Methods: The medical records of a total of 34 patients (24 males, 10 females; mean age: 55.4+13 years; range, 23 to 76 years) with malignant tracheobronchial fistulas treated with airway stenting between February 2014 and August 2020 were retrospectively analyzed. Data including demographic features, diagnosis, symptoms, treatment, complications and outcomes were recorded.
Results: Thirty-eight airway stents were inserted in 34 patients with malignant tracheobronchial fistulas, including 19 patients with malignant tracheobronchial esophageal fistulas and 15 patients with bronchopleural fistulas. The clinical success and the technical success rates were 91% and 100%, respectively. No perioperative death or severe complications occurred. Chronic complications (>24 h) occurred in eight (23%) patients with malignant tracheobronchial fistula. Median follow-up was 3.5 (range, 1.4 to 5.5) months in patients with malignant tracheobronchial esophageal fistulas and 18 (range, 9.5 to 26.5) months in patients with bronchopleural fistulas. Mortality rates were 79% and 61%, respectively.
Conclusion: Airway stent insertion provides a secure and effective treatment for patients with malignant tracheobronchial fistulas.
In the present study, we aimed to evaluate the efficacy, tolerance, and safety of palliative stenting for MTBF patients and to investigate its impact on survival.
Location of fistulas
Fistulas were classified according to their location
(L) in eight groups: (i) L- I, upper third of the trachea; (ii) L- II, middle third of the trachea; (iii) L- III, lower
third of the trachea; (iv) L- IV, main carina; (v) L- V,
right main bronchus; (vi) L- VI, left main bronchus;
(vii) L- VII, distal part of right main bronchus;
(viii) L- VIII, distal part of left main bronchus.
Stenting technique
We used a bronchoscope to decide the type
and shape of the stent to be placed. The location,
diameter, and length of the fistulas (a); the status
of airway stenosis and the percentage (b) if present;
and whether mechanical debulking, argon plasma
coagulation (APC), or cryotherapy (c) would be
of assistance were recorded. The patients were
intubated with a rigid bronchoscope (RB) (Efer
Endoscopy, La Ciotat; Paris, France) of appropriate
size followed by loading of the stent into a specifically
designed introducer and which was deployed using
the applicator. Stents used were silicone stents
(Volutam; Medical Epsilon, Istanbul, Türkiye)
and covered airway self-expanding metallic stents
(SEMS; Leufen, Medical GmbH, Berlin, Germany).
Stent shapes included Y-shaped, I-shaped, J-shaped,
and Oki stents. The Oki and Y stents were modified
according to the fistula localization and length by
tailoring or drilling. Some patients with MTBEF
were referred to our center following insertion
of self-expanding esophageal metallic stents by
gastroenterologists.
Follow-up
Respiratory failure requiring mechanical
ventilation, arrhythmia, hemorrhages, and death within
24 h after the procedure were considered to be acute
complications. All patients underwent surveillance
bronchoscopies at one month of the procedure or
earlier according to the patient's symptoms for
detecting chronic complications, such as stent fracture,
granulation tissue formation, migration and mucostasis.
The primary outcomes of the present study were the
assessment of clinical and technical success of AS and
their complications. Technical success was described
as successful insertion of the stent at the appropriate
site in a single bronchoscopic session. Clinical success
was defined as dramatic improvement in symptoms
and/or successful repair of fistula, within one month
after stent placement without complications or death.
Statistical analysis
Statistical analysis was performed using the
R software version 3.5.1/2018-7-01 (Bell Laboratories,
Lucent Technologies, New Jersey, USA). Descriptive
data were expressed in mean ± standard deviation (SD), median (min-max) or number and frequency, where
applicable. The Student t-test and Mann-Whitney
U test were used to continuous data, respectively.
Categorical data were compared using the chi-square
and Fisher exact test. The date of stenting was
considered as zero-day, last check date or date of
death was considered as last day on survival analysis.
The Kaplan-Meier survival analysis was performed
for univariate survival analysis. Cut-off values for
continuous variables were identified using the receiver
operating characteristic (ROC) analysis. Variables
that were associated with survival at p<0.15 in the
univariate analysis were included in multivariate
analysis. The Cox proportional risk model was used for multivariate analysis of these factors that were
likely to affect the survival. A p value of < 0.05 was
considered statistically significant.
