Gastroesophageal-junction CancerNCT02085564
Significance of Peritoneal Washing Cytology Before and After Neoadjuvant Chemotherapy in Patients With Esophagogastric-junction Cancer
An observational study of Gastroesophageal-junction Cancer, run by Copenhagen University Hospital, Rigshospitalet at 1 site in Denmark.
Trial summary
Background: The prevalence of gastroesophageal-junction cancer (cancer between the distal part of the oesophagus, and proximal part of the stomach/GEJ-cancer) is increasing in Denmark with more than 400 patients per year. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Gastroesophageal-junction Cancer
- What is being tested?
- Peritoneal washing cytology
- Type of treatment
- Surgery or procedure
- How many people
- 87 participants
- Where
- 1 siteDenmark
- Study dates
- Mar 2014to Jun 2015
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients with biopsy verified GEJ-cancer referred from peripheral hospitals in the region of Sjælland and the Capitol. (The treatment of GEJ-cancer is centered at Rigshospitalet. All of our patients are referred from other hospitals)
Who may be able to join
- patients with biopsy verified GEJ-cancer referred to the department of surgical gastroenterology, Rigshospitalet, which is considered resectable at MDT-conference.
- >18 years old
- informed consent
Who cannot join
- < 18 years old
- Not informed consent
Trial locations and contacts
1 site in 1 country.
Denmark1 site
Department of surgical gastroenterology, Rigshospitalet
Copenhagen, Kbh Ø, 2100
About this study
Background:
The prevalence of gastroesophageal-junction cancer (cancer between the distal part of the oesophagus, and proximal part of the stomach/GEJ-cancer) is increasing in Denmark with more than 400 patients per year. The 5-year overall survival is less than 10% for the 2/3 of the patients, which are not considered resectable. Even for the 1/3, which is treated with surgical intervention and neoadjuvant chemotherapy the overall-survival is approximately 30%.
Read more
The current Danish intended curative treatment consists of esophagectomy (surgical resection of the oesophagus with extended lymphadenectomy in abdomen and thorax (removal of lymphnodes)). Furthermore, perioperative chemotherapy consists of 6 series neoadjuvant chemotherapy (3 series before, and 3 series after operation).
Unresectable patients receive palliative chemotherapy and no resection. Peritoneal washing cytology (PWC) is a recommended prediagnostic modality in gastric cancer patients. The method is used to detect free peritoneal cancer cells in the abdominal cavity even when macroscopic carcinomatosis is not present (i.e. the cancer has spread to other parts of the abdomen).
Carcinomatosis can be found in up to 19% in gastric cancer patients often in the peritoneum. Positive peritoneal cytology (C1) can be identified in up to 7% of gastric cancer patients without metastases (C1M0), i.e. malignant cells can be identified in the peritoneal washing, but tumor spread has not been identified.
Lots of studies indicate that C1-disease is an independent prognostic predictor for decreased survival, and increased recurrence rate, comparable with M1 patients (i.e. patients with distant metastases).
The American Joint Committee on cancer recommends that C1 patients should be treated non-surgically - even when M1 disease has not been identified.
On the basis of the above, PWC can be used to identify patients at greater risk for recurrence, and thereby not candidates for intended curative treatment.
It is a fact, though, that C1M0 patients have a better survival than C1M1 patients. Currently, there is no level-1 evidence for specific treatment of C1M0 patients, why further research is required to approach this patient group in the most comprehensive way. The focus group of our study is therefore C1M0 patients, because of the difference in opinions. Furthermore most evidence is based on gastric carcinomas, why GEJ-cancer patients are the group, we will examine.
Purpose:
Peritoneal washing cytology (PWC) is performed as a standard prediagnostic modality at Rigshospitalet, for patients with gastric- and GEJ cancer, considered resectable at preceding multidisciplinary conference. Most studies in the past 20-years have focused on gastric cancer, and not specifically GEJ-cancer.
This study will determine the usefulness of peritoneal washing cytology, and thereby verifying our own standard regarding GEJ-cancer. Furthermore, we will determine the effect of neoadjuvant chemotherapy on free peritoneal tumor cells and its correlation with overall survival.
This study is intended as a validation of our own standard.
