Abstract 3171
Background
New efficacious systemic therapies for advanced melanoma have been practice changing. More recently these therapies have been tested in the adjuvant setting for stage III disease with positive results. With recent FDA and EMA approvals for stage III disease we wished to evaluate current uptake of adjuvant therapies for stage III melanoma. Such benchmark data will be important in testing our ability to integrate clinical trial data into clinical practice.
Methods
We identified 34,376 stage III patients from the National Cancer Database (NCDB) diagnosed 2004-2015 with known extent of LN surgery and no prior invasive cancer. Use of adjuvant chemotherapy (including targeted therapy), immunotherapy and radiation therapy was assessed. Cochran-Armitage trend tests were used to test for changes in proportions over time overall and stratified by substage.
Results
Of the 34,376 patients, median age 57 years, 21,093 (61.4%) were male and 33,300 Caucasian (97.7%). The median (mean) number of positive nodes was 1 (2.1), IQR 1-2, range 1-81. Overall, 9,180 patients (27.4%) received adjuvant immunotherapy, 2,467 (7.5%) adjuvant chemotherapy and 3,088 (9.1%) adjuvant radiation. Any adjuvant therapy use declined over time from 41.9% in 2004 to 35.8% in 2015 (p < 0.001), as did immunotherapy specifically (30.6% in 2004 to 25.3% in 2015, p < 0.001). Use of any adjuvant therapy correlated with disease burden (49.9% for ≥2LN+ vs 34.6% for 1LN+, p < 0.001) and substage: Stage IIIA 33.3%, Stage IIIB 38.8%, Stage IIIC 51.7%. Use of any adjuvant therapy significantly decreased from 2004 to 2015 in both IIIA (39.9% to 22.9%) and IIIB substages (44.0% to 35.4%), each p < 0.001, while stable among Stage IIIC patients (50.6% to 52.4%, p = 0.50). Use of immunotherapy followed a similar trend (Stage IIIA 33.4% to 19.1%, p < 0.001, Stage IIIB 31.1% to 27.5%, p < 0.001, Stage IIIC 30.6% to 31.7%, p = 0.76).
Conclusions
These data provide benchmarks for adjuvant therapy uptake for stage III melanoma patients reflective of general clinical practice. Future study with integration of adjuvant systemic therapies tested in clinical trials into the general cancer population should utilize these data to test the uptake of newer adjuvant treatments.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
3140 - Phase 2 study of olaparib in previously treated advanced solid tumors with homologous recombination repair mutation (HRRm) or homologous recombination repair deficiency (HRD): LYNK-002
Presenter: David Hyman
Session: Poster Display session 3
Resources:
Abstract
2655 - The K-BASKET trial: A prospective phase II biomarker-driven multiple basket trial in Korean solid cancer patients.
Presenter: Seul Kim
Session: Poster Display session 3
Resources:
Abstract
5938 - Cambridge Liquid biopsy “CALIBRATION” study: Can changes in circulating tumour DNA (ctDNA) predict durable tumour responses in patients with advanced oesophageal cancer receiving MEDI4736?
Presenter: Constanza Linossi
Session: Poster Display session 3
Resources:
Abstract
3799 - Validation of a tumour mutational burden workflow on routine histological samples of colorectal cancer and assessment of a cohort with synchronous hepatic metastases
Presenter: Andrea Mafficini
Session: Poster Display session 3
Resources:
Abstract
4647 - Microsatellite Instability Testing and Lynch Syndrome Screening For Colorectal Cancer Patients Through Tumor Sequencing
Presenter: Li Liu
Session: Poster Display session 3
Resources:
Abstract
3231 - "Liquid Withdarw" technique in CT-guided cutting needle lung biopsy: decreased incidence of complications and increased tissue amount for lung cancer molecular testing.
Presenter: Xue Wang
Session: Poster Display session 3
Resources:
Abstract
3282 - WGS Implementation in standard cancer Diagnostics for Every cancer patient (WIDE)
Presenter: Paul Roepman
Session: Poster Display session 3
Resources:
Abstract
5905 - Known and unknown gene fusion detection capabilities of solid tumor laboratories conducting next generation sequencing in 6 countries
Presenter: Steph Finucane
Session: Poster Display session 3
Resources:
Abstract
4238 - Clinical and Analytical Accuracy of a 523 Gene Panel Next-Generation Sequencing (NGS) Assay on Formalin-Fixed Paraffin-Embedded (FFPE) Solid Tumor Samples
Presenter: Ina Deras
Session: Poster Display session 3
Resources:
Abstract
2493 - Methylation analysis of MLH1 using droplet digital PCR and methylation sensitive restriction enzyme.
Presenter: Celine De Rop
Session: Poster Display session 3
Resources:
Abstract