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Application of micro flow control technology in the treatment of advanced lung cancer

Application of micro flow control technology in the treatment of advanced lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-PNC-16009995
Enrollment
Unknown
Registered
2016-11-24
Start date
2016-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Interventions

experimental group:Microfluidic sorting of tumor cells+chemotherapy
control group:chemotherapy

Sponsors

Shanghai Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years old, male and female; 2. there was no late stage (stage III B and not to be treated) and metastatic (stage IV) NSCLC in the presence of an inability to be operated by histopathology or cytology; 3. patients with tumors lacking EGFR sensitive mutation (i.e. deletion of exon 19, exon 21 and exon 21 of L858R, L861Q, exon 18 or G719X exon 20 S7681 mutation) and ALK rearrangement, or the corresponding targeted drug treatment failure; 4. patients with advanced lung cancer were able to obtain fresh tumor tissue or pleural effusion samples; 5. At least 5 of 1 lesions (who had not received radiotherapy), baseline by CT accurate measurement showed the longest diameter over 10mm (lymph nodes except short axis lymph node must be greater than or equal to 15mm), and RECIST v1.1 in accordance with the guidelines, the focus for repeated measurement; 6. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1, the expected survival should be more than 3 months; 7. signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Can not or refuse to collect tumor samples, including tumor tissue blocks, or malignant pleural effusion, or circulating tumor cells, etc.; 2. Refused to accept the relevant treatment or follow-up programs

Design outcomes

Primary

MeasureTime frame
Objective remission rate;

Secondary

MeasureTime frame
Survival Time;Toxic and side effects;

Countries

China

Contacts

Public ContactZhiwei Chen

Shanghai Chest Hospital

drchenzhiwei@163.com+86 13916251926

Outcome results

None listed

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