Gastroesophageal Junction Cancer Clinical Trial
Official title:
PET/MR-imaging and Circulating Tumour Cells to Evaluate the Response of Chemotherapy in Patients With Gastroesophageal Junction Cancer
The incidence of malignity in the gastroesophageal junction (GEJ) is rising in Denmark, 400
new cases annually 1. 60% of the patients with GEJ cancer have disseminated disease
(M1-stage) at time of diagnosis and are consequently unable to undergo curative intended
surgery. The prognosis is poor, with 5-year survival rates of approximately 2 % for these
60% and the treatment only consists of palliative therapy 1. For the remaining approximately
40 % who are assessed as candidates for curative intended surgery, the 5-year survival rate
is 33 % 1. This emphasizes the need for further research and knowledge concerning tumour
biology and spontaneous course of the disease.
In Denmark, all cancer patients are enrolled in a specific cancer program. The primary
diagnostic work-up for GEJ cancers includes gastroscopy with biopsy, blood samples,
ultrasonography scan, Positronemissionstomography (PET) and Computed tomography (CT) alone
or PET/CT in combination 2. From these parameters physicians determine resectability and
TNM-stage (tumour staging), which is substantial for the prognosis and future treatment. The
primary goal is to achieve a macroscopically resection of tumour and lymphnodes in relation
to the stomach and oesophagus (Esophagectomi a.m. Ivor Lewis and D1+ lymphadenectomy in the
abdomen and thorax). In addition to surgery, patients receive perioperative chemotherapy,
which consist of three series of chemotherapy preoperative and three series postoperative
approximately 21-28 days after surgery.
Approximately 12.6 % of patients receiving perioperative chemotherapy prior to surgery will
have disease progression due to chemotherapy resistance during the therapy 3. This
unintentionally leads to shifting these patients from the resectable group to non-resectable
group (palliative treatment). Thus, the possibility for detecting response to perioperative
chemotherapy is of great interest. A paradigm shift towards an individualised tailored
therapy form has emerged in recent years, which potentially require a higher need for
diagnosis on molecular level. Today most molecular biological methods apply tissue samples
for in-vitro analyses, but new radiological tools provide opportunity for non-invasive
examinations; for example PET can with a radioactive sugar compound: Flour-18 deoxyglucose
(18F-FDG). This compound is injected through a catheter in a larger vein (media cubiti vein)
and absorbed in cells with increased metabolism - especially cancer cells. A PET scanner
registers the absorption; this radiology modality can provide valid information, which is
essential for non-invasive tumour staging and monitoring response under a specific therapy.
A new diagnostic modality is PET scan combinated with magnetic resonance (PET/MR)
simultaneously. So far, no studies have conducted an evaluation of simultaneous PET/MR scan
to assess the perioperative chemotherapy response in patients with GEJ cancer. However, some
studies suggest that commercially available PET/MR scanner might contribute in a diagnostic
elucidation 6. Simultaneous PET/MR scan might in theory minimize the misinterpretations of
potential response changes after chemotherapy, which can appear in the interval between
separate PET, CT and MR scans 4,5,7. Studies have found PET scan of GEJ cancer could be
helpful as a prognostic tool to differentiate between responders and non-responders during
chemotherapy 9. Standardized uptake value (SUV) is a unit that display the absorption of
18F-FDG and is used routinely to quantify tumour glucose metabolism in PET scan 8. A change
of more than 35 % in SUV measurements before and after the induction of chemotherapy is
considered as the definition of responders and non-responders in earlier studies 9.
The MR technique is based on magnetic fields and radio waves. Diffusion Weighted Imaging
(DWI) is a non-invasive MR-modality, which measures the changes in water diffusion (Brownian
movements) throughout tissue. These changes are measured in Apparent Diffusion Coefficient
(ADC), a parameter derived from DWI and reflects the change in diffusion 7. ADC and DWI can
be used to differentiate between benign and malignant tumours, due to a larger cell density
in malignant tumours. Consequently, malignant tissue has a decreased diffusion relative to
normal tissue. ADC has been used as a factor in some studies to predict the response to
chemotherapy 10. A single study has shown a rise in ADC-value two weeks after initiation of
chemotherapy in patients with GEJ cancer, and demonstrated that the percentage change in
ADC-value between the groups (responders and non-responders) is significantly different 11.
Simultaneous PET- and MR scan might be very useful to evaluate the response to chemotherapy
in patients with GEJ cancer compared with these parameters alone. The opportunity for a more
individualised tailored treatment in future might be possible with PET/MR.
n/a
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