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Advanced Lung CancerNCT06326086

Differences in Rate of Decline in CT-defined Skeletal Muscle Mass and Physical Performance in Patients With Advanced Non-small Cell Lung Cancer Receiving Chemotherapy and Targeted Therapy/Immunotherapy, Before and After Treatment.

An observational study of Advanced Lung Cancer and Sarcopenia, run by Prince of Songkla University at 1 site in Thailand.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Lung cancer is a common disease leading to 18 % of cancer deaths worldwide. Despite various improvement in treatment, there still remains low 5-year survival rate of 10-20 % in advanced lung cancer patients. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Advanced Lung Cancer, Sarcopenia
What is being tested?
Chemotherapy drug, Targeted Agent and Immunotherapy
How many people
240 participants
Where
1 siteThailand
Study dates
1 Aug 2022to 1 Aug 2024
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
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Stage III and IIIC (if patients are treated with TKI/IO), and Stage IV non-small cell lung cancer patients who are receiving chemotherapy or targeted therapy/immunotherapy (TKI/IO) treated in Songklanagarind Hospital.

Who may be able to join

  • Age >18years old,
  • Stage IIIB and IIIC (if patients are treated with TKI/IO), and Stage IV non-small cell lung cancer patients confirmed by histopathology.
  • Patients should be either on chemotherapy, molecular targeted therapy or immunotherapy.

Who cannot join

  • Unable to perform CT scan due to various reasons.
  • Patients with metastatic disease at L3 vertebral level.
  • If unable to perform SPPB test due to physical disability or patient's refusal.
  • Patients with known other primary malignancies. 5 . Patients who have underwent definitive surgery.
  • 6. Pregnant patients. 7. Patients with physical deformities/neurological deficits which restricts their physical movements.

Trial locations and contacts

1 site in 1 country.

Shiva R Timsina, MBBS contact

+660623898980

timsinasraj@gmail.com

Thailand1 site, 1 recruiting
  • Prince of Songkla University

    Hat Yai, Changwat Songkhla, 90110

    Recruiting

Other trials in Thailand

About this study

Lung cancer is a common disease leading to 18 % of cancer deaths worldwide. Despite various improvement in treatment, there still remains low 5-year survival rate of 10-20 % in advanced lung cancer patients. Skeletal muscle mass and physical performance have been shown to effect overall survival and prognosis in lung cancer. This research focuses on effects of different treatment of lung cancer such as chemotherapy, targeted therapy and immunotherapy on skeletal muscle mass and physical performance.

Read the detailed description

Lung cancer is a common disease leading to 18% of all cancer deaths worldwide. Prognosis of lung cancer depends on various factors like disease stage, socioeconomic factors, body composition factors such as sarcopenia have been shown to be associated with poor prognosis and survival. Sarcopenia is defined as decline in muscle strength, muscle quantity/quality (skeletal muscle mass) and physical performance. Diagnosis of sarcopenia is confirmed by demonstrating reduced skeletal muscle mass while physical performance can be used to assess severity of sarcopenia. In past 5 years there are some studies indicating an association between treatment of lung cancer and decline in parameters of sarcopenia. Although remarkable improvements in medical treatments for non-small cell lung cancer (NSCLC) based on chemotherapy, targeted therapy and immunotherapy have been made, advanced lung cancer patients still have low five-year survival rate at 10-20 percent. Notably with a high prevalence of 43%, sarcopenia is shown to be a significant predictor of worsening overall survival and poor prognosis in NSCLC patients.

Cancer patients have expedited decline in skeletal muscle mass as compared to normal age-related decline in patients without cancer. Majority of older studies on NSCLC patients show that there is decrease in skeletal muscle mass during chemotherapy. Data on changes in skeletal muscles in NSCLC patients receiving targeted therapy and immunotherapy are limited, however studies suggest that patients experience decline in skeletal muscle mass while receiving these therapies as well. During treatment, in addition to decline in skeletal muscle mass, non-small cell lung cancer patients also exhibit decline in other parameters of sarcopenia i.e., muscle strength and physical performance as well. The impact of decline in parameters of sarcopenia leads to functional impairment with poor response to treatment, increased drug toxicities and poor quality of life. The value of measuring sequential decline in parameters of sarcopenia is not clearly understood. It is believed that interventions to treat sarcopenia can evolve if we can understand effects of different cancer therapies on sarcopenia. Early screening and treatment of sarcopenia in these patients may help to prevent functional impairment and improve overall survival.

