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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
Chifeng Municipal Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Small Cell Lung Cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. patients 18-75 years of age.
  2. A metastatic or recurrent advanced SCLC confirmed by histology or cytology and did not receive any other treatment;
  3. a measurable disease
  4. an Eastern Cooperative Oncology Group PS of 0-1;
  5. an estimated survival duration of >6 months;

Exclusion Criteria:

  1. 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

    First Posted
    March 24, 2019
    Last Updated
    March 25, 2019
    Sponsor
    Chifeng Municipal Hospital
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    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

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    Clinical Study of First-line Treatment of Small Cell Lung Cancer (SCLC) With Anlotinib Hydrochloride

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