triple negative breast cancer being treated by preoperative chemotherapy
Conditions
Interventions
None listed
Sponsors
Hyogo Cancer Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All the patients those who receive KN522 regimen for the treatment of stage II - III TNBC
Exclusion criteria
Exclusion criteria: Those who not gave written informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| prevalence of fevrile events, FN (true-FN, surrogate-FN), antibiotics usage, number of unplanned visits, irAE (including ILD), arthralgia, usage of pain medication, PPI usage, all adverse events Grade 2-4 (CTCAE ver.5), RDI, pCR, and laboratory data | — |
Countries
Japan
Contacts
Public ContactMitsunori Morita
Hyogo Cancer Center Division of Medical Oncology
Outcome results
None listed