Although there are other causes of sarcopenia in cancer patients such as impaired nutritional intake, low physical activity, causes relating to cancer therapies are not well established. There still remains a wide knowledge gap in understanding decline in different parameters of sarcopenia while patients are on different types of lung cancer treatment. Therefore, we aim to study a prospective cohort to evaluate differences in rate of decline in skeletal muscle mass and physical performance in advanced NSCLC patients receiving chemotherapy and targeted therapy/immunotherapy. The skeletal muscle mass and physical performance will be evaluated using computed tomography (CT) and short physical performance battery (SPPB) respectively. There is lack of validated cut-off values for CT-defined skeletal muscle mass in Thai population. Therefore, in Thai population, we aim to validate the cutoff values set by Japanese Society of Hepatology(JSH) based on recommendation of Asian Working Group for Sarcopenia (AWGS). As latest consensus on sarcopenia highlights importance of physical performance, if there exist an association between CT-defined skeletal muscle mass and physical performance, the former can be used in predicting physical functioning of patients. Therefore, we intend to determine baseline association between CT-defined skeletal muscle mass and physical performance as well. As far as we know there are no previous studies done to evaluate the differences in decline in skeletal muscle mass in patients who are unable to complete their first line chemotherapy and receive other line of chemotherapy (chemotherapy agents which are not considered first line), therefore we intent to study these differences too. Finally, this study also includes an evaluation of overall response rate of chemotherapy in patients with low CT-defined skeletal muscle mass.

This study is based in Songklanagarind Hospital and enrollment of participants will be as per our inclusion criteria which includes advanced lung cancer patients who are more than 18 years old treated with either chemotherapy, targeted therapy or immunotherapy. The sample size required for the study was estimated using simulation in Stata, with an estimated total N=240. According to treatment recommended by primary chest physician, participants will be divided into groups of chemotherapy (CMT) and targeted/immunotherapy (TKI/IO). Measurement of variables will take place in four different time period. Baseline characteristics will be measured before starting the treatment. The outcome variables our study i.e., computed tomography (CT)-defined skeletal muscle mass, short physical performance battery (physical performance) and health related quality of life using Thai Version of EQ-5D-5L Health Questionnaire (EQ-5D-5L) will be measured before starting treatment (T1), after 3rd, 6th and 9th months (T2, T3 and T4) of treatment. Additionally, after 3rd cycle of treatment "response evaluation criteria in solid tumors" (RECIST v1.1) will be recorded to evaluate response rate of chemotherapy. For patients who are unable to tolerate first line chemotherapy, they will be recruited for our 1st secondary objective and patients in this group will be evaluated only for CT-defined skeletal muscle mass in subsequent time period. At the end of our study, we will have three groups of patients i.e., patients receiving first line chemotherapy (CMT) patients on first line targeted/immunotherapy (TKI/IO) and patients on other line chemotherapy (OCMT).

