Efficacy and Safety of Omadacycline Versus Linezolid in Acute Bacterial Skin and Skin Structure Infections in Persons Who Inject Drugs.

INTRODUCTION: Acute bacterial skin and skin structure infections (ABSSSI) represent one of the most common reasons for emergency department visits, and are frequent complications of intravenous drug use in persons who inject drugs (PWID). This study examined the efficacy and safety of omadacycline, versus linezolid, in PWID and persons who do not inject drugs, in the Phase 3 Omadacycline in Acute Skin and Skin Structure Infection (OASIS-1, OASIS-2) studies.
METHODS: Eligible participants were aged ≥ 18 years with qualifying skin infections: wound infection, cellulitis, erysipelas, or major abscess. The primary efficacy endpoint was early clinical response (ECR) in the modified intent-to-treat (mITT) population, defined as survival with ≥ 20% reduction in lesion size at 48-72 h after the first dose of omadacycline or linezolid. Key secondary endpoints included investigator-assessed clinical response at the post-treatment evaluation (PTE) in the mITT and clinical per-protocol populations, and clinical response at PTE in the micro-mITT population. Safety was assessed based on adverse events (AEs) and standard clinical laboratory tests. Efficacy endpoints of clinical response at ECR and PTE were analyzed for the mITT and clinically evaluable (CE) PTE populations.
RESULTS: In total, 1380 patients (822 PWID, 558 non-PWID) were included in this secondary analysis. Wound infections were reported more frequently in the PWID subgroup (72.8%) at baseline; cellulitis or erysipelas (43.9%) and major abscess (37.4%) were the most frequently reported baseline infections in the non-PWID subgroup. Clinical success rates at ECR and PTE in the mITT population, and at PTE in the CE population, were high for patients receiving omadacycline or linezolid. Severe or serious treatment-emergent AEs (TEAEs), and TEAEs leading to discontinuation, were infrequent.
CONCLUSION: This subgroup analysis showed that omadacycline was effective and well tolerated, regardless of PWID status.

Key Summary Points

Introduction

Acute bacterial skin and skin structure infections (ABSSSI) represent one of the most common reasons for emergency department visits worldwide [1, 2]. ABSSSI include cellulitis, erysipelas, wound infections, and major cutaneous abscesses, most of which are caused by Gram-positive organisms [3, 4]. Although most ABSSSI can be treated on an outpatient basis, infections with methicillin-resistant Staphylococcus aureus (MRSA) are highly prevalent, representing about half of purulent skin infection and abscesses in the United States, and more often lead to complications and hospitalizations [5, 6]. Between 2001 and 2009, S. aureus-related ABSSSI incidence more than doubled in the USA, from 57 to 117 infections per 100,000 people [7]. The average associated cost of an S. aureus-related ABSSSI hospitalization was US$11,622 per patient, with total estimated annual costs exceeding $4 billion [7].

Over the past two decades, increased levels of intravenous (IV) drug use in the USA have been associated with an elevated incidence of chronic viral infections, including hepatitis B and C, and human immunodeficiency virus [8]. Despite the increase in IV drug use, robust clinical data are limited in this population, and few recent studies have examined the incidence, microbiology, and characteristics of skin infections among persons who inject drugs (PWID) [2]. However, earlier studies suggest that ABSSSI are frequent, morbid, and costly complications of IV drug use, and are among the most common causes of hospital admissions in PWID [6, 9, 10]. In addition, the prevalence of ABSSSI in PWID may be underestimated, as many PWID are admitted for bacterial endocarditis rather than for the associated skin infection [11]. Studies performed in the USA and UK have found that almost 70% of PWID with a current skin infection report a history of past infections [12-14].

Cultures obtained from abscesses in PWID show that, similar to the general population, most infections are likely to be caused by S. aureus, including MRSA [15]; however, causative pathogens may be more diverse than seen in the general population, and dependent on injection practices [15, 16].

A barrier to proper treatment in the PWID population is the perception by healthcare providers that PWID are more difficult to care for and have poorer outcomes in medical care than non-PWID. Perceived issues include lack of insurance coverage and non-adherence to treatment, including patient-directed discharge [17-19]. The perception that PWID are less adherent to treatment regimens may lead providers to prescribe a suboptimal therapy that is easier for the patient to follow than the preferred therapy [19]. Additionally, there is a perceived risk that IV catheters are misused by PWID at outpatient treatment centers, although this can be overcome by patient selection, tamper-proof seals, counseling, and careful monitoring of patients [17].

