Abstract

ObjectivesComplete resection of thymic neoplasms is important for achieving a favorable prognosis; however, the efficacy of neoadjuvant therapy remains controversial. We investigated the effect of induction therapy on complete resection and survival using 3-dimensionally reconstructed images to measure tumor volume.MethodsEighty-nine patients who underwent surgical resection for Masaoka-Koga stage III–IV thymic neoplasms between January 2000 and December 2013 were enrolled, including 71 and 18 in the primary surgery and neoadjuvant therapy groups, respectively. Baseline characteristics, postoperative outcomes, and survival rates were analyzed. Moreover, baseline and post-neoadjuvant therapy tumor volumes were compared among patients in the neoadjuvant group.ResultsAdjacent mediastinal structure invasion was significantly rarer in the primary surgery group than in the neoadjuvant group (1.27±1.09 vs. 2.61±1.42, p<0.001). On subgroup analysis of patients who underwent neoadjuvant therapy, tumor volumes decreased significantly from 206.08±132.32 cm3 to 81.25±71.24 cm3 post-therapy (p = 0.001). Interestingly, only the pre-neoadjuvant tumor volume was significantly associated with complete resection, while the post-neoadjuvant volume was not (p = 0.012 and p = 0.458, respectively). Moreover, despite significantly reduced tumor volumes, patients in the neoadjuvant therapy group did not exhibit significantly different R0 resection rates (odds ratio 1.490, p = 0.581) or overall survival (p = 0.285) compared to those in the primary surgery group.ConclusionsNeoadjuvant therapy does not significantly influence the R0 resection rate or overall survival relative to primary surgery. Nevertheless, it may by useful for patients planning surgical resection because it significantly reduces the presurgical tumor volume and extent of invasion.

Highlights

  • Thymic neoplasms are rare tumors with an annual incidence of 1–5 per million people [1]

  • According to the International Thymic Malignancy Interest Group, approximately 30% of thymic neoplasms are of Masaoka-Koga stage III–IVa [2]

  • The optimal treatment for advanced thymic tumors remains controversial [3]; in patients with locally advanced disease, achieving complete resection is a critical determinant of recurrence and overall survival [4]

Read more

Summary

Introduction

Thymic neoplasms are rare tumors with an annual incidence of 1–5 per million people [1]. The optimal treatment for advanced thymic tumors remains controversial [3]; in patients with locally advanced disease, achieving complete resection is a critical determinant of recurrence and overall survival [4]. That patients with locally advanced thymic tumors have poorer outcomes than those with early-stage disease is evidence for the clinical necessity of multimodal approaches [5]. Cisplatin-based induction chemotherapy is generally well tolerated, and patients with advanced thymic tumors have exhibited favorable responses to it in several prospective clinical trials [4, 6]. A previous meta-analysis revealed that thymomas exhibited marked chemosensitivity with clinical response rates of 49–70%; complete resection rates ranged from 67% to 79% [4]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call