Journal Thoracic Oncology
WCLC2016-Abstract-Book_vF-WEB_revNov17-1
WCLC2016-Abstract-Book_vF-WEB_revNov17-1
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Abstracts <strong>Journal</strong> of <strong>Thoracic</strong> <strong>Oncology</strong> • Volume 12 Issue S1 January 2017<br />
strong specificity detection in patients with NSCLC, while it also indicated<br />
that the lower frequency in tumor tissue, the less possibility to be detected<br />
in plasma.<br />
Keywords: EGFR, Quantstudio 3D digital PCR, ctDNA, Ion Proton<br />
POSTER SESSION 2 – P2.04: MESOTHELIOMA/THYMIC<br />
MALIGNANCIES/ESOPHAGEAL CANCER/OTHER THORACIC<br />
MALIGNANCIES<br />
Thymic Malignancies Clinical & Translational –<br />
TUESDAY, DECEMBER 6, 2016<br />
P2.04-001 A COMPARATIVE ANALYSIS OF LONG-TERM OUTCOME<br />
OF THYMOMA BETWEEN VIDEO-ASSISTED SURGERY AND OPEN<br />
RESECTION FROM MULTI-CENTER STUDY DATA<br />
Su Kyung Hwang 1 , Dong Kwan Kim 1 , Chang Hyun Kang 2 , Chang Young Lee 3 ,<br />
Jong Ho Cho 4<br />
1 Department of <strong>Thoracic</strong> and Cardiovascular Surgery, Asan Medical Center,<br />
University of Ulsan College of Medicine, Seoul/Korea, Republic of, 2 <strong>Thoracic</strong> and<br />
Cardiovascular Surgery, Seoul National University Hospital, Seoul/Korea, Republic<br />
of, 3 Yonsei University College of Medicine, Seoul/Korea, Republic of, 4 <strong>Thoracic</strong> &<br />
Cardiovascular Surgery, Samsung Medical Center, Seoul/Korea, Republic of<br />
Background: To compare the oncologic results between video-assisted<br />
thoracoscopic surgery and open resection in early and locally advanced<br />
thymomas from multi-center study database using propensity score matching<br />
analysis. Methods: Data from 1546 participants in the Korean Association<br />
for Research on the Thymus were used to analysis for video-assisted<br />
thoracoscopic surgery(VATS) versus open resection from January 2003 to<br />
December 2013. We performed propensity score matching analysis for the<br />
outcomes of video-assisted thoracoscopic surgery versus thoracotomy lung<br />
resection (based on age, gender, MG symptom, tumor size, WHO histologic<br />
type, receiving neoadjuvant chemotherapy). Results: We excised the<br />
thymoma using VATS in 513 patients, while 1033 patients underwent open<br />
procedures. There were not significant differences between the 2 groups<br />
for the 5-year overall survival (p=.61), recurrence-free survival (p=.25),<br />
and complete resection (p=.38). The operative times, the hospital stay<br />
duration, and the chest tube indwelling time were significantly shorter in<br />
the VATS group compared to in the open group. Median follow-up duration<br />
was 50.13 months (IQR 26.61-79.60). The Masaoka-Koga stage was I/II/<br />
III, IV in 556/604/384 patients, respectively. We analyzed on the basis of<br />
propensity score matching. There were no significant difference in survival<br />
rate (p=0.882/0.632/0.597), recur-free survival (p=0.120/0.104/0.488), and R0<br />
resection (p=0.945/0.656/0.007) between 3 grups in multivariable analysis.<br />
Conclusion: Patients undergoing VATS thymectomy had shorter the operative<br />
time and the hospital stay duration. Moreover, survival rate and recurrencefree<br />
survival are equivalent between VATS and open resection. Therefore,<br />
video-assisted thoracosopic surgery is feasible approach for early and locally<br />
advanced stage thymoma.<br />
Keywords: minimal invasive surgery, Thymoma, Thymic carcinoma<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 />
