Patient-level pooled analysis of adjudicated gastrointestinal outcomes in celecoxib clinical trials: meta-analysis of 51,000 patients enrolled in 52 randomized trials

Patients seeking effective pain relief from chronic and acute painful conditions such as osteoarthritis (OA), rheumatoid arthritis (RA), postsurgical pain, and dysmenorrhea may be prescribed nonselective (ns) nonsteroidal antiinflammatory drugs (NSAIDs) (for example, naproxen, diclofenac, and ibuprofen) or cyclooxygenase (COX)-2 selective NSAIDs (for example, celecoxib). The benefits and risks of each medication vary according to both the clinical setting and individual patient characteristics. Some patients respond well to NSAID use, whereas others receive little benefit [1]. However, all patients using NSAIDs run the risk of associated adverse events (AEs).

The AEs associated with NSAID use include upper and lower gastrointestinal (GI) adverse outcomes [2‐6] and cardiovascular events [7‐10]. Assessment of both upper- and lower-GI complications is important, as a number of studies have shown that the use of NSAIDs increases the risk of lower-GI AEs [5, 11, 12]. The novel end point of clinically significant upper-and lower-GI events (CSULGIEs) extends the traditional assessment of upper-GI complications (perforations, obstructions and bleeding in the esophagus, stomach, and duodenum) by also including events (perforation, bleeding, and clinically significant anemia) from the lower-GI tract (small/large bowel) [2].

Unlike nsNSAIDs that inhibit both the constitutive and inducible forms of the COX enzyme (COX-1 and COX-2), celecoxib is selective for the COX-2 enzyme. Inhibition of the COX-1 enzyme is responsible for the associated GI toxicity of nsNSAIDs [13], and the selective COX-2 inhibitory activity of celecoxib is believed to be associated with a lower risk of GI AEs than are the nsNSAIDs [14].

The GI safety of celecoxib has been investigated in observational studies, randomized controlled trials (RCTs), and meta-analyses of RCTs. An observational study found a lower short-term risk of upper-GI toxicity for celecoxib than for nsNSAIDs, as measured in hospitalization rates due to upper-GI bleeds [15]. Two large RCTs, Celecoxib Long-term Arthritis Safety Study (CLASS) and SUccessive Celecoxib Efficacy and Safety Study (SUCCESS), compared the GI safety of celecoxib with that of nsNSAIDs by using the upper-GI ulcer-complications measurement. CLASS found celecoxib to be no different from comparator nsNSAIDs in the incidence of upper-GI ulcer complications [16], whereas SUCCESS showed superior GI safety of celecoxib over nsNSAIDs [17]. A third large RCT, Celecoxib vs Omeprazole and Diclofenac in Patients with Osteoarthritis and Rheumatoid Arthritis (CONDOR), compared the total (upper and lower) GI safety of celecoxib with that of the nsNSAID diclofenac in patients with OA and RA at increased gastrointestinal risk. This was the first clinical trial to show that the risk of clinical outcomes throughout the GI tract was significantly reduced in patients treated with celecoxib compared with diclofenac-treated patients [18].

Meta-analyses of RCTs, comparing celecoxib with nsNSAIDs for upper-GI events, also concluded that celecoxib is superior to comparator nsNSAIDs for GI safety [19‐21]. The review by Deeks et al. (2002) was limited to nine trials and 15,187 patients; the review by Moore et al. (2005) was a more comprehensive analysis of 31 RCTs and 39,605 patients based on Pfizer study reports, but did not assess ulcer complications; and the Rostom et al. (2007) review was not limited to celecoxib trials. None of these meta-analyses, however, included patient-level data with independent adjudication.

Although the safety of celecoxib has previously been investigated in observational studies, RCTs, and meta-analyses, limited data are available on complications affecting the entire (upper and lower) GI tract. To date, no patient-level comprehensive meta-analysis or pooled analysis of both upper- and lower-GI outcomes with COX-2 selective NSAIDs has been published. The present pooled analysis evaluating the upper- and lower-GI safety of celecoxib in RCTs fills this evidence gap.

An independent blinded expert committee adjudicated all end points by using predefined GI-complications criteria (gastroduodenal, small bowel, or large bowel perforation; gastric outlet obstruction; gastroduodenal hemorrhage; large bowel hemorrhage; small bowel hemorrhage; clinically significant anemia of defined GI origin; acute GI hemorrhage of unknown origin, including presumed small bowel hemorrhage; and clinically significant anemia of presumed occult GI origin, including possible small bowel blood loss) as well as available reported AEs, laboratory data, vital signs, and case narratives, where available.

The adjudication committee consisted of two external, independent gastroenterologists and one external independent rheumatologist. The two gastroenterologists acted as adjudicators, and the rheumatologist acted as a facilitator only for cases in which agreement was not initially reached between the adjudicators. The adjudicators advised on the proper definition of potential and suspected outcomes; they provided guidance on the selection of events to be adjudicated, guidance regarding evaluation, and collection of information necessary to adjudicate suspected GI outcomes and guidance on the screening methods to be applied to potential events before adjudication. Additionally, the adjudicators validated the screening method of the potential events, reviewed, in a blinded fashion, and where necessary, rereviewed all suspected GI outcomes by using the clinical information supplied in supporting documentation, and provided final classification of the primary and secondary events as an end point or not an end point. Adjudication of CSULGIEs could be made satisfactorily only when clinical information in the form of a narrative was available. The facilitator coordinated consensus between adjudicators in cases of discordance, but did not adjudicate any end points.

