Non-Small-Cell Lung CancerNCT06833632
Detection of Circulating Tumour Cells, Spread Through Air Space in Patients With Lung Cancer
An observational study of Non-Small-Cell Lung Cancer, run by IRCCS Azienda Ospedaliero-Universitaria di Bologna at 1 site in Italy.
Trial summary
The aim of this study is to evaluate the prognostic impact of the presence of circulating tumour cells Circulating Tumour Cells (CTCs), Spread Through Air Space (STAS) and lymph node micrometastases in patients undergoing radical surgery for non-small cell lung neoplasia Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Non-Small-Cell Lung Cancer
- How many people
- 100 participants
- Where
- 1 siteItaly
- Study dates
- 25 May 2023to 11 Sep 2025
- How long will I take part?
- 2 Years
- 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: The study is low-risk, human-tissue, prospective, single-center experimental study conducted on patients undergoing surgery for removal of stage I-IIA NSCLC.
Who may be able to join
- obtaining voluntary written informed consent
- diagnosis of NSCLC
- clinical stage I-IIA cN0
- Candidates for surgical resection
Who cannot join
- Pregnancy
- Induction therapy for pulmonary neoplasia
- Patients who have received systemic treatment for previous cancers in the last three years prior to lung surgery
- Any previous surgery for lung cancer
- Patients with other active neoplasms
- Infiltration of the chest wall
Trial locations and contacts
1 site in 1 country.
Italy1 site, 1 recruiting
- Recruiting
IRCCS - Azienda Ospedaliero Universitaria di Bologna
Bologna, Emilia-Romagna, 40138
Pietro Bertoglio, MD, 051 647 8362 ext. +39, pietro.bertoglio@ausl.bologna.it
About this study
Official title: Detection of Circulating Tumour Cells, Spread Through Air Space and Lymph-nodal Micrometastasis in Patients With Lung Cancer Undergoing Surgical Resection With Curative Intent
The aim of this study is to evaluate the prognostic impact of the presence of circulating tumour cells Circulating Tumour Cells (CTCs), Spread Through Air Space (STAS) and lymph node micrometastases in patients undergoing radical surgery for non-small cell lung neoplasia
Read the detailed description
Non-small cell lung cancer (NSCLC) is one of the leading causes of cancer deaths worldwide. Patients diagnosed with early-stage NSCLC are candidates for radical surgical resection with curative intent. However, disease recurrence after surgery is common, with 5-year recurrence rates ranging from about 20% in patients with stage I disease to about 50% in those with stage III disease. In detail, in patients operated with radical resection (R0), the loco-regional recurrence rate varies from 4.6 to 24%, with a significantly higher incidence in the first two years after surgery.
To date, only a few risk factors have been correlated with an increased propensity to develop recurrences, namely stage and some loco regional aggressiveness (e.g. pleural invasion, high-grade growth pattern, lymphovascular invasion), but there are still no certain elements that allow us to understand in advance the biology of the early spread of the disease and thus identify patients at high risk of relapse.
of relapse; the presence of these elements would have the potential advantage of playing a role both in recommending new therapeutic approaches for adjuvant treatment and in acting as biomarkers to anticipate the diagnosis or recurrence of lung cancer.
Until 2022, lobectomy was considered the standard of care for any type of lung neoplasm that was a candidate for surgery. Recent studies, however, have shown that even sublobar resections may allow adequate oncological radicality for tumours peripheral tumours of small size (<2 cm) . Moreover, in the last decade, technological development has allowed a gradual replacement of traditional open techniques with mini-invasive techniques (videothoracoscopy, Video Assisted Thoracic Surgery (VATS), or robotic, Robotic Assisted Thoracic Surgery (RATS)).
Circulating tumour cells (CTCs) are considered to be the site of origin for possible disease recurrence in several cancers, showing a higher rate of disease recurrence in the case of high CTC levels. Despite this, their specific clinical role in lung cancer has not yet been clarified. CTCs from the peripheral blood of patients with breast cancer, melanoma, NSCLC and small cell lung cancer can form tumours in mice immunocompromised mice, confirming their carcinogenic potential. Furthermore, the presence of CTCs has also been correlated with manipulation of the lung during surgery, which would seem to favour dissemination, although the clinical significance is uncertain.
