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Concurrent Nab-P/Carboplatin and Thoracic Radiotherapy in Inoperable Stage III Squamous Cell Lung Cancer

A perspective, open, multi-center phase II Study of Nab-P/Carboplatin and Thoracic Radiotherapy for Stage III Squamous Cell Lung Cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018674
Enrollment
Unknown
Registered
2018-10-02
Start date
2018-12-01
Completion date
Unknown
Last updated
2018-10-10

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

Conditions

Squamous Cell Lung Cancer

Interventions

Case series:Nab-P+CBP

Sponsors

Zhongnan Hospital, Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 Years to 75 years; 2. Performance status of 0 to 1 on the Eastern Cooperative Oncology Group (ECOG) Scale; 3. Previously untreated, histological documented, inoperable stage III squamous cell carcinoma of lung, excluding those with pericardial, pleural effusion, and those with contralateral hilar or contralateral supraclavicular lymph nodes; 4. Patients must have measurable disease according to RECIST criteria, and all detectable tumor can be encompassed by radiation therapy fields; 5. Patient must have adequate blood, liver, lungs and kidney function within the requirements of this study; 6. Female patients of child-bearing potential must test negative for pregnancy at the time of enrollment based on a serum pregnancy test. Male and female patients must agree to use a reliable method of birth control during and for 3 months following the last dose of study drug; 7. Patients must sign a study-specific informed consent form prior to study entry.

Exclusion criteria

Exclusion criteria: 1. Previous chemotherapy or previous biologic response modifiers for current lung cancer; 2. Patient has previously had thoracic radiation therapy; 3. Prior or concurrent malignancy except non-melanomatous skin cancer unless disease-free for five years or more; 4. Serious concomitant disorders that would compromise the safety of the patient, or compromise the patient's ability to complete the study, at the discretion of the investigator.

Design outcomes

Primary

MeasureTime frame
PFS;

Secondary

MeasureTime frame
OS;ORR;LCR;Safety;QoL;

Countries

China

Contacts

Public ContactConghua Xie

Department of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University

chxie_65@hotmail.com+86 027 67812607

Outcome results

None listed

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