting long-term HT (that is, earlier in the time course of the disease and synchronously with standard androgen ablation).

Design issues

The addition of HT plus abiraterone means that STAMPEDE has become a five-arm trial from mid-November 2011. The design parameters for STAMPEDE in Table 1 relate to each pairwise comparison of research arm against control arm. The same parameters and targets for the new comparison of abiraterone versus control have been chosen; these will only be made within contemporaneously recruited patients. That is, patients allocated to a new research arm are compared against control arm patients randomized after a new research arm was added.

Inevitably, analyses of new comparisons will be later than for the original comparisons. It is anticipated that completing accrual to the new research comparison (and possibly further additional arms) may occur before the primary survival results from the initial comparisons are known.

The key question was how many patients are required to attain these parameters? This depends on traditional and MAMS-specific factors, including recruitment rate, power and significance level for each stage. We realized that accrual would start strongly because the new comparison would quickly be activated in many sites. Furthermore, accrual to the new comparison would be boosted when recruitment to the original research arms stopped. A survey of participating sites (unpublished) suggested that overall accrual could even be boosted by including an ‘attractive’ new research arm. Accrual rates have increased throughout the trial (Figure 2) and could continue to increase regardless of the addition of a new arm.

For the sample size calculations, this comparison was first treated as if it were a two-arm multi-stage trial using nstage [8, 9] to obtain the control arm events required to trigger the end of each stage. The duration of the trial was then estimated using ARTPEP [10] to estimate when these events would be attained. ARTPEP offers much flexibility in accrual rates, follow-up duration and loss-to-follow-up.

Figure 3 (left) shows projected cumulative accrual to the new comparison (not the full trial) in the basic scenario. A boost to the accrual rate for the comparison is seen when the original research arms complete accrual, here after 12 months of co-recruitment, a 2:2 allocation ratio is shown so the green and purple lines depicting accrual to each arm are overlaid. A 2:1 allocation ratio was chosen for the original comparisons. It is more efficient to have more patients allocated to the control arm when there are more research arms co-recruiting [7]. Accrual to the abiraterone comparison will continue after accrual to the original research arms completes. An equal allocation ratio is more efficient in a two-arm setting, bringing forward maturity by a few months. We further considered that a 2:1 allocation ratio favoring the control arm might negatively impact accrual and duration.

Figure 3
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An example of accrual scenarios for the new comparison and project of cont rol arm events.

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Figure 3 (right) shows cumulative FFS events and deaths expected on the control arm. The dashed lines mark the number of control events required to trigger the intermediate and final analyses and the approximate calendar time of these analyses (rounded to the nearest quarter-year) in this scenario. On both sides of the graph, the vertical, dashed, black line represents the end of accrual.

The TMG has constructed and stored many such scenarios for the original trial, including increasing or decreasing the accrual rate, the accrual period, the follow-up period, the length of co-recruitment with the original arms and the median FFS and overall survival times, as well as introducing one or two further research arms later in the trial.

Accrual to this comparison is planned to stop at the sooner of (i) 1,500 new patients allocated to control or abiraterone or (ii) three years after activating the abiraterone comparison. The comparison should mature in around five years, depending on the mix of metastatic and non-metastatic patients joining the trial. Importantly, accrual to this comparison should complete before the original comparisons mature for the definitive primary outcome measure.

Practical experience

The abiraterone comparison was formally launched on Tuesday 15 November 2011. A total of 31 patients joined STAMPEDE by the end of the first full week, with 18 allocated to arms A or G (around the 4 of 7 expected). We describe the steps that we took to reach this point.

Janssen’s first formal results for abiraterone in late-stage prostate cancer were published in April 2011 [27] and updated at the American Society of Clinical Oncology (ASCO) 2011 [29], with abiraterone being licensed in Europe in September 2011. Discussions between the TMG and Janssen were formally initiated much earlier in March 2010 with an application by the trial team for an investigator-initiated study. In July 2010, the main funding body, Cancer Research United Kingdom, organized a scientific peer review of the revised trial application to conditionally amend STAMPEDE pending successful negotiations and a successful results from the Janssen’s COU-AA-301 trial. This included findings reflecting broad enthusiasm among investigators and patients to assess abiraterone, plus the TMG’s enthusiasm for this new approach.

