Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
A prospective, real-world clinical study of the efficacy and safety of camrelizumab combined with pemetrexed and bevacizumab in the treatment of newly diagnosed driver-gene-negative advanced non-squamous non-small cell lung cancer
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
A prospective, open-label, one-arm clinical study of pemetrexed in combination with platinum-based regimens in patients with advanced non-squamous non-small cell lung cancer treated with apatinib after 4-6 cycles of chemotherapy
Excerpt:...If the genetic test (EGFR/ALK) is an EGFR-sensitive mutation or an ALK fusion gene-positive patient, it is necessary to receive targeted therapy for the first-line treatment; if there is no mutation, it is necessary to be a first-line patient; 4. ...
More C2 evidence

Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
The Effectiveness and Safety of Sintilimab Plus Bevacizumab Combined with Pemetrexed and Platinum-Based Drugs in Retrospective Analysis for Advanced Non-Small Cell Lung Cancer Patients Without Targeted Therapy
Excerpt:...Histologically confirmed absence of EGFR gene sensitive mutation, ALK gene fusion, ROS1 gene mutation, and RET gene mutation; 4. ...
Evidence Level:Sensitive: C2 – Inclusion Criteria
Title:
A single-center, randomized, phase II superiority clinical trial of concurrent radiotherapy and intrathecal pemetrexed followed by long-term intrathecal maintenance chemotherapy in patients with refractory leptomeningeal metastases from lung adenocarcinoma
Less C2 evidence

Evidence Level:Resistant: C3 – Early Trials
Title:
Impact of prior ALK-tyrosine kinase inhibitor on pemetrexed-based chemotherapy in patients with advanced ALK positive non-small cell lung cancer.
Excerpt:...28 ALK positive NSCLC patients who had received pemetrexed-based chemotherapy...OS from pemetrexed-based chemotherapy of ALK-TKI treated group was also significantly shorter than ALK-naïve group...Pemetrexed-based chemotherapy might be less effective in ALK-positive NSCLC patients previously treated with ALK-TKI.
DOI:10.1200/JCO.2021.39.15_suppl.e21113