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Published on: September 25, 2018
Programmed cell death 1 inhibitor plus chemotherapy vs. chemotherapy in advanced drive-gene-negative non-small-cell
Ying Li1, Peng Yang2, Xiao Zhou3
1Respiratory Medicine, Daqing Oilfield General Hospital, Daqing, China.
Objective:
Programmed cell death 1 (PD-1) inhibitor has been in the market in China for several years, which lacks sufficient domestic evidence regarding its application in lung cancer. Thus, this study intended to assess the treatment outcome and tolerance of PD-1 inhibitor plus chemotherapy in advanced, driver-gene-negative, nonsquamous, non-small-cell lung cancer (NSCLC) patients in a real clinical setting.
Methods:
This retrospective cohort study analyzed 68 advanced driver-gene-negative nonsquamous NSCLC patients, among which 38 cases received PD-1 inhibitor plus chemotherapy and 30 cases adopted chemotherapy alone. Disease control rate (DCR), objective response rate (ORR), progression-free survival (PFS), overall survival (OS), and adverse events were reviewed.
Results:
Generally, PD-1 inhibitor plus chemotherapy achieved a more satisfying ORR compared with chemotherapy alone (52.6% vs. 30.0%, P = 0.061), while the DCR did not vary between PD-1 inhibitor plus chemotherapy and chemotherapy (84.2% vs. 73.3%, P = 0.271). Patients receiving PD-1 inhibitor plus chemotherapy exhibited favorable PFS (median: 10.1 vs. 7.1 months, P = 0.040) and OS (median: 17.4 vs. 13.9 months, P = 0.049) than patients adopting chemotherapy alone. Additionally, after adjustment using multivariable Cox's analyses, PD-1 inhibitor plus chemotherapy (vs. chemotherapy) could independently realize prolonged PFS (P = 0.020) and OS (P = 0.029). Moreover, the majority of adverse events were manageable; meanwhile, grade 3-4 adverse events included leukopenia (13.2%), neutropenia (13.2%), nausea and vomiting (7.9%), anemia (5.3%), elevated transaminase (5.3%), thrombopenia (2.6%), anorexia (2.6%), peripheral neuropathy (2.6%), and rash (2.6%).
Conclusion:
PD-1 inhibitor plus chemotherapy exhibits a better efficacy and equal tolerance compared with chemotherapy alone in advanced driver-gene-negative nonsquamous NSCLC patients.
Insights
Programmed cell death 1 (PD-1) inhibitor combined with chemotherapy shows improved outcomes for advanced non-small-cell lung cancer (NSCLC) patients. This combination therapy demonstrated better progression-free survival and overall survival compared to chemotherapy alone.
Area of Science:
- Oncology
- Immunotherapy
- Thoracic Surgery
Background:
- Programmed cell death 1 (PD-1) inhibitors are increasingly used in cancer treatment.
- Limited domestic evidence exists for PD-1 inhibitor use in Chinese lung cancer patients.
- Advanced, driver-gene-negative, nonsquamous NSCLC presents a specific treatment challenge.
Purpose of the Study:
- To evaluate the efficacy and safety of PD-1 inhibitor plus chemotherapy in real-world NSCLC patients.
- To compare treatment outcomes between combination therapy and chemotherapy alone.
- To assess the tolerance and adverse events associated with PD-1 inhibitor combination therapy.
Main Methods:
- Retrospective cohort study of 68 advanced driver-gene-negative nonsquamous NSCLC patients.
- Comparison between 38 patients receiving PD-1 inhibitor plus chemotherapy and 30 receiving chemotherapy alone.
- Analysis of disease control rate (DCR), objective response rate (ORR), progression-free survival (PFS), overall survival (OS), and adverse events.
Main Results:
- PD-1 inhibitor plus chemotherapy showed a higher ORR (52.6% vs. 30.0%) and significantly improved PFS (median 10.1 vs. 7.1 months) and OS (median 17.4 vs. 13.9 months).
- Multivariable Cox's analyses confirmed PD-1 inhibitor plus chemotherapy as an independent predictor of prolonged PFS and OS.
- The majority of adverse events were manageable, with common grade 3-4 events including leukopenia and neutropenia.
Conclusions:
- PD-1 inhibitor plus chemotherapy offers superior efficacy compared to chemotherapy alone in advanced driver-gene-negative nonsquamous NSCLC.
- The combination therapy demonstrates comparable tolerance to chemotherapy alone.
- Real-world data supports the use of PD-1 inhibitor plus chemotherapy for this patient population.
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