Read the detailed description
- Background: The prevalence of gastroesophageal-junction cancer is increasing in Denmark with more than 400 patients per year. The 5-year overall survival is less than 10% for the 2/3 of the patients, which are not considered resectable. Even for the 1/3, which is treated with surgical intervention and neoadjuvant chemotherapy, the overall-survival is approximately 30%. The current Danish intended curative treatment consist of esophagectomy a.m. Ivor Lewis with extended lymphadenectomy in the abdomen and thorax. Furthermore, perioperative chemotherapy consists of 6 series neoadjuvant chemotherapy. Unresectable patients receive palliative chemotherapy and no resection. Peritoneal washing cytology is a recommended prediagnostic modality in gastric cancer. The method is used to detect free peritoneal cancer cells in the abdominal cavity, even when macroscopic carcinomatosis is not present. Carcinomatosis can be found in up to 19% in gastric cancer patients, often in the peritoneum. Positive peritoneal cytology (C1) can be identified in up to 7% of gastric cancer patients without metastases (C1M0). Lots of studies indicate that C1-disease is an independent prognostic predictor for decreased survival, and increased recurrence rate, comparable with M1 patients (i.e. patients with distant metastases). The American Joint Committee on cancer recommends that C1 patients should be treated non-surgically - even when M1 disease is not identified. On the basis of the above, PWC can be used to identify patients at greater risk for recurrence, and thereby not candidates for intended curative treatment. It is a fact, though, that C1M0 patients have a better survival than C1M1 patients. Currently, there is no level-1 evidence supporting specific treatment of C1M0 patients, why further research is required to approach this patient group in the most comprehensive way. Therefore, the focus group of our study is C1M0 patients, because of the differences in opinions. Furthermore, most evidence is based on gastric carcinomas, why GEJ-cancer patients are the group, we will examine. Results from other investigators regarding treatment of C1M0 patients: Lee et al. found a median survival of 21 months and 4 months in gastrectomized versus non-gastrectomized patients. Lorentzen et al. found a median 5-year survival of 71,4% and 25% in gastrectomized patients, who had C1 at staging laparoscopy and converted after preoperative chemotherapy versus persistent C1-disease after preoperative chemotherapy. Another interesting treatment modality for C1M0 patients is extensive intraperitoneal lavage (EIPL) examined by a Japanese study group. 88 C1M0 patients were randomized into three group; 1. Gastrectomy only, 2. Gastrectomy + intraperitoneal chemotherapy (IPC), and 3. Gastrectomy + IPC + EIPL. Group 3 compared to group 2 had a significant better 5 year overall survival of 43,8% versus 4,6% (p<0,0001). Further research is required to establish specific guideline for C1M0 patients.
- Purpose: Peritoneal washing cytology (PWC) is performed as a standard prediagnostic modality at Rigshospitalet for patients, with gastric- and GEJ cancer, considered resectable at preceding multidisciplinary conference. Most studies in the past 20-years have focused on gastric cancer, and not specifically GEJ-cancer. This study will determine the usefulness of peritoneal washing cytology, and thereby, verify our own standard regarding GEJ-cancer. Furthermore, we will determine the effect of neoadjuvant chemotherapy on free peritoneal tumor cells, correlated with overall survival. See outcome measures for more detailed description. This study is intended as a validation of our own standard.
- Methods Our current algorithm includes peritoneal washings performed at two different time points:
- Staging laparoscopy using one port technique
- After pneumoperitoneum and oversight of the abdomen is established, a puncture is created subhepatically in the midclavicular line with a pigtail catheter ch. 10.
- 500ml of sterile 37°C NaCl is injected through the catheter and manually dispersed throughout the abdomen by positioning the operating table in different positions.
- At least 200ml of fluid is aspirated subhepatically through the catheter.
- 100ml is analysed by an experienced pathologist for any malignant cancer cells.
- Initially, before operation (transthoracic esophagectomy): either open operation or robot assisted o Robot assisted: same technique as above o Open operation: • After abdominal incision and exploration 500ml °C of sterile NaCl is manually dispersed in the abdominal cavity.
