^
Association details:
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Phase II Clinical Study for Advanced Non-small Cell Lung Cancer Harboring HER2 Amplification or Mutations Treated with Pyrotinib and Apatinib

Excerpt:
...1) Aged 18 to 70 years; 2) Histologically or cytologically confirmed non-small cell lung cancer with stage IV disease; 3) HER2 exon 20 insertion mutations, primary HER2 missense mutations or primary HER2 amplification (HER2 copy number detected by NGS testing >= 3.62 or HER2 FISH+) confirmed by tumor tissue or plasma, pleural effusion, cerebrospinal fluid or other specimens; 4) Pretreated with first-line chemotherapy or ErbB-TKI targeted therapy and had experienced disease progression; 5) At least one radiographically measurable lesion exists; 6) Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1; 7) Life expectancy of more than 12 week; 8) Left ventricular ejection fraction (LVEF) >= 50 percent (%) by echocardiogram (ECHO); 9) Adequate hepatic, renal, and hematologic functions are required including following parameters; a. ANC>= 1.5 x 10^9/L (1,500/mm3) b. Platelet count: >= 100 x 10^9/L (100,000/mm3) c. Hemoglobin >= 80 g/L (8 g/dL) d. SCr<= 1.5 x upper limit of normal (ULN) or creatine clearance rate >= 60 mL/min e. Total bilirubin <= 1.5 x ULN f. ALT and AST <= 2 x ULN or ALT and AST <= 5 x ULN for patients with liver metastasis g. INR <= 1.5 x UNL, PT and APTT <= 1.5 x UNL; h. Urine protein < 2+and if urine protein >= 2+, 24-hour urine protein quantitation shows that protein must be <= 1g; 10) Provide written, informed consent to participate in the study and follow the study procedures....
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Phase II Clinical Trial for Advanced Non-Small Cell Lung Cancer Harboring HER2 Amplification or Mutations Treated with First-Line Pyrotinib plus Apatinib Targeted Therapy

Excerpt:
...HER2 insertion mutation, primary HER2 point mutation or primary HER2 amplification confirmed by genetic testing of tumor tissue or blood, pleural effusion, cerebrospinal fluid and other specimens (including HER2 copy number amplification >=3.62 detected by NGS or positive FISH detection ); 4. ...
Less C2 evidence
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Pyrotinib combined with apatinib for targeting metastatic non-small cell lung cancer with HER2 alterations: a prospective, open-label, single-arm phase 2 study (PATHER2)

Published date:
08/29/2022
Excerpt:
Pyrotinib plus apatinib demonstrated promising antitumor activity and a manageable safety profile in HER2-mutated or HER2-amplified metastatic NSCLC patients.
DOI:
https://doi.org/10.1186/s12916-022-02470-6
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Efficacy and safety of pan-ErbB inhibitor pyrotinib combined with antiangiogenic agent apatinib for HER2-mutant or amplified metastatic NSCLC: A phase II clinical study.

Published date:
05/19/2021
Excerpt:
Metastatic NSCLC patients...harboring primary HER2 amplification, exon 20 insertion or activating missense mutations who had failed to prior chemotherapies or anti-HER2 TKIs were eligible to be enrolled...the overall ORR and DCR were 45.5% (15/33) and 93.9% (31/33), respectively. The median PFS was 6.8 (95%CI: 5.4-8.2) months. The median DoR and OS were 5.3 (95%CI: 0-11.8) and 12.9 (95%CI: 8.6-17.2) months, respectively....Pyrotinib combined with apatinib showed potent anti-tumor activity and acceptable safety profile in metastatic NSCLC with HER2 amplification or activating mutations.
DOI:
10.1200/JCO.2021.39.15_suppl.9035
Evidence Level:
Sensitive: C3 – Early Trials
Title:

Pyrotinib Combined with Apatinib for HER2-Mutant Non-Small Cell Lung Cancer: Interim Analysis from a Phase II Clinical Study

Published date:
01/12/2021
Excerpt:
Patient characteristics at baseline and response for pyrotinib with apatinib...Pyrotinib in combination with apatinib showed favorable antitumor activity and acceptable safety in heavily pretreated NSCLC patients with diverse HER2 mutations.