Pyrotinib Plus Thalidomide in Advanced NSCLC Patients Harboring HER2 Exon 20 Insertions

  • STATUS
    Recruiting
  • End date
    Apr 3, 2023
  • participants needed
    39
  • sponsor
    Shanghai Chest Hospital
Updated on 3 February 2021

Summary

Various driver gene mutations have been identified in lung cancer. Among them, human epidermal growth factor 2 (HER2) was identified in approximately 2% of non-small-cell lung cancers. Pyrotinib is an oral tyrosine kinase inhibitor targeting both HER-1 and HER-2 receptors. This is a prospective, single-arm, open-label phase II study, designed to evaluate the efficacy and safety of pyrotinib combined with thalidomide in advanced non-small-cell lung cancer patients with HER2 exon 20 insertions.

Details
Condition Non-Small Cell Lung Cancer, nsclc
Treatment pyrotinib combined with thalidomide
Clinical Study IdentifierNCT04382300
SponsorShanghai Chest Hospital
Last Modified on3 February 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Aged 18-80 years
ECOG performance status 0-1
Life expectancy 12 weeks
At least one measurable lesion according to RECIST 1.1
Histologically or cytologically confirmed advanced (IIIB or IV) non-small-cell lung cancer according to the 7th edition of TNM classification and staging system for lung cancer published by IASLC
HER2 exon 20 insertions confirmed by next generation sequencing or polymerase chain reaction (if blood samples are used, the mutation abundance should be 10%)
Disease progression during or after platinum-based chemotherapy, or refusing chemotherapy (patients are allowed to have prior therapy with PD-1/PD-L1 inhibitors and/or antiangiogenic agents)
No more than two prior chemotherapy regimens (a. replacing platinum drug due to toxicity is considered as a new regimen; b. adjuvant chemotherapy is not considered as a prior regimen if disease recurrence occurred at more than 6 months after the last dose)
No radiotherapy within 3 months, or prior radiotherapy with radiation area <25% of bone marrow area at least 4 weeks before enrollment
Required laboratory values including following parameters
ANC: 1.5 10^9/L, Platelet count: 90 10^9/L, Hemoglobin: 90 g/L, INR: 1.5
APTT: 1.5 ULN, Total bilirubin: 1.5 ULN, ALT and AST: 2 ULN for liver
metastases, BUN and creatine: 1.5 ULN, creatine clearance rate: 50 mL/min
LVEF: 50%, QTcF: < 470 ms for female, < 450 ms for male
Willingness to use highly effective contraception from the start of the study to 90 days after the last dose of study drug
Written informed consent

Exclusion Criteria

Prior HER2-targeting therapies
Other gene alterations with available targeted drugs, such as EGFR mutations, T790M resistance mutations, ALK fusions, ROS1 fusions, RET rearrangements, BRAF V600E mutations, NTRK fusions, and MET exon 14 skipping
Factors influencing the oral administration of drugs, such as inability to swallow, chronic diarrhea, intestinal obstruction, or other gastrointestinal diseases or abnormalities
With third space effusion that can not be controlled by drainage or other methods
Radiotherapy, chemotherapy, surgery, or other targeted therapy for non-small-cell lung adenocarcinoma within 4 weeks
Active brain metastases, meningeal metastases, spinal compression, or CT or MRI revealing brain or leptomeningeal diseases at screening (patients with symptomatically stable brain metastases can be enrolled if no cerebral hemorrhage is found by brain MRI, CT or venography)
Uncontrolled hypokalemia or hypomagnesemia
Allergy history to the components of study drug
History of immunodeficiency disease (including positive test of human immunodeficiency virus, active hepatitis B/C, or other acquired or congenital immunodeficiency disease) or organ transplantation
History of cardiac diseases, including angina, arrhythmia requiring drug therapy or of clinical significance, myocardial infarction, heart failure, and other cardiac diseases unsuitable for this trial as judged by the investigator
Patients with thrombotic disease or previous history of thrombosis
Other malignancies within 5 years, except for cured cervical cancer in situ, skin basal cell cancer, and skin squamous cell cancer
History of neurological or mental disorders, such as epilepsy and dementia
Respiratory syndrome (dyspnea grade 2 using NCI CTCAE 5.0)
Coagulation disorders (INR >1.5, prothrombin time >ULN + 4 s, or APTT >1.5ULN), with bleeding tendency or receiving thrombolytic or anticoagulant therapy
Renal dysfunction (urine protein ++, or 24-hour proteinuria 1.0 g)
Participating in other clinical trials within 4 weeks
Pregnant or lactating woman
Concomitant diseases seriously affecting the patient safety or the completion of study as judged by the investigator, such as uncontrolled severe hypertension, severe diabetes mellitus, and active infection
Any other condition unsuitable for the study as judged by the investigator
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