key: cord-0003540-cpl7zf7f
authors: Provoost, Judith; Valour, Florent; Gamondes, Delphine; Roux, Sandrine; Freymond, Nathalie; Perrot, Emilie; Souquet, Pierre-Jean; Kiakouama-Maleka, Lize; Chidiac, Christian; Lina, Gérard; Dumitrescu, Oana; Sénéchal, Agathe; Ader, Florence
title: A retrospective study of factors associated with treatment decision for nontuberculous mycobacterial lung disease in adults without altered systemic immunity
date: 2018-12-14
journal: BMC Infect Dis
DOI: 10.1186/s12879-018-3559-x
sha: a5fdb40f1b5bddf4ab24efaddedc40d441e3a130
doc_id: 3540
cord_uid: cpl7zf7f

BACKGROUND: Nontuberculous mycobacteria (NTM) lung diseases are increasingly recognized as chronic opportunistic infections, occurring in individuals with a wide variety of underlying conditions. In the absence of systemic immunodeficiency, decision of NTM lung disease treatment must relies on a careful risk/benefit assessment, given the requirement of long-term administration of multidrug therapies supported by limited evidence. The primary objective was to identify the factors associated with anti-NTM treatment initiation. Clinical and radiological outcome upon treatment were studied. METHODS: This retrospective, single center study (2013–2016, 45 months) addressed the criteria supporting treatment decision among adults with NTM lung disease without systemic immunodeficiency at our institution, with the assigned goal to harmonize the practice. All patients matched the current international definitions of NTM lung disease according to the American Thoracic Society criteria. Factors associated with anti-NTM treatment were investigated by conditional logistic regression. Clinical and radiological outcomes of treated and untreated NTM-disease cases were examined. Mortality rate was assessed. An expert radiologist conducted a blinded computed tomography (CT)-scan review of the treated and untreated patients. RESULTS: Among 51 cases of NTM lung diseases, 25 (49%) received anti-NTM treatment. In univariate analysis, a body mass index (BMI) < 18 kg/m(2) (odds ratio (OR), 4.2 [95% confidence interval (CI) 1.2–15.2]; p = 0.042), hemoptysis (OR, 11.8 [95% CI 1.35–12.9]; p = 0.026), excavation(s) (OR, 4.8 [95% CI 1.4–16.4], p = 0.012), prior anti-NTM treatment (OR, 5.65 [95% CI 1.06–29.9]; p = 0.042), Aspergillus spp. co-infection (OR, 6.3 [95% CI 1.8–22.2]; p = 0.004) were associated with treatment initiation. In multivariate analysis, Aspergillus spp. co-infection was the only independent determinant of treatment initiation (OR, 5.3 [95% CI 1.1–25.4]; p = 0.036). Twenty-one (81%) patients received ≥3 anti-NTM drugs. Median treatment duration and follow-up were 36.3 (interquartile range [IQR], 13.1–64.4) weeks and 17.1 (IQR, 8.7–27.1) months, respectively. Regarding radiological outcome, 85 CT-scans were reviewed, showing similar rates of regression or stabilization in treated and untreated patients. Overall mortality rate was not different in treated and untreated patients. CONCLUSION: The most relevant variable associated with anti-NTM treatment initiation was Aspergillus spp. co-infection. Radiological regression or stabilization of pulmonary lesions was not different between the treated and untreated patients.

Nontuberculous mycobacteria (NTM) are ubiquitous bacteria of environmental origin including a widely diverse number of species (> 160), some of which cause disease in humans [1] [2] [3] . Prevalence of NTM lung diseases is unexpectedly increasing in industrialized countries, as consistently uncovered by recent studies [3, 4] . The key issue remains to determine whether NTM are the true and single promoter of an evolving lung disease or chronic airway colonizers, among others. To standardize the diagnosis of NTM lung disease, the guidelines for NTM diagnosis of the American Thoracic Society (ATS)/Infectious Disease Society of America (IDSA) and the British Thoracic Society (BTS) require isolation and growth of the same NTM strain on at least two separate samples from the patient [5, 6] .

Human host and pathogenic NTM relationship is still poorly understood, as NTM virulence is highly variable from one species to another. NTM lung disease is strongly associated with pre-existing pulmonary conditions such as chronic obstructive pulmonary disease (COPD), cystic fibrosis, idiopathic bronchiectasis, prior active tuberculosis or pneumoconiosis [6] . It is also frequently associated with genetic or acquired systemic immune deficiency such as defects in the pathways of inflammatory cytokines interleukin (IL)-12, tumor necrosis factor (TNF)-α or interferon (IFN)-γ, immunosuppressive treatments (including anti-TNF-α therapy or corticosteroids), solid-organ transplantation, or acquired immune deficiency syndrome (AIDS)/human immunodeficiency virus (HIV) infection [1] [2] [3] [4] [5] [6] [7] . However, it may also occur in individuals without recognized severe immune local or systemic deficiency. In the absence of patent predisposition, NTM diseases are overrepresented among the specific morphotype of slender women with a low body fat [8] .

