Lixisenatide Improves Glycemic Control in Asian Type 2 Diabetic Patients Inadequately Controlled With Oral Antidiabetic Drugs: An Individual Patient Data Meta-Analysis.

INTRODUCTION: Lixisenatide is a novel GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus (T2DM). Its efficacy and safety have been assessed in a series of phase 3 studies included in the GetGoal program. In these studies, lixisenatide was found to be superior to placebo in glycemic control. The aim of this meta-analysis was to assess the safety and efficacy of lixisenatide as an adjunct therapy in Asian patients with T2DM in adequately controlled with oral antidiabetic drugs (OADs).
METHODS: We performed a meta-analysis from five lixisenatide phase 3 studies. In each of these multiethnic studies, patients with T2DM inadequately controlled (glycated hemoglobin, HbA1c ≥7%) with established OADs were randomized to lixisenatide or placebo for 24 weeks, with a balanced distribution of Asian patients in these two arms (503 and 338 patients in the intent-to-treat population, respectively).
RESULTS: Lixisenatide was superior to placebo in reducing HbA1c (weighted, total mean difference -0.57%; P = 0.002). More patients treated with lixisenatide versus placebo achieved HbA1c targets of ≤7% (49.1% vs. 28.4%, P = 0.003). Lixisenatide was superior to placebo in lowering 2-h postprandial glucose (PPG) (weighted, total mean difference -5.50 mmol/l, P = 0.0005). More patients treated with lixisenatide versus placebo achieved 2-h PPG targets of ≤7.8 mmol/l (39.2% vs. 2.2%, P < 0.0001). More patients treated with lixisenatide versus placebo achieved both an HbA1c target of ≤7% and a 2-h PPG target of ≤10 mmol/l (34.8% vs. 2.69%, P < 0.00001). The body weight of the lixisenatide group tended to decrease. Lixisenatide was generally well tolerated.
CONCLUSION: Lixisenatide as an adjunct therapy can significantly improve the glycemic control of Asian patients with type 2 DM who do not meet targets for glycemic control with an established OAD regimen. FUNDING: Sanofi (China) Investment Co., Ltd., Shanghai, China.

RCT Entities:   Population Interventions Outcomes

Introduction

Globally, effective strategies for the clinical management of type 2 diabetes mellitus (T2DM) are receiving urgent attention as the world’s T2DM population is nearly 400 million. In Asia, the unprecedented rise in the prevalence of T2DM is particularly alarming. For instance, in China, the prevalence of T2DM increased from 3.2% in 1996 to ca. 9.7% in 2013, with the Chinese T2DM population at nearly 100 million, which represents approximately a quarter of the world’s diabetic population [1, 2].

Currently there is genuine concern about the extent of poor glycemic control in a large portion of the Asian T2DM population; for instance, recent evidence has shown that approximately two-thirds of patients in China who are treated with oral antidiabetic drugs (OADs) do not achieve the glycated hemoglobin (HbA1c) targets of ≤6.5 or ≤7% [3-5].

Patients from East Asia with T2DM share common pathophysiologic characteristics, which are distinct from those of their European counterparts. In East Asian countries diabetes occurs at a much lower BMI than elsewhere in the world [6], and the majority of East Asians with prediabetes have impaired glucose tolerance as opposed to impaired fasting glucose [7]. Another feature characterizing T2DM in Asian populations is the tendency to develop young-onset diabetes. Studies conducted in different East Asian populations have found a mean age of diagnosis of T2DM typically around 50 years [8]. Impaired beta cell function plays an important role in the pathogenesis of diabetes in Asians, especially in those who are not overweight or have a positive family history. Importantly, HbA1c values seem to be higher among Asians than Europeans, which is likely related to genetic similarities [9]. In addition to shared genetic and pathophysiological characteristics, East Asians have similar dietary habits. Therefore, a common treatment strategy for this population is indicated.

Currently in East Asia, patients with T2DM are commonly prescribed metformin/sulfonylurea, and the initiation of insulin therapy is often delayed [4, 5]. Because inadequately controlled T2DM can give rise to serious, irreversible medical complications, there is thus an urgent need to identify alternative treatment strategies that would improve glycemic control in the East Asian T2DM population.