- Peritoneal washings is aspirated subhepatically
- Further algorithm as described above
- Recruiting of patients:
90 consecutive patients with biopsy verified GEJ-cancer will be included. Because PWC is already a standard guideline for this group of patients at Rigshospitalet, there will be no direct inclusion of patients.
- Study design: Prospective feasibility study. Patients considered candidates for intented curative therapy, according to The Danish Esophagus-,GEJ- and Gastric Cancer Association (DECV), is included. Furthermore, patients must have undergone evaluation of a multidisciplinary panel of specialist including the specialties surgical gastroenterology, thoracic surgery, oncology, pathology, radiology, and clinical nuclear medicine.
- Data: Patient data will be obtained from internal systems of Rigshospitalet including OPUS, LABKA, PatologiWEB, and ORBIT.
The following preoperative data will be obtained:
- age, sex, initial symptoms, tumour staging (TNM version 7) and histology characteristics, disease anamnesis, chemotherapy treatment, medicine anamnesis, comorbidity, postoperative complications, mortality, specifics regarding PWC such as injected volume of NaCl, procedure time, aspirated amount of fluid, and cytology findings.
- Approval: Authorization of data retreatment is approved by The Danish Data Protection Agency.
Approval of The Danish Ethics Committee has not been applied, because the study is a validation of our own standard guideline.
- Finances:
The following contributors have financed the study:
The Danish Cancer Society Research Center, Mogens Andreasen Fonden, Familien Erichsens familiefond, and Rigshospitalet.
All expenses have been covered.
- Results Both negative and positive results will be published in a national and/or international journal.
- Practical feasibility The relevant patients and the medical expertise are to find at the surgical gastroenterology department of Rigshospitalet. 120 staging laparoscopies are being performed per year in the handling of gastric cancer patients. Persons and departments involved in the study have agreed to allocate time and resources to the study. Furthermore, our department has a technician affiliated with our institution on full time basis, who is going to provide development, optimization, and assistance of projects associated with GEJ-cancer.
- Conditions
- Gastroesophageal-junction Cancer
- Being tested
- Peritoneal washing cytology
- Keywords
- Gastroesophageal-junction cancer, neoadjuvant chemotherapy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Peritoneal washing cytologyProcedure or surgery
Also called Peritoneal lavage
The methode is describes in the detailed study description
| Study group | Role | What they receive |
|---|---|---|
| GEJ-cancer patients consideres resectable | All patients have biopsy verified GEJ-cancer, and has been considered for intend curative resection by a multidisciplinary panel of specialists. Receives: Procedure: Peritoneal washing cytology |
What is being measured
The primary outcome is the main question the study is designed to answer.
The effect of neoadjuvant chemotherapy (NAC) on free peritoneal cancer cells (FPCCs)
Peritoneal washings will be performed at two time points. The first at the time of staging laparoscopy and the second initially before esophagectomy. Thereby, we will gain a measure for the effect of NAC on FPCC.
We are interested in the following:
- patients converting from positive cytology at staging laparoscopy to negative before surgery or reverse.
- patients with persisting negative cytology at both measure points or persisting positive.
These measurements for these 4 groups will be correlated with overall survival (up to 5 years).
Measured: 1 year
Secondary outcomes (2)
Postoperative complications
Minor complications:
atelectasis, pleural effusion, pneumonia, chylothorax, pulmonary embolism, pneumothorax, empyema, wound infection, supraventricular arrhythmia, radiographic anastomotic leakage
Severe complications:
Respiratory insufficiency requiring reintubation, heart failure, cerebrovascular incidents, renal insufficiency, AMI, sepsis, death
Measured: 2 weeks after surgery
Overall survival
Overall survival will be determined after 5 years postoperatively. In the meantime, we will assess survival after 1,2,3,4 and 5 years
Measured: up to 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Mar 2014 (estimated)
- Study startMar 2014
- Primary completionJun 2015
- Study completionJun 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Gastroesophageal-junction CancerStudies of the same condition, open and under way.
