Abstract 5364: Neutrophilic skin infiltrates in patients with acute myeloid leukemia (AML) are clonal and associate with poor overall survival.

Abstract Background: Acute myeloid leukemia (AML) is an aggressive hematologic malignancy. While blast infiltration (leukemia cutis, LC) is a known extramedullary disease, reactive neutrophilic dermatoses (like Sweet's syndrome) are common, but their etiology remains unclear. We aimed to determine if these lesions represent an atypical leukemic process. Methods: We analyzed the clinical and molecular characteristics, including survival outcomes, in 1,019 consecutive AML patients for histopathologically evaluated skin lesions (10 days prior and up to 60 days post-diagnosis). Patients with reactive neutrophilic dermatoses underwent confirmation for absence of leukemic blasts. We then performed paired tumor/normal whole-exome sequencing on bone marrow (BM) and FFPE-derived skin biopsy tissues for 8 such patients. Results: Dermatology consultation was required in 31% of patients. While reactive inflammation generally showed high complete remission (CR) rates (91%), patients with reactive neutrophilic dermatoses had the shortest disease-free survival (DFS) of all patient groups, with a median DFS of only 13 months. Clinically, these patients frequently harbored NPM1 (27%), IDH1/2 (41%), and FLT3-ITD (23%) mutations. Next, we sequenced paired samples from 4 patients whose skin lesions were confirmed as blast-free. Remarkably, sequencing of the skin lesions revealed AML gene mutations identical to those found in the BM blasts, with near-identical variant allele fractions (VAFs) in both tissues. Three of four patients also harbored mutations in genes encoding keratin-associated proteins. Conclusions: Morphologically normal, mutationally clonal, neutrophilic infiltrates represent a distinct extramedullary manifestation of leukemia that differs from classical leukemia cutis but has significant clinical and biological relevance (poor survival). A similar phenomenon is known for chronic myelomonocytic leukemia (CMML). If validated, this may identify an underappreciated type of leukemic involvement and possible escape mechanism. Citation Format: Gabby Tesfaye, Yazan Abu-Shihab, Deedra Nicolet, Jill Buss, Andrea Laganson, Catherine Chung, SANAM LOGHAVI, Benjamin Kaffenberger, Ann-Kathrin Eisfeld. Neutrophilic skin infiltrates in patients with acute myeloid leukemia (AML) are clonal and associate with poor overall survival [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5364.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-5364
Primary Topic
Autoimmune and Inflammatory Disorders
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article
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article

Abstract 5364: Neutrophilic skin infiltrates in patients with acute myeloid leukemia (AML) are clonal and associate with poor overall survival.

Andrea Laganson, Jill Buss, Benjamin Harris Kaffenberger, Deedra Nicolet et al.
Cancer Research
Autoimmune and Inflammatory Disorders
article

Abstract 5364: Neutrophilic skin infiltrates in patients with acute myeloid leukemia (AML) are clonal and associate with poor overall survival.

Andrea Laganson, Jill Buss, Benjamin Harris Kaffenberger, Deedra Nicolet, Gabby Tesfaye, Ann-Kathrin Eisfeld, Catherine Chung, Yazan Abu-Shihab, SANAM LOGHAVI
article en

Abstract

Abstract Background: Acute myeloid leukemia (AML) is an aggressive hematologic malignancy. While blast infiltration (leukemia cutis, LC) is a known extramedullary disease, reactive neutrophilic dermatoses (like Sweet's syndrome) are common, but their etiology remains unclear. We aimed to determine if these lesions represent an atypical leukemic process. Methods: We analyzed the clinical and molecular characteristics, including survival outcomes, in 1,019 consecutive AML patients for histopathologically evaluated skin lesions (10 days prior and up to 60 days post-diagnosis). Patients with reactive neutrophilic dermatoses underwent confirmation for absence of leukemic blasts. We then performed paired tumor/normal whole-exome sequencing on bone marrow (BM) and FFPE-derived skin biopsy tissues for 8 such patients. Results: Dermatology consultation was required in 31% of patients. While reactive inflammation generally showed high complete remission (CR) rates (91%), patients with reactive neutrophilic dermatoses had the shortest disease-free survival (DFS) of all patient groups, with a median DFS of only 13 months. Clinically, these patients frequently harbored NPM1 (27%), IDH1/2 (41%), and FLT3-ITD (23%) mutations. Next, we sequenced paired samples from 4 patients whose skin lesions were confirmed as blast-free. Remarkably, sequencing of the skin lesions revealed AML gene mutations identical to those found in the BM blasts, with near-identical variant allele fractions (VAFs) in both tissues. Three of four patients also harbored mutations in genes encoding keratin-associated proteins. Conclusions: Morphologically normal, mutationally clonal, neutrophilic infiltrates represent a distinct extramedullary manifestation of leukemia that differs from classical leukemia cutis but has significant clinical and biological relevance (poor survival). A similar phenomenon is known for chronic myelomonocytic leukemia (CMML). If validated, this may identify an underappreciated type of leukemic involvement and possible escape mechanism. Citation Format: Gabby Tesfaye, Yazan Abu-Shihab, Deedra Nicolet, Jill Buss, Andrea Laganson, Catherine Chung, SANAM LOGHAVI, Benjamin Kaffenberger, Ann-Kathrin Eisfeld. Neutrophilic skin infiltrates in patients with acute myeloid leukemia (AML) are clonal and associate with poor overall survival [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5364.

Cancer ResearchVol. 86(7_Supplement)
The Ohio State University Wexner Medical Center (US), Ohio University (US), The Ohio State University (US)
No poverty
Openalex Percentile: Top 4%
Autoimmune and Inflammatory Disorders
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