Glucagon-like peptide-1 (GLP-1) receptor agonists increase insulin release, suppress glucagon secretion, and delay gastric emptying, which has been shown to be an effective strategy for improving glucose control in T2DM [10]. Furthermore, GLP-1 agonists are associated with a reduction in HbA1c levels, a low incidence of hypoglycemia, and a reduction in body weight [10]. GLP-1 receptor agonists are generally well tolerated, and side effects are mainly limited to mild gastrointestinal disturbances in a relatively small proportion of patients.

Lixisenatide is a novel, once-daily prandial GLP-1 receptor agonist for the treatment of T2DM [11-16]. Its efficacy has been assessed across the full spectrum of the natural history of T2DM in a series of lixisenatide phase 3 studies that were included in the GetGoal study programme. The GetGoal clinical study programme assessed glycemic control and safety following lixisenatide treatment in T2DM patients with uncontrolled glycemia despite diet and exercise interventions, single OADs, combinations of two or more OADs, or basal insulin. In the GetGoal studies, lixisenatide was found to be superior to placebo in reducing HbA1c and postprandial glucose (PPG) levels with a low incidence of hypoglycemia. Accordingly, lixisenatide was granted market authorization by the European Medicines Agency in 2013.

In the GetGoal study programme, one study enrolled only Asian patients who were inadequately controlled by OADs, and an additional four GetGoal randomized controlled trials (RCTs) included Asian patients in cohorts of mixed ethnicity. The primary objective of this meta-analysis was to amalgamate the safety and efficacy data of the Asian T2DM patients enrolled in those five RCTs, so as to broaden the database concerning the safety and efficacy of lixisenatide in Asian patients with T2DM who do not achieve adequate glycemic control with an established OAD regimen.

Methods

Data Sources

To identify relevant clinical studies, we performed a manual search on ClinicalTrials.gov. Firstly, we searched for lixisenatide phase 3 studies from the GetGoal programme. The terms used in the search were “phase 3”, “lixisenatide”, and “GetGoal” and a total of 13 studies were identified. Secondly, we also searched on ClinicalTrials.gov and pubmed.gov to make sure study primary results had been published previously. Thirdly, we further narrowed down to studies which had enrolled Asian patients and evaluated lixisenatide as an add-on treatment to OADs and compared with placebo. The terms used in this search were “Asian” and “OAD” and “placebo controlled”. Five studies were identified after this three-step search.

Analysis Design

The five randomized, placebo-controlled phase 3 studies of lixisenatide (GetGoal-M, GetGoal-F1, GetGoal-S, GetGoal-P, GetGoal-M-Asia) belonged to the GetGoal study programme, which was a series of 11 multinational RCTs that investigated the efficacy and safety profile of lixisenatide 20 µg once daily across the spectrum of patients with T2DM. All five of the RCTs included in the present meta-analysis enrolled, amongst others, Asian patients with T2DM who had inadequate glycemic control (HbA1c ≥7%) despite an established regimen of OADs. All patients received either lixisenatide or placebo as an adjunct to an established OAD regimen. Patients self-administered the study drug according to the regimens of the individual trials. The designs of each of the RCTs have been reported previously (see Table 1 for information on the individual studies). Briefly, GetGoal-M (NCT01169779) assessed the efficacy and safety of lixisenatide as an adjunct to metformin in patients with T2DM not adequately controlled with metformin. GetGoal-F1 (NCT00713830) assessed the efficacy and safety of four treatment schedules with lixisenatide—a one-step or two-step dose escalation, lixisenatide once daily for 12 weeks as a one-step dose increase (10 µg for 2 weeks, then 20 µg) or two-step dose increase (10 µg for 1 week, 15 µg for 1 week, then 20 µg)—as an adjunct to metformin in patients with T2DM not adequately controlled with metformin. GetGoal-P (NCT00763815) assessed the efficacy and safety of lixisenatide as an adjunct to pioglitazone in patients with T2DM not adequately controlled with pioglitazone. GetGoal-S (NCT00713830) assessed the efficacy and safety of lixisenatide as an adjunct to sulfonylurea in patients with T2DM not adequately controlled with sulfonylurea, and GetGoal-M-Asia (NCT01169779) assessed the efficacy and safety of lixisenatide in Asian patients with T2DM inadequately controlled by metformin (with or without sulfonylurea).

