Lung Cancer (NSCLC)LCabNCT07004868
Inflammation, Cachexia and Therapeutic Response in Lung Cancer Treated With Immune Checkpoint Inhibitors: Exploratory Observational Study
An observational study of Lung Cancer (NSCLC), run by University Hospital, Tours at 1 site in France.
Trial summary
Lung cancer is the leading cause of cancer-related death in France and globally, with 2.48 million new cases diagnosed in 2022, accounting for nearly 13% of global cancer incidence. Despite recent advances, it remains a major health issue due to late-stage diagnosis and high patient and societal burden. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Lung Cancer (NSCLC)
- How many people
- 150 participants
- Where
- 1 siteFrance
- Study dates
- 3 Jun 2025to Jun 2030
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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: Adult patients with a lung cancer treated with immune checkpoint inhibitors
Who may be able to join
- Age greater than or equal to 18 years
- Diagnosis of lung cancer, any histology, any stage
- Treatment with Ab ICI, with or without chemotherapy
- 1st administration of Ab ICI
Who cannot join
- Patient not followed at the CHRU de Tours
- Person under protective supervision
- Opposition to data processing
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
France1 site, 1 recruiting
- Recruiting
university hospital, Tours
Tours, 37000
Marion FERREIRA, Dr, 0247471640 ext. +33, marion.ferreira@chu-tours.fr
Marion FERREIRA, DR
About this study
Lung cancer is the leading cause of cancer-related death in France and globally, with 2.48 million new cases diagnosed in 2022, accounting for nearly 13% of global cancer incidence. Despite recent advances, it remains a major health issue due to late-stage diagnosis and high patient and societal burden. New insights into tumor and immune pathways have led to the development of targeted therapies, including tyrosine kinase inhibitors and therapeutic antibodies. Among these, immune checkpoint inhibitors (ICIs) such as nivolumab, pembrolizumab, atezolizumab, and durvalumab have significantly improved outcomes for some patients by reactivating T-cell responses.
The LCAb (Lung Cancer Antibodies) research project focuses on studying the interindividual variability of clinical response to ICI in lung cancer. These therapies are now used across various lung cancer types and stages, including early and advanced disease. Most ICIs are administered at fixed doses, without considering patient-specific factors as blood concentrations, tumor burden, body weight or nutritional status. The study hypothesizes that fixed dosing may affect treatment response and survival outcomes, highlighting the need for more personalized approaches.
Read the detailed description
Lung cancer is the leading cause of cancer-related death in France and worldwide. Its incidence is significant, with 2.48 million new cases diagnosed in 2022, representing nearly 13% of the total global cancer incidence. Despite recent therapeutic advances, it remains a major public health issue due to its frequent diagnosis at a metastatic stage, which results in high morbidity and mortality for patients and significant costs for society.
A better understanding of tumor and immune signaling pathways has recently led to the discovery of new molecular targets, such as immune checkpoints. The therapeutic arsenal against lung cancer has thus expanded to include new molecules such as tyrosine kinase inhibitors and therapeutic antibodies (Abs). The latter represent the majority of anticancer biotherapies, with more than 50 approved agents for solid or hematologic cancers.
In particular, antibodies targeting immune checkpoints (ICIs - immune checkpoint inhibitors), such as nivolumab, pembrolizumab, atezolizumab, and durvalumab, have revolutionized the management of certain lung cancer patients by reversing T-cell exhaustion, allowing some of them to become long-term responders.
The research project "Pharmacokinetics of Immune Checkpoint Inhibitor Antibodies Used in Lung Cancer" (LCAb - Lung Cancer Antibodies) aims to study the blood concentrations and pharmacokinetics of various ICI-type antibodies used in the treatment of lung cancer.
Lung cancer is characterized by multiple histological types, stages, and molecular profiles, each associated with different therapeutic options. ICI-type antibodies have numerous indications in lung cancer, and these indications have continued to expand in recent years. They are now used not only in metastatic stages but also in localized and locally advanced stages. These molecules have led to a marked improvement in the prognosis of lung cancer patients. However, their effectiveness varies from one patient to another.
The study focuses on anti-PD-1 and anti-PD-L1 ICI antibodies used routinely in lung cancer, regardless of histology or stage, whether administered alone or in combination with chemotherapy. Most of these antibodies are administered at a fixed dose, without adjustment for age, weight, general health, or nutritional status of the patients.We hypothesize that the use of fixed-dose ICIs in lung cancer may influence therapeutic response and patient survival.
- Conditions
- Lung Cancer (NSCLC)
- Keywords
- immune checkpoint inhibitors, inflammation, cachexia
- Medical subject headings
- Lung Neoplasms, Carcinoma, Non-Small-Cell Lung, Inflammation, Cachexia
What is being measured
The primary outcome is the main question the study is designed to answer.
time to progression
time between 1st administration of Ab ICI and progression or death from any cause.
Measured: Month 36
Secondary outcomes (5)
weight
Measured: from day 0 to month 36 at each patient visit
Serum CRP concentration
Measured: from day 0 to month 36 at each patient visit
Serum Ab ICI concentration
measured using validated ELISA (Enzyme-Linked Immunosorbent Assay) techniques
Measured: from day 0 to month 36 at each patient visit
Drug toxicity
Measured: from day 0 to month 36 at each patient visit
Overall survival
time between first administration of Ab ICI and death from any cause.
Measured: from day 0 to month 36 at each patient visit
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Jun 2025
- Study start3 Jun 2025
- Primary completionJun 2030 (estimated)
- Study completionJun 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Lung Cancer (NSCLC)Studies of the same condition, open and under way.
