A Study of Trastuzumab and Pyrotinib in HER2 Positive Locally Advanced or Metastatic Urothelial Carcinoma

Last updated: March 31, 2022
Sponsor: Chinese Academy of Medical Sciences
Overall Status: Active - Recruiting

Phase

2

Condition

Carcinoma

Treatment

N/A

Clinical Study ID

NCT05318339
NCC3398
  • Ages > 18
  • All Genders

Study Summary

A open-label, single-arm, phase II trial to study was designed to evaluate the effectiveness and safety of trastuzumab and pyrotinib in treating HER2 positive patients who have previously treated, locally advanced, or metastatic urothelial carcinoma.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Sign the informed consent form
  • Locally advanced or metastatic histologically confirmed transitional cell carcinoma ofthe urothelium, including the bladder, urethra, ureter, or renal pelvis
  • 18 years and older
  • HER2 expression (3+ or 2+) as determined by immunohistochemistry or gene amplificationby fluorescent in situ hybridization
  • Relapsed from or failed at least one prior standard systemic chemotherapy regimen,including immunotherapy, HER2 ADC durgs, and chemothearpy containing cisplatin,carboplatin, paclitaxel, docetaxel, or gemcitabine
  • At least 1 measurable lesion could be evaluated by RECIST v1.1
  • Performance status: ECOG 0-1
  • Life expectancy more than 12 weeks
  • Ejection fraction at least 50% (or lower limit of normal) by echocardiogram
  • Good organ function: Blood routine: hemoglobin ≥80g/L, neutrophil ≥1.5×10^9/L, platelet ≥75×10^9/L; Renalfunction: creatinine≤1.5×upper limit of normal (UNL) or creatinine clearance ≥50ml/min;Liver function: total bilirubin (TBIL)≤1.5×upper limit of normal (UNL); ALT≤2.5×UNL,AST≤2.5×UNL, ALT≤5×UNL and AST≤5×UNL for patients with liver metastasis

Exclusion

Exclusion Criteria:

  • Have received trastuzumab or pyrotinib treatment in the past
  • Known to have allergic reactions to any ingredients or excipients of experimentaldrugs
  • Radiotherapy, RFA, interventional therapy or surgery were performed within 28 daysbefore the first medication (except for previous diagnostic biopsy)
  • Other active malignant tumors, excluding those who have been disease free for morethan 5 years or in situ cancer considered to have been cured by adequate treatment
  • Clinically significant ascites
  • Brain metastasis or meningeal metastasis with neurological symptoms
  • Diabetes was not controlled, defined as HbA1c > 7.5% after anti-diabetic drugs orhypertension was not controlled, defined as systolic / diastolic blood pressure > 140 / 90 mmHg after antihypertensive drug
  • Myocardial infarction, severe/unstable angina, New York Heart Association (NYHA) classIII or IV congestive heart failure in the past 12 months
  • Known to be infected with human immunodeficiency virus (HIV), have acquiredimmunodeficiency syndrome (AIDS) related diseases, have active hepatitis B orhepatitis C
  • Pregnant or nursing
  • May increase the risk associated with participation in the study or administration ofthe study drug or mental illness that may interfere with the interpretation ofresearch results
  • There are other serious diseases that the researchers believe patients cannot beincluded in the study

Study Design

Total Participants: 30
Study Start date:
March 10, 2022
Estimated Completion Date:
December 10, 2024

Connect with a study center

  • National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

    Beijing,
    China

    Active - Recruiting

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