Omadacycline is an aminomethylcycline antibiotic, available in oral and IV formulations, approved in the USA for the treatment of ABSSSI and community-acquired bacterial pneumonia in adults. For the treatment of ABSSSI, omadacycline was non-inferior to linezolid in two Phase 3 studies (ClinicalTrials.gov identifiers NCT02378480, NCT02877927) [20, 21]. The post hoc secondary analysis presented here describes the PWID population from two pooled Phase 3 studies, and examines the efficacy and safety of omadacycline in PWID and in persons who do not inject drugs (non-PWID).

Methods

Study Designs

The OASIS-1 and OASIS-2 study designs, including full inclusion and exclusion criteria, have been previously described [20, 21] and are briefly summarized in Table 1. Both studies were conducted in accordance with Good Clinical Practice guidelines and provisions of the Declaration of Helsinki. The institutional review board or ethics committee at each participating site approved the protocol and amendments, and written informed consent was obtained from all participants prior to enrollment. In brief, eligible patients had one of the following qualifying skin infections, as judged by the investigator: wound infection (e.g., from IV drug use or trauma), cellulitis, erysipelas, or major abscess (capped at ≤ 30% of randomly assigned patients) that had a contiguous surface area of ≥ 75 cm2 and exhibited clear evidence of erythema, edema, or induration, as well as evidence of inflammatory response. Wound infection was defined as an infection characterized by purulent drainage from a wound with surrounding erythema, edema, and/or induration extending ≥ 5 cm in the shortest distance from the peripheral margin of the wound; cellulitis/erysipelas was defined as a diffuse skin infection characterized by spreading areas of erythema, edema, and/or induration; and major abscess was defined as an infection characterized by a collection of pus within the dermis or deeper with surrounding erythema, edema, and/or induration extending ≥ 5 cm in the shortest distance from the peripheral margin of the abscess.

Table 1

Summary of OASIS-1 and OASIS-2 phase 3 randomized clinical trials

Study design	OASIS-1 (NCT02378480)	OASIS-2 (NCT02877927)
	Double-blind, 1:1 randomization	Double-blind, 1:1 randomization
Participant age	≥ 18 years	≥ 18 years
Qualifying infections	Wound infection, cellulitis/erysipelas, or major abscess	Wound infection, cellulitis/erysipelas, or major abscess
Treatment arms	Omadacycline: 100 mg IV q12h for two doses, followed by 100 mg IV every 24 h q24h Linezolid: 600 mg IV q12h Option to transition to 300 mg omadacycline orally q24h/linezolid 600 mg orally q12h after ≥ 3 days	Omadacycline: 450 mg orally once daily for two doses, then 300 mg orally once daily Linezolid 600 mg orally twice daily
Randomization	1:1	1:1
Study duration	7–14 days	7–14 days

Patient Population Classification and Subgroup Analyses

The modified intent-to-treat (mITT) population included all randomized patients without a baseline sole Gram-negative ABSSSI pathogen. The micro-mITT population included all patients in the mITT population who had at least one Gram-positive causative bacterial pathogen identified from the primary ABSSSI site. Clinically evaluable (CE) patients met protocol-specified criteria including a clinical response that was not indeterminate [19, 20]. The safety population included all patients who received at least one dose of the study drug. Safety was assessed based on adverse events (AEs) and standard clinical laboratory tests.

The primary efficacy endpoint for both OASIS-1 and -2 was early clinical response (ECR) in the mITT population, which defined success as survival with ≥ 20% reduction in lesion size at 48–72 h after the first dose of the study drug. The secondary endpoint was an investigator-assessed clinical response at the post-treatment evaluation (PTE) visit (assessed 7–14 days after the last dose of the study drug) in the mITT, CE, and micro-mITT populations. Clinical success at PTE was defined as survival with resolution of signs and symptoms of infection, such that further antibacterial therapy was not needed.

In this secondary analysis, participants in OASIS-1 and -2 were classified as PWID or non-PWID based on whether the patient reported the primary etiology of infection was due to IV drug use. Bacterial pathogens were identified from culture samples taken from the infection site or blood specimens. Treatment compliance was calculated as 100 × (number of IV doses and oral tablets actually received)/(number of IV doses and oral tablets expected).