Table 1

Individual study information

Study codeShort name	Duration of treatment	Test drug and treatment regimen	Overall patient number (ITT) N	Number of Asian patients analyzed for primary endpoint (HbA1c) (ITT)
				Lixisenatide n	Placebo n	All N
EFC6014 GetGoal-F1	24 weeks followed by a ≥52-week double-blind extension	OAD + lixisenatide 10–20 μg (one-step), qd; or OAD + lixisenatide 10–15–20 μg (two-step), qd; or OAD + placebo (one-step), qd; or OAD + placebo (two-step), qd	479	14	7	21
EFC10743 GetGoal-P		OAD + lixisenatide 20 μg, qd; or OAD + placebo qd	484	22	9	31
EFC6017 GetGoal-G-M		OAD + lixisenatide 20 μg, qd (morning) qd; or OAD + lixisenatide 20 μg, qd (evening) qd; or OAD + placebo, qd (morning) or OAD + placebo, qd (evening)	680	40	11	51
EFC6015 GetGoal-S		OAD + lixisenatide 20 μg, qd; or OAD + placebo qd	856	242	123	365
EFC11321 GetGoal-G-M-Asia	24 weeks	OAD + lixisenatide 20 μg, qd; or OAD + placebo qd	388	185	188	373
Overall			2887	503	338	841

ITT intent-to-treat

For the meta-analysis, the data on Asian patients included in the five GetGoal studies were extracted, amalgamated, and analyzed according to the protocol of the meta-analysis. The GetGoal programme was a series of phase 3, randomized, placebo-controlled trials conducted at centers across the globe. All studies were sponsored by Sanofi.

Inclusion Criteria

Only GetGoal studies that included Asian adults (men and women) with a confirmed diagnosis of T2DM (as defined by the World Health Organization, WHO) at least 1 year prior to study entry were eligible for inclusion in the meta-analysis. All patients had inadequate glycemic control (HbA1c levels ≥7%) despite an established regimen of OADs and were in the intent-to-treat populations. In all of the included studies, patients were randomly assigned to either lixisenatide or placebo as an adjunct to their usual OAD(s), and they self-administered the study drug. The OADs that were allowed in the studies included in this meta-analysis were either metformin (1.0–1.5 mg/day) ± sulfonylurea (at least half of the maximum recommended dose as per the package insert) or pioglitazone (at least 30 mg/day).

Endpoints

The primary endpoint of this meta-analysis (and of the five GetGoal trials) was the mean change in HbA1c from baseline to week 24.

Secondary endpoints included the number of patients who achieved HbA1c target levels of ≤7% at week 24; the mean change in 2-h PPG values after a standardized meal test from baseline to week 24; the number of patients who achieved a PPG of ≤7.8 mmol/l at week 24; the number of patients who achieved an HbA1c target of ≤7% as well as a 2-h PPG of 10 mmol/l at week 24; the mean change in fasting plasma glucose (FPG); the mean change in body weight from baseline to week 24; and the number (%) of patients who experienced treatment-emergent adverse events (TEAEs) or serious TEAEs.

The data items extracted from each of the selected studies are listed in Table 2, and the main findings of the individual studies included in the meta-analysis with regard to HbA1c (percentage reduction), number of patients who achieved HbA1c targets of ≤6.5% or ≤7%, 2-h PPG, and safety are listed in Tables S1–4 in the supplementary material.

Table 2

Data items extracted from selected studies

Demographics	Age
	Gender
	Body weight and body mass index
	HbA1c at study entry (baseline)
	FPG at study entry (baseline)
Efficacy parameters	Change in HbA1c % from baseline (week 1) to end of treatment (week 24)
	Number (%) of patients who achieved an HbA1c target of ≤7% at week 24
	Change in 2-h PPG after a standardized meal administered at baseline and at the end of treatment (week 24)
	Number (%) of patients who achieved PPG ≤7.8 mmol/l at week 24
	Change in FPG from baseline (week 1) to end of treatment (week 24) Number (%) of patients who achieved FPG of ≤6.1 and ≤7.0 mmol/l
	Change in body weight from baseline (week 1) to end of treatment (week 24)
Safety parameters	Number (%) of patients with TEAEs and serious TEAEs

HbA1c glycated hemoglobin, FPG fasting plasma glucose, PPG postprandial glucose

Statistical Methods

All meta-analyses were performed using RevMan, version 5.3 (Cochrane Collaboration, Copenhagen). RevMan 5.3 was also used to generate forest plots.

