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Pembrolizumab-Induced Cold Agglutinin Disease

Patient: Female, 58-year-old Final Diagnosis: Cold agglutinin disease • lung adenocarcinoma Symptoms: Anemia • fatigue • GI bleeding • neck mass • thrombocytopenia Medication:— Clinical Procedure: — Specialty: Hematology • General and Internal Medicine • Oncology OBJECTIVE: Unusual clinical course B...

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Autores principales: Atiq, Osman, Atiq, Saad O., Atiq, Zainab O., Patel, Vijay, Atiq, Mohammad O., Atiq, Omar T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491957/
https://www.ncbi.nlm.nih.gov/pubmed/32887867
http://dx.doi.org/10.12659/AJCR.924283
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author Atiq, Osman
Atiq, Saad O.
Atiq, Zainab O.
Patel, Vijay
Atiq, Mohammad O.
Atiq, Omar T.
author_facet Atiq, Osman
Atiq, Saad O.
Atiq, Zainab O.
Patel, Vijay
Atiq, Mohammad O.
Atiq, Omar T.
author_sort Atiq, Osman
collection PubMed
description Patient: Female, 58-year-old Final Diagnosis: Cold agglutinin disease • lung adenocarcinoma Symptoms: Anemia • fatigue • GI bleeding • neck mass • thrombocytopenia Medication:— Clinical Procedure: — Specialty: Hematology • General and Internal Medicine • Oncology OBJECTIVE: Unusual clinical course BACKGROUND: The introduction of immunotherapy in the management of metastatic lung cancer appears to be changing their natural history. Most patients tolerate immunotherapy without any significant adverse events. Nevertheless, a significant number of patients still experience adverse effects. Autoimmune hemolytic anemia has been described as mostly related to warm autoantibodies. The following case report describes cold agglutinin disease with hemolysis secondary to Pembrolizumab therapy for the treatment of metastatic lung cancer. CASE REPORT: A 58-year-old woman noted a left neck mass 4 months prior to her presentation. A biopsy confirmed the presence of metastatic adenocarcinoma, consistent with primary lung cancer. Further evaluation revealed the tumor to be PDL-1-positive. She was started on Pembrolizumab, Pemetrexed, and carboplatin chemotherapy regimen. Her CBC was within normal limits when she started therapy, but within 4 weeks hemoglobin dropped to 4.3 g/dL. Further evaluation showed high cryoglobulin levels and a high cold agglutinin titer. Complement C3 DAT was positive. A peripheral smear showed clumps of red cells and the serum IgM was elevated. The diagnosis of CAD was made. She was then started on Rituximab. Imaging showed a significant response, with decreased disease burden. CONCLUSIONS: Our case shows a unique presentation of CAD, initially presumed to be myelosuppression secondary to chemo-therapy. Instead, a peripheral smear revealed Pembrolizumab to be the cause of cold agglutinin disease. Due to the relatively unknown association between these 2 entities, patient care was delayed. Finally, after initiation of Rituximab therapy, the patient’s CBC began to recover.
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spelling pubmed-74919572020-09-28 Pembrolizumab-Induced Cold Agglutinin Disease Atiq, Osman Atiq, Saad O. Atiq, Zainab O. Patel, Vijay Atiq, Mohammad O. Atiq, Omar T. Am J Case Rep Articles Patient: Female, 58-year-old Final Diagnosis: Cold agglutinin disease • lung adenocarcinoma Symptoms: Anemia • fatigue • GI bleeding • neck mass • thrombocytopenia Medication:— Clinical Procedure: — Specialty: Hematology • General and Internal Medicine • Oncology OBJECTIVE: Unusual clinical course BACKGROUND: The introduction of immunotherapy in the management of metastatic lung cancer appears to be changing their natural history. Most patients tolerate immunotherapy without any significant adverse events. Nevertheless, a significant number of patients still experience adverse effects. Autoimmune hemolytic anemia has been described as mostly related to warm autoantibodies. The following case report describes cold agglutinin disease with hemolysis secondary to Pembrolizumab therapy for the treatment of metastatic lung cancer. CASE REPORT: A 58-year-old woman noted a left neck mass 4 months prior to her presentation. A biopsy confirmed the presence of metastatic adenocarcinoma, consistent with primary lung cancer. Further evaluation revealed the tumor to be PDL-1-positive. She was started on Pembrolizumab, Pemetrexed, and carboplatin chemotherapy regimen. Her CBC was within normal limits when she started therapy, but within 4 weeks hemoglobin dropped to 4.3 g/dL. Further evaluation showed high cryoglobulin levels and a high cold agglutinin titer. Complement C3 DAT was positive. A peripheral smear showed clumps of red cells and the serum IgM was elevated. The diagnosis of CAD was made. She was then started on Rituximab. Imaging showed a significant response, with decreased disease burden. CONCLUSIONS: Our case shows a unique presentation of CAD, initially presumed to be myelosuppression secondary to chemo-therapy. Instead, a peripheral smear revealed Pembrolizumab to be the cause of cold agglutinin disease. Due to the relatively unknown association between these 2 entities, patient care was delayed. Finally, after initiation of Rituximab therapy, the patient’s CBC began to recover. International Scientific Literature, Inc. 2020-09-05 /pmc/articles/PMC7491957/ /pubmed/32887867 http://dx.doi.org/10.12659/AJCR.924283 Text en © Am J Case Rep, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Atiq, Osman
Atiq, Saad O.
Atiq, Zainab O.
Patel, Vijay
Atiq, Mohammad O.
Atiq, Omar T.
Pembrolizumab-Induced Cold Agglutinin Disease
title Pembrolizumab-Induced Cold Agglutinin Disease
title_full Pembrolizumab-Induced Cold Agglutinin Disease
title_fullStr Pembrolizumab-Induced Cold Agglutinin Disease
title_full_unstemmed Pembrolizumab-Induced Cold Agglutinin Disease
title_short Pembrolizumab-Induced Cold Agglutinin Disease
title_sort pembrolizumab-induced cold agglutinin disease
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491957/
https://www.ncbi.nlm.nih.gov/pubmed/32887867
http://dx.doi.org/10.12659/AJCR.924283
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