Recent studies have highlighted the importance of the molecular profile of neoplasms lung neoplasms that could change the standard of care with regard to neoadjuvant or adjuvant therapies. Molecular assessment is usually performed on biopsies or on the operative specimen of the primary tumour, but could potentially be performed on circulating tumour cells. Weak evidence on the clinical role of CTCs also includes their role in defining the molecular profile of the tumour.
In addition to haematogenous spread of which CTCs could be a warning sign, NSCLC can potentially spread via the airway and lymphatic route. Spread via the airway and through the alveolar spaces has recently been observed, especially in the adenocarcinoma histotype, and codified by the World Health Organisation (WHO 2021) as Spread Through Air Space (STAS); as for lymphatic invasion lymphatic invasion, in addition to intrapulmonary lymphatic vessel invasion, it is manifested by the presence of lymph node metastases or micrometastases.
In detail, STAS are defined as tumour cells existing within alveolar spaces in the lung parenchyma beyond the edge of the main neoplasm, in close proximity to the edge of the main neoplasm. STAS can be found mainly, but not only, in lung adenocarcinomas and in about 35-40% of early stage clinical NSCLC; some studies have shown their correlation with a worse prognosis than in patients without STAS .
Micrometastases, in other body districts such as breast and axillary locoregional lymph node metastases, on the other hand, are defined as tumour aggregates between between 0.2 and 2.0 mm. In the literature, data on the incidence of lymph node micrometastases in NSCLC are inconsistent and range from 10-80%. Compared to patients with macroscopic lymph node involvement, micrometastases seem to be related to a better prognosis, but, on the other hand, outcomes seem to be worse than in N0 pathological patients.
The objectives of the study are to :
- Check whether the presence and/or levels of CTC is associated with disease-free survival (DFI)
- To assess the pattern of recurrence in patients with CTC, STAS and lymph node micrometastases
Secondary objectives
- Quantify the difference in intraoperative release of CTC into the bloodstream based on the intraoperative variables:
- Resection sequence of the hilar structure (first vein or artery)
- Lung management according to different surgical techniques (open, VATS, RATS)
- Type of resection: segmentectomy, lobectomy, pneumonectomy
- Check for association between CTC, presence of STAS and presence of lymph node micrometastases
- Check whether the presence and/or levels of CTC, STAS and lymph node micrometastases are associated with long-term outcomes (DFI, OS)
- Compare the molecular profile of CTCs and the primary tumour
- Conditions
- Non-Small-Cell Lung Cancer
- Medical subject headings
- Carcinoma, Non-Small-Cell Lung
What is being measured
The primary outcome is the main question the study is designed to answer.
Overall survival (OS)
Overall survival (in months) will be assessed for each patient enrolled in the study from the day of surgery to the last follow-up or death whichever comes first
Measured: Through study completion, up to 36 months.
Disease-free survival (DFS)
DFS (in months) will be assessed for each patient enrolled in the study: the relapse is defined as the first evidence of recurrence of disease on instrumental examinations instrumental examinations performed in the follow-up.
Measured: Through study completion, up to 36 months.
Global recurrence rate
Percentage of patients with any recurrence
Measured: Through study completion, up to 36 months.
Type of recurrence
Number of patients with local, regional distant or multiple recurrence
Measured: Through study completion, up to 36 months.
Secondary outcomes (5)
Circulating Tumour Cells (CTC)
Presence or absence, level of CTCs measured as median value with interquartile range
Measured: Through study completion, the day before surgery and 30 days after surgery, up to 36 months.
Spread through air space (STAS)
Presence or absence of STAS
Measured: Through study completion, at the time of pathological analysis of surgical specimen (approximately 36 months)
Micrometastases at lymph nodes
Presence or absence of micrometastasis
Measured: Through study completion, at the time of pathological analysis of surgical specimen (approximately 36 months)
Molecular mutations in EGFR, ALK, ROS1, KRAS genes
Counting of mutations though multigenic panels
Measured: Through study completion, at the time of pathological analysis of surgical specimen (approximately 36 months)
PD-L1 expression
Assessment of level of expression of PD-KL1 gene in CTCs and tumour
Measured: Through study completion, at the time of pathological analysis of surgical specimen (approximately 36 months)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 Feb 2025
- Study start25 May 2023
- Primary completion11 Sep 2025 (estimated)
- Study completion11 Sep 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Non-Small-Cell Lung CancerStudies of the same condition, open and under way.
