Risultati per: Terapia sistemica del carcinoma epatocellulare
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EP14 DIFFERENCE OF EXHALED BREATH VOLATILE ORGANIC COMPOUNDS BETWEEN ESOPHAGEAL SQUAMOUS CELL CARCINOMA PATIENTS AND HEALTHY POPULATION BY FACE MASK LAYERED WITH NANOPARTICLES: A PILOT STUDY
Su1586 STATIN DECREASES THE RISK OF HEPATOCELLULAR CARCINOMA IN METABOLIC DYSFUNCTION-ASSOCIATED STEATOTIC LIVER DISEASE PATIENTS. A SYSTEMATIC REVIEW AND META-ANALYSIS,
163 A PRACTICAL POINTS-BASED MODEL TO PRIORITIZE LIVER TRANSPLANT CANDIDATES WITH HEPATOCELLULAR CARCINOMA IN THE MODERN ERA
525 CRISPR/CAS99-MEDIATED TLR4 KNOCKOUT ATTENUATES HEPATOCELLULAR CARCINOMA PROGRESSION IN MICE VIA THE KINETICS OF MYELOID-DERIVED SUPPRESSOR CELL SUBSETS DYNAMICS
526 VIRULENCE-PROTEIN-MEDIATED CROSS-TALK OF ENTEROCLOSTER BOLTEAE AND CANCER CELLS PROMOTES HEPATOCELLULAR CARCINOMA PROGRESSION
465 CARBAMOYL PHOSPHATE SYNTHETASE 1 HETEROGENEITY POTENTIATES METASTASIS OF HEPATOCELLULAR CARCINOMA VIA REWRITING ASPARTATE METABOLISM
Mo1474 MTF-1 FACILITATES REMODELING OF THE TUMOR IMMUNE MICROENVIRONMENT BY REGULATING FERROPTOSIS AND LACTATION MODIFICATIONS IN HEPATOCELLULAR CARCINOMA
Sa1544 MACHINE LEARNING MODELS TO PREDICT THE CHARACTERISTICS OF UNSCREENED HEPATOCELLULAR CARCINOMA
Sa1583 ENDOSCOPIC VARICEAL LIGATION VERSUS PROPRANOLOL FOR THE PRIMARY PREVENTION OF OESOPHAGEAL VARICEAL BLEEDING IN PATIENTS WITH HEPATOCELLULAR CARCINOMA: AN OPEN-LABEL, TWO-CENTRE, RANDOMISED CONTROLLED TRIAL
1052 PAAM FOR HEPATOCELLULAR CARCINOMA RISK STRATIFICATION IN PATIENTS WITH CIRRHOSIS: MULTICENTER PHASE 3 BIOMARKER VALIDATION STUDIES IN THE U.S.
Sa1536 ASSOCIATION OF CIRCULATING FATTY ACIDS WITH RISK OF HEPATOCELLULAR CARCINOMA AND CHRONIC LIVER DISEASE MORTALITY: EVIDENCE FROM THE UK BIOBANK COHORT STUDY
Considerations Regarding Mohs Surgery for Early-Stage Merkel Cell Carcinoma
To the Editor We read with interest the analysis comparing unadjusted overall survival (OS) of Mohs micrographic surgery (MMS) vs excision using the National Cancer Database (NCDB) for stage 1 and 2 Merkel cell carcinoma (MCC). MMS was associated with improved OS vs wide local excision (WLE) with an approximately 40% reduction in deaths. However, we cannot endorse the authors’ conclusion that MMS “may provide a more effective treatment for MCC” as it is inconsistent with what is known about MCC. A systematic review of 31 studies (retrospective and case series) comparing WLE and MMS for MCC did not show a difference in outcomes. A recent NCDB analysis of early-stage MCC during an overlapping period (2004-2014 vs 2004-2018 as in the current study) failed to detect a survival advantage with MMS. The present study was larger than the prior NCDB analysis and required pathologic nodal staging. Of the 2312 patients analyzed, 4.5% underwent MMS vs 95.5% who underwent a form of excision (narrow margin excision or WLE). Compared with the MMS group, the WLE group had an approximately 2-fold higher incidence of lymphovascular invasion (13.9% vs 7.7%), a comorbidity index of 2 or higher (4.6% vs 1.9%), and pT2 MCC (20.8% vs 11.5%). Although a multivariable regression model considering these covariates found improved OS with MMS, it is likely that the unidentified confounding variables were associated with the difference. Patients with stage 1 and 2 MCC have high disease-specific survival, with most MCC-specific deaths occurring within 3 years and many deaths due to intercurrent disease. In the present study, the OS differences were not detected until 3 years or later, suggesting other-cause mortality for the difference. The study also examined adjuvant radiotherapy (RT) use. National Comprehensive Cancer Network guidelines recommend that most patients with MCC be considered for adjuvant RT. Seventy percent of patients in the MMS group had MCC of the head and neck (H/N). However, RT was recorded for only 45%. The H/N location is considered a high-risk feature for MCC recurrence and death, and a recent study found that adjuvant RT for stage 1 H/N MCC may be associated with decreased recurrence rates. We are concerned that RT is being underused or underreported. The authors of the present study acknowledged several limitations of using the NCDB, including the lack of disease-specific survival data and the small MMS cohort. We advise caution when interpreting the results, mostly because observed survival differences may not reflect MCC-specific deaths.
Keratoacanthoma and Cutaneous Squamous Cell Carcinoma With PD-1 and PD-L1 Inhibitor Use
This cross-sectional study assesses risk of dermatological immune-related adverse events associated with immunotherapy for cancer.
Considerations Regarding Mohs Surgery for Early-Stage Merkel Cell Carcinoma—Reply
In Reply We appreciate the interest in our article by Faries and Venna et al as well as their comments on the analysis. While we agree that there are inherent limitations to retrospective studies of survival outcomes using registry data, we believe that it is prudent to glean what insights we can from these datasets given the lack of large-scale studies of rare cancers, such as Merkel cell carcinoma (MCC), in the existing literature.
Considerations Regarding Mohs Surgery for Early-Stage Merkel Cell Carcinoma
To the Editor I read with interest the recent article by Cheraghlou and colleagues regarding primary tumor excision techniques in Merkel cell carcinoma (MCC). The article’s central observation, an association between the use of Mohs surgery and improved overall survival (OS) compared with wide excision, appears to be accurate. However, the assertion that Mohs surgery provides a “more effective treatment for MCC primary tumors than conventional” wide local excision does not appear to be supported by the presented data.