ISSN : 1301-5680
e-ISSN : 2149-8156
Turkish Journal of Thoracic and Cardiovascular Surgery     
Risk factors for malignancy-unrelated long-term respiratory events after pneumonectomy
Ümit Aydoğmuş1, Erhan Uğurlu2, Serkan Değirmencioğlu3, Figen Türk1, Gökhan Yuncu4
1Departments of Thoracic Surgery, Medical Faculty of Pamukkale University, Denizli, Turkey
2Departments of Chest Diseases, Medical Faculty of Pamukkale University, Denizli, Turkey
3Departments of Medical Oncology, Medical Faculty of Pamukkale University, Denizli, Turkey
4Department of Thoracic Surgery, Liv Hospital, İstanbul, Turkey
DOI : 10.5606/tgkdc.dergisi.2017.12680

Abstract

Background: In this study, we aimed to evaluate late-onset, malignancyunrelated respiratory events following pneumonectomy.

Methods: The medical data of 78 patients (73 males, 5 females; mean age 55.6±9.6 years; range, 32 to 79 years) who underwent pneumonectomy in our clinic between January 2009 and September 2014 were retrospectively analyzed. Preoperatively, data including smoking habits, comorbidities, the American Society of Anesthesiologists risk score, the EuroSCORE, neoadjuvant chemotherapy need, cancer cell type, and clinical stage were recorded. Postoperatively, data included complications and treatment modalities were recorded.

Results: The mean follow-up was 35.2±22.0 months (range 9 to 104 months). Malignancy-related respiratory events such as local relapse and a second primary lung tumor developed in 21 patients (35.0%). Non-malignancy-related respiratory events were seen in 18 patients (31.6%). Long-term, non-malignancy-related morbidity was more prevalent in the patients with high American Society of Anesthesiologists scores (p=0.01), preoperative forced expiratory volume in one second <60% (p=0.05), and a high EuroSCORE (p=0.04). In multivariate analysis, non-malignancy-related respiratory events were found to be statistically significantly more frequent in the patients with high American Society of Anesthesiologists scores (p=0.01) and preoperative forced expiratory volume in one second <60% (p=0.03).

Conclusion: Our study results suggest that patients undergoing pneumonectomy may develop both short-term and long-term respiratory morbidities, and patients with high preoperative American Society of Anesthesiologists scores and low forced expiratory volume in one second are at an increased risk for non-malignancy-related morbidity.

Pneumonectomy is a surgical procedure of which complication rates are still high, and it has been recently performed mostly in the case of malignancy.[1] Furthermore, as it involves the loss of an organ, pneumonectomy is a debilitating surgery which often includes comorbidities that negatively affect the quality of life of patients.[1]

Some patients undergoing pneumonectomy may die due to morbidities related to circulatory and respiratory failure in the long-term.[2] Accordingly, some authors advocate the evaluation of data about mortality between 90 days and six months in patients undergoing pneumonectomy for the non-malignancyrelated mortality risk.[3,4] Many studies have focused on short-term morbidity and mortality of pneumonectomy, and the complication rates are still high.[1,4,5] In addition, a number of studies have examined the factors related to long-term survival.[6-8] However, the incidence and the mechanism of circulatory and respiratory failure in the long-term is unclear.

In this study, we aimed to evaluate possible risk factors for the development of long-term nonmalignancy- related respiratory events in patients undergoing pneumonectomy.

Methods

An ethical approval was obtained from the institutional Ethics Board on Human Experiments of Medical Faculty of Pamukkale University, with the approval number 60116787-020/35871. The medical data of 83 patients who underwent pneumonectomy in our clinic between January 2006 and September 2014 were retrospectively analyzed. Two patients were excluded due to missing data, while three patients were excluded due to mortality within the first 90 days following the operation. As a result, 78 patients (73 males, 5 females; mean age 55.6±9.6 years; range 32 to 79 years) were included in the study.