P2.04-002 THE EFFICACY OF POSTOPERATIVE RADIOTHERAPY<br />
AGAINST THYMIC EPITHELIAL TUMORS ACCORDING TO MASAOKA<br />
STAGING AND WHO CLASSIFICATION<br />
Kai Obayashi, Kimihiro Shimizu, Toshireru Nagashima, Yoichi Ohtaki, Seshiru<br />
Nakazawa, Yoko Azuma, Misaki Iijima, Takayuki Kosaka, Toshiki Yajima, Akira<br />
Mogi, Hiroyuki Kuwano<br />
Division of General <strong>Thoracic</strong> Surgery, Integrative Center of General Surgery, Gunma<br />
University Hospital, Maebashi/Japan<br />
Background: Postoperative radiotherapy (PORT) against thymic epithelial<br />
tumors is mainly performed based on Masaoka staging. However there is no<br />
definite indication for PORT, and its efficacy is still controversial. Meanwhile,<br />
the relationship between the efficacy of PORT and WHO classification is<br />
also unclear. This study aimed to clarify the efficacy of PORT in association<br />
with both Masaoka staging and WHO classification. Methods: A 262 patients<br />
with thymic epithelial tumors surgically treated in our institute from April<br />
1990 to December 2015 were reviewed. The clinicopathological data were<br />
retrospectively evaluated for prognosis and recurrence. Results: There were<br />
86 patients with stageI, 121 with stageII, 35 with stage III, 13 with stage IVa,<br />
and 7 with stage IVb thymic epithelial tumors according to Masaoka staging.<br />
As for histological type, 37 patients had type A, 50 had type AB, 59 had type<br />
B1, 43 had type B2, 44 had type B3, and 29 had type C (thymic carcinoma)<br />
according to WHO classification (2004). Eighty cases (30.5%) underwent<br />
PORT. Although PORT showed no association with OS (hazard ratio [HR],<br />
0.565; 95% confidence interval [CI], 0.298 to 1.070; p=0.080), there was no<br />
recurrence in patients who received PORT. Subgroup analysis of Masaoka<br />
staging (stageI-II: HR, 2.445; 95% CI, 0.905-6.607; p=0.078, stage III-IV: HR,<br />
0.434; 95% CI, 0.145 to 1.302, p=0.137,) or WHO classification (type A-B1: HR,<br />
2.859; 95% CI, 1.050-7.719, p=0.030, type B2-C: HR, 1.460; 95% CI, 0.502 to<br />
4.248; p=0.488) alone showed no association with prognosis either. However<br />
in thymoma patients who were classified in both stageIII-IV and type B2-C<br />
group, PORT was associated with better OS (HR, 0.189; 95% CI, 0.049 to 0.724;<br />
p=0.015). Conclusion: PORT is effective in patients with thyimic epithelial<br />
tumors who are classified in both stageIII-IV and type B2-C.<br />
Keywords: postoperative radiotherapy, WHO Classification, thymic epithelial<br />
tumor, Masaoka staging<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 />
P2.04-003 CHEMOTHERAPY IN ADVANCED THYMIC EPITHELIAL<br />
TUMORS: INSIGHTS FROM THE RYTHMIC PROSPECTIVE COHORT<br />
Claire Merveilleux Du Vignaux 1 , Maria Bluthgen 2 , Laurent Mhanna 3 , Eric<br />
Dansin 4 , Laurent Greillier 5 , Eric Pichon 6 , Hervé Léna 7 , Christelle Clément-<br />
Duchêne 8 , Gilbert Massard 9 , Virginie Westeel 10 , Marie Robert 11 , Xavier<br />
Quantin 12 , Gérard Zalcman 13 , Luc Thiberville 14 , Thierry Molina 15 , Julien<br />
Mazieres 3 , Benjamin Besse 16 , Nicolas Girard 17<br />
1 Hospices Civils de Lyon, Lyon/France, 2 Gustave Roussy, Villejuif/France,<br />
3 University Hospital, Toulouse/France, 4 Cancer Center, Lille/France, 5 University<br />
Hospital, Marseille/France, 6 University Hospital, Tours/France, 7 University<br />
Hospital, Rennes/France, 8 Cancer Center, Nancy/France, 9 University Hospital,<br />
Strasbourg/France, 10 University Hospital, Besançon/France, 11 Cancer Center,<br />
