Monocyte to lymphocyte ratios and cancer-specific mortality for patients with renal cell carcinoma and inferior vena cava tumor thrombus.

Authors

null

Maxwell Sandberg

Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, NC

Maxwell Sandberg , Rory Ritts , Mary Namugosa , Davis Temple , Wyatt Whitman , Claudia Marie Costa , Justin Refugia , Benjamin Eilender , Reza Mehrazin , Rafael Ribiero Zanotti , Patricio Garcia Marchiñena , Stenio Cassio Zequi , Alejandro Rodriguez

Organizations

Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, NC, Atrium Health Wake Forest Baptist Medical Center, Winston Salem, NC, Wake Forest University School of Medicine, Winston-Salem, NC, Mount Sinai Hospital System, New York, NY, Tisch Cancer Institute at the Icahn School of Medicine at Mount Sinai, New York, NY, A.C. Camargo Cancer Center, São Paulo, Brazil, Hospital Italiano de Buenos Aires, Buenos Aires, Brazil

Research Funding

No funding sources reported

Background: Renal cell carcinoma (RCC) with inferior vena cava (IVC) tumor thrombus carries a poor prognosis and presents complex medical management to urologists. Long-term data examining RCC with IVC tumor thrombus is sparse. Specifically, markers predicting cancer-specific survival are lacking. Recently, immune cell markers in cancer, such as neutrophils, lymphocytes, and monocytes, have come into focus. These cell counts and/or ratios may provide a window into cancer-specific outcomes. The purpose of this study was to examine the use of immune cell ratios in patients with RCC and IVC tumor thrombus to predict survival outcomes through a collaboration project across North and South America. Methods: Patients were included in this study if they had a diagnosis of RCC with IVC tumor thrombus and underwent nephrectomy with IVC thrombectomy for their RCC. Data was reviewed and entered into a multi-institutional/continental database. Complete blood counts taken as close to the date prior to/date of surgery were used to calculate immune cell ratios. Neutrophil to (/) lymphocyte ratios were done by dividing patients’ neutrophil cell count by their lymphocyte count. Monocyte/lymphocyte ratios were calculated in the same manner. Independent samples t-test was used to test for significance in cause of death post-operatively (RCC versus non-RCC cause) based on immune cell ratio. Results: There were 107 patients included in the study with long-term follow-up data (Mean: 2.6 years; Range: 0-16-years). Of all patients, 43/107 died by the end of the study, with 31/43 (72.1%) dying due to RCC and 12/43 (27.9%) from other causes. No difference existed in neutrophil/lymphocyte ratios based on cause of death (p=0.260). Monocyte/lymphocyte ratios were significantly lower in those who died from RCC relative to another cause (p=0.035). Conclusions: Immune cell ratios may have a role in predicting death from RCC. In our study, monocyte/lymphocyte ratios were significantly lower in patients who died from RCC compared to death from other reasons. Our results stem from a multi-continental/institutional study, and thus hold clinical utility as an increased focus is turned towards including diverse populations in research. Urologists may consider monocyte/lymphocyte ratios in the future when managing patients with RCC and an IVC thrombus.

Immune cell ratios and cause of death.

VariableDeath From RCC (standard dev.)Death From Other Reason (standard dev.)P-value
Neutrophil/Lymphocyte3.3 (1.4)4.2 (2.2)0.260
Monocyte/Lymphocyte0.39 (0.13)0.56 (0.2)0.035

Note: P-values are comparing immune cell ratios based on cause of death. Standard deviations are in parentheses.

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Abstract Details

Meeting

2024 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Renal Cell Cancer; Adrenal, Penile, and Testicular Cancers

Track

Renal Cell Cancer,Adrenal Cancer,Penile Cancer,Testicular Cancer

Sub Track

Translational Research, Tumor Biology, Biomarkers, and Pathology

Citation

J Clin Oncol 42, 2024 (suppl 4; abstr 444)

DOI

10.1200/JCO.2024.42.4_suppl.444

Abstract #

444

Poster Bd #

J5

Abstract Disclosures

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