Preoperative evaluation
All patients underwent thoracic computed tomography (CT), respiratory function test, electrocardiography, blood count analysis, and biochemistry tests preoperatively. Perfusion scintigraphy and cardiopulmonary stress tests were performed in patients in whom the highest forced expiratory volume in one second (FEV1) was below 2,000 mL. Pneumonectomy was canceled in cases with an estimated FEV1 capacity of the remaining lung lower than 800 mL or below 40%.

Data including smoking habits, comorbidities, American Society of Anesthesiologists (ASA) risk score, EuroSCORE, neoadjuvant chemotherapy need, cancer cell type, and clinical stage were recorded. Patients older than 65 years or who had related symptoms underwent an additional echocardiographic examination.

The patients were divided into three groups according to the EuroSCORE risk: class 1 (low risk): 0-2 points; class 2 (moderate risk): 3-5 points; class 3 (high risk): ≥6.

A total of 32 patients (41.0%) had comorbidities: diabetes mellitus in 12 patients (15.4%) and chronic obstructive pulmonary disease in nine patients (11.3%). Three patients have been taken bronchodilators.

The patients with lung cancer underwent positron emission tomography/CT (PET/CT) examination. The patients with lymphadenopathy, as assessed using PET/CT or CT underwent mediastinoscopy. Neoadjuvant treatment was given to the patients with Stage T1-2-3N2 and T4N0 at the discretion of the Thoracic Oncology Team.

Postoperative evaluation
All patients remained in the intensive care unit for at least one day following surgery. Routine monitoring of vital signs, daily blood counts, and biochemical tests were performed within the first three days. Daily posteroanterior lung X-rays were obtained within the first seven days. All complications, treatments applied, and management modalities related to the patients were recorded. Surgical mortality was defined as inhospital mortality or mortality within the first 90 days after surgery.

Long-term follow-up
Patients returned to the outpatient clinic for followup one week and one month after discharge from the hospital. All patients were scheduled for follow-up visits every three months for the first two years and every six months for subsequent years. Complaints and treatments received were recorded, and posteroanterior X-ray, blood count, erythrocyte sedimentation rate, and C-reactive protein tests were performed on a regular basis. In the long-term follow-up, medical records in our hospital, prescription records in the pharmacy, citizen registry records, and social security trust records were also evaluated.

Malignancy-related events were defined as respiratory problems in patients with locoregional relapse, pulmonary metastasis, malignant pleural effusion, or a secondary lung carcinoma. Non-malignancy-related long-term events were defined as in need of brochodilator, need for oxygen treatment, emergency department admittance, pulmonary embolism, tuberculosis, recurrent pneumonia, pneumothorax, or pleural effusion developing following surgery.

Statistical analysis
For statistical analysis, PASW 17.0 software for Windows (SPSS Inc., Chicago, IL, USA) was used to analyze outcomes. Descriptive data were expressed in mean and standard deviation. The chi-square and Fisher’s exact tests were performed to analyze data. Only variables with a p value of 0.2 without a correlation were included in the multivariate analysis. A p value of <0.05 was considered statistically significant.

Results

The mean follow-up was 35.2±22.0 (range, 9 to 104) months. Indications for pneumonectomy were a destroyed lung in five patients (6.4%) and non-small-cell lung cancer in 73 patients (93.6%).

A right pneumonectomy was performed in 35 patients (44.9%) and a left pneumonectomy was done in 43 patients (55.1%). The FEV1 value was lower than 60% in seven patients (8.9%).

The mean duration of hospitalization was 11.7±9.8 (range, 5 to 66) days. A standard pneumonectomy was performed in 68 patients (78.2%); 18 patients (23.1%) received induction chemotherapy, and 12 patients (15.4%) received induction chemo-radiotherapy. A total of 46 patients (59.0%) received adjuvant chemotherapy, while 15 patients (19.2%) received adjuvant radiotherapy. During follow-up, distant metastasis developed in 26 (33.3%), local-regional relapse in seven (9.7%), and secondary lung cancer in three patients (3.8%). In addition, 31 patients (39.7%) died during follow-up; causes of death were distant metastasis in 18 (23.1%), local relapse in six (7.7%), secondary lung cancer in one (1.3%), and non-malignancy-related causes in six patients (7.7%).

