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

Study to Evaluate the Efficacy and Safety of SHR6390 Combined With Pyrotinib in HER2+ Advanced Breast Cancer

Excerpt:
...- HER2-positive breast cancer(according to 2018 ASCO/CAP HER2 test guideline)....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Pyrotinib, Dalpiciclib(SHR6390) and Endocrine Therapy in Subjects With Dual-receptor Positive(ER+/HER2+) Advanced Breast Cancer

Excerpt:
......
Trial ID:
More C2 evidence
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Study to Evaluate the Efficacy and Safety of CDK4/6 Inhibitor SHR6390 Combined With Pyrotinib in the Treatment of HER2-positive Advanced Breast Cancer

Excerpt:
...- HER2-positive breast cancer(according to 2018 ASCO/CAP HER2 test guideline)....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Go to data
Title:

Study to Evaluate SHR6390 Combined With Pyrotinib in Patients With HER2 Positive Gastric Cancer

Excerpt:
...- Patients definitely diagnosed by pathology as Her2 positive stage III/IV gastric cancer...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

A single-arm, double-cohort, prospective, open-label, phase II exploratory study evaluating dalpiciclib combined with pyrotinib maleate in first-line treatment of HER2+ advanced breast cancer

Excerpt:
...Follow the 2018 ASCO-CAP HER2 positive Interpretation guidelines. ...
Less C2 evidence
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Pyrotinib combined with SHR6390 in the treatment of refractory advanced HER2 positive gastric cancer or solid tumors: Safety and efficacy results from a phase Id trial

Published date:
05/19/2021
Excerpt:
pyrotinib combined with SHR6390 in the treatment of refractory advanced HER2 positive gastric cancer or solid tumors (NCT03480256)...19 pts (14 gastric cancer, 3 colorectal cancer, 2 other solid tumors) were enrolled...overall response rate was 38.9%, with 7 PR (A: n = 3; E: n = 2; F: n = 2) and 7 SD. The median PFS was 3.83 months, with 2 pts received treatment over 12 months (A: n = 1; F: n = 1). Pyrotinib combined with SHR6390 had shown acceptable safety profile and encouraging efficacy in refractory advanced HER2 positive solid tumors.
DOI:
10.1200/JCO.2021.39.15_suppl.e16009
Trial ID: