18FDG PET Assessment of Therapeutic Response in Patients with Advanced or Metastatic Melanoma Treated with First-Line Immune Checkpoint Inhibitors

被引:5
作者
Rivas, Alexia [1 ]
Delyon, Julie [2 ,3 ]
Martineau, Antoine [1 ]
Blanc, Estelle [1 ]
Allayous, Clara [2 ]
Da Meda, Laetitia [2 ]
Merlet, Pascal [1 ,4 ]
Lebbe, Celeste [2 ,3 ]
Baroudjian, Barouyr [2 ]
Vercellino, Laetitia [1 ,5 ]
机构
[1] St Louis Hosp, AP HP, Dept Nucl Med, F-75010 Paris, France
[2] St Louis Hosp, AP HP, Dept Dermatol, F-75010 Paris, France
[3] Univ Paris Cite, INSERM, U976, F-75010 Paris, France
[4] Univ Paris Cite, F-75006 Paris, France
[5] Univ Paris Cite, INSERM UMR S942, F-75006 Paris, France
关键词
FDG PET; melanoma; immunotherapy; therapeutic response; immune checkpoint inhibitors; F-18-FDG PET/CT; LUNG-CANCER; CRITERIA; PEMBROLIZUMAB; IPILIMUMAB;
D O I
10.3390/cancers14133190
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary In a retrospective study of patients with advanced or metastatic melanoma treated with first-line immune checkpoint inhibitors, we investigated the value of metabolic criteria, PERCIST 5 (criteria used for conventional chemotherapy), and imPERCIST5 (criteria adapted for immunotherapy therapeutic evaluation). Responding patients according to both criteria had better overall survival than that of not-responding patients, with a 2 years OS of 91% versus 39%, respectively. Combining different approaches to assess response could help improve the confidence in the test aiming at evaluating the response to immunotherapy. Background: Immune checkpoint inhibitors (ICI) are currently the first-line treatment for patients with metastatic melanoma. We investigated the value of positron emission tomography (PET) response criteria to assess the therapeutic response to first-line ICI in this clinical context and explore the potential contribution of total tumor metabolic volume (TMTV) analysis. Methods: We conducted a retrospective study in patients treated with first-line ICI for advanced or metastatic melanoma, with 18F-FDG PET/CT performed at baseline and 3 months after starting treatment. Patients' metabolic response was classified according to PERCIST5 and imPERCIST 5 criteria. TMTV was recorded for each examination. Results: Twenty-nine patients were included. The median overall survival (OS) was 51.2 months (IQR 13.6-not reached), and the OS rate at 2 years was 58.6%. Patients classified as responders (complete and partial response) had a 90.9% 2-year OS rate versus 38.9% for non-responders (stable disease and progressive disease) (p = 0.03), for PERCIST5 and imPERCIST 5 criteria. The median change in metabolic volume was 9.8% (IQR -59-+140%). No significant correlation between OS and changes in TMTV was found. Conclusion: The evaluation of response to immunotherapy using metabolic imaging with PERCIST5 and imPERCIST5 was significantly associated with OS in patients with advanced or metastatic melanoma.
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页数:14
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