Abstract 1151P
Background
Cutaneous adnexal tumors comprise a heterogenous group of both benign and malignant tumors evolving from the four primary adnexal structures. Malignant adnexal tumors encompass a variety of histologic subtypes with varying clinical presentation. Due to the rarity of these conditions, incidence and prevalence is not well understood. In a retrospective analysis, estimated five-year Overall Survival (OS) and Disease-Free Survival (DFS) were estimated at 73% and 98%, respectively. There is a paucity of data surrounding the preferred clinical management of cutaneous adnexal tumors due to the rarity of these entities.
Methods
Patients with malignant adnexal tumors were identified using the National Cancer Database (NCDB). We examined demographic, clinicopathologic, and treatment information. Excluded from our cohort were patients with metastatic or unknown disease stage, positive or unknown margin status, unknown radiation and/or chemotherapy status, and unknown vital status. Chi-square analyses were used to assess differences across sebaceous versus non-sebaceous histologies. Multivariable Cox proportional hazard models were used to evaluate the effects of treatment modalities on overall survival after controlling for relevant covariates (age, race, and stage).
Results
3,694 patients were included in the final analysis. The most prevalent malignant cutaneous adnexal tumor included sebaceous carcinoma (n=1699, 46%), eccrine porocarcinoma (n = 568, 15.4%), and skin appendage carcinoma (n =415, 11.2%). In patients with fully resected cutaneous adnexal tumors with negative surgical margins, multivariable results showed that receipt of adjuvant radiation was associated with statistically significantly longer survival compared to not receiving radiation (HR .76 (95%CI 0.61 – 0.96)). Non-sebaceous histology was also associated with longer survival than sebaceous histology (HR 0.78 (95% CI 0.69 – 0.88)). After stratifying by histologic groups, adjuvant radiation was associated with longer overall survival in sebaceous carcinoma (HR 0.62 (95% CI 0.42 – 0.92)), while receipt of adjuvant radiation in non-sebaceous histology groups was not associated with overall survival (HR 0.85 (95% CI 0.65 – 1.13)). Use of adjuvant chemotherapy following R0 resection was not associated with overall survival in the sebaceous group, while in the non-sebaceous group, chemotherapy was associated with shorter overall survival (HR 3.92 (95% CI 1.94 – 7.92)).
Conclusions
Acknowledging the limitations of a retrospective evaluation of real-world data, there does not appear to be a benefit for adjuvant chemotherapy after R0 resection in cutaneous adnexal carcinomas. Alternatively, omission of adjuvant radiotherapy was associated with an increased risk of mortality.
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
1100P - Open-label non-randomized phase IB study to characterize the safety, tolerability and recommended dose of tinostamustin in combination with nivolumab in patients with advanced melanoma (ENIGMA)
Presenter: Markus Joerger
Session: Poster session 13
1101P - The effect of LNS8801 in combination with pembrolizumab in patients with treatment-refractory cutaneous melanoma
Presenter: Jordi Rodon
Session: Poster session 13
1102P - Evaluation of surrogate endpoints for overall survival within the RELATIVITY-047 trial
Presenter: Peter Mohr
Session: Poster session 13
1103P - Nivolumab (NIVO) plus relatlimab (RELA) vs NIVO in previously untreated metastatic or unresectable melanoma: 2-year subgroup analyses from RELATIVITY-047
Presenter: Georgina Long
Session: Poster session 13
1104P - Efficacy of immune checkpoint inhibition in metastatic or non-resectable melanoma after failure of adjuvant anti-PD1 treatment: A EUMelareg real-world evidence study
Presenter: Michael Weichenthal
Session: Poster session 13
1105P - First-line nivolumab plus ipilimumab in advanced melanoma patients previously treated with adjuvant systemic therapy
Presenter: Katarzyna Kozak
Session: Poster session 13
1106P - Anti-PD-1 (PD1) monotherapy or in combination with anti-CTLA-4 for metastatic melanoma (MM) patients (pts) with liver metastases (mets)
Presenter: Ines Pires da Silva
Session: Poster session 13
1107P - BRAF mutation status does not impact outcomes with tebentafusp in advanced cutaneous melanoma
Presenter: Alexander Shoushtari
Session: Poster session 13
1108P - Outcomes of patients with unresectable or metastatic melanoma after cessation of immunotherapy following complete response or toxicities
Presenter: Nur Sakinah Zulkifli
Session: Poster session 13