In addition, 11 patients required 14 invasive procedures during follow-up: five wedge resection of the lung, three tube thoracostomy, two rigid bronchoscopy, and four thoracentesis. The indication among the patients who received wedge resection was metastatic disease in three and a secondary lung carcinoma in two patients, and all of these patients survived at the time of the study completion.

During the study, morbidities which were reported are shown in Table 1. Four patients had more than one long-term respiratory incident. In three of the pleural effusion cases, collection was transudate, and in one patient, collection was regarded as having a parapneumonic effusion.

Table 1: Distribution of non-malignancy-related long-term morbidity

On the other hand, the probability of a long-term incident was not significantly different between the patients who had a right pulmonectomy (n=8, 22.9%) and those who had a left pneumonectomy (n=10, 23.3%) (p=0.99), between males (n=21, 28.8%) and females (n=1, 20%) (p=0.99), or between the patients who received standard resection (n=13, 28.8%) and extended resection (n=5, 29.4%) (p=0.52). Similarly, receiving induction therapy (p=0.75), pneumonectomy for non-small-cell lung cancer (p=0.33), smoking habits (p=0.76), having comorbidities (p=0.28), or receiving adjuvant chemotherapy (p=0.75) were not found to be risk factors (Table 2).

Table 2: Comparison of the non-malignancy related long-term morbidity with categorical variables

Long-term respiratory morbidity was higher in patients over 60 years of age (n=9, 34.6%) than in those below 60 years (n=9, 17.3%) (p=0.1) and, similarly, higher in patients with a higher EuroSCORE 66.7% in class 3 (n=2), 32.1% in class 2 (n=9), and 14.9% (n=7) in class 1 (n=7), (p=0.17). Only one of the patients who received adjuvant radiotherapy (6.7%) had long-term respiratory morbidity. Although long-term respiratory morbidity was not seen in the patients with an ASA score of 1, 16 patients with an ASA score of 2 (29.6%) and two patients with an ASA score of 3 (50%) had long-term morbidity (p=0.01). Similarly, long-term morbidity was found to be higher in patients with a preoperative FEV1 l ower t han 6 0% ( n=7, 5 7.1%) (p=0.05).

Multivariate analysis revealed that a higher ASA score was a significant risk factor for long-term postpneumonectomy morbidity unrelated to malignancy (p=0.005) (odds ratio = 2.93) (95% confidence interval: 0.08-0.43). Meanwhile, non-malignancy-related longterm respiratory morbidity was significantly lower in patients who had adjuvant radiotherapy (p=0.02) (OR=2.38). Long-term, non-malignancy-related respiratory morbidity was higher in patients older than 60 years (p=0.2) with a preoperative FEV1 lower than 60% (p=0.1) and with a higher cardiac risk score (p=0.08), although the difference was not significant (Table 3).

Table 3: Multivariate analysis of the non-malignancy related long-term morbidity

Discussion

Higher ASA scores, older age, neoadjuvant treatments, comorbidities (particularly COPD), right pneumonectomy, and extended resection were found to be associated risk factors for post-pneumonectomy morbidity.[1,4,7,9] However, the long-term implications of these risk factors are not well-known. Long-term survival after pneumonectomy is primarily associated with the stage of lung cancer.[8] In addition, there are studies utilizing the Short-Form 36 Health Survey (SF-36), which contains subjective evaluations for quality of life of patients undergoing thoracic surgery.[10,11] Other problems in assessing the long-term quality of life of patients are non-compliant patients and life quality of patients which declines during adjuvant therapies.[11] Lung function of the patients who underwent pneumonectomy may deteriorate, if they receive adjuvant radiotherapy.[12] In this study, objectively recorded, non-malignancy-related long-term morbidity in patients who underwent pneumonectomy was evaluated.

Rodríguez et al.[4] found that right pneumonectomy was associated with a higher rate of cardio-respiratory complications and death within the first postoperative six months. Recently, there is growing evidence suggesting that neoadjuvant treatment is not related to higher morbidity and mortality.[8,9] Our results also showed that factors such as right pneumonectomy, neoadjuvant therapy, smoking, and extended resection, which were previously related to postoperative morbidity, were not found to significantly increase non-malignancy-related long-term respiratory morbidity.