Subsequent months were spent discussing the dose and duration of abiraterone, steroid support, details of drug supply and distribution, safety reporting, research supports and contracts with Janssen’s United Kingdom, European and Global affiliates. The sample size estimates were then finalized and the protocol was conditionally updated.

The principle of adding a new arm was discussed at each IDMC and TSC meeting in 2010 and 2011. The TSC reviewed the protocol in August 2011. The new research arm G (hormone therapy plus abiraterone) was then submitted to the regulatory agency and ethics committee late in August 2011 as a substantial protocol amendment (version 8.0) along with an updated PIS. This updated protocol included some modified eligibility criteria pertinent to assessing abiraterone. All patients now needed histological confirmation of prostate cancer, something not previously required for the subset of patients with bone metastases and PSA >100 ng/ml. In the United Kingdom this affected only a small proportion of patients and fitted in with current National Institute for Health and Clinical Excellence (NICE) guidance recommending a biopsy where a patient may wish to enter a trial. This is also consistent with most trials of new agents in prostate cancer. Further clarifications on liver and renal function that are associated with fitness for abiraterone were also introduced but were unlikely to markedly affect the number of eligible patients.

The TMG also introduced an unrelated change for non-metastatic patients following recent results from SPCG-7 [30] and MRC PR07/NCIC PR.3 [31], which demonstrated a survival advantage to HT plus radiotherapy over HT alone in men with locally advanced, non-metastatic prostate cancer. Previously, radiotherapy had been encouraged for such men in STAMPEDE, but the trial has been updated to reflect the new standard-of-care.

The likely addition of abiraterone had been extensively promoted at conferences and investigator meetings in addition to the survey. The trial team started training participating sites in parallel with the contractual and regulatory processes. Regional launch and training meetings in Glasgow, London, Cardiff and Manchester in September 2011 and October 2011 were supplemented with teleconferences. This included making clear that there would be a formal switchover date to protocol version 8.0 and that centers would need new local approval to maintain accrual beyond this date. That is, all sites needed to provide evidence to be given permission to start randomizing again.

The ethics committee responded quickly and positively in September 2011, the regulatory agency gave approval in October 2011 within their 35-day window, and neither body requested changes.

The chosen date for the switchover was 15 November 2011, allowing sites 35 days from 12 October 2011 to attain local approvals. Figure 4 shows sites with local approvals for v8.0 over time. The first site gained approval within one week demonstrating the feasibility of quick amendments. By the time of final activation 83 of 104 sites had the necessary permissions in place. This denominator includes some sites that had not previously participated and were waiting for this protocol amendment. Four-fifths were ready within five weeks. This does not include centers in Switzerland, where the coordinating body, the Swiss Group for Clinical Cancer Research (Schweizerische Arbeitsgemeinschaft für Klinische Krebsforschung or SAKK), chose not to submit for approvals until after activation in the United Kingdom. All Swiss sites suspended accrual. Sites that were slower in activating include three that shared one R&D department, one where the PI had recently changed and one with unrelated pharmacy problems. The trial team ensured that all sites with approvals prior to switchover had access to abiraterone on-site from the day of activation.

Figure 4
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Activat ion of sites to new comparison.

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It is unlikely that any completely new trial could have 83 sites ready to recruit on activation day, something that would be a considerable achievement. Figure 2 shows (on the left axis) the number of sites recruiting their first patient to the trial, demonstrating how long de novo trials may take to activate sites. Site activation was deliberately limited during the original Pilot Phase, but new sites have continued to activate throughout, giving accelerated recruitment rates. Therefore, a new, separate trial of abiraterone would likely have taken much longer to get to the same rate of recruitment as STAMPEDE achieved immediately. The cost of a separate trial would also have been higher if the trial took longer to conduct. A separate trial would also potentially have become established as a competing trial, with the possibility of an adverse effect on recruitment to both trials. Combining the new comparison into STAMPEDE also brings efficiencies in costs regarding site training, site monitoring and database construction.

We anticipated that accrual would be ahead of the switchover with sites that might want to wait until after switchover to randomize new patients. However, in the last full week prior to switchover 18 patients were randomized and 4 further patients were randomized the day before switchover. On the day of activation, 15 November 2011, 6 patients were randomized and by the end of January 2011, 53 patients were allocated to arm G. Figure 5 summarizes the current design of the trial and projected timelines.