The following analysis populations were identified: (1) the HbA1c population, which included data from all randomized patients who had at least one dose of the study drug (lixisenatide or placebo) and one baseline and one post-baseline HbA1c result; (2) the 2-h PPG population, which included data from all randomized patients who had at least one dose of the investigational medicinal product (IMP) and one baseline and one post-baseline PPG result; (3) the FPG population, which included data from all randomized patients who had at least one dose of IMP and one baseline and one post-baseline FPG result; (4) the body weight analysis population, which included all randomized patients who had at least one dose of IMP and at least one baseline and one post-baseline body weight measurement; and (5) the safety population, which included all randomized patients who had at least one dose of study medication.

Descriptive statistics were used to measure and describe the clinical characteristics and patient demographic data, as well as to measure and describe the efficacy and safety outcomes. The number of patients and the associated percentage of the total number of patients with the relevant data reported were determined for dichotomous variables. The count, mean ± standard deviation (SD), and median were reported for continuous variables. Treatment arms within each group were compared with one another, with P values calculated using a Chi square (χ 2) test or analysis of variance test where appropriate.

Standard meta-analytic techniques were applied to assess the overall outcome measures using a random-effects model with an inverse variance method to determine weighted mean differences with 95% confidence intervals (CIs) for continuous variables and Mantel–Haenszel odds ratios for all dichotomous outcome data. A P value of 0.05 was used to determine the level of statistical significance.

Quantification of heterogeneity was examined with I 2 to measure the degree of total variation across trials owing to heterogeneity and establish the consistency of evidence. I 2 values greater than 50% indicate a substantial level of heterogeneity; if heterogeneity was observed, this was accommodated using a random-effects model.

Compliance with Ethics Guidelines

All procedures in the trials included in this current meta-analysis were in accordance with the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964, as revised in 2013. Informed consent was obtained from all patients for being included in the studies. This meta-analysis is based on previously conducted studies, and does not involve any new studies of human or animal subjects performed by any of the authors.

Results

In total, 883 Asian patients with T2DM were available from the five GetGoal studies for inclusion in the meta-analysis. All of the patients had inadequate glycemic control (HbA1c levels ≥7%) on an established regimen of OADs (metformin ± sulfonylurea or pioglitazone). Of the 883 patients, 536 were assigned to lixisenatide and 347 to placebo as an adjunct to the patients’ established OAD regimen. The demographics of the analysis populations for the meta-analysis are reported in Table 3. The mean (SD) value of age, BMI, weight, HbA1c, and FPG at baseline, and the percentages of male patients were well balanced between two treatment groups.