Although some studies reported that a higher ASA score was a significant indicator of postoperative morbidity, others found it to be irrelevant.[4,5] In our study, preoperative ASA scores were found to be a significant indicator for long-term morbidity. Poor respiratory-function test results were also found to be a risk factor for poorer long-term quality of life for patients who underwent lung excision.[10]

Low preoperative respiratory functional capacity and higher cardiac risk scores were found to be related potential risk factors for long-term respiratory morbidity.

Toxicity of postoperative radiotherapy to the lungs is well-known, and accordingly, it is not recommended for patients with early stage non-small cell lung cancer (Stage I-II).[13] In contrast, our results showed lower long-term respiratory morbidity in patients who received adjuvant radiotherapy. This discrepancy can be explained in two ways: first, toxic effects of the radiotherapy were not seen, as there was no lung tissue at the target area of radiotherapy; second, patients with a poor general condition did not receive radiotherapy in our series to prevent possible side effects.

Non-malignancy-related, long-term, postoperative respiratory morbidity is mostly due to cardiopulmonary insufficiency.[12] Indeed, the most important threat for the patients with lung cancer undergoing pneumonectomy, particularly those in the early stages, is intervening disease for five-year survival.[12] This finding is in consistent with the findings indicating that preoperative low FEV1 values were associated risk factors.

Furthermore, in patients undergoing cancer surgery, it is suggested to be used the ASA classification rather than Eastern Oncology Cooperative Group (ECOG).[14] In addition, the relationship among the ASA scoring, mortality and morbidity in early period in patients undergoing thoracic surgery is well-known.[16] For the Turkish society, this method was found with higher sensitivity and specificity according to other methods.[17] In our study, the patients with a high cardiac risk score had high respiratory problems in the late period. Thus, the EuroSCORE risk classification seems to be a good indicator of health problems in the late period. Cardiopulmonary system is affected in patients undergoing pneumonectomy and these patients who are at cardiac and pulmonary risks often experience impaired quality of life in the long-term.

The only problem of patients with pneumonectomy is not the failure of cardiopulmonary. Developing problems in the only remaining lung have almost always life-threatening aspect. These events which might threaten the life of a patient with a solitary lung were pneumonia (n=2), tuberculosis (n=1), and contralateral pneumothorax (n=2). Herniation of the remaining lung to the contralateral empty hemithorax and hyperinflation are also regarded as the underlying causative mechanisms for nonmalignancy- related, contralateral pneumothorax.[18] Although pneumothorax is mild, it must be drained carefully, since the patient may not tolerate the changes secondary to pneumothorax and drainage. In our study, both patients were managed with no further events by tube thoracostomy and underwater sealed drainage.

Nonetheless, cross-sectional design and retrospective nature of this study is the major limitation. Although it is a single-center study with close monitoring of the patients, small sample size is another limitation. As most of the studies in the literature have addressed into survival following pneumonectomy, we believe that our contribution evaluating non-malignancy-related long-term morbidities is valuable.

In conclusion, our study results showed that higher American Society of Anesthesiologists scores and lower forced expiratory volume in one second were related risk factors for non-malignancy-related long-term respiratory morbidities. Although pneumonectomy is a procedure with low morbidity and mortality in experienced hands, long-term morbidity is remarkable due to locoregional or distant tumor relapse or nonmalignancy- related cardiopulmonary morbidities.

Therefore, patients undergoing pneumonectomy require close and long-term monitoring.

Declaration of conflicting interests
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.

References

1) Marret E, Miled F, Bazelly B, El Metaoua S, de Montblanc J, Quesnel C, et al. Risk and protective factors for major complications after pneumonectomy for lung cancer. Interact Cardiovasc Thorac Surg 2010;10:936-9.

2) Grodzki T, Alchimowicz J, Kozak A, Kubisa B, Pieróg J, Wójcik J, et al. Additional pulmonary resections after pneumonectomy: actual long-term survival and functional results. Eur J Cardiothorac Surg 2008;34:493-8.

