An observational study in Lung Cancer in Normal and Malignant Tumors, sponsored by Fuzhou General Hospital. Not yet recruiting at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-03-31.
Sponsored by Fuzhou General Hospital · Observational
Pulmonary nodules are often an early indicator of lung cancer. With the widespread adoption of chest CT scans in routine physical examinations, an increasing number of pulmonary nodules are being detected, including a variety of small nodules such as inflammatory lesions, benign tumors, and malignant tumors. Currently, there is no unified international consensus on the diagnostic and treatment strategies for pulmonary nodules, as outlined by various global guidelines. Developing and implementing a comprehensive lung nodule and lung cancer screening program within public health management systems remains a complex and challenging endeavor. Advancing research and proposing lung cancer screening technologies that are highly sensitive, highly specific, simple, accessible, and cost-effective is an essential and pressing priority in modern healthcare.
Raman spectroscopy (RS), as a non-invasive and highly specific molecular detection technique, can be obtained at the molecular level to sensitively detect changes in biomolecules composed of proteins, nucleic acids, lipids, and sugars related to tumor metabolism in biological samples. The surface enhanced Raman spectroscopy (SERS) developed based on this technology is one of the feasible methods for high-sensitivity biomolecule analysis. Although SERS technology has shown good diagnostic efficacy in lots of preclinical studies in multiple tumors, it is limited to a generally small sample size and lacks external validation. There for, a clinical study of Raman spectra for tumor diagnosis is needed, which meets the following requirements: 1.An objective, fast and practical application of Raman spectral data processing is needed and deep learning method may be the best classification method; 2. It requires multicenter and large clinical samples to train deep learning diagnostic model, and verify its true efficacy through external data of prospective study.
In preliminary research, the investigators collected serum Raman spectroscopy data from a cohort of 191 patients with pulmonary nodules and developed an intelligent diagnosis system for distinguishing between benign and malignant pulmonary nodules using a machine learning model. The system achieved an accuracy of 89.7%. In order to obtain the highest level of clinical evidence and truly realize clinical transformation, this prospective, multi-center clinical study is designed to verify the intelligent diagnostic system for early diagnosis of prostate cancer.
In 2020, there were approximately 19.3 million new cancer cases and nearly 10 million cancer deaths worldwide. Among them, the number of new cases of lung cancer was approximately 2.21 million, accounting for 11.4% of the total number of new cancer cases. There were approximately 1.8 million deaths from lung cancer, ranking first among cancer deaths. In that year, the number of new cases of lung cancer in China was 816,000, accounting for 37% of the global total. In 2022, the latest number of lung cancer cases in China increased to 1.0606 million, and the number of lung cancer deaths was 733,000. In terms of the 5-year survival rate of lung cancer patients, the data released in 2018 in China (2012-2015) was 19.7%, which is still a large gap from the overall cancer 5-year survival rate of 46.6% by 2030 proposed in the "Healthy China Action-Cancer Prevention and Control Action Implementation Plan (2023-2030)". The prognosis of lung cancer at different stages is quite different. The 5-year survival rate of stage I lung cancer is 77%\~92%, and the 5-year survival rate of stage IIIA\~IVB lung cancer is 0\~36%. Therefore, early diagnosis and treatment of lung cancer is the key to improving the 5-year survival rate of lung cancer and improving the prognosis of patients. However, most lung cancer patients are already in the late stage of lung cancer when they are diagnosed, and they have missed the opportunity for radical treatment. The main reason is that the primary and secondary prevention work is not done enough. It is necessary to develop advanced technologies and integrate them into the consensus guidelines for wide promotion.
