Clinical Study of First-line Treatment of Small Cell Lung Cancer (SCLC) With Anlotinib Hydrochloride
Primary Purpose
Small Cell Lung Cancer
Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Anlotinib Hydrochloride
Sponsored by
About this trial
This is an interventional treatment trial for Small Cell Lung Cancer
Eligibility Criteria
Inclusion Criteria:
- patients 18-75 years of age.
- A metastatic or recurrent advanced SCLC confirmed by histology or cytology and did not receive any other treatment;
- a measurable disease
- an Eastern Cooperative Oncology Group PS of 0-1;
- an estimated survival duration of >6 months;
Exclusion Criteria:
- Have used erlotinib or other anti-vascular targeted drugs (eg, Endo, bevacizumab, etc.)2. Patients who have been treated with chemotherapy or radiotherapy for previous tumors.3.Have appeared or merged with other tumors within 5 years.4.Patients with no measurable lesions; 5.any severe and uncontrolled disease.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Clinical trial group
Arm Description
(Carboplatin/cisplatin + etoposide)+ (Anlotinib Hydrochloride 12 mg/day ,Each cycle was defined as 2 weeks on-treatment fol- lowed by 1 week off-treatment), after 4-6 cycles of treatment, the treatment was continued with anlotinib until disease progression.
Outcomes
Primary Outcome Measures
PFS
progression-free survival
Secondary Outcome Measures
OS
overall survival
ORR
Objective Response Rate
DCR
disease control rate
safety assessed by Adverse reactions
Adverse reactions
Full Information
NCT ID
NCT03890055
First Posted
March 24, 2019
Last Updated
March 25, 2019
Sponsor
Chifeng Municipal Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03890055
Brief Title
Clinical Study of First-line Treatment of Small Cell Lung Cancer (SCLC) With Anlotinib Hydrochloride
Official Title
Clinical Study of First-line Treatment of Small Cell Lung Cancer (SCLC) With Anlotinib Hydrochloride in in Combination With EC/EP
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Unknown status
Study Start Date
April 1, 2019 (Anticipated)
Primary Completion Date
April 1, 2020 (Anticipated)
Study Completion Date
October 1, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chifeng Municipal Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
This study was designed to investigate the efficacy and side effects of combining erlotinib with classical EC/EP chemotherapy regimens.
Detailed Description
Lung cancer is a common malignant tumor that poses a serious threat to human health. Small cell lung cancer accounts for about 20% of lung cancer. Precision medicine has recently been perfectly interpreted in many tumor types, but the treatment of small cell lung cancer is still bleak. The EC/EP regimen is the most classic chemotherapy regimen for small cell lung cancer with good results but is prone to drug resistance. In 2018, with the development of immunotargeting therapy, small molecule multi-target anti-angi drugs, PARP inhibitors, new chemotherapy drugs, etc., the treatment of small cell lung cancer has ushered in a new dawn. As a kind of highly selective multi-target anti-angiogenic TKI drugs,Anlotinib Hydrochloride is a kind of 1.1 innovative drugs with independent intellectual property rights in China, mainly acting on VEGFR, PDGFR, FGFR and c-Kit. The latest ALTER1202 study confirms that anlotinib is significantly improved for PSC and ORR in SCLC patients who have previously received at least 2-line chemotherapy. OS data is not yet mature, but the benefits of the anlotinib group were observed. The adverse effects of anlotinib were consistent with expectations, no new adverse events were found, and safety was tolerated. Nowadays, the effective combination of traditional chemical therapy with molecular targeting and immunotherapy is the future development direction of lung cancer treatment. Therefore, this topic is designed to combine the efficacy of safety and safety with the treatment of anlotinib with the classic EC/EP chemotherapy regimen. Expected to get longer PFS and OS for patient benefit.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Small Cell Lung Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Clinical trial group
Arm Type
Experimental
Arm Description
(Carboplatin/cisplatin + etoposide)+ (Anlotinib Hydrochloride 12 mg/day ,Each cycle was defined as 2 weeks on-treatment fol- lowed by 1 week off-treatment), after 4-6 cycles of treatment, the treatment was continued with anlotinib until disease progression.
Intervention Type
Drug
Intervention Name(s)
Anlotinib Hydrochloride
Other Intervention Name(s)
Focusv
Intervention Description
Best supportive care
Primary Outcome Measure Information:
Title
PFS
Description
progression-free survival
Time Frame
nine months
Secondary Outcome Measure Information:
Title
OS
Description
overall survival
Time Frame
12 months
Title
ORR
Description
Objective Response Rate
Time Frame
12 months
Title
DCR
Description
disease control rate
Time Frame
12 months
Title
safety assessed by Adverse reactions
Description
Adverse reactions
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients 18-75 years of age.
A metastatic or recurrent advanced SCLC confirmed by histology or cytology and did not receive any other treatment;
a measurable disease
an Eastern Cooperative Oncology Group PS of 0-1;
an estimated survival duration of >6 months;
Exclusion Criteria:
Have used erlotinib or other anti-vascular targeted drugs (eg, Endo, bevacizumab, etc.)2. Patients who have been treated with chemotherapy or radiotherapy for previous tumors.3.Have appeared or merged with other tumors within 5 years.4.Patients with no measurable lesions; 5.any severe and uncontrolled disease.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hongbo JI, postgraduate
Phone
18604868579
Email
docjihongbo@qq.com
First Name & Middle Initial & Last Name or Official Title & Degree
Lele Wang, Bachelor
Phone
18604868579
Email
15754816534@163.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
23182663
Citation
Han JY, Kim HY, Lim KY, Han JH, Lee YJ, Kwak MH, Kim HJ, Yun T, Kim HT, Lee JS. A phase II study of sunitinib in patients with relapsed or refractory small cell lung cancer. Lung Cancer. 2013 Feb;79(2):137-42. doi: 10.1016/j.lungcan.2012.09.019. Epub 2012 Nov 20.
Results Reference
result
Links:
URL
https://www.nih.gov/
Description
National Institutes of Heaith
Learn more about this trial
Clinical Study of First-line Treatment of Small Cell Lung Cancer (SCLC) With Anlotinib Hydrochloride
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