» Articles » PMID: 30483125

Cutaneous Leukemic Infiltrates Successfully Treated With Biomodulatory Therapy in a Rare Case of Therapy-Related High Risk MDS/AML

Overview
Journal Front Pharmacol
Date 2018 Nov 29
PMID 30483125
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Cutaneous manifestations in hematologic malignancies, especially in leukemia, are not common and may be very variable. Here we report a very unusual case of a patient (female, 70 years old) who was admitted to the hospital in 2016 because of skin lesions on the face, the trunk of the body and the extremities. She had a history of breast cancer in the year 2004 (pT1b, pN0, cM0, L0, V0, R0) which had been resected and treated with adjuvant radiation and chemotherapy (cyclophosphamide, methotrexate, 5-fluorouracile) as well as psoriasis treated with methotrexate and cyclosporine. Because of mild cytopenia a bone marrow aspirate/biopsy was performed showing myelodysplastic syndrome (MDS) with multilineage dysplasia. Cytogenetic review revealed a complex aberrant karyotype denoting adverse outcome. Simultaneously, a skin biopsy could confirm leukemic skin infiltration. Consequently, a therapy with azacitidine was started. After the first cycle the patient developed severe pancytopenia with a percentage of 13% peripheral blasts (previously 0-2%) as well as fever without evidence for infection which was interpreted as progressive disease. Therefore, the therapeutic regimen was changed to a biomodulatory therapy consisting of low-dose azacitidine 75 mg/day (given sc d1-7 of 28), pioglitazone 45 mg/day per os, and all-trans-retinoic acid (ATRA) 45 mg/m2/day per os. After cycle 1 of this combined biomodulatory therapy the patient showed hematologic recovery; besides a mild anemia (hemoglobin 11.1 g/dl) she developed a normal blood count. Moreover, the cutaneous leukemic infiltrates which had been unaffected by the azacitidine ameliorated tremendously after 2 cycles resulting in a complete remission of the skin lesions after cycle 6. In conclusion, we report a very unusual case with cutaneous infiltrates being the first clinical manifestation of hematologic disease, preceding the development of acute myeloid leukemia. While azacitidine alone was ineffective, a combined biomodulatory approach resulted in a complete remission of the cutaneous manifestation.

Citing Articles

Addressing Genetic Tumor Heterogeneity, Post-Therapy Metastatic Spread, Cancer Repopulation, and Development of Acquired Tumor Cell Resistance.

Harrer D, Luke F, Pukrop T, Ghibelli L, Reichle A, Heudobler D Cancers (Basel). 2024; 16(1).

PMID: 38201607 PMC: 10778239. DOI: 10.3390/cancers16010180.


Low-dose azacitidine, pioglitazone and all- retinoic acid is safe in patients aged ≥60 years with acute myeloid leukemia refractory to standard induction chemotherapy (AMLSG 26-16/AML-ViVA): results of the safety run-in phase.

Heudobler D, Luke F, Hahn J, Grube M, Schlosser P, Kremers S Haematologica. 2023; 109(4):1274-1278.

PMID: 37881883 PMC: 10985427. DOI: 10.3324/haematol.2023.283864.


Advantages of the Combinatorial Molecular Targeted Therapy of Head and Neck Cancer-A Step before Anakoinosis-Based Personalized Treatment.

Kleszcz R Cancers (Basel). 2023; 15(17).

PMID: 37686523 PMC: 10486994. DOI: 10.3390/cancers15174247.


Drug Repurposing by Tumor Tissue Editing.

Luke F, Harrer D, Pantziarka P, Pukrop T, Ghibelli L, Gerner C Front Oncol. 2022; 12:900985.

PMID: 35814409 PMC: 9270020. DOI: 10.3389/fonc.2022.900985.


Clinical characteristics, treatment, and prognosis of 118 cases of myeloid sarcoma.

Zhao H, Dong Z, Wan D, Cao W, Xing H, Liu Z Sci Rep. 2022; 12(1):6752.

PMID: 35474239 PMC: 9042854. DOI: 10.1038/s41598-022-10831-7.


References
1.
Hart C, Vogelhuber M, Wolff D, Klobuch S, Ghibelli L, Foell J . Anakoinosis: Communicative Reprogramming of Tumor Systems - for Rescuing from Chemorefractory Neoplasia. Cancer Microenviron. 2015; 8(2):75-92. PMC: 4542828. DOI: 10.1007/s12307-015-0170-1. View

2.
Montalban-Bravo G, Garcia-Manero G, Jabbour E . Therapeutic choices after hypomethylating agent resistance for myelodysplastic syndromes. Curr Opin Hematol. 2017; 25(2):146-153. DOI: 10.1097/MOH.0000000000000400. View

3.
Patel L, Maghari A, Schwartz R, Kapila R, Morgan A, Lambert W . Myeloid leukemia cutis in the setting of myelodysplastic syndrome: a crucial dermatological diagnosis. Int J Dermatol. 2012; 51(4):383-8. DOI: 10.1111/j.1365-4632.2011.05297.x. View

4.
Tabe Y, Konopleva M, Andreeff M, Ohsaka A . Effects of PPARγ Ligands on Leukemia. PPAR Res. 2012; 2012:483656. PMC: 3364693. DOI: 10.1155/2012/483656. View

5.
Thomas S, Schelker R, Klobuch S, Zaiss S, Troppmann M, Rehli M . Biomodulatory therapy induces complete molecular remission in chemorefractory acute myeloid leukemia. Haematologica. 2014; 100(1):e4-6. PMC: 4281320. DOI: 10.3324/haematol.2014.115055. View