Table 1: Demographic and clinical details of the patients with MTBF
The MTBEF patients included 16 cases of esophageal cancer and three cases of lung cancer. Seven patients with MTBEF who had AS inserted were previously treated with esophageal stents. Four (21%) patients had a history of surgery. Mucosal tumor infiltration at the fistula side was observed in 15 (79%) patients.
A total of 38 ASs were inserted with a technical success rate of 100% (Figures 1 and 2, Video 1). Stents were inserted in a single session in 88% of the patients and the remaining in two sessions (12%). Thirteen of the stents were SEMS and 25 were silicon stents (Table 2).
Table 2: Characteristics of stents implanted in patients with MTBF
The clinical success rate was 95% in patients with MTBEF (n=1 migration) and 86% in patients with MBPF (n=2 migration). The median survival time was 3.5 (range, 1.7 to 8.5) months in patients with MTBEF and 18 (range, 7.2 to 51) months in patients with MBPF (Figure 3). The 3, 6, and 12-month survival rates were 64%, 27%, and 18% in patients with MTBEF, and 83%, 66%, and 38% in patients with MBPF, respectively.
Factors significantly affecting survival in patients with M TBEF u sing t he u nivariate a nalysis w ere t he diameter of the fistula (p=0.08), stage of the tumor (p=0.02), degree of airway obstruction (p=0.11), and the presence of esophageal stent (p=0.02). Multivariate analysis showed that the stage of the tumor (p=0.04) and the presence of esophageal stent (p=0.02) were both independent predictors of survival (Table 3).
Factors significantly affecting survival in patients with MBPF using the univariate analysis were histological tumor type (p=0.02), degree of airway obstruction (p=0.14), stage of the tumor (p=0.03), diameter of the fistula (p=0.08), and the site of the fistula (p=0.09). Multivariate analysis revealed that no factor was an independent predictor of survival (Table 4).
There were no major acute complications. Three patients had minor complications: two had mild hemorrhage and the other had hypercarbic respiratory failure requiring non-invasive mechanical ventilation for 4 h. Chronic complications (>24 h) occurred in nine (26%) of 34 patients with fistulas. Additionally, four patients needed stent reinsertion: three for stent migration and one for mucostasis (Table 5). Chronic complications were not correlated with the stent type, stent shape, fistula location, or fistula size.
Malignant tracheobronchial esophageal fistulas can develop secondary to tumoral invasion or after cancer treatment or pressure necrosis caused by a previously implanted stent.[1] These fistulas can be lethal, and many patients are not surgical candidates due to their poor general condition.[8] The AS insertion is an alternative to surgery and can sometimes afford better symptomatic relief. The MTBEF cases lacking airway obstruction receive esophageal stents. If such stents (not ASs) are placed in patients with airway obstructions, airway stenosis can worsen. In such cases, AS should be placed first.[12,13] A combination of an esophageal stent and an AS is more effective than either stent alone.[14,15] All of our MTBEF patients had esophageal or lung cancer. Most previously received chemotherapy and radiotherapy. Of 19 patients with MTBEF, seven were initially treated with ESs.
Furthermore, MTBEF are always poorly prognostic.[4,6,16] Most patients die within three to four months from frequent airway aspiration, malnutrition, or life-threatening hemoptysis.[4,6] Stenting enables such patients to breathe normally, facilitates oral nutrition, and improves quality of life and survival.[6,17,18] Freitag et al.[17] found that 30 patients with MTBEF survived for a mean of 110 days after esophageal stent and AS placement, but patients survived for a mean of only 24 days after AS placement alone. Herth et al.[18] found that MTBEF patients survived for a mean of seven months, and survival was longer in those with bilateral stents. The mean survival time of our patients was 3.5 months and was longer in patients with both esophageal stents and ASs (4.7 months) than patients with AS alone (two months), similar to the literature. In our study, the presence of an ES was found to be one of the factors that independently affected survival positively in the multivariate analysis of patients with MTBEF.