Table 3

Demographics of the analysis populations

Parameter	Analysis population
	HbA1c		PPG		FPG		Body weight		Safety
	Lixisenatide n = 503	Placebo n = 338	Lixisenatide n = 250	Placebo n = 186	Lixisenatide n = 250	Placebo n = 185	Lixisenatide n = 517	Placebo n = 341	Lixisenatide n = 536	Placebo n = 347
Age, years, mean (SD)	54.6 (10.12)	55.1 (10.56)	54.8 (10.32)	55.9 (10.80)	54.6 (10.08)	55.1 (10.55)	54.6 (10.10)	55.1 (10.57)	54.7 (10.13)	55.2 (10.59)
Male, n (%)	270 (53.7)	174 (51.5)	135 (54.0)	96 (51.6)	279 (53.2)	178 (51.7)	277 (53.6)	176 (51.6)	283 (52.8)	180 (51.9)
BMI, kg/m2, mean (SD)	26.7 (4.21)	27.0 (3.98)	26.5 (4.00)	26.9 (4.05)	26.7 (4.20)	27.0 (3.97)	26.7 (4.19)	27.0 (3.97)	26.7 (4.17)	27.0 (3.97)
Weight, kg, mean (SD)	71.2 (13.74)	71.8 (14.37)	71.3 (13.60)	72.3 (15.33)	70.9 (13.67)	71.7 (14.35)	71.1 (13.67)	71.8 (14.33)	70.9 (13.62)	71.6 (14.35)
HbA1c, mean (SD) %	8.2 (0.88)	8.1 (0.84)	8.2 (0.86)	8.1 (0.81)	8.2 (0.88)	8.1 (0.84)	8.2 (0.88)	8.1 (0.84)	8.2 (0.88)	8.1 (0.84)
FPG, mg/dl, mean (SD)	8.9 (2.08)	8.9 (2.04)	8.8 (1.97)	8.9 (1.92)	8.8 (2.07)	8.9 (2.06)	8.8 (2.08)	8.9 (2.05)	8.8 (2.07)	8.9 (2.05)

HbA1c %

Compared with placebo, lixisenatide 20 µg once daily as an adjunct to an established OAD regimen significantly reduced HbA1c from baseline to week 24 in patients with inadequate glycemic control (weighted, total mean difference −0.57%; P = 0.002; Table 4). The potential heterogeneity of the primary endpoint was high (I 2 = 79%), but this was accommodated by the randomized-effects model.

Table 4

Forest plot for meta-analysis of least-squares mean difference between lixisenatide plus an OAD regimen and placebo plus an OAD regimen in terms of change in HbA1c (mITT population)

Study	Mean difference	SE	Lixisenatide total	Placebo total	Weight (%)	Mean difference IV, random, 95% CI	Mean difference IV, random, 95% CI
GetGoal-F1	–0.71	0.345	22	9	14.7	–0.71 (–1.39, –0.03)
GetGoal-M-Asia	–0.36	0.099	185	188	29.0	–0.36 (–0.55, –0.17)
GetGoal-M	–0.33	0.348	40	11	14.6	–0.33 (–1.01, 0.35)
GetGoal-S	–0.92	0.09	242	123	29.4	–0.92 (–1.10, –0.74)
GetGoal-P	–0.37	0.404	14	7	12.3	–0.37 (–1.16, 0.42)
Total (95% CI)			503	338	100	–0.57 (–0.93, –0.22)
Heterogeneity: τ2 = 0.10; χ 2 = 18.94, df = 4 (P = 0.0008); I 2 = 79%
Test for overall effect: Z = 3.16 (P = 0.002)

Random-effects model

CI confidence interval, df degrees of freedom, HbA1c glycated hemoglobin, IV inverse variance, mITT modified intent-to-treat population, SE standard error

Number (%) of Patients Achieving HbA1c Targets of ≤7%

Significantly more patients in the lixisenatide versus the placebo treatment group achieved the HbA1c targets of ≤7% (49.1% vs. 28.4%, P = 0.003) (Table 5). The odds ratios (ORs) for HbA1c ≤7% were 0.18 (0.06, 0.57, random-effects model).

Table 5

Forest plots for lixisenatide versus placebo in terms of percentage of patients with HbA1c values ≤7%

Study	Lixisenatide		Placebo		Weight (%)	Odds ratio M-H, 95% CI	Odds ratio M-H, random, 95% CI
	Events	Total	Events	Total
GetGoal-F1	11	22	1	9	14.0	0.13 (0.01, 1.17)
GetGoal-M-Asia	107	185	84	188	30.3	0.59 (0.39, 0.89)
GetGoal-M	21	40	1	11	14.7	0.09 (0.01, 0.77)
GetGoal-S	100	242	9	123	27.9	0.11 (0.05, 0.23)
GetGoal-P	8	14	1	7	13.2	0.13 (0.01, 1.33)
Total (95% CI)		503		338	100	0.18 (0.06, 0.57)
Total events	247		96
Heterogeneity: τ2 = 1.05; χ 2 = 19.31; df = 4 (P = 0.0007); I 2 = 79%
Test for overall effect: Z = 2.94 (P = 0.003)