Pulmonary nodules are early manifestations of lung cancer. With the popularization of chest CT screening in physical examination items, more and more lung nodules are found in physical examinations, including various types of small nodules, such as inflammatory lesions, benign tumor lesions, and malignant tumor lesions. In order to identify these types of nodules, clinicians often judge the two-dimensional imaging features of nodules based on their personal experience, such as plane diameter, whether there are burrs, lobes, calcification and other features to assess the probability of malignancy of lung nodules, but the accuracy of judging the benign and malignant nodules in this way is closely related to the experience and seniority of clinicians, and different doctors have different judgments on the same nodules. At present, there is no unified consensus on the diagnosis and treatment strategies of lung nodules recommended by multiple international consensus guidelines. In public health management facilities, the development and implementation of a comprehensive lung nodule lung cancer screening program is a complex and challenging task. Researching and proposing high-sensitivity and high-specificity, as well as simple, easy-to-popular and low-cost lung cancer screening technologies is an indispensable part of the healthcare system. In addition, due to the inconsistency of guidelines for the diagnosis and treatment strategies of lung nodules, the phenomenon of overdiagnosis and treatment of lung nodules is also common in clinical practice. How to avoid overdiagnosis and treatment needs more attention. Therefore, it is our responsibility to actively improve the accuracy of prediction of lung nodule canceration, reduce the rate of overdiagnosis and treatment, and increase the rate of early lung cancer intervention. Among the existing screening methods for early lung cancer, laboratory tests (especially the use of blood, urine or other liquid biopsies) are a low-cost, non-invasive and easily repeatable early prediction method compared with imaging or histopathological examinations, by detecting specific cancer biomarkers such as circulating tumor DNA, proteins, cancer metabolites, and even cell-derived exosomes and circulating tumor cells. However, there are still many challenges, including: 1) There are no effective and abundant tumor biomarkers for lung cancer; 2) There is no simple and feasible cancer detection method, especially in the asymptomatic stage; 3) There is no comprehensive analysis platform for large data sets to distinguish between healthy and lung cancer populations.
Raman spectroscopy (RS) is a non-invasive and highly specific material molecular detection technology that can be obtained at the molecular level to sensitively detect changes in biomolecules composed of proteins, nucleic acids, lipids and sugars related to tumor metabolism in biological samples. Surface-enhanced Raman spectroscopy (SERS) developed based on this technology is one of the feasible methods for highly sensitive biomolecular analysis technology. Although SERS technology has shown good diagnostic effects in a large number of preclinical studies of multiple tumors, it is limited by the generally small sample size and lack of external verification. Therefore, it is necessary to conduct clinical research on the use of Raman spectroscopy for tumor diagnosis, which meets the following requirements: 1. Objective, fast and practical Raman spectroscopy data processing methods are required, and machine and deep learning methods may be the best classification methods; 2. Multi-center, large-sample clinical samples are needed to train deep learning diagnostic models, and their true efficacy is verified by external data from prospective studies.
In previous study, the investigators collected serum Raman spectroscopy data from a cohort of 191 patients with pulmonary nodules, and built a Raman intelligent diagnosis system for benign and malignant pulmonary nodules based on a machine learning model. The accuracy of this intelligent diagnosis system reached 89.7%. In order to obtain the highest level of clinical evidence and truly achieve clinical transformation, this prospective, multi-center clinical study aims to verify the use of this intelligent diagnosis system for the early diagnosis of malignant pulmonary nodules.
10,818 studies on the registry are indexed under Neoplasms; 2,324 are open to participants now.
This study's planned enrollment of 200 is close to the median of 200 across 2,638 observational studies indexed under Neoplasms.
Browse Neoplasms studies →Fuzhou General Hospital is the lead sponsor of 40 studies on the registry; 9 are open to participants now.
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Chest CT reveals the presence of pulmonary nodules in the patient and plans to undergo surgical treatment
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
COPD
Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Chest CT confirmed the presence of pulmonary nodules in the patient and ultimately underwent surgical intervention. The pulmonary nodules had the final pathological results.
Diagnostic Test: Serum Raman spectroscopy intelligent diagnostic system
1. Screening interested participants should sign the appropriate informed consent (ICF) prior to completion any study procedures. 2. The investigator will review symptoms, risk factors, and other non-invasive inclusion and exclusion criteria. 3. The following is the general sequence of events during the 3 months evaluation period: 4. Completion of baseline procedures Participants were assessed for 3 months and completed all safety monitoring.
Postoperative pathological results
After undergoing surgical resection of pulmonary nodules, the final pathological nature of the pulmonary nodules was determined through pathological examination.
Time frame: through study completion, an average of 1 year
Diagnostic accuracy
Determine whether there is hematogenous metastasis in enrolled lung cancer patients through RAMAN intelligent diagnostic system
Time frame: through study completion, an average of 1 year
Time to RAMAN diagnosis
The time to perform RAMAN testing and obtain diagnostic results after obtaining serum
Time frame: up to 30 days
Safety assessment Results
AEs and SAEs through Day 30
Time frame: up to 30 days
Plan to share: Yes — Age, gender, smoking history, and tumor type of the enrolled patients
Supporting information: Study protocol, Statistical analysis plan
Access criteria: For any reasonable needs related to scientific research, please contact the project leader for specific data consultation.
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This study is not yet recruiting, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.
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Fuzhou General Hospital