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The effect of Qi tonifying and Yin nourishing method combined with PD-1 monoclonal antibody on immune function in patients with advanced lung adenocarcinoma undergoing chemotherapy

The effect of Qi tonifying and Yin nourishing method combined with PD-1 monoclonal antibody on immune function in patients with advanced lung adenocarcinoma undergoing chemotherapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000302
Enrollment
Unknown
Registered
2025-02-16
Start date
2024-09-02
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung caner

Interventions

control group:Pemetrexed combined with cisplatin chemotherapy, PD-1 monoclonal antibody, bevacizumab
Experimental group:On the basis of the control group the experimental group was given a traditional Chinese medicine formula based on Shamaidong Tang at the same time orally for two weeks stopped for

Sponsors

Jinshazhou Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: a. Pathologically diagnosed as lung adenocarcinoma with distant metastasis; b. EGFR wild-type and ALK negative; c. Traditional Chinese medicine syndrome differentiation is characterized by deficiency of both qi and yin: fatigue and weakness in the mind dry mouth and insufficient drinking red or pale tongue and weak pulse; d. Age range from 18 to 80 years old (including 18 and 80 years old) regardless of gender; e. The expected survival period exceeds three months; f. No previous use of pemetrexed combined with cisplatin chemotherapy and currently suitable for this chemotherapy regimen; g. ECOG score = 2 points; h. Sign an informed consent form

Exclusion criteria

Exclusion criteria: a. Existence of brain metastasis; b. Severe liver and kidney dysfunction (Child C liver function stage 4-5 kidney disease); c. Application of other immune preparations; d. Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
INF-?;T lymphocyte subpopulation;

Secondary

MeasureTime frame
PFS(Progression Free Survival);Adverse reactions;

Countries

China

Contacts

Public ContactXiang Li

Jinshazhou Hospital of Guangzhou University of Chinese Medicine

L1095468223@163.com+86 177 0193 2179

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026