Lung cancer is the leading cause of cancer death in China1. Generally, 65%–70% of lung cancer patients are already at an advanced, inoperable stage at diagnosis. Therefore, there has been a surge in drug development to address the unmet medical needs of lung cancer. In recent years, benefiting from the precise molecular classification of lung cancer, the number of clinical trials testing drugs in lung cancer has increased rapidly in China, enhancing R&D capacities and the impactful regulatory reform. It thus has led to significant improvements in drug accessibility.
From 2013 to 2021, there were 2114 lung cancer-related clinical trials registered in China, including 751 phase I‒II trials (35.5%), 261 phase III trials (12.3%), 143 phase IV trials (6.8%), and 959 other types of trials (investigator initiating trials accounting for 45.4%) (Fig. 1). Among them, there were 150 multi-regional clinical trials (MRCTs), which consisted of 33 phase I‒II clinical trials (22.0%), 114 phase III clinical trials (76.0%) and 3 other types of trials (2.0%). The top three targets most investigated were EGFR, PD1, and VEGFR, accounting for 16.4% (346), 12.0% (254), and 10.6% (225), respectively (Fig. 1), consistent with their success in the international market.
Figure 1.
Lung cancer-related clinical trials in China from 2013 to 2021.
From the perspective of drug approval, there has been a marked increase in drug approvals for lung cancer since 2018 (Table 1). Notably, one imported and seven domestic drugs had been granted marketing authorizations to treat lung cancer in 2021 in China.
Table 1.
Approved drugs for lung cancer in China and the US.
| Target | FDA-approved new drug (approved year) | Domestic NMPA-approved domestic new drug (approval year) | Time difference of first approval/year |
|---|---|---|---|
| EGFR | Erlotinib (2004), afatinib (2013), gefitinib (2015) | Icotinib (2011) | 7 |
| VEGFR | Bevacizumab (2006) | Anlotinib (2018), QL1101 (2019), IBI305 (2020), LY01008 (2021), BP102 (2021) | 12 |
| Endostatin | – | Endostar (2006) | ‒ |
| ALK | Crizotinib (2011), ceritinib (2014), alectinib (2015), brigatinib (2020), lorlatinib (2020) | Ensartinib (2020) | 9 |
| EGFR-T790M | Osimertinib (2015) | Almonertinib (2020), furmonertinib (2021) | 5 |
| PD1 | Nivolumab (2015), pembrolizumab (2016), cemiplimab (2021) | Camrelizumab (2020), sintilimab (2021), tislelizumab (2021) | 5 |
| PD-L1 | Atezolizumab (2016) | Sugemalimab (2021) | 5 |
| ROS1 | Crizotinib (2016), lorlatinib (2018), entrectinib (2019) | – | ‒ |
| BRAF V600E | Dabrafenib+trametinib (2016) | – | ‒ |
| NTRK | Larotrectinib (2018), entrectinib (2019) | – | ‒ |
| RET | Selpercatinib (2020) | Pralsetinib (licensed-in, 2021) | 1 |
| KRAS G12C | Sotorasib (2020) | – | |
| MET exon 14-skipping mutation | Capmatinib (2020), tepotinib (2021) | Savolitinib (2021) | 1 |
| EGFR exon 20 insertion mutations | Mobocertinib (2021), amivantamab (2021) | – | ‒ |
‒Not applicable.
In the meantime, the time lag in drug development between China and the international market is dramatically shortened. For example, the US Food and Drug Administration (FDA) approved capmatinib for lung cancer with MET-14 exon skipping mutation in 2020. One year later, the National Medical Products Administration (NMPA) of China approved savolitinib, another new drug for the same target.
The approval of the homegrown targeted and immunotherapeutic drugs has been speeded up in China; meanwhile, new indications have been added. From 2004 to 2020, most lung cancer drugs approved by the FDA are for the treatment of advanced lung cancer, but few for postoperative adjuvant therapy of early-stage lung cancer, of which the current standard treatment is still chemotherapy2. However, adjuvant chemotherapy only improves the 5-year survival rate by 5.3%3. In 2018, China's researchers found that EGFR-TKI can decrease the risk of postoperative recurrence for patients with early-stage lung cancer4,5; it thus has changed the treatment protocol. In April 2021, the NMPA-approved osimertinib for postoperative adjuvant therapy of lung cancer with EGFR mutation, based on the result of ADAURA trial (ClinicalTrials.gov identifier, NCT02511106) led by Prof. Yilong Wu6. In June 2021, based on the outcome of EVIDENCE trial (ClinicalTrials.gov identifier, NCT02448797)7, icotinib was approved by the NMPA for the postoperative adjuvant treatment of early-stage lung cancer with EGFR mutation.
In terms of immune checkpoint inhibitors, the FDA-approved atezolizumab for postoperative adjunctive therapy of lung cancer in October 2021, based on the result of IMpower-010 trial (ClinicalTrials.gov identifier, NCT02486718)8. In addition, clinical studies of sintilimab, tislelizumab, and toripalimab for perioperative immunotherapy have been carried out in China (Supporting Information Table S1).
The result of CheckMate-816 trial (ClinicalTrials.gov identifier, NCT02998528) released in November 2021 indicates that nivolumab combined with chemotherapy significantly improved the overall complete remission rate of operation for early-stage lung cancer. Additionally, the positive results of sintilimab and toripalimab were revealed in the clinical trials for the same indication (Supporting Information Table S2).
While patients benefit from EGFR, ALK, and ROS1 targeted drugs in advanced lung cancer, the drug resistance of targeted therapies and brain metastasis have been concerned. Drug combinations and rare targets could provide a potential solution to these issues. For patients without driver mutations, it needs to identify which groups can benefit from immunochemotherapy, and select a safe and effective plan. For early-stage lung cancer, EGFR-targeted therapy and immunotherapy in the perioperative period can improve patients’ outcomes. Future studies should be performed to explore the targeted therapies besides EGFR and the combination with immunotherapy. There are still many challenges to be overcome, such as whether chemotherapy is needed before immunotherapy, what is the best course of medication, how to achieve long-term survival benefits, and how to identify people at high risk of recurrence after surgery.
Footnotes
Peer review under responsibility of Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences.
Supporting data to this article can be found online at https://doi.org/10.1016/j.apsb.2022.01.010.
Appendix A. Supplementary data
The following is the Supplementary data to this article:
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