Cyramza™ (ramucirumab) when combined with Taxotere® (docetaxel) extends overall survival in patients with non-small cell lung cancer (NSCLC) compared to standard second-line therapy with Taxotere alone. When combined with Tarceva in EGFR positive NSCLC patients, Cyramza also delays cancer progression compared to Tarceva alone.(1,2)
Cyramza is a targeted therapy that inhibits the growth of new blood vessels in tumors and, therefore, slows tumor growth.
As part of the REVEL trial, Dr. Maurice Perol et al tested the combination therapy against the standard Taxotere therapy in 1253 stage IV NSCLC patients who had progressed either during or after previous treatment.(1)
Overall survival for the combination therapy was 10.5 months, while that of the Taxotere arm was 9.1 months. Progression-free survival was 4.5 months versus 3 months. The combination therapy showed an objective response rate of 23%response compared to 14% for Taxotere.
There were a number of grade 3 adverse events associated with the Cyramza treatment, including neutropenia, febrile neutropenia, fatigue, leukopenia, hypertension, and pneumonia. The number of treatment-related adverse events that led to death was comparable.
In June 2019 it was also announced that the phase 3 RELAY study of Cyramza met its primary endpoint of progression-free survival (PFS), when used in combination with Tarceva (erlotinib) compared to Tarceva alone as a first-line treatment in patients with metastatic NSCLC whose tumors have activating EGFR mutations.(2)
- Perol M, et al. REVEL: A randomized, double-blind, phase III study of docetaxel and ramucirumab versus docetaxel and placebo in the second-line treatment of stage IV non-small cell lung cancer following disease progression after one prior platinum-based therapy. ASCO 2014; Abstract LBA8006.