The findings of this retrospective pooled analysis of 52 RCTs and more than 51,000 patients show that celecoxib is associated with a significantly lower risk of all clinically significant GI events throughout the entire GI tract when compared with nsNSAIDs, however defined. This is consistent with previously published meta-analyses [19‐21] and observational studies [15, 22].

A major strength of this patient-level pooled analysis was the inclusion of more than 51,000 patients with active disease (OA/RA, chronic low-back pain, ankylosing spondylitis, Alzheimer disease, or cancer), giving a robust sample size. It included all the methodologically sound randomized trials of celecoxib performed of at least 4 weeks' duration and concluded by October 2007. Further strengths included the independent evaluation of both upper- and lower-GI complications, together with the blinded adjudication of cases.

Caution should be exercised, however, because many of the clinical trials included in this analysis were not designed to study serious GI outcomes, and, at the time, detailed clinical information was not available on all suspected end points. In addition, the quality and the availability of the narratives varied (that is, some narratives were not available, and some were more fully descriptive of the serious AEs than were others). The members of the adjudication committee used their best clinical judgments based on available data for these adjudications. Furthermore, analysis of trials solely from the Pfizer Celecoxib Clinical Database might exclude relevant trials conducted elsewhere.

One additional issue is that the number of primary outcome events (patients experiencing CSULGIEs) was, at 89, below the limits of about 200 to eliminate random-chance effects suggested for adverse-event determinations [23]. For secondary outcomes, the number of events was > 200. The primary and secondary events were influenced in the same direction and to much the same extent.

Statistical heterogeneity between trials is not unexpected when the number of events is small, as in the case of rare adverse events [24]. The primary analysis method using a stratified log-rank test adjusting for studies was prespecified. Small numbers of events produce uncertainty over results [25], with subgroup analysis based on small numbers producing incorrect results; therefore, the advice is not to consider subgroup analyses in this circumstance [26]. For these reasons, together with the adjudication of CSULGIEs as a specific definition rather than by site of injury (upper or lower gastrointestinal tract), no subgroup analyses were attempted.

Systematic reviews generally should have a cut-off date beyond which additional information for new studies is not added. This is especially necessary when a detailed program of adjudication is required, as it was for this analysis of more than 1,000 patients. Medicines like celecoxib, with ongoing investigations into their benefits and safety, require the findings from meta-analyses to be continually compared with results from studies completed after the meta-analysis study inclusion cut-off date. This is particularly the case when the number of patients exposed or the duration of exposure would have added significantly to the total number available in the meta-analysis: here, 28,614 patients were exposed to celecoxib for 12,276 years. Several studies that were completed after the cut-off date are relevant, and show similar trends (Figure 4)

A large clinical research program of three studies (CONDOR, GI-REASONS, and PRECISION) to assess both the GI and/or cardiovascular safety of celecoxib and commonly used nsNSAIDs was ongoing at the cut-off date of this meta-analysis. The CONDOR and GI-REASONS studies have now been completed, whereas the PRECISION trial is still ongoing. The CONDOR trial, which compared the total GI safety of celecoxib with diclofenac plus omeprazole by using the novel composite GI end point of CSULGIEs, was completed in May 2009 [18]. OA and RA patients (n = 4,484) were randomized either to celecoxib or to diclofenac plus omeprazole for 6 months. The rate of CSULGIEs was significantly lower with celecoxib than with diclofenac plus omeprazole (0.9% versus 3.8%), and the majority of the events were related to anemia (decrease in hemoglobin ≥ 2 g/dl).

The GI-REASONS study, which was completed in November 2010, assessed the incidence of CSULGIEs in OA patients (n = 8,067) randomized to celecoxib or nsNSAIDs for 6 months [27]. The rate of CSULGIEs was significantly lower with celecoxib (1.3%) than with nsNSAIDs (2.4%), and the majority of events were also related to anemia (decrease in hemoglobin, ≥ 2 g/dl).

These two studies used the same end point as did our meta-analysis, used an adjudication committee, and reached essentially the same conclusion, that celecoxib was associated with a significantly lower rate of GI tract events than were nsNSAIDs. Other trials involving celecoxib have been reported since 2007, but none of a size or concentration on GI-tract outcomes that would allow comparison with results from our meta-analysis.

When compared with nsNSAIDs, celecoxib is associated with a significantly lower risk of all clinically significant GI events throughout the entire GI tract. This pooled analysis of patient-level data from 52 RCTs significantly advances the understanding of the cumulative upper- and lower-GI safety profile of celecoxib and its potential benefits to patients. Future NSAID safety studies should consider analyzing the cumulative incidence of clinically significant upper- and lower-GI events.