Random-effects model

CI confidence interval, df degrees of freedom, HbA1c glycated hemoglobin, OR odds ratio

Two-hour PPG

Two-hour PPG was measured in three of the five GetGoal studies only (GetGoal-M-Asia, GetGoal-M, and GetGoal-S). Overall, lixisenatide was superior to placebo in lowering 2-h PPG at the end of the 24-week treatment period (weighted, total mean difference −5.50 mmol/l, P = 0.0005). Table 6 shows the change in 2-h PPG for lixisenatide versus placebo for all the treatment groups. The potential heterogeneity for the primary endpoint was relatively high (I 2 = 89%), but this was accommodated using a random-effects model.

Table 6

Forest plot for meta-analysis of least-squares mean difference between lixisenatide plus an OAD regimen and placebo plus an OAD regimen in terms of change in 2-h PPG (mITT population)

Study	Mean difference	SE	Lixisenatide total	Placebo total	Weight (%)	Mean difference IV, random, 95% CI	Mean difference, IV, random, 95% CI
GetGoal-M-Asia	–4.28	0.548	107	116	41.1	–4.28 (–5.35, –3.21)
GetGoal-M	–3.03	2.72	19	4	18.9	–3.03 (–8.36, 2.30)
GetGoal-S	–7.91	0.675	122	66	40.0	–7.91 (–9.23, –6.59)
Total (95% CI)			248	186	100	–5.50 (–8.59, –2.41)
Heterogeneity: τ 2 = 5.76; χ2 = 18.39, df = 2 (P = 0.0001); I 2 = 89% Test for overall effect: Z = 3.49 (P = 0.0005)

Random-effects model

CI confidence interval, df degrees of freedom, SE standard error

Number (%) of Patients Achieving 2-h PPG Targets of ≤7.8

Significantly more patients treated with lixisenatide versus placebo achieved 2-h PPG targets of ≤7.8 (39.2% vs. 2.2%, P < 0.0001). The OR for achieving a target of ≤7.8 mmol/l was 0.06 (95% CI 0.01, 0.22), at the end of the 24-week treatment period (random-effects model; see Table 7).

Table 7

Forest plots for lixisenatide versus placebo in terms of percentage of patients with PPG ≤7.8 mmol/l

Study	Lixisenatide		Placebo		Weight (%)	Odds ratio M-H, 95% CI	Odds ratio M-H, random, 95% CI
	Events	Total	Events	Total
GetGoal-M-Asia	37	109	4	116	63.8	0.07 (0.02, 0.20)
GetGoal-M	7	19	0	4	16.8	0.19 (0.01, 3.94)
GetGoal-S	54	122	0	66	19.4	0.01 (0.00, 0.16)
Total (95% CI)		250		186	100	0.06 (0.01, 0.22)
Total events	98		4
Heterogeneity: τ 2 = 0.46; χ 2 = 2.70, df = 2 (P = 0.26); I 2 = 26% Test for overall effect: Z = 4.14 (P < 0.0001)

Random-effects model

CI confidence interval, df degrees of freedom, HbA1c glycated hemoglobin, OR odds ratio, PPG postprandial glucose

Number (%) of Patients Achieving an HbA1c Target of ≤7% and a 2-h PPG Target of ≤10 mmol/l

Significantly more patients treated with lixisenatide versus placebo achieved both an HbA1c target of ≤7% as well as a 2-h PPG target of ≤10 mmol/l (34.8% vs. 2.69%, respectively, P < 0.00001). The OR for achieving this composite endpoint was 0.07 (95% CI 0.03, 0.18) at the end of the 24-week treatment period (random-effects model; see Table 8).

