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Journal Thoracic Oncology

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Abstracts <strong>Journal</strong> of <strong>Thoracic</strong> <strong>Oncology</strong> • Volume 12 Issue S1 January 2017<br />

grading was WHO B3 (33%) followed by AB (25%). 58% had surgical margins < 1<br />

mm, with tumour at margin in 24%. 39 patients (51%) had adjuvant<br />

radiotherapy, with median follow-up of 5.1 years for these patients. A<br />

radiotherapy dose of 45 – 50.4 Gy in 1.8 Gy fractions was used. 5-year survival<br />

for the whole cohort was 68% after surgery alone, and 86% with adjuvant<br />

radiotherapy, but the difference was not statistically significant. There were<br />

no deaths during follow-up in patients who had clear surgical margins, with or<br />

without radiotherapy. If surgical margins < 1 mm, there was a trend towards<br />

improved overall survival with adjuvant radiotherapy (5-year survival 88%),<br />

compared to surgery alone (5-year survival 50%) (log-rank test chisquare 3.7, p<br />

= 0.056) (Fig. 1).<br />

Conclusion: Thymomas had a significantly better prognosis than thymic<br />

carcinomas suggesting that these are 2 different disease processes. The<br />

variability in treatments received reflects the lack of information and general<br />

consensus. Given the rarity of these tumours, greater emphasis must be<br />

placed on collaborative efforts, to increase patient numbers and obtain<br />

meaningful results that will increase our understanding of this challenging<br />

group of patients and improve outcomes.<br />

Keywords: Thymoma, Thymic carcinoma<br />

Conclusion: The long-term outcomes of thymic epithelial tumours are<br />

excellent after complete surgical excision. There is a trend towards improved<br />

overall survival with adjuvant radiotherapy in patients with surgical margins<br />

less than 1 mm. Routine referral of patients with close surgical margins for<br />

consideration of radiotherapy is recommended.<br />

Keywords: Radiotherapy, Thymoma, thymectomy<br />

POSTER SESSION 2 – P2.04: MESOTHELIOMA/THYMIC MALIGNANCIES/ESOPHAGEAL<br />

CANCER/OTHER THORACIC MALIGNANCIES<br />

THYMIC MALIGNANCIES CLINICAL & TRANSLATIONAL –<br />

TUESDAY, DECEMBER 6, 2016<br />

P2.04-011 TUMOURS OF THE THYMUS: NORTHERN IRELAND 11<br />

YEAR EXPERIENCE<br />

Anastasia Papafili 1 , Lynn Campbell 2 , Rosie Douglas 1<br />

1 Northern Ireland Cancer Centre, Belfast City Hospital, Belfast/United Kingdom, 2 Ni<br />

Cancer Centre, Belfast City Hospital, Belfast/United Kingdom<br />

Background: Tumours of the thymus are rare and consensus on their<br />

management is lacking. We aimed to assess outcomes of patients diagnosed<br />

over the last 11 years. Methods: We identified all patients diagnosed with<br />

thymic tumours in Northern Ireland between January 2004 and December<br />

2015 as recorded in the Cancer Registry. Electronic Care Records were used for<br />

data collection. Results: Fifty-seven patients were identified, including 9<br />

thymic carcinomas, 44 thymomas, 3 neuroendocrine tumours and 1 with small<br />

cell features. Mean age at diagnosis was 62 (16-82) and 26% presented with<br />

paraneoplastic phenomena. Of the thymoma patients, the majority presented<br />

with early stage disease (45.5% stage 1, 31.8% stage 2) and 86% had surgery.<br />

Ten patients received adjuvant radiotherapy (XRT), most received 50G in 20<br />

fractions (#). Of those with advanced disease, only 3 received palliative<br />

chemotherapy. Various platinum-based regimes were used. Only 1 patient<br />

received any subsequent line of therapy. Generally thymic carcinomas<br />

presented later, with > 75% with stage 3 or 4 disease. Despite this, almost half<br />

