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Study of Thalidomide in Treatment of Advanced Nsclc (Dream-003)

Primary Purpose

Advanced Nsclc

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Thalidomide
pemetrexed
cisplatin
carboplatin
Sponsored by
Qilu Hospital of Shandong University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Advanced Nsclc focused on measuring thalidomide, pemetrexed, nsclc, maintenance treatment

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. stage Ⅳ non-squamous NSCLC with epidermal growth factor receptor wild-type or unknown mutation status confirmed by molecular biology and histology.
  2. age 18-70 years.
  3. Eastern Cooperative Oncology Group performance status of 0 or 1 and life expectancy greater than 3 months.
  4. no previous treatment with chemotherapy or radiotherapy
  5. adequate bone marrow, hepatic, and renal function
  6. measurable or evaluable disease
  7. informed consent
  8. negative pregnancy test and adequate contraception for the duration of treatment

Exclusion Criteria:

  1. malignancy during the 5 years previous to the diagnosis of NSCLC (unless nonmelanoma skin cancer or early cervical cancer)
  2. surgery within 4 weeks
  3. history of major hemoptysis
  4. recent history of bleeding or thrombotic events
  5. brain metastasis
  6. uncontrolled hypertension
  7. ongoing therapeutic anticoagulation

Sites / Locations

  • Qilu hospital of Shandong UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

P+Cisplatin/Carboplatin+T

P+Cisplatin/Carboplatin

Arm Description

Induction therapy (Platinum based chemotherapy combined with antiangiogenic therapy 4-6 cycles): Pemetrexed + Platinum + Thalidomide [pemetrexed (500mg/m^2)+cisplatin(75mg/m^2)or carboplatin(AUC=5) on day 1 of 21-days cycle, ivgtt +thalidomide 100-200mg/d ,oral, qn ] Continue maintenance therapy (It is defined when a drug included in the induction treatment is used as maintenance .Patients who had not progressed during induction phase will be in this phase): Thalidomide 100mg/d ,oral, qn, until either disease progression or unacceptable toxicity.

Induction therapy ( Platinum based chemotherapy 4-6 cycles): Pemetrexed + Platinum [pemetrexed (500mg/m^2)+cisplatin(75mg/m^2)or carboplatin(AUC=5) on day 1 of 21-days cycle,ivgtt ] Maintenance therapy (It is defined when a drug included in the induction treatment is used as maintenance .Patients who had not progressed during induction phase will be in this phase): Pemetrexed (500mg/m^2) on day 1 of 21-days cycle, ivgtt.until either disease progression or unacceptable toxicity

Outcomes

Primary Outcome Measures

progression-free survival (PFS)
Addition of thalidomide to chemotherapy and as single maintenance treatment is associated with similar PFS with Control Arm.

Secondary Outcome Measures

objective response rate(ORR)
Response rates are similar in the two treatment groups
weight
Thalidomide can increase the weight of the patient
vascular endothelial growth factor (VEGF) VEGF
Thalidomide can decrease the level of VEGF

Full Information

First Posted
February 7, 2017
Last Updated
June 3, 2019
Sponsor
Qilu Hospital of Shandong University
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1. Study Identification

