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International Journal of Scientific and Research Publications

IJSRP, Volume 12, Issue 4, April 2022 Edition [ISSN 2250-3153]


An Immunohistochemical Study Of The Relationship Between Programmed Cell Death Ligand-1 (PD-L1) And Clinicopathological Characteristics Of Malignant Melanoma In General Hospital Haji Adam Malik Medan
      Febri Susanto, Ibnu Alferraly, Delyuzar
Abstract: Malignant melanoma is a potentially aggressive and lethal malignancy deriving from melanocytic cells. Although it comprises only 3% of all cutaneous malignancies diagnosed each year, malignant melanoma contributes to 75% of all skin cancer deaths. In the last decades, there have been advances in immune checkpoint inhibitor (ICPI) development in treating melanoma metastases. ICPI such as programmed cell death ligand-1 (PD-L1) is primary membrane-bound protein expressed in dendritic cells and monocytes. Programmed cell death protein- 1 (PD-1) inhibitors or PD-L1 inhibitors will clinically improve treatment response and overall survival rates in many types of tumors. Nowadays, PD-L1 is being intensively used in cancer patient management revolution, especially in melanoma and non small cell lung cancer. Therefore, the researchers were interested in assessing the relationship between PD-L1 immunohistochemical expression and clinicopathology of malignant melanoma patients in General Hospital Haji Adam Malik Medan. Objective: To analyse the relationship between PD-L1 immunohistochemical expression and clinicopathology characteristics of malignant melanoma in General Hospital Haji Adam Malik Medan.

Reference this Research Paper (copy & paste below code):

Febri Susanto, Ibnu Alferraly, Delyuzar (2022); An Immunohistochemical Study Of The Relationship Between Programmed Cell Death Ligand-1 (PD-L1) And Clinicopathological Characteristics Of Malignant Melanoma In General Hospital Haji Adam Malik Medan; International Journal of Scientific and Research Publications (IJSRP) 12(4) (ISSN: 2250-3153), DOI: http://dx.doi.org/10.29322/IJSRP.12.04.2022.p12408
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