Clinical Outcomes of the POPCORN Study: Pharmacodynamics of Pre-Operative PD1 CheckpOint Blockade and Receptor Activator of NF-κB Ligand (RANKL) Inhibition in Non-Small Cell Lung Cancer (NSCLC)-A Phase 1B/2 Trial.
2/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
추출되지 않음
I · Intervention 중재 / 시술
two cycles of nivolumab with denosumab or nivolumab alone prior to surgical resection
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] Our results support the feasibility of neoadjuvant systemic therapy in resectable NSCLC and explore the novel combination of nivolumab with denosumab. CD8 T-cell infiltration correlates with pathological response, warranting ongoing translational research to better understand patient selection for such novel combinations.
OpenAlex 토픽 ·
NF-κB Signaling Pathways
Bone Metabolism and Diseases
Melanoma and MAPK Pathways
[BACKGROUND] There is a growing body of evidence supporting neoadjuvant systemic therapy to improve outcomes for people with early-stage non-small cell lung cancer (NSCLC).
- 추적기간 38.1 months
APA
Elizabeth Ahern, Cassie Turner, et al. (2026). Clinical Outcomes of the POPCORN Study: Pharmacodynamics of Pre-Operative PD1 CheckpOint Blockade and Receptor Activator of NF-κB Ligand (RANKL) Inhibition in Non-Small Cell Lung Cancer (NSCLC)-A Phase 1B/2 Trial.. Asia-Pacific journal of clinical oncology. https://doi.org/10.1111/ajco.70107
MLA
Elizabeth Ahern, et al.. "Clinical Outcomes of the POPCORN Study: Pharmacodynamics of Pre-Operative PD1 CheckpOint Blockade and Receptor Activator of NF-κB Ligand (RANKL) Inhibition in Non-Small Cell Lung Cancer (NSCLC)-A Phase 1B/2 Trial.." Asia-Pacific journal of clinical oncology, 2026.
PMID
41957527 ↗
Abstract 한글 요약
[BACKGROUND] There is a growing body of evidence supporting neoadjuvant systemic therapy to improve outcomes for people with early-stage non-small cell lung cancer (NSCLC). However, not all patients will respond, necessitating the need to explore novel combinations and predictors of response to neoadjuvant therapies.
[PATIENTS AND METHODS] In this open-label Phase 1B/2 signal-seeking trial, we recruited people with resectable Stage IB-IIIA NSCLC. Participants received two cycles of nivolumab with denosumab or nivolumab alone prior to surgical resection. Key clinical outcomes included the degree of pathological response, radiological overall response rate, recurrence-free survival, and overall survival. Tumor-immune correlates with pathological response were also investigated.
[RESULTS] Ten participants were recruited between August 2019 and September 2021, with five participants allocated to each treatment arm using minimization for tumor stage and histopathology. Two participants (20%) achieved a pathological complete response, with a further one patient achieving a major pathological response. Density of infiltrating CD8 T cells correlated with the degree of pathological response to neoadjuvant therapy. With a median follow-up of 38.1 months, all patients remained alive at data cutoff. The 36-month recurrence-free survival was 80%. Treatment-related adverse events were reported in three patients (30%), all of which were Grade 1-2.
[CONCLUSION] Our results support the feasibility of neoadjuvant systemic therapy in resectable NSCLC and explore the novel combination of nivolumab with denosumab. CD8 T-cell infiltration correlates with pathological response, warranting ongoing translational research to better understand patient selection for such novel combinations.
[PATIENTS AND METHODS] In this open-label Phase 1B/2 signal-seeking trial, we recruited people with resectable Stage IB-IIIA NSCLC. Participants received two cycles of nivolumab with denosumab or nivolumab alone prior to surgical resection. Key clinical outcomes included the degree of pathological response, radiological overall response rate, recurrence-free survival, and overall survival. Tumor-immune correlates with pathological response were also investigated.
[RESULTS] Ten participants were recruited between August 2019 and September 2021, with five participants allocated to each treatment arm using minimization for tumor stage and histopathology. Two participants (20%) achieved a pathological complete response, with a further one patient achieving a major pathological response. Density of infiltrating CD8 T cells correlated with the degree of pathological response to neoadjuvant therapy. With a median follow-up of 38.1 months, all patients remained alive at data cutoff. The 36-month recurrence-free survival was 80%. Treatment-related adverse events were reported in three patients (30%), all of which were Grade 1-2.
[CONCLUSION] Our results support the feasibility of neoadjuvant systemic therapy in resectable NSCLC and explore the novel combination of nivolumab with denosumab. CD8 T-cell infiltration correlates with pathological response, warranting ongoing translational research to better understand patient selection for such novel combinations.
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🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반
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