- More trials run by IRCCS Azienda Ospedaliero-Universitaria di BolognaThe 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
- 100 participants (estimated)
- Target duration
- 2 Years
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Pietro Bertoglio, MD, Principal investigator, IRCCS Azienda Ospedaliero-Universitaria di Bologna
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06833632
- Sponsor's protocol ID
- CTC22
- Status last verified
- Oct 2024
- First submitted
- 28 Nov 2024
- Last updated
- 19 Feb 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 19 Feb 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Detection of Circulating Tumour Cells, Spread Through Air Space and Lymph-nodal Micrometastasis in Patients With Lung Cancer Undergoing Surgical Resection With Curative Intent
- ClinicalTrials.gov ID
- NCT06833632
- Acronym / sponsor ID
- CTC22
- Conditions
- Non-Small-Cell Lung Cancer
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- IRCCS Azienda Ospedaliero-Universitaria di BolognaUniversity, hospital or other
- Study start
- 25 May 2023 (actual)
- Primary completion
- 11 Sep 2025 (estimated)
- Study completion
- 11 Sep 2025 (estimated)
- First posted
- 19 Feb 2025 (actual)
- 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.
The aim of this study is to evaluate the prognostic impact of the presence of circulating tumour cells Circulating Tumour Cells (CTCs), Spread Through Air Space (STAS) and lymph node micrometastases in patients undergoing radical surgery for non-small cell lung neoplasia
Detailed description
Non-small cell lung cancer (NSCLC) is one of the leading causes of cancer deaths worldwide. Patients diagnosed with early-stage NSCLC are candidates for radical surgical resection with curative intent. However, disease recurrence after surgery is common, with 5-year recurrence rates ranging from about 20% in patients with stage I disease to about 50% in those with stage III disease. In detail, in patients operated with radical resection (R0), the loco-regional recurrence rate varies from 4.6 to 24%, with a significantly higher incidence in the first two years after surgery.
To date, only a few risk factors have been correlated with an increased propensity to develop recurrences, namely stage and some loco regional aggressiveness (e.g. pleural invasion, high-grade growth pattern, lymphovascular invasion), but there are still no certain elements that allow us to understand in advance the biology of the early spread of the disease and thus identify patients at high risk of relapse.
of relapse; the presence of these elements would have the potential advantage of playing a role both in recommending new therapeutic approaches for adjuvant treatment and in acting as biomarkers to anticipate the diagnosis or recurrence of lung cancer.
Until 2022, lobectomy was considered the standard of care for any type of lung neoplasm that was a candidate for surgery. Recent studies, however, have shown that even sublobar resections may allow adequate oncological radicality for tumours peripheral tumours of small size (<2 cm) . Moreover, in the last decade, technological development has allowed a gradual replacement of traditional open techniques with mini-invasive techniques (videothoracoscopy, Video Assisted Thoracic Surgery (VATS), or robotic, Robotic Assisted Thoracic Surgery (RATS)).
Circulating tumour cells (CTCs) are considered to be the site of origin for possible disease recurrence in several cancers, showing a higher rate of disease recurrence in the case of high CTC levels. Despite this, their specific clinical role in lung cancer has not yet been clarified. CTCs from the peripheral blood of patients with breast cancer, melanoma, NSCLC and small cell lung cancer can form tumours in mice immunocompromised mice, confirming their carcinogenic potential. Furthermore, the presence of CTCs has also been correlated with manipulation of the lung during surgery, which would seem to favour dissemination, although the clinical significance is uncertain.
Recent studies have highlighted the importance of the molecular profile of neoplasms lung neoplasms that could change the standard of care with regard to neoadjuvant or adjuvant therapies. Molecular assessment is usually performed on biopsies or on the operative specimen of the primary tumour, but could potentially be performed on circulating tumour cells. Weak evidence on the clinical role of CTCs also includes their role in defining the molecular profile of the tumour.
In addition to haematogenous spread of which CTCs could be a warning sign, NSCLC can potentially spread via the airway and lymphatic route. Spread via the airway and through the alveolar spaces has recently been observed, especially in the adenocarcinoma histotype, and codified by the World Health Organisation (WHO 2021) as Spread Through Air Space (STAS); as for lymphatic invasion lymphatic invasion, in addition to intrapulmonary lymphatic vessel invasion, it is manifested by the presence of lymph node metastases or micrometastases.