Treatment decision for NTM lung disease is challenging. There is debate as to which patients should benefit the most from treatment according to medical background, comorbidities, clinical status, radiologic features and causal NTM strain. Assessment of clinical, microbiologic, and radiologic response to treatment is not standardized as well. We focused on NTM lung diseases in adults without systemic immunodeficiency that met the ATS criteria guidelines. Based on the comparison of a group of treated and untreated patients, the primary objective was to identify the factors associated with physician decision of initiating anti-NTM treatment. Secondary objectives were to study the outcome upon treatment and to propose a standardized evaluation for the diagnosis and decision making to treatment of NTM lung diseases in adults without systemic immunodeficiency.

We conducted a retrospective, observational, single-center study between January 2013 and February 2016 (45 months) among adults (≥ 18 year-old) without systemic immunosuppression presenting NTM lung disease. Exclusion criteria were HIV infection, cystic fibrosis, primary ciliary dyskinesia, active malignant disease, solid-organ transplantation or ongoing immunosuppressant treatments such as TNF inhibitor or high-dose corticosteroid (≥ 1 mg/kg more than 21 days). Case identification was based on cross-referencing the databases of the mycobacteria laboratory and the departments of infectious and pulmonary diseases. Patients eligible for inclusion in the NTM lung disease cohort were those who matched the criteria previously defined by the ATS/IDSA and the BTS guidelines with the minimum requirement of clinical and microbiologic following criteria: (i) pulmonary symptoms associated with multifocal bronchiectasis with multiple small nodules on computed tomography (CT)-scan; (ii) proper exclusion of other diagnoses; (iii) NTM-positive culture results from at least two separate expectorated sputum samples or a NTM-positive culture result from at least one bronchial wash or lavage [5, 6] . Patients' characteristics at diagnosis were collected in order to perform analysis on 146 selected variables: demographics; history of predisposing factors; underlying pulmonary diseases; comorbidities; pulmonary function testing; respiratory bacterial or mycological co-infection(s), which definition was similar to NTM criteria, namely positive culture isolation of the same species from at least two separate expectorated sputum samples or a positive culture result from at least one bronchial wash or lavage; immunologic status; nutritional status; clinical features; microbiologic assessment through identification of NTM species on positive NTM cultures and sample culture conversions; radiologic features on high-resolution CT-scans (fibrocavitary disease or nodular/bronchiectasis disease); prior treatment for NTM lung disease, treatment combination and duration; outcome. Because of the retrospective observational nature of the study and the lack of any modification in patients' management, the need for informed consent was waived with the authorization of the Ethics Committee of Lyon University Hospital (Comité d'Ethique, Hospices Civils de Lyon), which approved the study under the number 17-207.

An independent expert chest radiologist, blinded to the patient information, retrospectively reviewed the CT-scans performed without injection of intravenous contrast media, assigned in random order at diagnosis and six to 24 months after treatment or during the follow up of the untreated patients. The number and size of cavity(ies) and their wall thickness were evaluated in the lung window setting. Nodular opacity(ies) (≥ 10 mm), cluster(s) of small nodules (≤ 5 mm), the tree-in-bud pattern, the presence of bronchiectasis in any of the lobes or multifocal bronchiectasis were evaluated. Based on the number and size of the lesions, the expert classified the lesions as improved, stable or worsening.

The primary endpoint was to identify the factors significantly involved in the decision of initiating anti-NTM treatment by patient referent physician. Secondary endpoints were the assessment of clinical and radiological outcomes upon anti-NTM treatment in comparison with no treatment. Based on these findings, a standardized appraisal was proposed to assist diagnosis management and treatment decision for NTM lung diseases in adults without altered systemic immunity.

Descriptive data were used to estimate the frequencies of the study variables. There were expressed as count (percentage, %) for dichotomous variables and as medians (interquartile range [IQR]) for continuous values. The number of missing values was excluded from the denominator. Non-parametric statistical methods Fisher exact test, χ2 test and Mann-Whitney U test were used to compare groups, where appropriate. The probability of treatment initiation over time was evaluated by Kaplan-Meier survival curve analysis, with group comparison using the log-rank (Mantel-Cox) test. Stepwise binary logistic regression analysis was used to assess the determinants for treatment initiation, expressed as odd ratios (OR) with 95% confidence intervals (95% CI). After checking the variables for interactions, variables with medical meaning and with p-values obtained in the univariate analysis of < 0.15 were included in the final multivariate model. A value of p < 0.05 was considered significant. All analyses were performed using SPSS software version 24.0 (SPSS. Chicago. IL).

