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Pathological response and prognostic factors of neoadjuvant PD-1 blockade combined with chemotherapy in resectable oesophageal squamous cell carcinoma.
- Source :
-
European Journal of Cancer . Jun2023, Vol. 186, p196-210. 15p. - Publication Year :
- 2023
-
Abstract
- We aimed to investigate the pathological changes, clinicopathological correlation and prognostic factors of neoadjuvant programmed cell death 1 (PD-1) blockade camrelizumab combined with carboplatin and nab-paclitaxel (CCNP) which we have proved its effectiveness in previous research for resectable esophageal squamous cell carcinoma (ESCC). 108 patients of resectable ESCC, with a mean follow-up of 13 m (ranging 1–30 m), treated with neoadjuvant CCNP from March 2020 to October 2022 in the First Affiliated Hospital of Sun Yat-sen University were enrolled. One year overall survival (OS) and disease-free survival (DFS) were 96.4% and 84.7% respectively. Pathological complete response or major pathological response (pCR/MPR) of the primary tumour (T-pCR/T-MPR) and the metastatic lymph node (N-pCR/N-MPR) were 58.3% and 47.5%. Pathological response of both primary tumours (PT) and lymph nodes (LN) metastasis correlated with DFS. LN pathological response was consistent with PT in 70.0% and inconsistent in 30.0% metastatic cases. Higher ratio of CD8+ to FoxP3+ tumour-infiltrating lymphocytes (TILs), earlier ypT stage and PT invasion not beyond circular muscle correlated with better pathological response. Four types of regression patterns of PT and two types of metastatic LN regression were found. A total of 18 (16.7%) out of 108 developed recurrence with a mean time of 6.9 ± 5.3 months. PT pathological response plus ypN and PT invasion beyond circular muscle or not were independent prognostic factors of DFS. This study suggested that camrelizumab plus chemotherapy had a high rate of T-pCR/T-MPR for resectable ESCC. T-pCR/T-MPR plus ypN0 and tumour invasion not beyond circular muscle predicted better DFS. • Neoadjuvant camrelizumab plus chemotherapy is effective for ESCC. • Pathological response of PT was inconsistent with metastatic LN in 30% cases. • Higher ratio of CD8+ to FoxP3+ TILs correlated with better pathological response. • Tumour regression patterns of both PT and metastatic LN were summarised. • PT pathological response and ypN and circular muscle penetration were independent prognostic factors. [ABSTRACT FROM AUTHOR]
- Subjects :
- *THERAPEUTIC use of monoclonal antibodies
*THERAPEUTIC use of antineoplastic agents
*PROGRAMMED cell death 1 receptors
*PATHOGENESIS
*CARBOPLATIN
*CANCER chemotherapy
*CANCER invasiveness
*METASTASIS
*LYMPH nodes
*CANCER relapse
*TREATMENT effectiveness
*DESCRIPTIVE statistics
*COMBINED modality therapy
*PACLITAXEL
*PROGRESSION-free survival
*SQUAMOUS cell carcinoma
*ESOPHAGEAL cancer
*OVERALL survival
Subjects
Details
- Language :
- English
- ISSN :
- 09598049
- Volume :
- 186
- Database :
- Academic Search Index
- Journal :
- European Journal of Cancer
- Publication Type :
- Academic Journal
- Accession number :
- 163714976
- Full Text :
- https://doi.org/10.1016/j.ejca.2023.03.008