AI Article Synopsis

  • Myelophthisis caused by melanoma is very rare, and there hasn't been much research on how to treat it effectively, especially using immune checkpoint inhibitors like pembrolizumab.
  • In a unique case, a patient with serious melanoma that spread to their bone marrow (causing low blood cell levels) responded well to treatment with an anti-PD-1 drug.
  • This is the first reported instance showing that immune checkpoint inhibitors can help treat myelophthisis, indicating that doctors should consider these treatments even in tough cases where bone marrow is heavily affected.

Article Abstract

Background: Myelophthisis due to melanoma is a rare phenomenon. Treatment strategies for patients with this serious complication of malignancy have not been well documented, and none have previously reported efficacy of immune checkpoint inhibition. Since bone metastases are not measurable lesions per standard response criteria, the efficacy of immune checkpoint inhibition in the bones is also not well described.

Case Presentation: We describe a patient with widespread melanoma metastases involving the bone marrow causing myelophthisis and pancytopenia who responded to immune checkpoint inhibition with the anti-programmed cell death-1 (PD-1) inhibitor pembrolizumab.

Conclusions: This is the first report to our knowledge of disease response to immune checkpoint inhibition in a patient with myelophthisis. Clinical trials have recently emerged describing the efficacy of PD-1 inhibition for disorders regularly involving the bone marrow, such as hematologic malignancies, suggesting the importance of better understanding the bone marrow as an immunologically active compartment. Clinicians should be aware that immune checkpoint inhibition alone may be effective in treating malignancy involving the bone marrow, even in cases of extensive involvement resulting in pancytopenia due to myelophthisis from a solid tumor as our case suggests.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394614PMC
http://dx.doi.org/10.1186/s40425-017-0236-3DOI Listing

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