Statistical Analysis

Efficacy endpoints of clinical response at ECR and PTE were analyzed for the mITT and CE-PTE populations. For each subgroup, the 95% confidence interval (CI) for the difference in success rates (omadacycline minus linezolid) was computed using the Miettinen–Nurminen method [22]. No formal statistical comparisons were made between PWID and non-PWID subgroups.

Results

Patient Demographics and Baseline Characteristics

In total, 1380 patients received at least one dose of the study drug (safety population) and were included in this secondary analysis: 822 in the PWID subgroup and 558 in the non-PWID subgroup (Fig. 1). Approximately 98%, 80%, and 74% of patients qualified for the mITT, CE, and micro-mITT populations, respectively. Patient demographics and baseline characteristics of the safety population are presented in Table 2. Both PWID and non-PWID were predominately male and white. In general, the PWID population was younger, and had lower body mass index, higher rates of liver disease and elevated liver transaminases, and lower rates of chronic conditions such as diabetes and hypertension than the non-PWID population. In the non-PWID subgroup, more patients randomized to omadacycline (28.3%) than linezolid (16.0%) had elevated liver enzymes at baseline. In the PWID subgroup, 21.0% had a medical history of prior skin infection compared with 7.4% in the non-PWID.

Fig. 1

Subject disposition. CE clinically evaluable, mITT modified intention-to-treat, micro-mITT all mITT subjects with ≥ 1 Gram-positive causative pathogen at baseline, PWID persons who inject drugs

Table 2

Patient baseline demographics and characteristics (safety population)

	PWID (n = 822)			Non-PWID (n = 558)
	Omadacycline (n = 411)	Linezolid (n = 411)	All (n = 822)	Omadacycline (n = 280)	Linezolid (n = 278)	All (n = 558)
Mean age (SD)	41.7 (11.5)	42.4 (11.3)	42.0 (11.4)	49.1 (16.4)	50.1 (16.6)	49.6 (16.5)
Sex, n (%)
Female	136 (33.1)	140 (34.1)	276 (33.6)	110 (39.3)	116 (41.7)	226 (40.5)
Male	275 (66.9)	271 (65.9)	546 (66.4)	170 (60.7)	162 (58.3)	332 (59.5)
Categorical BMI (kg/m2), n (%)
n	411	411	822	280	277	557
< 25	178 (43.3)	170 (41.4)	348 (42.3)	82 (29.3)	75 (27.1)	157 (28.2)
25–30	137 (33.3)	147 (35.8)	284 (34.5)	84 (30.0)	96 (34.7)	180 (32.3)
> 30	96 (23.4)	94 (22.9)	190 (23.1)	114 (40.7)	106 (38.3)	220 (39.5)
Race, n (%)
White	368 (89.5)	382 (92.9)	750 (91.2)	253 (90.4)	259 (93.2)	512 (91.8)
Non-white	43 (10.5)	29 (7.1)	72 (8.8)	27 (9.6)	19 (6.8)	46 (8.2)
Comorbidities, n (%)a
Diabetes	4 (1.0)	8 (1.9)	12 (1.5)	34 (12.1)	59 (21.2)	93 (16.7)
Liver diseaseb	186 (45.3)	196 (47.7)	382 (46.5)	21 (7.5)	23 (8.3)	44 (7.9)
Liver enzyme elevation	135 (33.0)	114 (27.7)	249 (30.3)	79 (28.3)	44 (16.0)	123 (22.0)
Hypertension	50 (12.2)	55 (13.4)	105 (12.8)	71 (25.4)	85 (30.6)	156 (28.0)
Prior skin infection, n (%)	83 (20.0)	89 (21.9)	172 (21.0)	13 (5.0)	26 (9.8)	39 (7.4)
Creatinine clearance,c n (%)	409	410	819	279	274	553
< 60 mL/min	2 (0.5)	7 (1.7)	9 (1.1)	19 (6.8)	14 (5.1)	33 (6.0)
60–89 mL/min	29 (7.1)	20 (4.9)	49 (6.0)	35 (12.5)	31 (11.3)	66 (11.9)
> 89 mL/min	378 (92.4)	383 (93.4)	761 (92.9)	225 (80.6)	229 (83.6)	454 (82.1)
Lesion size, n (%)
≤ 300 cm2	164 (39.9)	179 (43.6)	343 (41.7)	166 (59.3)	163 (58.6)	329 (59.0)
> 300–600 cm2	154 (37.5)	156 (38.0)	310 (37.7)	75 (26.8)	68 (24.5)	143 (25.5)
> 600–1000 cm2	70 (17.0)	55 (13.4)	125 (15.2)	17 (6.1)	17 (6.1)	34 (6.1)
> 1000 cm2	23 (5.6)	21 (5.1)	44 (5.4)	22 (7.9)	30 (10.8)	52 (9.3)
Body temperature, n (%)
< 36 °C	4 (1.0)	5 (1.2)	9 (1.1)	2 (0.7)	2 (0.7)	4 (0.7)
36 to ≤ 38 °C	403 (98.1)	403 (98.1)	806 (98.1)	198 (70.7)	193 (69.4)	391 (70.1)
> 38 °C	4 (1.0)	3 (0.7)	7 (0.9)	80 (28.6)	83 (29.9)	163 (29.2)
White blood cell count, n (%)	405	407	812	274	273	547
≤ 4000 cells/mm3	6 (1.5)	2 (0.5)	8 (1.0)	2 (0.7)	2 (0.7)	4 (0.7)
> 4000 to < 10,000 cells/m3	141 (34.8)	171 (42.0)	312 (38.4)	108 (39.4)	105 (38.5)	213 (38.9)
≥ 10,000 cells/mm3	258 (63.7)	234 (57.5)	492 (60.6)	164 (59.9)	166 (60.8)	330 (60.3)