- More trials run by Copenhagen University Hospital, RigshospitaletThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 87 participants (actual)
Sponsor and investigators
- Lead sponsor
- Copenhagen University Hospital, Rigshospitalet
- Sponsor type
- University, hospital or other
- Collaborators
- Danish Cancer Society
- Responsible party
- Principal investigator, Rune Broni Strandby, Copenhagen University Hospital, Rigshospitalet
- Investigators
- Lars Bo Svendsen, Prof., MD., DMSc., Study director, Department of surgical gastroenterology, RigshospitaletMichael Patrick Achiam, MD. phD., Study chair, Department of surgical gastroenterology, RigshospitaletRune Broni Strandby, Junior researcher, Principal investigator, Department of surgical gastroenterology, Rigshospitalet
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02085564
- Sponsor's protocol ID
- 050314-Rstrandby1
- Status last verified
- Jun 2015
- First submitted
- 11 Mar 2014
- Last updated
- 3 Jun 2015
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Jun 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Significance of Peritoneal Washing Cytology Before and After Neoadjuvant Chemotherapy in Patients With Esophagogastric-junction Cancer
- ClinicalTrials.gov ID
- NCT02085564
- Acronym / sponsor ID
- 050314-Rstrandby1
- Conditions
- Gastroesophageal-junction Cancer
- Keywords
- Gastroesophageal-junction cancer, neoadjuvant chemotherapy
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 87 participants (actual)
- Lead sponsor
- Copenhagen University Hospital, RigshospitaletUniversity, hospital or other
- Collaborators
- Danish Cancer Society
- Study start
- Mar 2014
- Primary completion
- Jun 2015 (actual)
- Study completion
- Jun 2015 (actual)
- First posted
- 13 Mar 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Background:
The prevalence of gastroesophageal-junction cancer (cancer between the distal part of the oesophagus, and proximal part of the stomach/GEJ-cancer) is increasing in Denmark with more than 400 patients per year. The 5-year overall survival is less than 10% for the 2/3 of the patients, which are not considered resectable. Even for the 1/3, which is treated with surgical intervention and neoadjuvant chemotherapy the overall-survival is approximately 30%.
The current Danish intended curative treatment consists of esophagectomy (surgical resection of the oesophagus with extended lymphadenectomy in abdomen and thorax (removal of lymphnodes)). Furthermore, perioperative chemotherapy consists of 6 series neoadjuvant chemotherapy (3 series before, and 3 series after operation).
Unresectable patients receive palliative chemotherapy and no resection. Peritoneal washing cytology (PWC) is a recommended prediagnostic modality in gastric cancer patients. The method is used to detect free peritoneal cancer cells in the abdominal cavity even when macroscopic carcinomatosis is not present (i.e. the cancer has spread to other parts of the abdomen).
Carcinomatosis can be found in up to 19% in gastric cancer patients often in the peritoneum. Positive peritoneal cytology (C1) can be identified in up to 7% of gastric cancer patients without metastases (C1M0), i.e. malignant cells can be identified in the peritoneal washing, but tumor spread has not been identified.
Lots of studies indicate that C1-disease is an independent prognostic predictor for decreased survival, and increased recurrence rate, comparable with M1 patients (i.e. patients with distant metastases).
The American Joint Committee on cancer recommends that C1 patients should be treated non-surgically - even when M1 disease has not been identified.
On the basis of the above, PWC can be used to identify patients at greater risk for recurrence, and thereby not candidates for intended curative treatment.
It is a fact, though, that C1M0 patients have a better survival than C1M1 patients. Currently, there is no level-1 evidence for specific treatment of C1M0 patients, why further research is required to approach this patient group in the most comprehensive way. The focus group of our study is therefore C1M0 patients, because of the difference in opinions. Furthermore most evidence is based on gastric carcinomas, why GEJ-cancer patients are the group, we will examine.
Purpose:
Peritoneal washing cytology (PWC) is performed as a standard prediagnostic modality at Rigshospitalet, for patients with gastric- and GEJ cancer, considered resectable at preceding multidisciplinary conference. Most studies in the past 20-years have focused on gastric cancer, and not specifically GEJ-cancer.
This study will determine the usefulness of peritoneal washing cytology, and thereby verifying our own standard regarding GEJ-cancer. Furthermore, we will determine the effect of neoadjuvant chemotherapy on free peritoneal tumor cells and its correlation with overall survival.
