Review Article Volume 2 Issue 1
Department of Surgical Oncology, India
Correspondence: Ravi Arjunan, Associate Professor in Surgical Oncology at Kidwai Memorial Institute of Oncology, Department of Surgical Oncology, Bangalore, India
Received: January 19, 2014 | Published: January 27, 2015
Citation: Arjunan R, Kurpad V, Vimalathithan V, et al. Thymoma: a retrospective review of 55 cases of thymoma treated at a regional cancer center. J Cancer Prev Curr Res. 2015;2(1):8-10. DOI: 10.15406/jcpcr.2015.02.00025
We have reviewed the results of 55 consecutive cases of Thymoma treated at Kidwai Memorial Institute of Oncology in terms of surgical approach, removal of tumour with adequate clearance, the related complications, adjuvant treatment and the survival for the different stages of Thymoma.
Keywords: thymoma, median sternotomy, thoracotomy, thymectomy
TET, thymic epithelial tumors; SVC, superior vena vava; KMIO, Kidwai memorial institute of oncology
Thymoma is the most common neoplasm of the anterior mediastinum, originates within the epithelial cells of the thymus.1 Thymomas are typically slow-growing tumors that spread by local extension. Metastases are usually confined to the pleura, pericardium, or diaphragm, whereas extra thoracic metastases are uncommon. The most widely used staging system for thymomas is Masaoka and recently by WHO staging, both were included in our studies. Surgery remains the mainstay of treatment regardless of stage for all thymic neoplasms (16). Blalock described removal of the thymus initially in 1941.2,3 The preferred surgical approach is median sternotomy with complete thymectomy.4-10 Complete thymectomy is favored even in cases of only partial thymic gland involvement because of reports of improved survival and multifocal thymoma. 40% of the cases invade surrounding structures which may limit the ability to achieve R0 margins.2 In advanced tumors, especially if the lung or pleural space is invaded, the extension of a sternotomy to a hemi clamshell incision or a full clamshell incision can be suitable. The oncologic equivalency of thoracoscopic and robotic assisted approaches has been reported, so long as capsule integrity has been maintained and tumour seeding has been prevented.11-14 Masaoka stages III and IV, histological types B2, B3, and C, and incomplete resection were independent risk factors for poor prognosis. Complete resection was feasible in all early stage TETs in our patients. The goals of surgery were achieved safely with very few serious complications and no surgical deaths. Completeness of resection is the most commonly cited statistically significant prognostic factor in thymoma. Our experience also proves that both the WHO criteria and the modified Masaoka staging are prognostic factors of TETs. Long-term disease-specific survival can be expected not only after surgery for early stage thymoma but also after surgery for advanced disease and also including histopathology sub types.
To investigate the role of surgery in the management of thymomas and investigate prognostic indicators after surgery for thymoma.
We retrospectively reviewed 55 thymic epithelial tumors diagnosed during the period of 1998 to 2008 at our (KMIO) institute. 55 patients were diagnosed as thymoma, 50 patients were include in our study, 5 patients were determined to have either World Health Organization type C disease or Masaoka stage IV-B disease and were excluded from analysis were examined the histological specimens using the current World Health Organization classification. Patient characteristics, surgical procedures, and postoperative courses were studied. Staging was performed according to the modified Masaoka system based on surgical and pathological findings; all the histological specimens were reexamined using the current WHO criteria for TET classification for the purpose of the study. Preoperative workup included a complete history and physical examination, laboratory tests, chest roentgenogram, computed tomographic scan. Our strategy for clinically suspected TET patients without any clinical evidence of dissemination was surgery oriented (i.e., surgical exploration for histological diagnosis and potential resection). The surgical procedure consisted of a total thymectomy, together with excision of invaded tissue when possible, through a median sternotomy or a thoracotomy based on the tumor location. Patients were operated on with every effort to remove the tumor. If complete resection was not feasible, then a partial resection (debulking) was carried out. When even a debulking was difficult, the procedure turned into a mere biopsy. Surgical specimens were further examined by our pathologists to determine the histology as well as the margins of resection. The most common surgical approach was sternotomy, which was utilized in 32(64%) patients in our series. In addition to total thymectomy, 4 of our patients additionally had partial pleurectomy, wedge resections of lung & lobectomy.
Cough |
17 |
Dyspnea |
12 |
Incidental/asymptomatic |
10 |
Chest pain |
8 |
SVC obstruction |
3 |
Table 1 Demographic characteristics of the 50 patients
Masoka Stage |
Number of Patients |
Stage 1 |
22 ( 44% ) |
Stage 2 |
16 (32% ) |
Stage 3 |
07 (14% ) |
Stage 4-A |
05 (10% ) |
Table 2 Results showing Masoka stage
Completely Resected |
35 |
||
Partially Resected |
11 |
||
Biopsy Only |
4 |
||
|
Completely Resected |
Partially Resected |
Biopsy |
35 |
11 |
4 |
|
Stage 1 |
20 |
2 |
- |
Stage 2 |
11 |
5 |
- |
Stage 3 |
3 |
4 |
0 |
Stage 4 |
1 |
0 |
4 |
Table 3 Showing resection rates
Post Op Complications |
8 Patients |
Myasthenic Crisis |
4 |
Respiratory Failure |
2 |
Pneumonia |
2 |
Mortality |
2 Patients |
Myasthenic Crisis |
1 |
Cardiac Arrest |
1 |
Table 4 Morbidity and Mortality
Incompletely Resected |
15 |
Patients Underwent Rt |
18 |
Completed Rt |
6 |
Partial Response/ On Follow Up |
4 |
Non Responders |
2 |
Table 5 Adjuvant treatment
Patient Alive |
33(66 %) |
Patient Died |
8 (16%) |
Not Able to Contact |
9 (18%) |
Table 6 After a mean follow-up of 60 months
*Five yrs survival was 66%.
None.
Authors declare that there is no conflict of interest.
©2015 Arjunan, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.