BMI body mass index, PWID persons who inject drugs, SD standard deviation

a10 patients (1.1%) in the PWID group and 42 (7.5%) in the non-PWID group had heart disease

bDefined as (chronic) hepatitis B, (chronic) hepatitis C, hepatic steatosis, alcoholic liver disease, hepatic cirrhosis, non-alcoholic steatohepatitis, or hepatic failure

cCalculated using the Cockcroft–Gault formula

Baseline Infections and Pathogens in the Micro-mITT Population

Wound infections were reported more frequently in the PWID subgroup (72.7%) than the non-PWID (19.0%) subgroup (Table 3). Cellulitis/erysipelas and major abscess were reported by 44.0% and 37.0% of participants in the non-PWID subgroup, and by 5.4% and 21.9% in the PWID group, respectively. Median lesion size in PWID and non-PWID was 341 cm2 (range 78–2601) and 248 cm2 (75–6739), respectively. Non-PWID presented with fever more frequently than PWID (29% vs. < 1%). In total, 88.7% (133/150) and 70.7% (87/123) of patients with major abscesses underwent incision and drainage in the PWID and non-PWID subgroups, respectively. In patients from whom a pathogen could be isolated, monomicrobial Gram-positive infection predominated in all infection types (Table 3). Gram-positive aerobes were the most common pathogen types at baseline, isolated from 96.9% of all patients (Table 3). S. aureus was the most common baseline pathogen, isolated from 74% of patients in the PWID and non-PWID subgroups; methicillin-susceptible S. aureus (MSSA) infections occurred in greater number than MRSA infections in both groups. The Streptococcus anginosus group was identified in 25% of PWID but only 5% of non-PWID. Group A Streptococcus (S. pyogenes) was an infrequent cause of infections (4.8% PWID; 6.6% non-PWID). Gram-positive and Gram-negative anaerobes were each identified in ≤ 10% of infections in both PWID and non-PWID in the micro-mITT population (Table 4).

