Paul Zarogoulidis1,2, Haidong Huang3, Zhenli Hu3, Ning Wu3, Jiannan Wang3, Dimitris Petridis4, Kosmas Tsakiridis5, Dimitris Matthaios6, Christoforos Kosmidis2, Wolfgang Hohenforst-Schmidt7, Christos Tolis8, Ioannis Boukovinas9, Nikolaos Courcoutsakis10, George Nikolaidis11, Chrysanthi Sardeli12, Chong Bai3, Chrysanthi Karapantzou13. 1. Pulmonary Department, "Bioclinic" Private Hospital, Thessaloniki, Greece. 2. 3 rd University General Hospital, "AHEPA" University Hospital, Thessaloniki, Greece. 3. Department of Respiratory & Critical Care Medicine, Changhai Hospital, The Second Military Medical University, Shanghai, China. 4. Department of Food Technology, School of Food Technology and Nutrition, Alexander Technological Educational Institute, Thessaloniki, Greece. 5. Thoracic Surgery Department, "Interbalkan" European Medical Center, Thessaloniki, Greece. 6. Oncology Department, General Hospital of Rhodos, Rhodos, Greece. 7. Sana Clinic Group Franken, Department of Cardiology/Pulmonology/Intensive Care/Nephrology, "Hof" Clinics, University of Erlangen, Hof, Germany. 8. Private Oncology Cabinet, Ioannina, Greece. 9. Oncology Department, "Bioclinic" Private Hospital, Thessaloniki, Greece. 10. Radiology Department, University General Hospital of Alexandroupolis, Democritus University of Thrace, Alexandroupolis, Greece. 11. Surgery Department, "General Clinic Euromedica" Private Clinic, Thessaloniki, Greece. 12. Department of Pharmacology & Clinical Pharmacology, School of Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece. 13. Ear, Nose and Throat (ENT) Department, Ludwig-Maximilians University of Munich, Munich, Germany.
Several patients are admitted to hospitals with different symptoms and radiology exams often reveal lesions in the thorax. Computed tomography (CT) of the thorax with or without intravenous contrast can be easily used in every tertiary hospital. Positron emission tomography (PET-CT) has been added in our diagnostic algorithm the last 12 years. It has been evaluated for several diseases both for benign and malignant diseases. It can be used either for initial diagnosis or initial staging, but also for the restaging of non-small cell lung cancer (NSCLC) disease 1-5. PET-CT has a substantial diagnostic value for single nodules of ≥0.8 mm. Several centers take a delayed second examination 20-30 minutes after the initial examination in order to identify malignancies with low metabolic rate. However; there are still issues where malignancies cannot be identified to the low metabolic rate 6. There is also still an issue with benign disease such as; sarcoidosis where PET-CT is under evaluation as a diagnostic tool 7. Endobronchial ultrasound (convex) is an endoscopic tool again with more than 10 years in service with 22G, 21G and 19G needles for biopsy. It is an excellent tool for initial diagnosis and staging in different diseases 8-10. The sample size is enough to perform gene investigation for several cancer types 11, 12. The role of PET-CT and EBUS-TBNA has been for several malignancies and an algorithm has been set. However; we do not have an algorithm to follow for undiagnosed mesothorax lymphadenopathy. Should we first perform PET-CT or we can proceed directly to biopsy. There is the issue of cost-effect regarding the needle that we have to use and the unnecessary PET-CT examinations which have a high cost. We performed a retrospective study to identify an algorithm through several institutions following the same diagnostic protocol and examination costs.
Patients and Methods
We enrolled 450 patients from our oncology and pulmonary outpatient cabinets. These patients came to our cabinets either with a CT of the thorax performed with intravenous contrast or PET-CT. The investigational review board (IRB) of the 3rd University General Hospital, “AHEPA” University Hospital, Thessaloniki, Greece provided us with the authorization of our study. A CT of the thorax with contrast costs 160 euros and a PET-CT 1150 euros. All patients had mesothorax lymphadenopathy. Endobronchial ultrasound (convex probe) was performed with a PENTAX EB-1970UK, EPK-1000 video processor and a Hitachi EUB-7500HV ultrasound source. The following needles were used; a) 22G Mediglobe®, b) 22G upgraded Mediglobe®, c) 21G Olympus® and d) 19G Olympus®. The costs for the needles were as follows: a) 170 euros, b) 330 euros, c) 440 euros and d) 520 euros. The EBUS procedure without the needles had a cost of 1300euros in every department including anesthesiology drugs, medical staff (nurse, anesthesiologist and doctor), pathology result and all other materials necessary for the examination. There was an extra cost of 350 euros for next generation sequencing (NGS) when this was necessary, but this was not information included in our study. Patients that had before the EBUS a PET-CT their examination had a total cost as follows for each needle: a) 259.475 euros, b) 280.780 euros, c) 289.000 euros and d) 112860 euros. All 344 patients that had an initial PET-CT before EBUS had a diagnosis and no false negative result. The rest of the 106 patients had only a CT of the thorax with intravenous contrast and the cost of the examination was as follows for each needle: a) 63.570 euros, b) 41.170 euros, c) 64.600 euros and d) 15.840 euros. All 106 patients did not have a diagnosis, and PET-CT was performed and then re-biopsy with EBUS-TBNA with the same needles in different puncture point where the PET-CT was highly positive with an SUV ≥3. The cost for the new examination of these patients after the PET-CT was as follows: a) 108.420 euros, b) 67.620 euros, c) 103.700 euros and d) 25.040 euros. The time between the new re-biopsy was 15 days for each patient. The money loss in total for the 106 patients was 304.780 euros. The total cost of the 344 patients was 942.115 euros (Table ).