This study is intended as a validation of our own standard.
Detailed description
- Background: The prevalence of gastroesophageal-junction cancer is increasing in Denmark with more than 400 patients per year. The 5-year overall survival is less than 10% for the 2/3 of the patients, which are not considered resectable. Even for the 1/3, which is treated with surgical intervention and neoadjuvant chemotherapy, the overall-survival is approximately 30%. The current Danish intended curative treatment consist of esophagectomy a.m. Ivor Lewis with extended lymphadenectomy in the abdomen and thorax. Furthermore, perioperative chemotherapy consists of 6 series neoadjuvant chemotherapy. Unresectable patients receive palliative chemotherapy and no resection. Peritoneal washing cytology is a recommended prediagnostic modality in gastric cancer. The method is used to detect free peritoneal cancer cells in the abdominal cavity, even when macroscopic carcinomatosis is not present. Carcinomatosis can be found in up to 19% in gastric cancer patients, often in the peritoneum. Positive peritoneal cytology (C1) can be identified in up to 7% of gastric cancer patients without metastases (C1M0). Lots of studies indicate that C1-disease is an independent prognostic predictor for decreased survival, and increased recurrence rate, comparable with M1 patients (i.e. patients with distant metastases). The American Joint Committee on cancer recommends that C1 patients should be treated non-surgically - even when M1 disease is not identified. On the basis of the above, PWC can be used to identify patients at greater risk for recurrence, and thereby not candidates for intended curative treatment. It is a fact, though, that C1M0 patients have a better survival than C1M1 patients. Currently, there is no level-1 evidence supporting specific treatment of C1M0 patients, why further research is required to approach this patient group in the most comprehensive way. Therefore, the focus group of our study is C1M0 patients, because of the differences in opinions. Furthermore, most evidence is based on gastric carcinomas, why GEJ-cancer patients are the group, we will examine. Results from other investigators regarding treatment of C1M0 patients: Lee et al. found a median survival of 21 months and 4 months in gastrectomized versus non-gastrectomized patients. Lorentzen et al. found a median 5-year survival of 71,4% and 25% in gastrectomized patients, who had C1 at staging laparoscopy and converted after preoperative chemotherapy versus persistent C1-disease after preoperative chemotherapy. Another interesting treatment modality for C1M0 patients is extensive intraperitoneal lavage (EIPL) examined by a Japanese study group. 88 C1M0 patients were randomized into three group; 1. Gastrectomy only, 2. Gastrectomy + intraperitoneal chemotherapy (IPC), and 3. Gastrectomy + IPC + EIPL. Group 3 compared to group 2 had a significant better 5 year overall survival of 43,8% versus 4,6% (p<0,0001). Further research is required to establish specific guideline for C1M0 patients.
- Purpose: Peritoneal washing cytology (PWC) is performed as a standard prediagnostic modality at Rigshospitalet for patients, with gastric- and GEJ cancer, considered resectable at preceding multidisciplinary conference. Most studies in the past 20-years have focused on gastric cancer, and not specifically GEJ-cancer. This study will determine the usefulness of peritoneal washing cytology, and thereby, verify our own standard regarding GEJ-cancer. Furthermore, we will determine the effect of neoadjuvant chemotherapy on free peritoneal tumor cells, correlated with overall survival. See outcome measures for more detailed description. This study is intended as a validation of our own standard.
- Methods Our current algorithm includes peritoneal washings performed at two different time points:
- Staging laparoscopy using one port technique
- After pneumoperitoneum and oversight of the abdomen is established, a puncture is created subhepatically in the midclavicular line with a pigtail catheter ch. 10.
- 500ml of sterile 37°C NaCl is injected through the catheter and manually dispersed throughout the abdomen by positioning the operating table in different positions.
- At least 200ml of fluid is aspirated subhepatically through the catheter.
- 100ml is analysed by an experienced pathologist for any malignant cancer cells.
- Initially, before operation (transthoracic esophagectomy): either open operation or robot assisted o Robot assisted: same technique as above o Open operation: • After abdominal incision and exploration 500ml °C of sterile NaCl is manually dispersed in the abdominal cavity.
