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Phase II clinical study for Sintilimab in the maintenance therapy after first-line chemotherapy of advanced lung squamous cell carcinoma

Phase II clinical study for Sintilimab in the maintenance therapy after first-line chemotherapy of advanced lung squamous cell carcinoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900026448
Enrollment
Unknown
Registered
2019-10-10
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-10-14

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

Conditions

Lung cancer

Interventions

Case series:Sintilimab for maintenance therapy

Sponsors

Fujian Province Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. pathology diagnosed with advanced lung squamous cell carcinoma without surgery or concurrent radiotherapy,meet any of the following criteria: (1) Systemic treatment for advanced or metastatic disease other than first-line GP regimen chemotherapy,EGFR and ALK gene test results were negative; (2) The first-line gemcitabine combined with cisplatin regimen after 4 cycles of chemotherapy was evaluated as SD or PR patients; 2. Aged >=18 years old; 3. Expected survival time >=12 weeks; 4. There are at least 1 measurable or evaluable lesion according to the solid tumor efficacy evaluation standard version 1.1 (RECIST v1.1); 5. According to the US Eastern Oncology Group, the physical status score (ECOG PS score) 0-2; 6. The planned treatment plan includes the salibizumab; 7. Normal main organs function.

Exclusion criteria

Exclusion criteria: 1. Received a live attenuated vaccine within 4 weeks prior to enrollment or during the study period; 2. Active, known or suspected autoimmune diseases; 3. A history of primary immunodeficiency is known; 4. History of allogeneic organ transplantation and history of allogeneic hematopoietic stem cell transplantation; 5. Female patients who are pregnant or breastfeeding; 6. Untreated acute or chronic active hepatitis B or hepatitis C infection. In the case of patients receiving antiviral therapy, in the case of monitoring the number of copies of the virus, the doctor judges whether or not the enrollment is met according to the individual condition of the patient; 7. Uncontrolled concurrent diseases, including but not limited to: (1) HIV-infected (HIV-positive); (2) Severe infections that are active or have poor clinical control; (3) severe or uncontrollable systemic diseases (such as severe mental, neurological, epilepsy or dementia, unstable or uncompensated respiratory, cardiovascular, hepatic or renal diseases, uncontrolled hypertension) Evidence of greater than or equal to CTCAE grade 2 hypertension after drug treatment]; 8. Active bleeding or new thrombotic disease is taking a therapeutic amount of anticoagulant or bleeding.

Design outcomes

Primary

MeasureTime frame
progression-free survival;progression-free survival;

Secondary

MeasureTime frame
Disease control rate;overall survival;Objective remission rate;Quality of life score;

Countries

China

Contacts

Public ContactZhuang Wu

Fujian Province Cancer Hospital

zhuangwu2008@126.com+86 13805900871

Outcome results

None listed

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