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Application of RecistBM Criteria in Efficacy Evaluation of Bone Metastasis from Non-Small Cell Lung Cancer

Application of RecistBM Criteria in Efficacy Evaluation of Bone Metastasis from Non-Small Cell Lung Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122916
Enrollment
Unknown
Registered
2026-04-20
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Non-small cell lung cancer (NSCLC) with bone metastases

Interventions

Immune/Targeted Therapy Observation Group:None

Sponsors

The Army Specialty Medical Center of the People's Liberation Army of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients with histologically or cytologically confirmed non-small cell lung cancer (NSCLC, including adenocarcinoma, squamous cell carcinoma, and other NSCLC subtypes), aged = 18 years, regardless of gender, with an expected survival = 3 months; 2.Patients with suspected bone metastases diagnosed by CT, PET-CT, MRI, or bone scan prior to enrollment; 3.Received first-line immunotherapy or targeted therapy for NSCLC, with regimens consistent with the recommendations of the Chinese Society of Clinical Oncology (CSCO) Guidelines for the Diagnosis and Treatment of Non-Small Cell Lung Cancer; 4.Presence of at least one measurable non-bone lesion; 5.Voluntarily signed informed consent, with good communication skills and compliance, able to cooperate with scheduled follow-up visits and relevant examinations as required by the study

Exclusion criteria

Exclusion criteria: 1.Concurrent malignanc; 2.Severe dysfunction of vital organs including heart, liver and kidney, or active infection, unable to tolerate protocol-specified treatment and follow-up; 3.Previous exposure to immunotherapy or targeted therapy, or receipt of local radiotherapy for bone metastases prior to study treatment; 4.Uncertain diagnosis of bone metastases; 5.Presence of psychiatric disorders, cognitive impairment or communication barriers, unable to cooperate with follow-up and data collection; 6.Female patients who are pregnant or lactating;

Design outcomes

Primary

MeasureTime frame
Progression-free survival (PFS);Efficacy;Bone Efficacy;Bone Progression-Free Survival (Bone PFS);

Secondary

MeasureTime frame
Overall survival (OS);

Countries

China

Contacts

Public ContactYang,xueqin

The Army Specialty Medical Center of the People's Liberation Army of China

yxq92@163.com+86 23 68746550

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026