- Peritoneal washings is aspirated subhepatically
- Further algorithm as described above
- Recruiting of patients:
90 consecutive patients with biopsy verified GEJ-cancer will be included. Because PWC is already a standard guideline for this group of patients at Rigshospitalet, there will be no direct inclusion of patients.
- Study design: Prospective feasibility study. Patients considered candidates for intented curative therapy, according to The Danish Esophagus-,GEJ- and Gastric Cancer Association (DECV), is included. Furthermore, patients must have undergone evaluation of a multidisciplinary panel of specialist including the specialties surgical gastroenterology, thoracic surgery, oncology, pathology, radiology, and clinical nuclear medicine.
- Data: Patient data will be obtained from internal systems of Rigshospitalet including OPUS, LABKA, PatologiWEB, and ORBIT.
The following preoperative data will be obtained:
- age, sex, initial symptoms, tumour staging (TNM version 7) and histology characteristics, disease anamnesis, chemotherapy treatment, medicine anamnesis, comorbidity, postoperative complications, mortality, specifics regarding PWC such as injected volume of NaCl, procedure time, aspirated amount of fluid, and cytology findings.
- Approval: Authorization of data retreatment is approved by The Danish Data Protection Agency.
Approval of The Danish Ethics Committee has not been applied, because the study is a validation of our own standard guideline.
- Finances:
The following contributors have financed the study:
The Danish Cancer Society Research Center, Mogens Andreasen Fonden, Familien Erichsens familiefond, and Rigshospitalet.
All expenses have been covered.
- Results Both negative and positive results will be published in a national and/or international journal.
- Practical feasibility The relevant patients and the medical expertise are to find at the surgical gastroenterology department of Rigshospitalet. 120 staging laparoscopies are being performed per year in the handling of gastric cancer patients. Persons and departments involved in the study have agreed to allocate time and resources to the study. Furthermore, our department has a technician affiliated with our institution on full time basis, who is going to provide development, optimization, and assistance of projects associated with GEJ-cancer.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| GEJ-cancer patients consideres resectable | – | Procedure: Peritoneal washing cytologyAll patients have biopsy verified GEJ-cancer, and has been considered for intend curative resection by a multidisciplinary panel of specialists. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with biopsy verified GEJ-cancer referred from peripheral hospitals in the region of Sjælland and the Capitol. (The treatment of GEJ-cancer is centered at Rigshospitalet. All of our patients are referred from other hospitals)
Key inclusion criteria (3 listed)
- patients with biopsy verified GEJ-cancer referred to the department of surgical gastroenterology, Rigshospitalet, which is considered resectable at MDT-conference.
- >18 years old
- informed consent
Key exclusion criteria (2 listed)
- < 18 years old
- Not informed consent
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Peritoneal washing cytologyAlso: Peritoneal lavageThe methode is describes in the detailed study description | Procedure or surgery | GEJ-cancer patients consideres resectable |
Primary outcome
The effect of neoadjuvant chemotherapy (NAC) on free peritoneal cancer cells (FPCCs)
Time frame: 1 year
Peritoneal washings will be performed at two time points. The first at the time of staging laparoscopy and the second initially before esophagectomy. Thereby, we will gain a measure for the effect of NAC on FPCC. We are interested in the following: * patients converting from positive cytology at staging laparoscopy to negative before surgery or reverse. * patients with persisting negative cytology at both measure points or persisting positive. These measurements for these 4 groups will be correlated with overall survival (up to 5 years).
2 secondary outcomes
Postoperative complications
Time frame: 2 weeks after surgery
Overall survival
Time frame: up to 5 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Jun 2015.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Lars Bo Svendsen, Prof., MD., DMSc. study director
Department of surgical gastroenterology, Rigshospitalet
Michael Patrick Achiam, MD. phD. study chair
Department of surgical gastroenterology, Rigshospitalet
Rune Broni Strandby, Junior researcher principal investigator
Department of surgical gastroenterology, Rigshospitalet
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Gastroesophageal-junction Cancer, run by Copenhagen University Hospital, Rigshospitalet at 1 site in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 3 Jun 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The effect of neoadjuvant chemotherapy (NAC) on free peritoneal cancer cells (FPCCs) (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Jun 2015.