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18FDG-PET-CT identifies histopathological non-responders after neoadjuvant chemotherapy in locally advanced gastric and cardia cancer: cohort study
by
Lehmann, Kuno
, Schneider, Paul M.
, Eshmuminov, Dilmurodjon
, Veit-Haibach, Patrick
, Rordorf, Tamara
, Weber, Achim
, Vetter, Diana
, Bauerfeind, Peter
, Samaras, Panagiotis
in
Adjuvant chemotherapy
/ AEG
/ Biomedical and Life Sciences
/ Biomedicine
/ cancer imaging
/ Cancer Research
/ Care and treatment
/ Cohort analysis
/ Gastric cancer
/ Health Promotion and Disease Prevention
/ Histopathologic regression
/ interventional therapeutics
/ Medicine/Public Health
/ Oncology
/ PET-CT
/ Research Article
/ Stomach cancer
/ Surgical Oncology
2018
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18FDG-PET-CT identifies histopathological non-responders after neoadjuvant chemotherapy in locally advanced gastric and cardia cancer: cohort study
by
Lehmann, Kuno
, Schneider, Paul M.
, Eshmuminov, Dilmurodjon
, Veit-Haibach, Patrick
, Rordorf, Tamara
, Weber, Achim
, Vetter, Diana
, Bauerfeind, Peter
, Samaras, Panagiotis
in
Adjuvant chemotherapy
/ AEG
/ Biomedical and Life Sciences
/ Biomedicine
/ cancer imaging
/ Cancer Research
/ Care and treatment
/ Cohort analysis
/ Gastric cancer
/ Health Promotion and Disease Prevention
/ Histopathologic regression
/ interventional therapeutics
/ Medicine/Public Health
/ Oncology
/ PET-CT
/ Research Article
/ Stomach cancer
/ Surgical Oncology
2018
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18FDG-PET-CT identifies histopathological non-responders after neoadjuvant chemotherapy in locally advanced gastric and cardia cancer: cohort study
by
Lehmann, Kuno
, Schneider, Paul M.
, Eshmuminov, Dilmurodjon
, Veit-Haibach, Patrick
, Rordorf, Tamara
, Weber, Achim
, Vetter, Diana
, Bauerfeind, Peter
, Samaras, Panagiotis
in
Adjuvant chemotherapy
/ AEG
/ Biomedical and Life Sciences
/ Biomedicine
/ cancer imaging
/ Cancer Research
/ Care and treatment
/ Cohort analysis
/ Gastric cancer
/ Health Promotion and Disease Prevention
/ Histopathologic regression
/ interventional therapeutics
/ Medicine/Public Health
/ Oncology
/ PET-CT
/ Research Article
/ Stomach cancer
/ Surgical Oncology
2018
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18FDG-PET-CT identifies histopathological non-responders after neoadjuvant chemotherapy in locally advanced gastric and cardia cancer: cohort study
Journal Article
18FDG-PET-CT identifies histopathological non-responders after neoadjuvant chemotherapy in locally advanced gastric and cardia cancer: cohort study
2018
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Overview
Background
Pathologic response to neoadjuvant chemotherapy (neoCTX) is a prognostic factor in many cancer types, and early prediction would help to modify treatment. In patients with gastric and esophagogastric junction (AEG) cancer, the accuracy of FDG PET-CT to predict early pathologic response after neoadjuvant chemotherapy (neoCTX) is currently not known.
Methods
From a consecutive cohort of 72 patients, 44 patients with resectable, locally-advanced gastric cancer or AEG Siewert type II and III received neoCTX after primary staging with endoscopic ultrasound, PET-CT and laparoscopy. Overall, 14 patients did not show FDG uptake, and the remaining 30 were restaged by PET-CT 14 days after the first cycle of neoCTX. Metabolic response was defined as decrease of tumor standardized uptake value (SUV) by ≥35%. Major pathologic regression was defined as less than 10% residual tumor cells.
Results
Metabolic response after neoCTX was detected in 20/30 (66.7%), and non-response in 10/30 (33.3%) patients. Among metabolic responders,
n
= 10 (50%) showed major and n = 10 (50%) minor pathologic regression. In non-responders,
n
= 9 (90%) had minor and 1 (10%) a major pathologic regression. This resulted in a sensitivity of 90.9%, specificity 47.3%, positive predictive value 50%, negative predictive value 90% and accuracy of 63.3%.
Conclusion
Response PET-CT after the first cycle of neoCTX does not accurately predict overall pathologic response. However, PET-CT reliably detects non-responders, and identifies patients who should either immediately proceed to resection or receive a modified multimodality therapy.
Trial registration
The trial was registered and approved by local ethics committee PB_2016–00769.
Publisher
BioMed Central,BioMed Central Ltd,BMC
Subject
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