Table 3

Most frequently occurring baseline infection types in the subgroups (micro-mITT population)

Infection type	PWID (n = 686)			Non-PWID (n = 332)
	Omadacycline (n = 347)n (%)	Linezolid (n = 339)n (%)	All (n = 686)n (%)	Omadacycline (n = 157)n (%)	Linezolid (n = 175)n (%)	All (n = 332)n (%)
Wound infection	252 (72.6)	247 (72.9)	499 (72.7)	26 (16.6)	37 (21.1)	63 (19.0)
Monomicrobial Gram-positive infection	158 (62.7)	178 (72.1)	336 (67.3)	14 (53.8)	26 (70.3)	40 (63.5)
Polymicrobial Gram-positive infection	51 (20.2)	32 (13.0)	83 (16.6)	5 (19.2)	5 (13.5)	10 (15.9)
Polymicrobial mixed infection	43 (17.1)	37 (15.0)	80 (16.0)	7 (26.9)	6 (16.2)	13 (20.6)
Major abscess	72 (20.7)	78 (23.0)	150 (21.9)	67 (42.7)	56 (32.0)	123 (37.0)
Monomicrobial Gram-positive infection	51 (70.8)	57 (73.1)	108 (72.0)	47 (70.1)	47 (84.0)	94 (76.4)
Polymicrobial Gram-positive infection	13 (18.1)	16 (20.5)	29 (19.3)	11 (16.4)	5 (8.9)	16 (13.0)
Polymicrobial mixed infection	8 (11.1)	5 (6.4)	13 (8.7)	9 (13.4)	4 (7.1)	13 (10.6)
Cellulitis/erysipelas	23 (6.6)	14 (4.1)	37 (5.4)	64 (40.8)	82 (46.9)	146 (44.0)
Monomicrobial Gram-positive infection	19 (82.6)	12 (85.7)	31 (83.8)	51 (79.7)	63 (76.8)	114 (78.1)
Polymicrobial Gram-positive infection	3 (13.0)	0	3 (8.1)	8 (12.5)	6 (7.3)	14 (9.6)
Polymicrobial mixed infection	1 (4.3)	2 (14.3)	3 (8.1)	5 (7.8)	13 (15.9)	18 (12.3)

mITT modified intention-to-treat, PWID persons who inject drugs

Table 4

Baseline pathogen types in the subgroups (micro-mITT population)

Pathogen typea	PWID (n = 686)			Non-PWID (n = 332)
	Omadacycline (n = 347)n (%)	Linezolid (n = 339)n (%)	All (n = 686)n (%)	Omadacycline (n = 157)n (%)	Linezolid (n = 175)n (%)	All (n = 332)n (%)
Gram-positive aerobes	338 (97.4)	328 (96.8)	666 (97.1)	152 (96.8)	169 (96.6)	321 (96.7)
Staphylococcus aureus	257 (74.1)	256 (75.5)	513 (74.8)	119 (75.8)	128 (73.1)	247 (74.4)
MRSA	110 (31.7)	100 (29.5)	210 (30.6)	63 (40.1)	57 (32.6)	120 (36.1)
MSSA	150 (43.2)	160 (47.2)	310 (45.2)	58 (36.9)	72 (41.1)	130 (39.2)
Streptococcus pyogenes	24 (6.9)	15 (4.4)	39 (5.7)	16 (10.2)	19 (10.9)	35 (10.5)
Streptococcus anginosus group	96 (27.7)	73 (21.5)	169 (24.6)	8 (5.1)	9 (5.1)	17 (5.1)
Streptococcus anginosus	31 (8.9)	23 (6.8)	54 (7.9)	4 (2.5)	4 (2.3)	8 (2.4)
Streptococcus intermedius	32 (9.2)	40 (11.8)	72 (10.5)	3 (1.9)	2 (1.1)	5 (1.5)
Streptococcus constellatus	33 (9.5)	18 (5.3)	51 (7.4)	1 (0.6)	3 (1.7)	4 (1.2)
Enterococcus faecalis	3 (0.9)	4 (1.2)	7 (1.0)	15 (9.6)	21 (12.0)	36 (10.8)
Gram-positive anaerobes	22 (6.3)	24 (7.1)	46 (6.7)	11 (7.0)	8 (4.6)	19 (5.7)
Gram-negative aerobesb	37 (10.7)	32 (9.4)	69 (10.1)	15 (9.6)	21 (12.0)	36 (10.8)
Escherichia coli	5 (1.4)	0 (0.0)	5 (0.7)	1 (0.6)	4 (2.3)	5 (1.5)
Klebsiella pneumoniae	9 (2.6)	9 (2.7)	18 (2.6)	2 (1.3)	2 (1.1)	4 (1.2)
Gram-negative anaerobesb	21 (6.1)	19 (5.6)	40 (5.8)	7 (4.5)	6 (3.4)	13 (3.9)