Unique Protocol Identification Number
NCT03062800
Brief Title
Study of Thalidomide in Treatment of Advanced Nsclc (Dream-003)
Official Title
Study of Thalidomide With First-line Chemotherapy and as Maintenance Treatment of Advanced Nonsquamous NSCLC With Epidermal Growth Factor Receptor Wild-Type or Unknown Mutation Status: A Multicenter, Randomized, Prospective Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Unknown status
Study Start Date
December 2016 (undefined)
Primary Completion Date
December 2020 (Anticipated)
Study Completion Date
November 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Qilu Hospital of Shandong University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The study for innovative strategies is warranted in the treatment of advanced non-squamous NSCLC with epidermal growth factor receptor wild-type or unknown mutation status because the outcomes remain unsatisfactory for most patients. Maintenance treatment after first-line chemotherapy is a very interesting strategy that has been largely investigated in the last years. This study is to evaluate the efficacy and toxicity of thalidomide in combination with chemotherapy and as maintenance treatment in patients with advanced non-squamous NSCLC.
Detailed Description
Lung cancer is the most common cancer and is the leading cause of cancer mortality in the world. Every year, more than one million people die from lung cancer in worldwide. NSCLC accounts for about 85% of all lung cancers diagnosis and continues to remain a major therapeutic challenge. Chemotherapeutic agents in the treatment of advanced NSCLC have reached a plateau of effectiveness when administered in the classic modality. In the first-line treatment of advanced non-squamous NSCLC with epidermal growth factor receptor wild-type, cisplatin plus pemetrexed is considered the best chemotherapeutic regimen. Recently, the PARAMOUNT trial has demonstrated that continuation maintenance with pemetrexed improves progression-free survival and overall survival after induction therapy with cisplatin plus pemetrexed in advanced non-squamous NSCLC with epidermal growth factor receptor wild-type. Bevacizumab, a pure humanized anti-VEGF monoclonal antibody (mAb) has improved the outcomes of chemotherapy alone when combined with chemotherapy as first-line therapy for advanced non-squamous NSCLC. A randomized phase Ⅲ trial named Eastern Cooperative Oncology Group E4559 has demonstrated that concurrent bevacizumab with chemotherapy followed by maintenance bevacizumab in previously untreated patients with advanced non-squamous NSCLC is associated with an increase in overall survival. In China, the cost of continuation maintenance with pemetrexed or bevacizumab is high in the current economic environment. Thalidomide is much cheaper than pemetrexed and bevacizumab, and has been shown to have activity in numerous malignancies. Although the exact anti-tumor mechanism is unknown, thalidomide exhibits both immuno-modulating and anti-angiogenic effects. Based on potentially synergistic mechanisms of action, thalidomide has the potential to enhance the activity of conventional chemotherapy. Results from previously published small studies in which thalidomide was given concurrently with conventional chemotherapy and was continued as maintenance therapy suggest that thalidomide might be effective in the treatment of patients with small cell lung cancer and NSCLC. Study and evaluation the efficacy and toxicity of thalidomide in combination with chemotherapy and as maintenance treatment in patients with advanced non-squamous NSCLC with epidermal growth factor receptor wild-type is necessary.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Advanced Nsclc
Keywords
thalidomide, pemetrexed, nsclc, maintenance treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
232 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
P+Cisplatin/Carboplatin+T
Arm Type
Experimental
Arm Description
Induction therapy (Platinum based chemotherapy combined with antiangiogenic therapy 4-6 cycles): Pemetrexed + Platinum + Thalidomide [pemetrexed (500mg/m^2)+cisplatin(75mg/m^2)or carboplatin(AUC=5) on day 1 of 21-days cycle, ivgtt +thalidomide 100-200mg/d ,oral, qn ] Continue maintenance therapy (It is defined when a drug included in the induction treatment is used as maintenance .Patients who had not progressed during induction phase will be in this phase): Thalidomide 100mg/d ,oral, qn, until either disease progression or unacceptable toxicity.
Arm Title
P+Cisplatin/Carboplatin
Arm Type
Experimental
Arm Description
Induction therapy ( Platinum based chemotherapy 4-6 cycles): Pemetrexed + Platinum [pemetrexed (500mg/m^2)+cisplatin(75mg/m^2)or carboplatin(AUC=5) on day 1 of 21-days cycle,ivgtt ] Maintenance therapy (It is defined when a drug included in the induction treatment is used as maintenance .Patients who had not progressed during induction phase will be in this phase): Pemetrexed (500mg/m^2) on day 1 of 21-days cycle, ivgtt.until either disease progression or unacceptable toxicity
Intervention Type
Drug
Intervention Name(s)
Thalidomide
Other Intervention Name(s)
H32026128
Intervention Description
100-200mg/d,oral ,qn
Intervention Type
Drug
Intervention Name(s)
pemetrexed
Other Intervention Name(s)
H20090232
Intervention Description
(500mg/m^2) on day 1 of 21-days cycle,ivgtt
Intervention Type
Drug
Intervention Name(s)
cisplatin
Other Intervention Name(s)
H20040813
Intervention Description
(75mg/m^2) on day 1 of 21-days cycle, ivgtt
Intervention Type
Drug
Intervention Name(s)
carboplatin
Other Intervention Name(s)
H20020180
Intervention Description
(AUC=5) on day 1 of 21-days cycle, ivgtt
Primary Outcome Measure Information:
Title
progression-free survival (PFS)
Description
Addition of thalidomide to chemotherapy and as single maintenance treatment is associated with similar PFS with Control Arm.
Time Frame
2 year
Secondary Outcome Measure Information:
Title
objective response rate(ORR)
Description
Response rates are similar in the two treatment groups
Time Frame
2 years
Title
weight
Description
Thalidomide can increase the weight of the patient
Time Frame
2 years
Title
vascular endothelial growth factor (VEGF) VEGF
Description
Thalidomide can decrease the level of VEGF
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: stage Ⅳ non-squamous NSCLC with epidermal growth factor receptor wild-type or unknown mutation status confirmed by molecular biology and histology. age 18-70 years. Eastern Cooperative Oncology Group performance status of 0 or 1 and life expectancy greater than 3 months. no previous treatment with chemotherapy or radiotherapy adequate bone marrow, hepatic, and renal function measurable or evaluable disease informed consent negative pregnancy test and adequate contraception for the duration of treatment Exclusion Criteria: malignancy during the 5 years previous to the diagnosis of NSCLC (unless nonmelanoma skin cancer or early cervical cancer) surgery within 4 weeks history of major hemoptysis recent history of bleeding or thrombotic events brain metastasis uncontrolled hypertension ongoing therapeutic anticoagulation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiuwen Wang, MD.PhD
Phone
+86 13791123979
Email
wangxiuwen@medmail.com.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Shuguang Li, MD.PhD
Phone
+86-0531-82169841
Email
lishuguang96@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiuwen Wang, MD.PhD
Organizational Affiliation
Qilu Hospital of Shandong University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Qilu hospital of Shandong University
City
Jinan
State/Province
Shandong
ZIP/Postal Code
250012
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shuguang Li, MD.
Phone
+86 18560082862
Email
lishuguang96@163.com
First Name & Middle Initial & Last Name & Degree
Xiuwen Wang, MD.