Table 8

Forest plot for lixisenatide versus placebo in terms of percentage of patients with both HbA1c ≤7% and PPG ≤10 mmol/l

Study	Lixisenatide		Placebo		Weight (%)	Odds ratio M-H, random, 95% CI	Odds ratio M-H, random, 95% CI
	Events	Total	Events	Total
GetGoal-M-Asia	39	109	5	116	81.7	0.08 (0.03, 0.21)
GetGoal-M	7	19	0	4	8.4	0.19 (0.01, 3.94)
GetGoal-S	41	122	0	66	9.9	0.01 (0.00, 0.24)
Total (95% CI)		250		186	100	0.07 (0.03, 0.18)
Total events	87		5
Heterogeneity: τ 2 = 0.00; χ 2 = 1.93; df = 2 (P = 0.38); I 2 = 0% Test for overall effect: Z = 5.80 (P < 0.00001)

Random-effects model

CI confidence interval, df degrees of freedom, HbA1c glycated hemoglobin, OR odds ratio, PPG postprandial glucose

FPG

Lixisenatide was superior to placebo in lowering FPG (P < 0.0001). The mean difference in FPG between the lixisenatide and placebo groups at the end of the 24-week treatment period was −0.51 mmol/l (−0.76, −0.26; random-effects model).

Change in Body Weight

Patients treated with lixisenatide generally had a stable body weight with a trend towards a decrease in body weight at the end of the 24-week treatment period [mean difference between groups –0.29 kg (−0.60, 0.01), both fixed and random-effects models].

Adverse Reactions

More patients in the lixisenatide versus placebo group experienced one or more TEAEs [OR 0.60; 95% CI (0.45, 0.81), both fixed and random-effects models].

In total, 12 of 347 (3.46%) patients in the placebo treatment group and 17 of 536 (3.17%) patients in the lixisenatide treatment group experienced at least one serious TEAE (P = 0.49). The risk ratios of serious adverse events did not show any statistically significant differences between lixisenatide and placebo group [OR 1.31; 95% CI (0.61, 2.79), both fixed and random-effects models].

Summary of Evidence

Overall, the evidence is sufficiently robust to confirm that lixisenatide as an adjunct therapy can improve glycemic control of HbA1c in Asian T2DM patients who do not achieve adequate glycemic control with OADs. Also, lixisenatide was superior to placebo in lowering 2-h PPG at the end of the 24-week treatment period. The improvements in glycemic control and the decrease in 2-h PPG were statistically significant and clinically meaningful.

Discussion

This meta-analysis of more than 800 Asian patients with T2DM shows that a once-daily dose of 20 µg of lixisenatide can substantially improve glycemic control in Asian patients who do not achieve an HbA1c target of 7% with an established regimen of OADs. Both HbA1c and 2-h PPG showed clinically meaningful reductions, with the 2-h PPG reduction being particularly large (−5.5 mmol/l) after the 24-week treatment course. Both HbA1c and PPG are important components of glycemic control, and the results of our meta-analysis provide evidence that lixisenatide has clinical application in Asian patients with T2DM who are inadequately controlled with OADs.

HbA1c Reduction

Our meta-analysis found that, compared with placebo, lixisenatide, on average, reduced HbA1c by 0.57% after a 24-week treatment period. This signifies a clinically meaningful improvement in glycemic control in Asian patients with T2DM who were inadequately controlled with an established OAD regimen.

In the GetGoal-S study, which enrolled 859 patients of mixed ethnic origin (ca. 45% of them were of Asian origin), the mean baseline HbA1c level was 8.2–8.3%, and the magnitude of the HbA1c reduction was 0.74%. This was more than double that reported in the GetGoal-M-Asia study, which enrolled 391 Asian patients (90% of them were Chinese) in China, Malaysia, Thailand, and Hong Kong [17, 18]. The mean baseline HbA1c of patients in that study was relatively low (7.85–7.95%), and the mean HbA1c reduction was considerably lower than that in other similar GetGoal studies that enrolled cohorts of mixed ethnic origin. The mean reduction in HbA1c in the present meta-analysis was greater than that reported in the GetGoal-M-Asia study (−0.36%). In our meta-analysis, the mean baseline HbA1c for the lixisenatide and placebo groups was 8.2% and 8.1%, respectively. Previous studies with GLP-1 receptor agonists showed that higher baseline HbA1c levels correlate with greater reductions in HbA1c [19-23].

The results of our meta-analysis therefore provide consolidated evidence for the value of lixisenatide in achieving glycemic control in Asian patients with T2DM who do not meet target HbA1c values despite an established OAD regimen.