In detail, STAS are defined as tumour cells existing within alveolar spaces in the lung parenchyma beyond the edge of the main neoplasm, in close proximity to the edge of the main neoplasm. STAS can be found mainly, but not only, in lung adenocarcinomas and in about 35-40% of early stage clinical NSCLC; some studies have shown their correlation with a worse prognosis than in patients without STAS .
Micrometastases, in other body districts such as breast and axillary locoregional lymph node metastases, on the other hand, are defined as tumour aggregates between between 0.2 and 2.0 mm. In the literature, data on the incidence of lymph node micrometastases in NSCLC are inconsistent and range from 10-80%. Compared to patients with macroscopic lymph node involvement, micrometastases seem to be related to a better prognosis, but, on the other hand, outcomes seem to be worse than in N0 pathological patients.
The objectives of the study are to :
- Check whether the presence and/or levels of CTC is associated with disease-free survival (DFI)
- To assess the pattern of recurrence in patients with CTC, STAS and lymph node micrometastases
Secondary objectives
- Quantify the difference in intraoperative release of CTC into the bloodstream based on the intraoperative variables:
- Resection sequence of the hilar structure (first vein or artery)
- Lung management according to different surgical techniques (open, VATS, RATS)
- Type of resection: segmentectomy, lobectomy, pneumonectomy
- Check for association between CTC, presence of STAS and presence of lymph node micrometastases
- Check whether the presence and/or levels of CTC, STAS and lymph node micrometastases are associated with long-term outcomes (DFI, OS)
- Compare the molecular profile of CTCs and the primary tumour
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 2 Years
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- The study is low-risk, human-tissue, prospective, single-center experimental study conducted on patients undergoing surgery for removal of stage I-IIA NSCLC.
Key inclusion criteria (4 listed)
- obtaining voluntary written informed consent
- diagnosis of NSCLC
- clinical stage I-IIA cN0
- Candidates for surgical resection
Key exclusion criteria (6 listed)
- Pregnancy
- Induction therapy for pulmonary neoplasia
- Patients who have received systemic treatment for previous cancers in the last three years prior to lung surgery
- Any previous surgery for lung cancer
- Patients with other active neoplasms
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Overall survival (OS)
Time frame: Through study completion, up to 36 months.
Overall survival (in months) will be assessed for each patient enrolled in the study from the day of surgery to the last follow-up or death whichever comes first
Disease-free survival (DFS)
Time frame: Through study completion, up to 36 months.
DFS (in months) will be assessed for each patient enrolled in the study: the relapse is defined as the first evidence of recurrence of disease on instrumental examinations instrumental examinations performed in the follow-up.
Global recurrence rate
Time frame: Through study completion, up to 36 months.
Percentage of patients with any recurrence
Type of recurrence
Time frame: Through study completion, up to 36 months.
Number of patients with local, regional distant or multiple recurrence
5 secondary outcomes
Circulating Tumour Cells (CTC)
Time frame: Through study completion, the day before surgery and 30 days after surgery, up to 36 months.
Spread through air space (STAS)
Time frame: Through study completion, at the time of pathological analysis of surgical specimen (approximately 36 months)
Micrometastases at lymph nodes
Time frame: Through study completion, at the time of pathological analysis of surgical specimen (approximately 36 months)
Molecular mutations in EGFR, ALK, ROS1, KRAS genes
Time frame: Through study completion, at the time of pathological analysis of surgical specimen (approximately 36 months)
PD-L1 expression
Time frame: Through study completion, at the time of pathological analysis of surgical specimen (approximately 36 months)
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Feb 2025.
- Individual participant dataSharing planned: Undecided
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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.
Pietro Bertoglio, MD principal investigator
IRCCS Azienda Ospedaliero-Universitaria di Bologna
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 Non-Small-Cell Lung Cancer, run by IRCCS Azienda Ospedaliero-Universitaria di Bologna at 1 site in Italy.
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 4 inclusion and 6 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: status not confirmed, as of the sponsor's last update on 19 Feb 2025. 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 Italy. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Pietro Bertoglio, MD (051 647 8362 ext. +39, pietro.bertoglio@ausl.bologna.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Overall survival (OS) (time frame: Through study completion, up to 36 months.). The study lists 4 primary outcomes in all. 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 19 Feb 2025.