Statistics
Methods
The efficiency of the positron emission tomography (PET) was investigated on patients with different cancer types using different needle sizes and dissecting various slices. The number of slices as affected by the needle size was detected using the 95% confidence interval plot of means based on ANOVA's error mean square. Also, the association among needle size, lesion size and cancer type was investigated employing a multiple correspondence analysis.The efficiency of the Modified electric convulsive treatment (MECT meaning patients that had PET-CT before the EBUS biopsy), was detected by plotting the slices mean against the lesion size and cancer type as similarly described above.
Results
For the PET apparatus Figure shows that the mean number of slices is twice much higher when needle 19 is used than those affiliated with the needles (22U) 22G upgraded Mediglobe® and 21G (equally performing) and the latter are again twice much higher than the mean slices associated with needle 22G (170 euros needle Mediglobe®).The multiple correspondence analysis pointed out an 85.25% explanation of inertia variation (Figure ) concerning the first two dimensions.Dimension 1 is best described by needle type 4 (19G Olympus® and cancer type 4 (Hodgkin) (see the partial contributions of coordinates in Figure ), both arranged at the right part of corresponding plot and far apart from the rest categories. Similarly, dimension 2 was best formed by lesion size 1 (≥1 cm) and cancer type 3 (higher contribution of the coordinates-Non-Hodgkin), both positioned at the lower part of the plot and also far apart from the other categories. Cancer type 2 (metastatic from other organs than the thorax) and lesion size 2 (≥2 cm) are also affiliated each other due to their close distance and moderate contributions for the axes formation.For the MECT (MECT meaning patients that had PET-CT before the EBUS biopsy) apparatus, the 95% confidence interval plot of slice means (Figure ) indicate that needles size 4 (19G Olympus®) produce the highest number of slices, those of size 2 (22G upgraded Mediglobe®) and 3 (21G Olympus®) intermediate ones and those of size 1 (≥1 cm) the lowest values (absent for lesion 4 ≥4 cm). Lesions show a similar pattern of slices in the needles across all lesion categories.The value of slices, needle type and cancer type in fact present a proportional cost-effectiveness due to the following reasons:The higher the number of slices, the larger the needle, the higher the cost;The cancer type Hodgkin, non-Hodgkin vs the other cancer types, increases the operation cost;Concerning the lesion size no cost-effective is reasonably expected thus, no real statistical information is possible to support an apparent effect as explained by the pre-explained reasons.
Discussion
Several studies have compared the cost-effectiveness and safety of EBUS-TBNA for diagnosis versus mediastinoscopy 13, 14. Certainly according to current guidelines for lung cancer PET-CT and EBUS-TBNA have an algorithm before mediastiscopy is performed 15. However; several patients refer to internal medicine doctors and general practitioners and not always to oncologists and pulmonary physicians. Currently there are no guidelines for undiagnosed lymphadenopathy of mesothorax. All our patients had malignancy because an initial work-up with medical history and because of the expertise of our departments patients referred to us were most likely to have malignancy. In other centers a part of these patients would include benign disease such post infection lymphadenopathy or sarcoidosis. We observed in our study again as it has been previously identified that 19G needle has larger biopsy sample almost double the size of a 22G needle 8, 16. The biopsy sample size was as follows in our study; d>c=b>a based on the needles. This observation was made with the number of cell block slices that were produced from each biopsy. The sample size did not differ among the different lesion size, this is due to the ebus technique where we have real time visualization of the lesion and several punctures can be made with safety indifferent of the needle. Needle size 19G we know from previous studies that is efficient for lymphomas 17. Cost-effectiveness is an issue for every health system and this is decided for each patient upon admission. A PET-CT is necessary to identify necrosis and the intensity of the lesions. Also, we can identify the part of the lesion which has the highest intensity in order to puncture this specific site (Figure ).We can observe in Figure that although someone could puncture lymphnode number 11L in this patient, no result would be available because there is no SUV uptake. This information would not available with a CT of the thorax even with i.v contrast.Several studies have been performed where elastography was used to identify the strain ratio of the lesions, however; without efficient results 18-20. Moreover; the use of the needle is another important cost, if we have the same number of block slices with less expenses then it would be preferred. However; health systems work different between Europe, China and the United States, and certainly PET-CT or EBUS-TBNA is not available in every hospital. The most important cost-effective decision is finally made by the initial physician and it would be preferred that these patients should be directed to centers of expertise with malignancies. A cost-effectiveness algorithm should be proposed by the scientific societies for the diagnostic work, not only for oncologists and pulmonary physicians, but also for other specialties (Figure ).
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