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24571650
Citation
Villa C, Cagle PT, Johnson M, Patel JD, Yeldandi AV, Raj R, DeCamp MM, Raparia K. Correlation of EGFR mutation status with predominant histologic subtype of adenocarcinoma according to the new lung adenocarcinoma classification of the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society. Arch Pathol Lab Med. 2014 Oct;138(10):1353-7. doi: 10.5858/arpa.2013-0376-OA. Epub 2014 Feb 26.
Results Reference
background
PubMed Identifier
20686429
Citation
Sandler A, Yi J, Dahlberg S, Kolb MM, Wang L, Hambleton J, Schiller J, Johnson DH. Treatment outcomes by tumor histology in Eastern Cooperative Group Study E4599 of bevacizumab with paclitaxel/carboplatin for advanced non-small cell lung cancer. J Thorac Oncol. 2010 Sep;5(9):1416-23. doi: 10.1097/JTO.0b013e3181da36f4.
Results Reference
background
PubMed Identifier
15019676
Citation
Iwasaki A, Kuwahara M, Yoshinaga Y, Shirakusa T. Basic fibroblast growth factor (bFGF) and vascular endothelial growth factor (VEGF) levels, as prognostic indicators in NSCLC. Eur J Cardiothorac Surg. 2004 Mar;25(3):443-8. doi: 10.1016/j.ejcts.2003.11.031.
Results Reference
background
PubMed Identifier
23259416
Citation
Gridelli C, Maione P, Rossi A. The PARAMOUNT trial: a phase III randomized study of maintenance pemetrexed versus placebo immediately following induction first-line treatment with pemetrexed plus cisplatin for advanced nonsquamous non-small cell lung cancer. Rev Recent Clin Trials. 2013 Mar;8(1):23-8. doi: 10.2174/15748871112079990040.
Results Reference
background
PubMed Identifier
23931282
Citation
Zhou S, Wang F, Hsieh TC, Wu JM, Wu E. Thalidomide-a notorious sedative to a wonder anticancer drug. Curr Med Chem. 2013;20(33):4102-8. doi: 10.2174/09298673113209990198.
Results Reference
background
PubMed Identifier
17920723
Citation
Lee SM, James L, Buchler T, Snee M, Ellis P, Hackshaw A. Phase II trial of thalidomide with chemotherapy and as maintenance therapy for patients with poor prognosis small-cell lung cancer. Lung Cancer. 2008 Mar;59(3):364-8. doi: 10.1016/j.lungcan.2007.08.032. Epub 2007 Oct 24.
Results Reference
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Study of Thalidomide in Treatment of Advanced Nsclc (Dream-003)

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