3) Kim AW, Boffa DJ, Wang Z, Detterbeck FC. An analysis, systematic review, and meta-analysis of the perioperative mortality after neoadjuvant therapy and pneumonectomy for non-small cell lung cancer. J Thorac Cardiovasc Surg 2012;143:55-63.

4) Rodríguez M, Gómez MT, Jiménez MF, Aranda JL, Novoa N, Varela G. The risk of death due to cardiorespiratory causes increases with time after right pneumonectomy: a propensity score-matched analysis. Eur J Cardiothorac Surg 2013;44:93-7.

5) Sağıroğlu G, Copuroglu E, Meydan B, Taşçı E, Karamustafaoğlu YA, Baysal A, et al. Risk factors for early mortality and morbidity after pneumonectomy, Turk Gogus Kalp Dama 2014;22:368-75.

6) Riquet M, Mordant P, Pricopi C, Legras A, Foucault C, Dujon A, et al. A review of 250 ten-year survivors after pneumonectomy for non-small-cell lung cancer. Eur J Cardiothorac Surg 2014;45:876-81.

7) Aydogmus U, Cansever L, Sonmezoglu Y, Karapinar K, Kocaturk CI, Bedirhan MA. The impact of the type of resection on survival in patients with N1 non-small-cell lung cancers. Eur J Cardiothorac Surg 2010;37:446-50.

8) Melek H, Erol MM, Bayram AS, Cetinkaya G, Evrensel T, Sarıhan S, et al. Pneumonectomy after neoadjuvant treatment. Turk Gogus Kalp Dama 2014;22:777-84.

9) Thomas PA, Berbis J, Baste JM, Le Pimpec-Barthes F, Tronc F, Falcoz PE, et al. Pneumonectomy for lung cancer: contemporary national early morbidity and mortality outcomes. J Thorac Cardiovasc Surg 2015;149:73-82.

10) Handy JR Jr, Asaph JW, Skokan L, Reed CE, Koh S, Brooks G, et al. What happens to patients undergoing lung cancer surgery? Outcomes and quality of life before and after surgery. Chest 2002;122:21-30.

11) Möller A, Sartipy U. Long-term health-related quality of life following surgery for lung cancer. Eur J Cardiothorac Surg 2012;41:362-7.

12) Kim DJ, Lee JG, Lee CY, Park IK, Chung KY. Long-term survival following pneumonectomy for non-small cell lung cancer: clinical implications for follow-up care. Chest 2007;132:178-84.

13) Veluswamy RR, Mhango G, Bonomi M, Neugut AI, Hershman DL, Aldridge MD, et al. Adjuvant treatment for elderly patients with early-stage lung cancer treated with limited resection. Ann Am Thorac Soc 2013;10:622-8.

14) Young J, Badgery-Parker T, Dobbins T, Jorgensen M, Gibbs P, Faragher I, et al. Comparison of ECOG/WHO performance status and ASA score as a measure of functional status. J Pain Symptom Manage 2015;49:258-64.

15) Berrisford R, Brunelli A, Rocco G, Treasure T, Utley M. The European Thoracic Surgery Database project: modelling the risk of in-hospital death following lung resection. Eur J Cardiothorac Surg 2005;28:306-11.

16) Nashef SA, Roques F, Michel P, Gauducheau E, Lemeshow S, Salamon R. European system for cardiac operative risk evaluation (EuroSCORE). Eur J Cardiothorac Surg 1999;16:9-13.

17) Fındık O, Haberal I, Akyıldız M, Aksoy T, Ertürk E, Zorman Y, et al. A comparision of the sensitivity and specificity of the EuroSCORE, Cleveland, and CABDEAL risk stratification systems in the Turkish population. Turk Gogus Kalp Dama 2012;20:458-66.

18) Staartjes WR, van Putte BP, Schramel FM. Contralateral pneumothorax draining via postpneumonectomy space. Ann Thorac Surg 2012;94:35-6.

Keywords : Cancer; long-term care; lung; pneumonectomy
Viewed : 6167
Downloaded : 1134