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

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

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03062800
Enrollment
232
Registered
2017-02-23
Start date
2016-12-31
Completion date
2021-11-30
Last updated
2019-06-05

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

Conditions

Advanced Nsclc

Keywords

thalidomide, pemetrexed, nsclc, maintenance treatment

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.

Interventions

DRUGThalidomide

100-200mg/d,oral ,qn

DRUGpemetrexed

(500mg/m\^2) on day 1 of 21-days cycle,ivgtt

DRUGcisplatin

(75mg/m\^2) on day 1 of 21-days cycle, ivgtt

DRUGcarboplatin

(AUC=5) on day 1 of 21-days cycle, ivgtt

Sponsors

Qilu Hospital of Shandong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
progression-free survival (PFS)2 yearAddition of thalidomide to chemotherapy and as single maintenance treatment is associated with similar PFS with Control Arm.

Secondary

MeasureTime frameDescription
objective response rate(ORR)2 yearsResponse rates are similar in the two treatment groups
weight2 yearsThalidomide can increase the weight of the patient
vascular endothelial growth factor (VEGF) VEGF1 yearThalidomide can decrease the level of VEGF

Countries

China

Contacts

Primary ContactXiuwen Wang, MD.PhD
wangxiuwen@medmail.com.cn+86 13791123979
Backup ContactShuguang Li, MD.PhD
lishuguang96@163.com+86-0531-82169841

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026