Nantes/France, 12 University Hospital, Montpellier/France, 13 University Hospital<br />
Bichat, Paris/France, 14 University Hospital, Rouen/France, 15 University Hospital<br />
Necker, Paris/France, 16 Department of Cancer Medicine, Gustave Roussy, Villejuif/<br />
France, 17 <strong>Thoracic</strong> <strong>Oncology</strong>, Hospices Civils de Lyon, Lyon/France<br />
Background: Thymic Epithelial Tumors (TET) are rare intrathoracic<br />
malignancies, which may be aggressive and difficult to treat. In the advanced<br />
setting, chemotherapy may be delivered as a primary/induction therapy<br />
before subsequent surgery or definitive radiotherapy, and/or as exclusive<br />
treatment in patients for whom no focal treatment is feasible, and/or in<br />
the setting of recurrences. As no randomized trial and a limited number of<br />
prospective studies are available, there is paucity of prospective, multicentre<br />
evidence regarding response rates and survival of patients. RYTHMIC<br />
is the nationwide network for TET in France. The RYTHMIC prospective<br />
database is hosted by the French Intergroup (IFCT), and collects data<br />
for all patients diagnosed with TET, for whom management is discussed<br />
at a national multidisciplinary tumor board (MTB) based on consensual<br />
recommendations. Primary, exclusive chemotherapy, and chemotherapy for<br />
recurrence accounted for 149 (11%), 37 (3%), and 67 (5%) questions of a total<br />
of 1401 questions raised at the MTB between 2012 and 2015. Methods: All<br />
consecutive patients for whom chemotherapy and/or systemic treatment<br />
was discussed at the RYTHMIC MTB from 2012 to 2015 were identified from<br />
the RYTHMIC prospective database. Main endpoints were response rates and<br />
progression-free and overall survival. Results: At the time of analysis, data<br />
were available for 156 patients (80 thymic carcinomas, and 76 thymomas),<br />
for whom the management led to raise 283 questions at the MTB: 67 (24%)<br />
for primary chemotherapy, 35 (11%) for exclusive chemotherapy, and 181<br />
(64%) for recurrences. For primary and exclusive chemotherapy, the most<br />
frequently administered regimen was CAP, producing response rates of 70%<br />
and 60%, respectively. A total of 104 patients received at least one line of<br />
chemotherapy for recurrence; 53 patients received second-line treatment,<br />
and 13 and 7 patients received third- and fourth line treatment. In the setting<br />
of first recurrence, carboplatine-paclitaxel combination was the most<br />
preferred regimen, administered to 54% of patients; overall response and<br />
disease control rates to systemic treatments for recurrences were 13% and<br />
42% in thymic carcinomas, and 19% and 43% in thymomas (p=0.38 and p=0.92,<br />
respectively). Median recurrence-free survival after primary chemotherapy<br />
was 16.6 months; median progression-free survival after exclusive<br />
chemotherapy, and first-, second-, and third-line chemotherapy for recurrence<br />
were 6.0 months, and 7.6 months, 6.2 months, and 6.0 months. Conclusion:<br />
Our data provide with a unique insight in the efficacy of chemotherapy for<br />
advanced thymic epithelial tumors in a real-life setting; our results help the<br />
decision-making to better define the optimal therapeutic strategies.<br />
Keywords: chemotherapy, Thymoma, Thymic carcinoma<br />
Copyright © 2016 by the International Association for the Study of Lung Cancer<br />
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