Out of 149 patients eligible to ATS/IDSA NTM lung disease criteria, 51 patients were included in the study, of who 25 (49%) received and 26 (51%) did not receive anti-NTM treatment (Fig. 1 ). The median age was 68 (interquartile range [IQR], 59-75) year-old with a male/ female ratio of 0.76. Etiologic NTM agents were Mycobacterium avium (n = 17, 33.3%), M. chimaerae (n = 14, 27.5%), M. xenopii (n = 9, 17.6%), M. intracellulare (n = 9, 17.6%), M. simiae (n = 3, 5.9%), M. kansasii (n = 1, 2%), and M. abscessus (n = 1, 2%), with three patients having ≥2 concomitant NTM lung diseases. Importantly, the evidence of NTM lung disease has led to diagnose six underlying chronic lung diseases, of which a genetically documented cystic fibrosis in a 61 year-old women. On descriptive analysis, patient's characteristics did not significantly differ, to the exception of a lower BMI (p = 0.023) and a higher number of previously known NTM lung disease (p = 0.038) in treated versus untreated patients (Table 1) . Notable percentages of missing data at diagnosis have to be acknowledged for active tobacco smoking (64.7%, n = 33), respiratory functional testing (23.5%, n = 12) with a very few patients having a 6-min walk test, baseline arterial blood oxygenation levels (58.8%, n = 30), CT-scan follow up within 24 months after diagnosis in untreated patients (46%, n = 12).

Factors leading the patient referent physician to initiate anti-NTM treatment were assessed using bivariate analysis. Table 3 ). The probability of treatment initiation over time according to the presence or not of targeted variables was investigated. The probability was significantly higher in case of BMI < 18 vs. > 18 kg/m 2 (p = 0.006), of hemoptysis vs. no hemoptysis (p = 0.009), of Aspergillus spp. co-infection vs. no co-infection (p = 0.029), of pulmonary excavation(s) vs. no excavation (p = 0.005) (Fig. 2a, b, c and d, respectively) . (Table 2) . Finally, all-cause mortality was not different between treated and untreated groups, although lost to follow-up was high in the untreated group (n = 10, 38.5%). Regarding the four patients that deceased (n = 3 in the treated group and n = 1 in the untreated group), the cause of mortality was linked to the underlying diseases rather than NTM-related mortality.

In the present study, treated patients were characterized by BMI < 18 kg/m 2 , presence of hemoptysis and excavation(s), Aspergillus spp. co-infection, and prior anti-NTM treatment. Aspergillus spp. co-infection was the only independent factor associated with treatment initiation. A single study from five English centers has recently addressed the factors that influence anti-NTM treatment initiation using similar retrospective design of treated and untreated cohort comparison inclusion criteria which allowed non-AIDS/HIV immunosuppressed patients (36 and 33% in the treated and untreated subsets, respectively) to be evaluated. In the multivariate analysis, patients had increased odds of anti-NTM treatment in case of cavitation on CT imaging, night sweats and weight loss [9] .

Here, three out of four criteria are part of guideline criteria leading to decision of anti-NTM treatment. They all reflect a degree of severity of NTM lung disease linked with progression of an impaired respiratory condition. The current problematic of NTM lung diseases shifts from distinguishing colonization from infection toward differentiating stable, poorly active vs. progressive active NTM disease, the latter being responsible for further structural lung damage(s). The risk/benefit analysis includes prescribing recommended long-term multidrug regimens with concerns over suboptimal cure rates and frequently reported drug-related side effects. To support these arguments, others have already shown that physician ATS/IDSA guideline [10] . Another study conducted in France has shown that among a cohort of 31 NTM lung diseases, only 12 (38.7%) received appropriate treatment matching ATS/IDSA guidelines [11] . Inappropriate prescriptions were mostly related to shorter treatment duration (6 months or less) and/or off-recommendation regimen, particularly those excluding macrolide from the combination or those using a single-drug macrolide regimen [10, 11] . It has to be acknowledged that guidelines specify that treatment for MAC-associated lung disease in HIV-negative individuals can be a three-times-weekly drug regimen upon culture conversion while on therapy for 1 year, which may favor treatment compliance [5, 12, 13] . Patients with bronchiectasis and NTM lung disease have a higher prevalence of being sensitized to Aspergillus than patients with NTM-free bronchiectasis [12] . Allergic airway manifestations in response to Aspergillus are termed Aspergillus-related lung diseases with a spectrum going from Aspergillus-induced hypersensitivity to the severe allergic bronchopulmonary aspergillosis (ABPA) [14] . By itself, the coexistence of NTM and Aspergillus in lung airway justifies the need for testing Aspergillus serology, total serum immunoglobulin (Ig)E and Aspergillus-specific IgE levels as well as mycological direct examination and culture of sputum or bronchial aspirates for presence of filamentous fungi in the diagnosis algorithm of patients with NTM lung diseases. Active co-infections with NTM and Aspergillus spp. have also been described, in which patients with NTM lung disease develop chronic forms of pulmonary aspergillosis which definitions and management have been revisited in recent updated guidelines [14] [15] [16] [17] .