mITT modified intention-to-treat, MRSA methicillin-resistant Staphylococcus aureus, MSSA methicillin-susceptible Staphylococcus aureus, PWID persons who inject drugs

aPatients may have had more than one pathogen at baseline

bPatients with a sole Gram-negative infection were excluded from the study, therefore patients represented in the Gram-negative rows are those with mixed infections. Includes Citrobacter koseri, Enterobacter aerogenes, Enterobacter cloacae, Escherichia coli, Escherichia vulneris, Klebsiella oxytoca, Klebsiella pneumoniae, Pantoea agglomerans, Proteus mirabilis, Raoultella planticola, and Serratia marcescens

Patient Disposition and Study Treatment Exposure

In total, 711/822 (86.5%) patients in the PWID subgroup and 516/558 (92.5%) patients in the non-PWID subgroup completed the study. In the PWID subgroup, reasons for study discontinuation (59/822 patients; 7.2%) included loss to follow-up (44/822; 5.4%) and withdrawal by patient (15/822; 1.8%). In the non-PWID subgroup, reasons for study discontinuation (17/558; 3.0%) included loss to follow-up (10/558; 1.8%), withdrawal by patient (6/558; 1.1%), and physician decision (1/558; 0.2%). Mean compliance with study drug was 98.4% in PWID and 98.8% in non-PWID, with similar rates observed in each treatment arm.

Most patients in both subgroups received treatment for 9–14 days. In the PWID subgroup, mean (standard deviation) treatment durations were 8.2 (2.7) and 8.0 (2.8) days for omadacycline and linezolid, respectively. In the non-PWID subgroup, mean (standard deviation) treatment durations were 9.3 (2.9) and 9.2 (3.0) days for omadacycline and linezolid, respectively.

Clinical Efficacy (mITT and CE-PTE Populations)

Clinical success rates exceeded 80% at ECR and PTE in the mITT population, and exceeded 90% at PTE in the CE-PTE population for both PWID and non-PWID receiving either omadacycline or linezolid (Fig. 2). In the non-PWID subgroup, the clinical success rate at PTE was higher for omadacycline than linezolid in the mITT (92.0% vs. 85.3%; 95% CI 1.3–12.3) and CE (97.8% vs. 94.3%; 95% CI 0.2–8.0) populations. The number of indeterminates in the PWID subgroup was 13.6% in the omadacycline group and 12.6% in the linezolid group. In the non-PWID subgroup, 3.5% in the omadacycline and 6.9% in the linezolid groups were classified as indeterminate.

Fig. 2

Clinical success at ECR and PTE endpoints in the subgroups (mITT and CE-PTE populations). CE clinically evaluable, CI confidence interval, ECR early clinical response, mITT modified intention-to-treat, PTE post-treatment evaluation, PWID persons who inject drugs

When assessed by individual study, clinical success rates across treatments were high in both studies. For PWID, clinical success rates at PTE were 79.1% and 81.2% in the mITT population and 94.2% and 96.7% in the CE-PTE population, in OASIS-1 and -2, respectively, whereas for non-PWID, clinical success rates at PTE were 91.0% and 85.4% in the mITT population and 95.6% and 96.7% in the CE-PTE population, in OASIS-1 and -2, respectively.

Clinical Response Per Baseline Pathogen and Pathogen Mix (Micro-mITT Population)

Clinical success rates by pathogen mix were ≥ 75% for both treatments in the PWID and non-PWID groups, with the exception of omadacycline for polymicrobial mixed infections in the PWID group (73.1%) (Table 5). In PWID with baseline S. aureus infections, rates of clinical success were 86.5% and 85.9% for omadacycline and linezolid, respectively, with similar rates of clinical success in patients with baseline MRSA or MSSA infections. In non-PWID, rates of clinical success for S. aureus were 89.9% and 80.5% for omadacycline and linezolid, respectively; however, in patients with MRSA, clinical success rates were 90.5% and 75.4%, respectively.

