The effect of neoadjuvant chemotherapy for hepatic colorectal metastases on the accuracy of FDG-PET scan

2005 ◽  
Vol 9 (4) ◽  
pp. 524-525
Author(s):  
N LUBEZKY ◽  
R NAKACHE ◽  
A FIGER ◽  
J KLAUZNER ◽  
M BENHAIM
2016 ◽  
Vol 28 (2) ◽  
pp. 95-99 ◽  
Author(s):  
Hany Abdel Rahman ◽  
Mohamed Sedky ◽  
Asmaa Hamoda ◽  
Tarek Raafat ◽  
Ayda Youssef ◽  
...  

2021 ◽  
Vol Publish Ahead of Print ◽  
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Abtin Doroudinia ◽  
Behnam Safarpour Lima ◽  
Mehrdad Bakhshayesh Karam ◽  
Niloufar Ghadimi ◽  
Farhad Yousefi

Blood ◽  
2012 ◽  
Vol 119 (7) ◽  
pp. 1665-1670 ◽  
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Craig H. Moskowitz ◽  
Matt J. Matasar ◽  
Andrew D. Zelenetz ◽  
Stephen D. Nimer ◽  
John Gerecitano ◽  
...  

Abstract We previously reported that remission duration < 1 year, extranodal disease, and B symptoms before salvage chemotherapy (SLT) can stratify relapsed or refractory Hodgkin lymphoma (HL) patients into favorable and unfavorable cohorts. In addition, pre-autologous stem cell transplant (ASCT) 18FDG-PET response to SLT predicts outcome. This phase 2 study uses both pre-SLT prognostic factors and post-SLT FDG-PET response in a risk-adapted approach to improve PFS after high-dose radio-chemotherapy (HDT) and ASCT. The first SLT uses 2 cycles of ICE in a standard or augmented dose (ICE/aICE), followed by restaging FDG-PET scan. Patients with a negative scan received a transplant. If the FDG-PET scan remained positive, patients received 4 biweekly doses of gemcitabine, vinorelbine, and liposomal doxorubicin. Patients without evidence of disease progression proceeded to HDT/ASCT; those with progressive disease were study failures. At a median follow-up of 51 months, EFS analyzed by intent to treat as well as for transplanted patients is 70% and 79%, respectively. Patients transplanted with negative FDG-PET, pre-HDT/ASCT after 1 or 2 SLT programs, had an EFS of > 80%, versus 28.6% for patients with a positive scan (P < .001). This prospective study provides evidence that the goal of SLT in patients with Hodgkin lymphoma should be a negative FDG-PET scan before HDT/ASCT. The study was registered at www.clinicaltrials.gov as NCT00255723.


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