Antidiabetic drugs that target GLP-1 are promising therapeutic options for Asian T2DM patients and it is postulated that GLP-1 receptor agonists increase glucose uptake, which, in turn, improves peripheral glucose utilization and measures of beta cell function [24, 25].

Two-hour PPG Reduction

The main antidiabetic effect of lixisenatide as a prandial GLP-1 receptor agonist is to delay gastric emptying, which, in turn, controls PPG excursions [10]. Our meta-analysis reported a large reduction in 2-h PPG (−5.5 mmol/l) after the 24-week treatment with lixisenatide, which was significantly better than that of the placebo group (weighted, total mean difference −0.57%; P = 0.0005). PPG control is a fundamental component of glycemic control in Asian T2DM because PPG excursions are thought to be more pronounced in Asians than in Westerners with T2DM [9, 26]. These disparities are usually ascribed to differences in eating/dietary habits, whereas physiological variances, such as a faster beta cell degeneration in Asian versus Western T2DM, may also have a role [26]. Consequently, in Asian T2DM, PPG is thought to be a more important contributor to HbA1c than FPG, and prandial GLP-1 receptor agonists are therefore a valuable addition to the treatment arsenal for Asian T2DM.

The reduction in PPG in our meta-analysis is aligned with the results of other studies with prandial GLP-1 agonists.

Body Weight

To date, GLP-1 receptor agonists have shown some benefits in terms of stable body weight or weight loss in T2DM patients. The effect of T2DM treatment regimens on body weight is an important consideration when selecting treatments for glycemic control because patients are often unwilling to commence, comply with, or intensify treatments that result in weight gain, in particular basal insulin. Treatment intensification with GLP-1 receptor agonists may therefore present a useful alternative to prandial insulin in patients insufficiently controlled with OADs. The results of this meta-analysis show that, at a minimum, body weight was stable over the 24-week treatment period. There was a tendency for weight loss at the end of the study, which might intensify if treatment is continued for a longer period. Nonetheless, another similar study in the GetGoal study programme (GetGoal-S) reported significantly larger reductions in body weight for patients treated with lixisenatide (mean reduction of 0.84 vs. –0.29 kg in this meta-analysis). In that study, the mean baseline body weight of patients was approximately 10 kg greater than that of patients in the meta-analysis.

In general, Asian individuals develop T2DM at a lower BMI than Westerners, and this could explain the generally lower mean body weight of the Asian cohort in our meta-analysis [23]. Nonetheless, in clinical practice, Asian individuals with T2DM do achieve high body weights and high BMIs, and these patients will most likely experience a reduction in body weight when treated with lixisenatide, similar to that of cohorts with a higher mean body weight in other GetGoal studies.

Safety

Although the incidence of TEAEs was higher in the lixisenatide than in the placebo group, the individual studies that were included in this meta-analysis showed that lixisenatide is generally well tolerated and the adverse events mostly mild to moderate in intensity. GLP-1 receptor agonists have a generally safe profile, and lixisenatide’s safety results are consistent with that of other GLP-1 receptor agonists [6].

Limitations

Observation can alter the behavior of both patients and physicians involved in clinical trials, and this may influence outcome measures, i.e., patients included in this meta-analysis were generally compliant with study protocols, and this may well not reflect real-world circumstances. For instance, in one of the GetGoal studies included in the meta-analysis, a relatively large placebo effect was observed in HbA1c, which is likely due to better patient compliance to diet and lifestyle changes because of more individualized care that is associated with study enrollment [17].

Conclusions

In the present meta-analysis, lixisenatide as an adjunct therapy was superior to placebo in lowering both HbA1c and 2-h PPG levels of Asian patients with T2DM who were inadequately controlled with an established regimen of OADs. A 24-week treatment period with lixisenatide resulted in a reduction of 0.57% in mean HbA1c and a large reduction in 2-h PPG (−5.5 mmol/l). Patients in the lixisenatide treatment group were significantly more likely than those in the placebo group to achieve HbA1c ≤7% and PPG targets. Lixisenatide is generally well tolerated and the adverse events mostly mild to moderate in intensity. Taken together, lixisenatide as an adjunct therapy has clinical application in Asian patients with T2DM who are inadequately controlled with OADs.

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 196 kb)