- More trials run by University Hospital, ToursThe 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
- Case only
- Time perspective
- Prospective
- Enrolment
- 150 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Tours
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Marion FERREIRA, Dr, Principal investigator, University Hospital, Tours
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07004868
- Sponsor's protocol ID
- DR240341 - LCab
- Acronym
- LCab
- Status last verified
- Aug 2025
- First submitted
- 26 May 2025
- Last updated
- 11 Aug 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 11 Aug 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Inflammation, Cachexia and Therapeutic Response in Lung Cancer Treated With Immune Checkpoint Inhibitors: Exploratory Observational Study
- ClinicalTrials.gov ID
- NCT07004868
- Acronym / sponsor ID
- LCab / DR240341 - LCab
- Conditions
- Lung Cancer (NSCLC)
- Keywords
- immune checkpoint inhibitors, inflammation, cachexia
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 150 participants (estimated)
- Lead sponsor
- University Hospital, ToursUniversity, hospital or other
- Study start
- 3 Jun 2025 (actual)
- Primary completion
- Jun 2030 (estimated)
- Study completion
- Jun 2030 (estimated)
- First posted
- 4 Jun 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.
Lung cancer is the leading cause of cancer-related death in France and globally, with 2.48 million new cases diagnosed in 2022, accounting for nearly 13% of global cancer incidence. Despite recent advances, it remains a major health issue due to late-stage diagnosis and high patient and societal burden. New insights into tumor and immune pathways have led to the development of targeted therapies, including tyrosine kinase inhibitors and therapeutic antibodies. Among these, immune checkpoint inhibitors (ICIs) such as nivolumab, pembrolizumab, atezolizumab, and durvalumab have significantly improved outcomes for some patients by reactivating T-cell responses.
The LCAb (Lung Cancer Antibodies) research project focuses on studying the interindividual variability of clinical response to ICI in lung cancer. These therapies are now used across various lung cancer types and stages, including early and advanced disease. Most ICIs are administered at fixed doses, without considering patient-specific factors as blood concentrations, tumor burden, body weight or nutritional status. The study hypothesizes that fixed dosing may affect treatment response and survival outcomes, highlighting the need for more personalized approaches.
Detailed description
Lung cancer is the leading cause of cancer-related death in France and worldwide. Its incidence is significant, with 2.48 million new cases diagnosed in 2022, representing nearly 13% of the total global cancer incidence. Despite recent therapeutic advances, it remains a major public health issue due to its frequent diagnosis at a metastatic stage, which results in high morbidity and mortality for patients and significant costs for society.
A better understanding of tumor and immune signaling pathways has recently led to the discovery of new molecular targets, such as immune checkpoints. The therapeutic arsenal against lung cancer has thus expanded to include new molecules such as tyrosine kinase inhibitors and therapeutic antibodies (Abs). The latter represent the majority of anticancer biotherapies, with more than 50 approved agents for solid or hematologic cancers.
In particular, antibodies targeting immune checkpoints (ICIs - immune checkpoint inhibitors), such as nivolumab, pembrolizumab, atezolizumab, and durvalumab, have revolutionized the management of certain lung cancer patients by reversing T-cell exhaustion, allowing some of them to become long-term responders.
The research project "Pharmacokinetics of Immune Checkpoint Inhibitor Antibodies Used in Lung Cancer" (LCAb - Lung Cancer Antibodies) aims to study the blood concentrations and pharmacokinetics of various ICI-type antibodies used in the treatment of lung cancer.
Lung cancer is characterized by multiple histological types, stages, and molecular profiles, each associated with different therapeutic options. ICI-type antibodies have numerous indications in lung cancer, and these indications have continued to expand in recent years. They are now used not only in metastatic stages but also in localized and locally advanced stages. These molecules have led to a marked improvement in the prognosis of lung cancer patients. However, their effectiveness varies from one patient to another.
The study focuses on anti-PD-1 and anti-PD-L1 ICI antibodies used routinely in lung cancer, regardless of histology or stage, whether administered alone or in combination with chemotherapy. Most of these antibodies are administered at a fixed dose, without adjustment for age, weight, general health, or nutritional status of the patients.We hypothesize that the use of fixed-dose ICIs in lung cancer may influence therapeutic response and patient survival.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adult patients with a lung cancer treated with immune checkpoint inhibitors
Key inclusion criteria (4 listed)
- Age greater than or equal to 18 years
- Diagnosis of lung cancer, any histology, any stage
- Treatment with Ab ICI, with or without chemotherapy
- 1st administration of Ab ICI
Key exclusion criteria (3 listed)
- Patient not followed at the CHRU de Tours
- Person under protective supervision
- Opposition to data processing
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
time to progression
Time frame: Month 36
time between 1st administration of Ab ICI and progression or death from any cause.
5 secondary outcomes
weight
Time frame: from day 0 to month 36 at each patient visit
Serum CRP concentration
Time frame: from day 0 to month 36 at each patient visit
Serum Ab ICI concentration
Time frame: from day 0 to month 36 at each patient visit
Drug toxicity
Time frame: from day 0 to month 36 at each patient visit
Overall survival
Time frame: from day 0 to month 36 at each patient visit
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Aug 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.
Marion FERREIRA, Dr principal investigator
University Hospital, Tours
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 Lung Cancer (NSCLC), run by University Hospital, Tours at 1 site in France.
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 3 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: looking for participants now, as of the sponsor's last update on 11 Aug 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 France. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Marion FERREIRA, Dr (0247471640 ext. +33, marion.ferreira@chu-tours.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
time to progression (time frame: Month 36). 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 11 Aug 2025.