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An exploration of Apatinib Plus IP solution as 2nd Line Treatment in Patients With Small Cell Lung Cancer

An exploration of Apatinib Plus IP solution as 2nd Line Treatment in Patients With Small Cell Lung Cancer

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018642
Enrollment
Unknown
Registered
2018-09-30
Start date
2018-10-01
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

Non-small Cell Lung Cancer

Interventions

Case series:apatinib mesylate combined with IP chemotherapy

Sponsors

Affiliated Cancer Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years male and female; 2. Histologically or cytologically confirmed,Second-line patient with small cell lung cancer; 3. At least one extracranial measurable lesion according to the evaluation criteria of solid tumor efficacy (RECIST 1.1), CT scan Long diameter of tumor=10mm; 4. ECOG score 0-2; 5. The main organ function is normal, and meet the following standards: (1) The standard of blood routine examination should be consistent: HB=80 g/L, ANC=1.5×10^9/L, PLT=80×10^9/L; (2) Biochemical tests should meet the following criteria: BIL50ml/min; 6. Estimated survival time=3 mouths; 7. Patients voluntarily entered the study and signed informed consent form (ICF); 8. Fertile woman must perform a pregnancy test (serum or urine) 7 days before screened, or voluntarily adopt proper methods of contraception during the observation period; For men, surgery should be sterilized or agreed to use appropriate methods of contraception during observation.

Exclusion criteria

Exclusion criteria: 1. pregnant or lactating women; 2. People with high blood pressure who cannot be reduced to the normal range by antihypertensive medication (systolic blood pressure >140 mmHg, diastolic blood pressure >90 mmHg); Arrhythmia with grade I or higher myocardial ischemia or myocardial infarction (including QTc interphase more than 440 MS) and I level cardiac insufficiency; 3. Have a variety of factors that affect the oral and absorption of drugs (such as can not swallow, after gastrointestinal resection, chronic diarrhea and intestinal obstruction, etc.); 4. Abnormal coagulation (PTorPT-INR>1.5ULN or APTT>1.5 ULN), bleeding tendency(such as: active gastrointestinal ulcer lesions) or receiving coagulation therapy; 5. There are clear gastrointestinal or other organ bleeding concerned (such as: local active ulcer lesions, fecal occult blood (++)), history of gastrointestinal bleeding within 6 months; 6. long nonunion or incomplete healing of the fracture; 7. urine protein positive patients (urine protein test 2+ or above, or 24 hours urine protein quantitative >1.0g); 8. patients with mental substance abuse history who are unable to quit or have mental disorders.

Design outcomes

Primary

MeasureTime frame
size of the lesions;

Countries

China

Contacts

Public ContactYan Wang

Affiliated Cancer Hospital of Harbin Medical University

wangyan86298263@163.com+86 18646112715

Outcome results

None listed

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