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Association of pathological response with long-term survival outcomes after neoadjuvant immunotherapy: A meta-analysis.
Wei, Chenyu; Sun, Haolin; Hu, Jiexuan; Ma, Zhongjun; Cao, Bangwei.
Afiliação
  • Wei C; Department of Oncology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
  • Sun H; Department of Oncology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
  • Hu J; Department of Oncology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
  • Ma Z; Department of Oncology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
  • Cao B; Department of Oncology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China. Electronic address: oncology@ccmu.edu.cn.
Int Immunopharmacol ; 133: 112078, 2024 May 30.
Article em En | MEDLINE | ID: mdl-38685176
ABSTRACT

BACKGROUND:

Complete pathological response (pCR) and major pathological response (MPR) have been proven to have a close association with improved event-free survival (EFS) and overall survival (OS) for patients accepting chemotherapy or chemoradiotherapy. However, further study focusing on neoadjuvant immunotherapy is limited. Here we provided an updated and comprehensive evaluation of the association between pathological response and long-term survival outcomes at patient level and trial level for neoadjuvant immunotherapy.

METHODS:

We systematically searched and assessed studies in PubMed, Embase, the Cochrane Library and relevant conference abstracts from inception to June 1, 2023. Studies reported EFS/OS results by pCR/MPR status were eligible.

RESULTS:

Forty-three studies comprising a total of 4100 patients were eligible for the analysis, which included 39 studies for the patient-level analysis and 5 randomized controlled trials for the trial-level analysis. Our results highlighted that pCR was associated with improved EFS (HR, 0.48 [95 % CI, 0.39-0.60]) and OS (HR, 0.55 [95 % CI, 0.41-0.74]). The magnitude of HRs by MPR status were similar to the results by pCR status (EFS HR, 0.31 [95 % CI, 0.18-0.53]) and OS HR, 0.43 [95 % CI, 0.19-0.96]). However, no association between pCR and EFS at trial level was found (P = 0.8, R2 = 0).

CONCLUSION:

Our meta-analysis demonstrates a strong association between pathological response and long-term survival outcomes at patient level across studies applying neoadjuvant immunotherapy in most solid tumors but we fail to validate the relationship at trial level. Therefore, an accepted surrogate endpoint applied to both patient and trial levels are waited for further search.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terapia Neoadjuvante / Imunoterapia Limite: Humans Idioma: En Revista: Int Immunopharmacol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terapia Neoadjuvante / Imunoterapia Limite: Humans Idioma: En Revista: Int Immunopharmacol Ano de publicação: 2024 Tipo de documento: Article