Complete Metabolic Response in FDG-PET-CT Scan before Discontinuation of Immune Checkpoint Inhibitors Correlates with Long Progression-Free Survival

被引:10
|
作者
Schank, Timo E. [1 ,2 ]
Forschner, Andrea [3 ]
Sachse, Michael Max [4 ]
Dimitrakopoulou-Strauss, Antonia [5 ]
Sachpekidis, Christos [5 ]
Stenzinger, Albrecht [6 ]
Volckmar, Anna-Lena [6 ]
Enk, Alexander [1 ,2 ]
Hassel, Jessica C. [1 ,2 ]
机构
[1] Univ Hosp Heidelberg, Dept Dermatol, D-69120 Heidelberg, Germany
[2] Univ Hosp Heidelberg, Natl Ctr Tumor Dis, D-69120 Heidelberg, Germany
[3] Univ Hosp Tubingen, Dept Dermatol, D-72076 Tubingen, Germany
[4] Hosp Bremerhaven Reinkenheide, Dept Dermatol Allergol & Phlebol, D-27574 Bremerhaven, Germany
[5] German Canc Res Ctr, Clin Cooperat Unit Nucl Med, D-69120 Heidelberg, Germany
[6] Univ Hosp Heidelberg, Dept Pathol, D-69120 Heidelberg, Germany
关键词
FDG-PET-CT scan; melanoma; outcome; checkpoint inhibitors; NIVOLUMAB PLUS IPILIMUMAB; ADVANCED MELANOMA; ANTI-PD-1; OUTCOMES; PEMBROLIZUMAB; CESSATION; CANCER;
D O I
10.3390/cancers13112616
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Immunotherapy is the standard of care in patients harboring metastasized melanoma. However, once further tumor growth is stopped it remains unclear when immunotherapy can be safely ceased. This clinical question is increasingly raised especially in patients with a strong desire to discontinue therapy or in patients who are forced to pause treatment due to severe immune-related side effects. With our study we aim to provide data which may be helpful for clinicians and patients when treatment discontinuation is considered. Further prospective, multicenter studies are needed to further address this important clinical issue. Checkpoint inhibitors have revolutionized the treatment of patients with metastasized melanoma. However, it remains unclear when to stop treatment. We retrospectively analyzed 45 patients (median age 64 years; 58% male) with metastasized melanoma from 3 cancer centers that received checkpoint inhibitors and discontinued therapy due to either immune-related adverse events or patient decision after an (F-18)2-fluoro-2-deoxy-D-glucose positron emission tomography (FDG-PET) combined with a low-dose CT scan (FDG-PET-CT) scan without signs for disease progression. After a median of 21 (range 1-42) months of immunotherapy an FDG-PET-CT scan was performed to evaluate disease activity. In these, 32 patients (71%) showed a complete metabolic response (CMR) and 13 were classified as non-CMR. After a median follow-up of 34 (range 1-70) months, 3/32 (9%) of CMR patients and 6/13 (46%) of non-CMR patients had progressed (p = 0.007). Progression-free survival (PFS), as estimated from the date of last drug administration, was significantly longer among CMR patients than non-CMR (log-rank: p = 0.001; hazard ratio: 0.127; 95% CI: 0.032-0.511). Two-year PFS was 94% among CMR patients and 62% among non-CMR patients. Univariable Cox regression showed that metabolic response was the only parameter which predicted PFS (p = 0.004). Multivariate analysis revealed that metabolic response predicted disease progression (p = 0.008). In conclusion, our findings suggest that patients with CMR in an FDG-PET-CT scan may have a favorable outcome even if checkpoint inhibition is discontinued.
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收藏
页数:11
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