(4/9) had surgery. Additionally, 2 received adjuvant XRT (between 40-50Gy)<br />

and 1 adjuvant chemoradiotherapy (Cisplatin/Etoposide, 50Gy 25#). 44.4% of<br />

these patients received palliative platinum-based chemotherapy, achieving<br />

modest partial responses at best. Median overall survival (OS) for thymoma<br />

(1) was 9.2 years compared to 6.2 years for thymic (2) carcinoma (p= 0.036)<br />

POSTER SESSION 2 – P2.04: MESOTHELIOMA/THYMIC MALIGNANCIES/ESOPHAGEAL<br />

CANCER/OTHER THORACIC MALIGNANCIES<br />

THYMIC MALIGNANCIES CLINICAL & TRANSLATIONAL –<br />

TUESDAY, DECEMBER 6, 2016<br />

P2.04-012 A RISK OF DEATH FROM A SECOND CANCER FOLLOWING<br />

COMPLETE RESECTION OF THYMOMA<br />

Masatsugu Hamaji, Kyoko Hijiya, Hideki Motoyama, Toshi Menju, Akihiro<br />

Aoyama, Toshihiko Sato, Fengshi Chen, Makoto Sonobe, Hiroshi Date<br />

Kyoto University, Kyoto/Japan<br />

Background: A portion of patients undergoing complete resection of<br />

thymoma develop recurrence of thymoma, while those undergoing<br />

thymectomy for thymoma are at risk of developing a second cancer, but it<br />

remains unknown whether those patients are more at risk of death from<br />

thymoma or from a second cancer. Methods: Retrospective chart review was<br />

performed on our prospectively maintained database of patients undergoing<br />

complete resection of thymoma at our institution between 1991 and 2016.<br />

Thymoma-specific survival was calculated from thymectomy to death of<br />

recurreence of thymoma. Second cancer-specific survival was calculated from<br />

thymectomy to death of a second cancer. Both were estimated with Kaplan-<br />

Meier method. Results: Follow-up ranged from 1 to 239 months (median: 54).<br />

One hundred and sixty-four patients were identified. During the follow-up,<br />

there were four thymoma deaths and 4 deaths from a second cancer. Five-year<br />

and 10-year thymoma specific survival was 97.8% and 96.1%, respectively.<br />

Five-year and 10-year second cancer specific survival was 98.2% and 96.1%,<br />

respectively. Conclusion: It appears that patients undergoing thymectomy<br />

for thymoma are at a similar risk of a second cancer death to that of thymoma<br />

death. However, there are too few events during the follow-up and a multiinstitutional<br />

database is required to more rigorously evaluate both risks.<br />

Keywords: Thymoma, survival, a second cancer<br />

POSTER SESSION 2 – P2.04: MESOTHELIOMA/THYMIC MALIGNANCIES/ESOPHAGEAL<br />

CANCER/OTHER THORACIC MALIGNANCIES<br />

THYMIC MALIGNANCIES CLINICAL & TRANSLATIONAL –<br />

TUESDAY, DECEMBER 6, 2016<br />

P2.04-013 PROGNOSIS FACTORS AND SURVIVAL ANALYSIS IN<br />

THYMIC EPITHELIAL TUMORS<br />

Luis Del Carpio 1 , Margarita Majem 2 , Laura López 3 , Josep Belda 4 , Elisabeth<br />

Martínez Tellez 4 , Joan Carles Trujillo 4 , Alfons Torrego 3 , Virginia Pajares 3 , Núria<br />

Farré 3 , Enrique Lerma 3 , Valle Camacho 3 , Alejandro Fernandez 3 , Ana Muñoz 3 ,<br />

Georgia Anguera 1<br />

1 Medical <strong>Oncology</strong>, Hospital de La Santa Creu I Sant Pau, Barcelona/Spain, 2 Medical<br />

<strong>Oncology</strong>, Hopital de La Santa Creu I Sant Pau, Barcelona/Spain, 3 Hospital de La<br />

Santa Creu I Sant Pau, Barcelona/Spain, 4 <strong>Thoracic</strong> Surgery, Hospital de La Santa<br />

S526 <strong>Journal</strong> of <strong>Thoracic</strong> <strong>Oncology</strong> • Volume 12 Issue S1 January 2017

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