Author/Authors :
Tacyildiz، Nurdan نويسنده Department of Pediatric Oncology, School of Medicine, Ankara University, Ankara, Turkey , , Tanyildiz، Hikmet Gulsah نويسنده Department of Pediatric Hematology/Oncology, Cerrahpasa
Medical Faculty, Istanbul University, Istanbul,
Turkey , , Dincaslan، Handan Ugur نويسنده Department of Pediatric Oncology, School of Medicine, Ankara University, Ankara, Turkey , , Yavuz، Gulsan نويسنده Department of Pediatric Oncology, School of Medicine, Ankara University, Ankara, Turkey , , Unal، Emel نويسنده Department of Pediatric Oncology, School of Medicine, Ankara University, Ankara, Turkey , , Ozkan، Elgin نويسنده Department of Nuclear Medicine, School of Medicine, Ankara University, Ankara, Turkey , , Soydal، Cigdem نويسنده Department of Nuclear Medicine, School of Medicine, Ankara University, Ankara, Turkey , , Kucuk، Ozlem نويسنده Department of Nuclear Medicine, School of Medicine, Ankara University, Ankara, Turkey , , Yildiz، Yusuf نويسنده Department of Orthopedics, School of Medicine, Ankara University, Ankara, Turkey ,
Abstract :
Background
The prognosis is still poor for patients with a metastatic bone tumor and new treatment approaches (anti-VEGF and tyrosine kinase inhibitors vs) are therefore needed.
Objectives
The aim of our study was to evaluate how the primary and metastatic lesions of our patients with a bone tumor were affected by these treatments and to determine the importance of the 18F-FDG PET method.
Patients and Methods
Twenty metastatic bone tumor cases were included. Sorafenib and anti-VEGF were added to the standard treatment in cases with widespread metastatic disease at diagnosis or after neoadjuvant chemotherapy showing less than 90% tumor necrosis in the surgical sample. Positron emission tomography (PET) imaging was performed at diagnosis, the preoperative period following neoadjuvant chemotherapy, during postoperative follow-up, and when treatment was discontinued.
Results
The primary treatment region median SUVmax level decreased from 7.35 to 2.5 in the living patients (n = 16) while there was no significant decrease in the patients who succumbed to the disease (P < 0.001). Comparison of the pre- and post-treatment metastasis region median SUVmax levels in patients with metastatic involvement showed a decrease from 2.1 to 0 in the surviving patients but only from 4.8 to 3.2 in the deceased patients (P < 0.01). Survival results indicated that 28.6% of the patients receiving classical treatment only died while all the patients receiving additional sorafenib and anti-VEGF survived.
Conclusions
18F-PET may be a useful technique before and during the follow-up of neoadjuvant treatment in pediatric metastatic bone tumor patients. The addition of sorafenib and anti-VEGF to classical treatment has a favorable contribution to the response and therefore the survival duration.