Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
Neoadjuvant Toripalimab for Non-squamous NSCLC With EGFR Mutation
Excerpt:...Harboring EGFR mutation (19del or L858R); 5....
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
The study of Triprilimab therapy with cytokine induced killer cells in advanced non-small cell lung cancer
More C2 evidence
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
The Effect of Toripalimab Plus Radiotherapy in Patients With Operable Stage II-IIIA (N+) Non Small Cell Lung Cancer
Excerpt:...histomolecular pathology confirming the absence of classic driver oncogene mutations in EGFR, ALK, or ROS1....
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
A Study of Toripalimab+ Pemetrexed Plus Carboplatin in Patients With EGFR-mutation Positive and T790M Negative After Progression on EGFR-TKI Treatment
Excerpt:...- Histologically and/or cytologically confirmed advanced or recurrent non-small cell lung cancer with EGFR sensitive mutation (exon 19 deletion, exon 21 L858R), and meeting the following conditions at the same time:...
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
Toripalimab in Combination With Platinum-based Chemotherapy for Mutation-negative Stage IV Oligometastatic NSCLC
Excerpt:...- Exact evidence confirms the presence of EGFR, ALK, ROS 1 gene mutations in non-small cell lung cancer....
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
neoadjuvant PD-1 inhibitor (Toripalimab) plus chemotherapy in stage Ⅱ-Ⅲ NSCLC (LungMate 002): an open-label, single-arm, phase 2 trial.
Excerpt:...Without specific driven gene mutation like EGFR, ALK, KRAS and so on. ...
Less C2 evidence
Evidence Level:Sensitive: C3 – Early Trials
Title:
Toripalimab plus chemotherapy as second-line treatment in previously EGFR-TKI treated patients with EGFR-mutant-advanced NSCLC: a multicenter phase-II trial
Excerpt:Toripalimab plus chemotherapy showed a promising anti-tumor activity with acceptable safety profiles as the second-line setting in patients with EGFR-mutant NSCLC.
DOI:https://doi.org/10.1038/s41392-021-00751-9