Table 5

Clinical success at PTE by baseline pathogen mix (micro-mITT population)

Baseline pathogen mix	PWID (n = 686)				Non-PWID (n = 332)				All patients (n = 1018)
	Omadacycline (n = 347)		Linezolid (n = 339)		Omadacycline (n = 157)		Linezolid (n = 175)		PWID (n = 686)		Non-PWID (n = 332)
	n	Clinical success (n, %)	n	Clinical success (n, %)	n	Clinical success (n, %)	n	Clinical success (n, %)	n	Clinical success (n, %)	n	Clinical success (n, %)
Monomicrobial Gram-positive infection	228	189 (82.9)	247	199 (80.6)	112	103 (92.0)	136	113 (83.1)	475	388 (81.7)	248	216 (87.1)
Polymicrobial Gram-positive infection	67	53 (79.1)	48	36 (75.0)	24	19 (79.2)	16	12 (75.0)	115	89 (77.4)	40	31 (77.5)
Polymicrobial Mixed (Gram-positive and Gram-negative) infection	52	38 (73.1)	44	34 (77.3)	21	20 (95.2)	23	19 (82.6)	96	72 (75.0)	44	39 (88.6)

mITT modified intention-to-treat, PTE post-treatment evaluation, PWID persons who inject drugs

Safety

Rates of severe or serious treatment-emergent AEs (TEAEs), discontinuation due to TEAEs, or death were infrequent (Table 6). Nausea and vomiting were frequently reported TEAEs for both PWID and non-PWID. Patients receiving omadacycline in both the PWID and non-PWID subgroups had higher numbers of TEAEs due to greater incidence of nausea and vomiting compared with patients receiving linezolid. TEAEs of increased liver transaminases were similar by treatment group in both PWID and non-PWID subgroups. Alanine transaminase increases post-baseline to > 3 × ULN were similar for omadacycline and linezolid in PWID (5.5% vs. 5.6%) and higher for omadacycline in non-PWID (3.6% vs. 1.9%). No patients met the criteria for Hy’s law. Skin infection TEAEs of wound infection and cellulitis were more common in PWID than non-PWID.

Table 6

Safety overview in the PWID and non-PWID subgroups (safety population)

	PWID (n = 822)		Non-PWID (n = 558)
	Omadacycline (n = 411)	Linezolid (n = 411)	Omadacycline (n = 280)	Linezolid (n = 278)
Participants with ≥ 1 TEAE (n, %)	232 (56.5)	189 (46.0)	121 (43.2)	95 (34.2)
Drug-related TEAE (n, %)	108 (26.3)	61 (14.8)	51 (18.2)	26 (9.4)
Severe TEAE (n, %)	3 (0.7)	4 (1.0)	2 (0.7)	7 (2.5)
Serious TEAE (n, %)	5 (1.2)	3 (0.7)	0 (0.0)	4 (1.4)
Drug-related serious TEAE (n, %)	0 (0.0)	0 (0.0)	0 (0.0)	0 (0.0)
TEAE leading to discontinuation (n, %)	5 (1.2)	5 (1.2)	3 (1.1)	1 (0.4)
Serious TEAE leading to death (n, %)	0 (0.0)	1 (0.2)	0 (0.0)	2 (0.7)
Nausea	108 (26.3)	43 (10.5)	43 (15.4)	17 (6.1)
Vomiting	58 (14.1)	17 (4.1)	21 (7.5)	10 (3.6)
Wound infection	26 (6.3)	21 (5.1)	4 (1.4)	1 (0.4)
Cellulitis	24 (5.8)	18 (4.4)	3 (1.1)	6 (2.2)
AST increased	19 (4.6)	21 (5.1)	6 (2.1)	3 (1.1)
ALT increased	18 (4.4)	22 (5.4)	10 (3.6)	3 (1.1)
Headache	12 (2.9)	12 (2.9)	11 (3.9)	9 (3.2)
Diarrhea	11 (2.7)	10 (2.4)	11 (3.9)	10 (3.6)

ALT alanine transaminase, AST aspartate transaminase, PWID persons who inject drugs, TEAE treatment-emergent adverse event

Discussion

The results of this analysis indicate that PWID can be successfully treated with the same therapy regimens as non-PWID, despite differences in patient and disease characteristics. The PWID group included more patients with a prior ABSSSI, more wound infections at baseline, more S. anginosus group identification, and higher AEs of subsequent skin infections likely due to IV drug injection practices. PWID had low treatment and study discontinuation levels (i.e., adherence), suggesting that perceived behaviors associated with IV drug use did not have a substantial impact on the efficacy outcomes. Similar findings have been observed in other studies involving ABSSSI in PWID [2, 23–25], which suggest that PWID can be treated in a similar manner to non-PWID. Therefore, PWID can be transitioned to oral therapy and discharged from inpatient care following achievement of ECR (as in OASIS-1), or be treated with oral-only therapy in the community (as in OASIS-2) [20, 26, 27].

In the current studies, compliance rates were very high and similar in PWID and non-PWID. PWID may benefit from increased engagement, follow-up, and access to care, as well as preventive interventions to reduce the need for hospitalization and emergency care, and to maximize treatment adherence [17, 28]. This could include the provision of primary care medical services for early identification of lesions and treatment of patients within the community, rather than requiring hospital admission [29, 30]. In one study that used a “package intervention” approach to facilitate treatment of PWID in an outpatient setting, 97% of patients were compliant with the entire duration of therapy [17].

Rates of clinical success for patients receiving omadacycline and linezolid in PWID and non-PWID were both high for the ECR and PTE endpoints. Either omadacycline or oxazolidinones may be considered for ABSSSI treatment in PWID. Omadacycline’s spectrum of activity, including its activity against MRSA and clinical response rates, suggests a role in the empiric treatment of PWID with any ABSSSI infection types [31]. The availability of both IV and oral formulations of omadacycline may be beneficial for treatment decisions in the emergency department for PWID, where patients often seek initial care. The prevalence of co-existing mental health comorbidities in PWID and in the general population [32], and widespread use of selective serotonin reuptake inhibitors, require alternatives to oxazolidinone antimicrobials in PWID and non-PWID populations.

Omadacycline was safe and well tolerated, regardless of PWID status. Nausea and vomiting were the most frequently occurring TEAEs in the subgroups, which is consistent with other studies using tetracyclines [33]. The increased rates of nausea and vomiting were generally associated with the 450-mg loading dose of omadacycline during the first 2 days of the oral-only OASIS-2 study, which then decreased after transition to the maintenance dose [19]. The rates for nausea and vomiting were greater in the PWID subgroup, suggesting that a population characteristic (e.g., continued drug use, withdrawal) may have had an additive effect on the nausea and vomiting incidence. Liver AEs were similar by treatment group in the PWID and non-PWID subgroups, despite greater baseline and post-baseline liver transaminase elevations in the non-PWID omadacycline treatment group.

Limitations

Limitations of this subgroup analysis involving PWID are similar to those previously described for the individual OASIS-1 and -2 studies [20, 21]. As this was an analysis of two randomized, controlled trials, selection of patients and therefore treatment adherence, compliance, and outcomes observed within the clinical trial setting may differ from those observed in real-world situations. Additionally, this secondary post hoc analysis had no inferential testing and was not powered to determine whether true differences existed between treatment groups or between PWID and non-PWID. Baseline pathogen identification used rigorous collection methods but could have identified a non-pathogen given the site of infection. However, the high monomicrobial Gram-positive identification, in particular the high rate of S. aureus, is consistent with our prior understanding of the etiology of ABSSSI. Finally, it is possible that an infection could be of mixed type and potentially misclassified; however, investigators were provided with infection type definitions and were instructed to classify each infection according to its predominant type.

Conclusions

Although IV drug use can create challenges in the treatment of ABSSSI, the results of this study indicate that IV or oral omadacycline can be successfully used in PWID, with high rates of clinical success and good tolerability, and may be helpful in shortening or preventing hospitalization in PWID with ABSSSI. Additional studies are warranted to determine the optimal management and cost-effectiveness of treating ABSSSI in PWID in both inpatient and outpatient settings.

Acute bacterial skin and skin structure infections (ABSSSI) are frequent complications of intravenous drug use in persons who inject drugs (PWID)

This study assessed the efficacy and safety of omadacycline versus linezolid for treatment of ABSSSI in PWID and persons who do not inject drugs in the Phase 3 OASIS-1 and OASIS-2 studies

Rates of clinical success were high for omadacycline and linezolid, and both drugs were well tolerated, regardless of PWID status

Although intravenous drug use can create challenges in the treatment of ABSSSI, clinical response rates were high and the drugs were well tolerated in PWID and non-PWID subgroups in this study, whether treated initially with intravenous or oral regimens