Unknown

Dataset Information

0

Predictive role of PD-L1 expression in the response of renal Medullary carcinoma to PD-1 inhibition.


ABSTRACT: Renal medullary carcinoma is one of the rarest malignancies arising from the kidney. Despite various aggressive therapeutic regimens, mortality remains significantly high (95%) with a median overall survival of 5 months. Furthermore, the scarcity of this malignancy renders randomized clinical trials impossible. We examined the expression of programmed death ligand 1 (PD-L1) in two new renal medullary carcinoma cases, investigated their responses to the PD-L1 inhibitor nivolumab and explored the predictive role of the rate of PD-L1 expression in such response.Two African-American patients (male and female) with sickle cell trait who presented to our center with hematuria and flank pain were diagnosed with metastatic renal medullary carcinoma. PD-L1 was expressed at rate of 25% and 60% in patient 1 and 2 respectively. Following nephrectomy, they were started on nivolumab. Patient 1 initially responded to the treatment with regression of metastatic lesions. However, following this early response, patient 1 who has been receiving nivolumab for more than 15 months, was noted to have a disease progression. Patient 2 had disease progression after 3 months of nivolumab therapy.Although PD-L1 is expressed in these patients with renal medullary carcinoma, response to nivolumab was only observed in patient 1 whose tumor has the lowest rate of PD-L1 expression. This may suggest that in RMC, response to PD-L1 inhibition therapy may not correlate with the rate of PD-L1 expression.

SUBMITTER: Sodji Q 

PROVIDER: S-EPMC5557570 | biostudies-other | 2017 Aug

REPOSITORIES: biostudies-other

Similar Datasets

| S-EPMC4674298 | biostudies-literature
| S-EPMC7697734 | biostudies-literature
| S-EPMC7336219 | biostudies-literature
| S-EPMC8011221 | biostudies-literature
| S-EPMC6480014 | biostudies-literature
| S-EPMC7409133 | biostudies-literature
| S-EPMC10210052 | biostudies-literature
| S-EPMC9481706 | biostudies-literature
| S-EPMC4647139 | biostudies-literature