Malingnant bronchopleural fistulas can trigger significant morbidity and prolonged hospitalization.[5] The treatment of choice is surgical closure, but this is risky in patients who have poor general health or an infection. In such cases, various endoscopic options have been utilized.[9] In many studies, AS insertion was successful using SEMS or silicon stents, without major complications.[10,11,19] T he success rate depends on the fistula diameter (optimal: <8 mm). Our patients had a mean fistula diameter of 6.9±2.2 mm. Most patients underwent chemotherapy and radiotherapy and were not indicated for surgery.
In the literature, MBPF-associated mortality rates range from 1 to 67%.[19-22] Several studies have been published investigating the effect of AS on survival in the treatment of BPF developing after lung cancer surgery.[10,11,19-21] Dutau et al.[19] treated large (>6 mm indiameter) fistulas that developed after pneumonectomy to treat lung cancer. In this study, SEMSs were placed in six patients who were not indicated for surgery, and all exhibited clinical improvement. The mortality rate was 57%. Another study compared surgical treatment and AS placement in fistulas >8 mm in diameter.[21] Although the early mortality rate was lower in the stented group, the two-year survival rates (76% vs. 70%, respectively) did not significantly differ. In our study, the six-month (83%) and one-year (66%) survival rates were similar to those reported in the literature.
Silicon stents and SEMSs have been widely used to treat MTBF.[6,10,11,17,18,19-21] However, ASs are foreign bodies that are prone to complications, despite their many benefits.[20] Hemorrhage and airway perforation are acute, but rare complications. Chronic complications include stenosis with granulation tissue formation, mucostasis, and stent migration/fracture.[22] We recorded no perioperative death and no severe acute complication. Minimal-to-moderate hemorrhage developed in two patients, but was easily controlled. Chronic complications were more common in patients with MTBF (33%) than MTBEF (21%). Additionally, migration was observed most frequently in patients with MBPF and granulation in patients with MTBEF. The higher complication rate in the former group of patients may reflect their longer follow-up period. The higher complication rates in patients with MBPF can be attributed to their longer follow-up period.
Silicon stents and SEMSs have unique advantages and disadvantages.[23] The first ones are easily repositioned or removed, minimally associated with granulation, and cost-effective. The latter ones are compatible with the airway anatomy, less prone to migration, and afford better mucociliary clearance.[23] Bronchoscopist experience, fistula location and size, and the bronchial anatomy influence the choice of (a silicone or metal) stent. Although modified silicon stents are available, a SEMS may be preferred, if the fistula is difficult to close and the bronchial structure is complex. An SEMS expands spontaneously to conform to the bronchial structure. In our study, we placed silicon stents in 66% and SEMSs in 34% of patients. We found no significant differences in complications between the stents. We consider that the extensive experience of our interventional unit, and fistula location and type, encouraged the use of SSs. The lack of any difference between stent types in terms of the development of complications may reflect the low number of cases. The stent should be chosen on the basis of bronchoscopist experience, fistula location and size, and the airway anatomy.
Our study has certain limitations, principally the relatively small sample size and the retrospective nature. Also, this was an observational study and we lacked a control group that was not stented.
In conclusion, our experience indicates that airway stents are safe and palliative, and are useful alternatives, when surgery is impossible or prohibitively risky.
Ethics Committee Approval: The study protocol was approved by the Health Sciences University, Hamidiye Scientific Research Ethics Committee Institutional Review Board (IRB committee A; 19.8.2020. 27817). The study was conducted in accordance with the principles of the Declaration of Helsinki.
Patient Consent for Publication: A written informed consent was obtained from each patient.
Data Sharing Statement: The data that support the findings of this study are available from the corresponding author upon reasonable request.
Author Contributions: Concept, supervision, writing - E.C.S.; Concept, desing, anaysis - D.T.; Data collection, interpretation critical reviews - M.A.Ö.; Materials, literature search - E.U.C.; Desing, materials literature search - G.Ö.; Research - E.Ç.
Conflict of Interest: The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.
Funding: The authors received no financial support for the research and/or authorship of this article.
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