Radiographic improvement may be hampered by concomitant lung disease and the limited potential for resolution of consolidated radiologic abnormalities. A previous study has investigated radiologic response to treatment showing consistent results with those found in the present study. Although anti-NTM treatment led to an improvement or stabilization of lesions for a majority of patients, these modifications were not significantly different from the untreated group who went through CT-scan follow up indicating that anti-NTM treatment did not lead to radiological abnormalities reversion [9] . The present study has strengths and limitations. The strength is the study of the largest cohort so far of NTM lung diseases in patients without systemic immunodeficiency with exhaustive data collection and blinded radiological assessment. We acknowledge the biases that contribute to mitigate conclusions from the study such as being conducted in a single center, the important differences in physician's management resulting in lack of consistency in treatment decision making, the number of missing data. In addition, the CT-scans were not performed at fixed intervals, particularly in the untreated subset of patients. Finally, treatment duration and outcome criteria were not standardized, which prevent to properly assess treatment efficacy. Useful consensus definitions for key outcome parameters to be used in the treatment of NTM lung diseases have been released very recently, which should harmonize data collection regarding NTM treatment [18] .

Future researches are necessary to better define criteria associated with progressive active NTM disease in the immunocompetent setting. Concretely, this preliminary study has led to implement in our institution a standardized appraisal for the diagnosis of NTM lung diseases in this particular setting ( Table 4 ). The aim is to provide a future basis for the development of a diagnosis scoring system supporting anti-NTM treatment decision. Future studies should focus as well on the most relevant CT imaging variables associated with response to treatment over time that may be applied in future clinical trials to assess treatment outcome.

In summary, the main factors supporting anti-NTM treatment decision in immunocompetent were low BMI, hemoptysis, lung excavation(s), prior anti-NTM treatment and Aspergillus pp. co-infection, the latter being the only independent factor. Anti-NTM treatment did not achieve radiological abnormalities reversion, as pulmonary lesions assessment showed no difference between the treated and the untreated patients. A diagnosis of NTM lung disease in an immunocompetent patient requires investigating the presence of a chronic pulmonary underlying disease. 

Pulmonary disease caused by non-tuberculous mycobacteria

Nontuberculous mycobacterial lung disease: the top ten essentials

Leveraging advances in tuberculosis diagnosis and treatment to address nontuberculous mycobacterial disease

Pulmonary nontuberculous mycobacterial disease prevalence and clinical features: an emerging public health disease

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Patients with nontuberculous mycobacterial lung disease exhibit unique body and immune phenotypes

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Are guidelines on the management of non-tuberculous mycobacteria lung infections respected and what are the consequences for patients? A French retrospective study from

Early results (at 6 months) with intermittent clarithromycin including regimens for lung disease due to Mycobacterium avium complex

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The authors gratefully acknowledge Pr Gilles Devouassoux for helpful insights.

No external funding was received for this study.

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request. 

Authors' contributions JP contributed to conception and design of the study, acquisition of the data, interpretation of the data, drafted the manuscript and approved the final version; FV carried out the statistical analysis, participated in revision of the paper for important intellectual content, and approved the final version; DG carried out the blinded review of 85 CT-scans with the examination of each imagery, she participated in revision of the paper for important intellectual content, and approved the final version; GL and OD are in charge of the Mycobacteria laboratory and have provided NTM strain identification and drug susceptibility tests. They participated in revision of the paper for important intellectual content, and approved the final version; SR, NF, EP, PJS, LKM, and CC contributed to acquisition of the data, revision of the paper for important intellectual content, and approved the final version; FA and AS are the project initiators, contributed to conception and design of the study, drafted the manuscript and approved the final version. FA coordinated the project until the submission of the article. All authors read and approved the final manuscript.

The Ethics Committee of Lyon University Hospital (Comité d'Ethique, Hospices Civils de Lyon) approved the study under the number 17-207. Because of the retrospective observational nature of the study and the lack of any modification in patients' management, the need for informed consent was waived with the authorization of the Ethics Committee of Lyon University Hospital (Comité d'Ethique, Hospices Civils de Lyon), which approved the study under the number 17-207.

Not applicable.

The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. No writing assistance was utilized in the production of this manuscript.

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.Author details 1 Département de Pneumologie, Hospices Civils de Lyon, Lyon, France.