Metastatic site and clinical outcome of patients with deficient mismatch repair metastatic colorectal cancer treated with an immune checkpoint inhibitor in the first-line setting

被引:4
|
作者
Saberzadeh-Ardestani, Bahar [1 ]
Jones, Jeremy C. [2 ]
McWilliams, Robert R. [3 ]
Tougeron, David [4 ]
Halfdanarson, Thorvardur R. [3 ]
Guimbaud, Rosine [5 ]
Hubbard, Joleen M. [3 ]
Flecchia, Clemence [6 ,11 ]
Shi, Qian [7 ]
Alouani, Emily [8 ]
Sonbol, Mohamad B. [9 ]
Ticku, Jonathan [10 ]
Jin, Zhaohui [3 ]
Taieb, Julien [11 ]
Sinicrope, Frank A. [1 ,3 ,12 ]
机构
[1] Mayo Clin, Gastrointestinal Res Unit, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Oncol, Jacksonville, FL USA
[3] Mayo Clin, Div Med Oncol, Rochester, MN USA
[4] Univ Poitiers Hosp, Dept Gastroenterol Hepatol, Poitiers, France
[5] Ctr Hospitalier Univ Toulouse, F-31400 Toulouse, France
[6] Paris Cite Univ, European Georges Pompidou Hosp, AP HP, Dept Gastroenterol & Digest Oncol, Paris, France
[7] Mayo Clin, Dept Quantitat Hlth Sci, Rochester, MN USA
[8] Toulouse Hosp Univ, Digest Med Oncol Dept, IUCT Rangueil, Toulouse, France
[9] Dept Oncol, Mayo Clin, Phoenix, AZ USA
[10] Mayo Clin Hlth Syst, La Crosse, WI USA
[11] Paris Cite Univ, Georges Pompidou European Hosp, AP HP, Dept Gastroenterol & Digest Oncol,SIRIC CARPEM Com, Paris, France
[12] Mayo Clin, Alix Sch Med, 200 First St SW, Rochester, MN 55905 USA
关键词
Immune checkpoint inhibitor; Pembrolizumab; Metastatic colorectal cancer; Liver; Metastatic site; LIVER METASTASIS; OPEN-LABEL; NIVOLUMAB; PEMBROLIZUMAB; COLON;
D O I
10.1016/j.ejca.2023.113433
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Only one-half of deficient mismatch repair (d-MMR) metastatic colorectal cancers (mCRC) demonstrate durable responses to immune checkpoint inhibitors (ICIs). Given preclinical data indicating that liver metastases sequester activated CD8+ T cells from systemic circulation, we examined clinical outcome by metastatic site.Patients and methods: In a retrospective cohort of patients with d-MMR mCRCs treated at multiple centers in France (n = 66), we sought to validate data from a U.S. cohort, and performed pooled analysis (n = 104). All patients received first-line ICI monotherapy. Metastatic site was analyzed in relationship to tumor response (RECIST version 1.1), and with progression-free survival (PFS) by multivariable stratified Cox regression after adjustment for covariates.Results: Objective responses were achieved in 38/66 (58%) of patients in the validation cohort. Best tumor response included 13 (20%) complete responses (CR), 25 (38%) partial responses (PR), 16 (25%) stable disease, and 11 (17%) progressive disease (PD). One-year and 5-year PFS rates were 73% and 67%, respectively; 18 (27%) patients progressed during immunotherapy. Best tumor response was attenuated in patients with liver metastasis (P = 0.03). Presence of liver metastasis, but not other sites, was associated with significantly poorer PFS after adjustment for covariates (HRadj 2.82; 95%CI, 1.08-7.39; Padj=0.03). In a pooled analysis, liver metastasis remained significantly and independently associated with poorer PFS (HRadj 3.18; 95%CI, 1.52-6.67; Padj=0.002) and with attenuated tumor best response (P = 0.01).Conclusions: Metastasis to the liver, but not other sites, was validated as an independent factor associated with poorer response and survival after ICI treatment in d-MMR mCRCs. These data underscore the need for novel therapeutic strategies in these patients.
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页数:7
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