Measuring skeletal muscle area (SMA) at L3 vertebral level using computed tomography scan is used to estimate total body skeletal muscle mass (SMM). Height adjusted SMA, also called skeletal muscle index (SMI) can be calculated by dividing SMA by patient's height square. As our study is based on Thai population, cut-off for diagnosis of CT-defined sarcopenia will be taken as L3 lumbar vertebra (L3SMI) <42cm2/m2 for men and <38 cm2/m2 for women. Short physical performance battery (SPPB) test will be used to evaluate physical performance. SPPB consists of set of three tests including balance test, gait test and 5 times chair stand test. Patients are asked to stand side-by-side, semi-tandem and tandem to measure balance. And then patients are asked to walk 4 meters to assess gait speed. Chair stand test is performed by asking the patient to fold their arms and stand up from seated position for five times. Points from 0 to 12 will be given according to time required to perform above tests. Health related quality of life will be measured using the Thai Version of EQ-5D-5L Health Questionnaire. This is validated tool for use in Thailand which has a self-completed questionnaire for adults consisting of 5 dimensions of mobility, self-care, usual activities, pain/discomfort and anxiety/depression The baseline characteristics will be presented with n (%) and mean (SD) or median (IQI) as appropriate. Chi-square test (or Fisher Exact test), Student t-test (or Kruskal-Wallis test) will be calculated to evaluate the differences of baseline data between CMT and TKI/IO groups. The baseline correlation between SPPB and SMI will be presented with scatter plot and LOWESS line. The change of SMI after 6th cycles of treatments and the differences of the change between CMT and TKI/IO groups will be calculated using Student t-test or Kruskal-Wallis test. Multivariable linear regression will be used to adjust the imbalance of baseline characteristics between these two-groups. Decline in SMI for CMT and OCMT will be calculated using same analysis. The rate of decline in SMI (and SPPB score) will be calculated using multilevel-linear regression (Mixed linear regression) and will be shown in two-way graph. The response rate to chemotherapy will be analyzed using logistic regression. The p-value of less the 0.05 will be considered statistically significant. The analysis and graphically figures will be shown using Stata/MP 17.0, StataCorp, 4905 Lakeway Dr, College Station, TX 77845, USA.

Being tested
Chemotherapy drug, Targeted Agent, Immunotherapy
Keywords
Chemotherapy, targeted therapy, immunotherapy, NSCLC, sarcopenia, physical performance.
Medical subject headings
Sarcopenia, Carcinoma, Non-Small-Cell Lung

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Chemotherapy drugDrug

    Chemotherapy drug as prescribed by primary treating physician

  • Targeted AgentDrug

    Targeted agents as prescribed by primary treating physician

  • ImmunotherapyDrug

    Immunotherapy as prescribed by primary treating physician

Study groups in NCT06326086
Study groupRoleWhat they receive
CMT for patients receiving chemotherapy,Not described
Receives: Drug: Chemotherapy drug
TKI/IO for patients receiving targeted and immunotherapyNot described
Receives: Drug: Targeted Agent; Drug: Immunotherapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To determine the differences in the rate of decline in CT defined skeletal muscle index at L3 vertebra and physical performance in advanced NSCLC patients receiving chemotherapy and targeted therapy/ immunotherapy, before and after treatment.

    To determine the differences in the rate of decline in CT defined skeletal muscle index at L3 vertebra and physical performance in advanced NSCLC patients receiving chemotherapy and targeted therapy/ immunotherapy, before and after treatment.

    Measured: 1 year

Secondary outcomes (1)
  1. To determine validity of gender based cut off for CT-defined skeletal muscle index at L3 lumbar vertebra (L3SMI) based on recommendation of JSH/AWGS in Thai population.

    1. To determine validity of gender based cut off for CT-defined skeletal muscle index at L3 lumbar vertebra (L3SMI) based on recommendation of JSH/AWGS in Thai population.

    Measured: 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Mar 2024
  2. Study start1 Aug 2022
  3. Primary completion1 Aug 2024 (estimated)
  4. Study completion1 Aug 2024 (estimated)

Resources

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
240 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06326086
Sponsor's protocol ID
REC.65-080-7-1
Status last verified
Mar 2024
First submitted
16 Mar 2024
Last updated
22 Mar 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Advanced Lung Cancer and Sarcopenia, run by Prince of Songkla University at 1 site in Thailand.

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 5 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 22 Mar 2024. 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 Thailand. 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 Shiva R Timsina, MBBS (+660623898980, timsinasraj@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To determine the differences in the rate of decline in CT defined skeletal muscle index at L3 vertebra and physical performance in advanced NSCLC patients receiving chemotherapy and targeted therapy/ immunotherapy, before and after treatment. (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 22 Mar 2024.

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