Predictive Value of Interim [18F]Fluorodeoxyglucose–Positron Emission Tomography in Advanced-Stage Hodgkin Lymphoma Is Not Well Established
Author:
Affiliation:
1. Hugo J.A. Adams, University Medical Center Utrecht, Utrecht, the Netherlands; and Thomas C. Kwee, University Medical Center Groningen, Groningen, the Netherlands
Publisher
American Society of Clinical Oncology (ASCO)
Subject
Cancer Research,Oncology
Link
https://ascopubs.org/doi/pdfdirect/10.1200/JCO.2016.68.1494
Reference10 articles.
1. US Intergroup Trial of Response-Adapted Therapy for Stage III to IV Hodgkin Lymphoma Using Early Interim Fluorodeoxyglucose–Positron Emission Tomography Imaging: Southwest Oncology Group S0816
2. Prognostic value of interim FDG-PET in Hodgkin lymphoma: systematic review and meta-analysis
3. The predictive role of interim positron emission tomography for Hodgkin lymphoma treatment outcome is confirmed using the interpretation criteria of the Deauville five-point scale
4. Early Interim 2-[18F]Fluoro-2-Deoxy-D-Glucose Positron Emission Tomography Is Prognostically Superior to International Prognostic Score in Advanced-Stage Hodgkin's Lymphoma: A Report From a Joint Italian-Danish Study
5. Importance of Histologic Verification of Positive Positron Emission Tomography/Computed Tomography Findings in the Follow-Up of Patients With Malignant Lymphoma
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Interim PET-results for prognosis in adults with Hodgkin lymphoma: a systematic review and meta-analysis of prognostic factor studies;Cochrane Database of Systematic Reviews;2020-01-13
2. Interim PET-results for prognosis in adults with Hodgkin lymphoma: a systematic review and meta-analysis of prognostic factor studies;Cochrane Database of Systematic Reviews;2019-09-16
3. Unproven value of end-of-treatment FDG-PET in Hodgkin lymphoma;European Journal of Nuclear Medicine and Molecular Imaging;2017-07-14
4. Reply: Interim PET in Hodgkin Lymphoma: Is It So Useless?;Journal of Nuclear Medicine;2017-03-09
5. Reply to H.J.A. Adams et al, E.A. Hawkes et al, and C.F. Hess et al;Journal of Clinical Oncology;2017-01-20
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