Figure 5
figure 5

Trial arms open to allocat ion and fur ther t imelines as of Nov 2011.

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Other issues

Randomization is achieved through minimization with a random element [32, 33] where 80% patients are allocated to a minimizing arm across a series of clinically-relevant stratification factors [7]. Therefore, at any moment in time, the groups allocated to each arm are well-balanced. After consideration, the TMG wiped the stratification tables clean when the new comparison was activated, effectively starting over again.

The possibility of the original research arms maturing while the new comparison was ongoing was discussed. Such data can be considered as if they are data emerging from an external trial. Indeed, there are some other trials which overlap partially with STAMPEDE in terms of both population and treatment. The trial team would react if change is needed, as demonstrated by the introduction of radiotherapy in non-metastatic disease.

The future

The STAMPEDE investigators appreciate that challenging and novel changes can only be made by working with enthusiastic researchers. The group has, therefore, encouraged discussions with sites from the outset and has repeatedly engaged sites to ensure clinician and patient input and ‘buy-in’. The potential changes have been presented in newsletters and at regional meetings over a long period. Furthermore, researchers have been encouraged to bring forward ideas for further arms that might be worthy of assessment in this trial population.

Indeed, the STAMPEDE TMG has started to consider further arms. In September 2011 the TMG prioritized potential questions. Any new comparison would take at least one year to develop and activate so it is important that such discussions start early if they are to be activated. Champions for potential new agents have been making contact with potential industry partners although the most favored question was radiotherapy for metastatic disease, which pertains only to a subgroup of patients. This provides a further challenge for our flexible design to address. Projections for various recruitment scenarios demonstrate that this could be achieved if participating centers are keen to formulate questions together. A questionnaire was distributed to sites in November 2011 and the concept was received positively. This has been approved by the trial committees and has been successfully peer-reviewed by Cancer Research United Kingdom. A formal amendment to activate this comparison will be developed during summer 2012. We estimated that undertaking this comparison within STAMPEDE would cost only about 60% as much as a separate stand-alone trial.

Conclusions

STAMPEDE is a high-profile adaptive randomized controlled trial (RCT). We believe the merits in this flexible approach are clearly apparent, and we encourage others to implement this or similar designs in other settings. In particular, the considerable costs associated with trial start up and close down can be substantially reduced by evaluating many new treatments simultaneously and also by using intermediate analyses to run a seamless phase II/III approach [3]. The ability to rapidly add new arms is also an important innovation. We have essentially set up a new phase III comparison of abiraterone in 100 centers in 18 months from the first idea to first patient; From protocol sign-off to opening was less than 4 months. The price in trial administration costs (ignoring drug associated costs which accrue whatever route one chooses) ran into tens of thousands of pounds sterling rather than the much larger sums normally associated with trial set up on this scale de novo. Experience shows that funders, regulators, investigators and, most importantly, patients can deal with the complex issues involved. Indeed, as the trial has progressed, companies wishing to have their drug included within the trial have started to approach us.

We hope that this very positive experience of an adaptive trial will encourage others to undertake further trials like STAMPEDE and that our experience will smooth the passage of further such trials.

In summary, the STAMPEDE trial has confirmed the notion that MAMS trials speed the evaluation of new treatments by testing many treatments simultaneously and by using lack-of-benefit analyses to focus research efforts towards the more promising research arms. It has also demonstrated that accrual and treatment of insufficiently active arms can be stopped successfully without this radical change affecting the continued evaluation of agents still undergoing testing in this setting. Finally, and importantly, we have demonstrated that adding additional research arms to enable new and rapid comparisons of novel agents either alone or in combination is possible, and that the modification of a complex protocol to accommodate changes in practice during the running of a MAMS study is achievable. This is particularly important in an ongoing trial of this type. We have shown that a major change to the protocol can be swiftly and effectively achieved in large numbers of centers, and high volume recruitment can be continued in a seamless, safe and efficient manner.

Disclosure

This manuscript is based on an oral presentation given at the first United Kingdom Clinical Trials Methodology Conference, Bristol, UK in October 2011 and subsequently presented as a poster as the Genitourinary Cancer Symposium, San Francisco, USA in February 2012.