Prognostic blood-based biomarkers in patients treated with neoadjuvant chemotherapy for urothelial carcinoma of the bladder: A systematic review

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Prognostic blood-based biomarkers in patients treated with neoadjuvant chemotherapy for urothelial carcinoma of the bladder: A systematic review. / Laukhtina, Ekaterina; Pradere, Benjamin; Mori, Keiichiro; Schuettfort, Victor M; Quhal, Fahad; Mostafaei, Hadi; Sari Motlagh, Reza; Aydh, Abdulmajeed; Moschini, Marco; Enikeev, Dmitry; Karakiewicz, Pierre I; Abufaraj, Mohammad; Shariat, Shahrokh F; European Association of Urology – Young Academic Urologists (EAU-YAU), Urothelial Carcinoma Working Group.

In: UROL ONCOL-SEMIN ORI, Vol. 39, No. 8, 08.2021, p. 471-479.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

Harvard

Laukhtina, E, Pradere, B, Mori, K, Schuettfort, VM, Quhal, F, Mostafaei, H, Sari Motlagh, R, Aydh, A, Moschini, M, Enikeev, D, Karakiewicz, PI, Abufaraj, M, Shariat, SF & European Association of Urology – Young Academic Urologists (EAU-YAU), Urothelial Carcinoma Working Group 2021, 'Prognostic blood-based biomarkers in patients treated with neoadjuvant chemotherapy for urothelial carcinoma of the bladder: A systematic review', UROL ONCOL-SEMIN ORI, vol. 39, no. 8, pp. 471-479. https://doi.org/10.1016/j.urolonc.2021.03.005

APA

Laukhtina, E., Pradere, B., Mori, K., Schuettfort, V. M., Quhal, F., Mostafaei, H., Sari Motlagh, R., Aydh, A., Moschini, M., Enikeev, D., Karakiewicz, P. I., Abufaraj, M., Shariat, S. F., & European Association of Urology – Young Academic Urologists (EAU-YAU), Urothelial Carcinoma Working Group (2021). Prognostic blood-based biomarkers in patients treated with neoadjuvant chemotherapy for urothelial carcinoma of the bladder: A systematic review. UROL ONCOL-SEMIN ORI, 39(8), 471-479. https://doi.org/10.1016/j.urolonc.2021.03.005

Vancouver

Bibtex

@article{13452ca0579a4a519a0d35141b4bf6c8,
title = "Prognostic blood-based biomarkers in patients treated with neoadjuvant chemotherapy for urothelial carcinoma of the bladder: A systematic review",
abstract = "PURPOSE: The present systematic review aimed to identify prognostic values of blood-based biomarkers in patients treated with neoadjuvant chemotherapy (NAC) for urothelial carcinoma of the bladder (UCB).MATERIAL AND METHODS: The PubMed, Web of Science, and Scopus databases were searched in August 2020 according to the PRISMA statement. Studies were deemed eligible if they compared oncological outcomes in patients treated with NAC for UCB with and without pretreatment laboratory abnormalities.RESULTS: Overall, ten studies, including 966 patients who underwent NAC, met our eligibility criteria. Six studies provided data on pretreatment neutrophil to lymphocyte ratio (NLR) with contradicting results on its association with pathologic response (PR) and complete pathologic response (pCR); some studies reported a strong association between a high level of pretreatment NLR and worse survival outcomes. Two studies reported that higher pretreatment platelet-lymphocyte ratio (PLR) is associated with a lower likelihood of achieving PR and/or pCR, while lymphocyte count alone had the opposite association. One study reported a negative association between pretreatment blood-based myeloid-derived suppressors cells and pCR. Patients who experienced a remission have been reported to have higher level of lymphocyte subsets (CD3+, CD4+, CD57+ cells, the ratio of CD4+/CD8+) compared to those who had progression. One study found that low pretreatment blood-based human chorionic gonadotrophin b subunit (hCGβ) was associated with improved overall survival (OS). High levels of epithelial tumor markers (CA-125, CA 19-9) were also associated with worse OS and recurrence-free survival in the NAC setting.CONCLUSION: Current evidence suggests that several readily available, easy measurable blood-based biomarkers hold promise to improve our selection of UCB patients who are likely benefit from NAC. However, their role as an adjunct to established histopathologic characteristics for clinical decision-making requires further validation along the biomarker phased approach.",
keywords = "Antineoplastic Agents/therapeutic use, Biomarkers, Tumor/blood, Humans, Male, Neoadjuvant Therapy/methods, Prognosis, Urinary Bladder Neoplasms/blood",
author = "Ekaterina Laukhtina and Benjamin Pradere and Keiichiro Mori and Schuettfort, {Victor M} and Fahad Quhal and Hadi Mostafaei and {Sari Motlagh}, Reza and Abdulmajeed Aydh and Marco Moschini and Dmitry Enikeev and Karakiewicz, {Pierre I} and Mohammad Abufaraj and Shariat, {Shahrokh F} and {European Association of Urology – Young Academic Urologists (EAU-YAU), Urothelial Carcinoma Working Group}",
note = "Copyright {\textcopyright} 2021 The Authors. Published by Elsevier Inc. All rights reserved.",
year = "2021",
month = aug,
doi = "10.1016/j.urolonc.2021.03.005",
language = "English",
volume = "39",
pages = "471--479",
journal = "UROL ONCOL-SEMIN ORI",
issn = "1078-1439",
publisher = "Elsevier Inc.",
number = "8",

}

RIS

TY - JOUR

T1 - Prognostic blood-based biomarkers in patients treated with neoadjuvant chemotherapy for urothelial carcinoma of the bladder: A systematic review

AU - Laukhtina, Ekaterina

AU - Pradere, Benjamin

AU - Mori, Keiichiro

AU - Schuettfort, Victor M

AU - Quhal, Fahad

AU - Mostafaei, Hadi

AU - Sari Motlagh, Reza

AU - Aydh, Abdulmajeed

AU - Moschini, Marco

AU - Enikeev, Dmitry

AU - Karakiewicz, Pierre I

AU - Abufaraj, Mohammad

AU - Shariat, Shahrokh F

AU - European Association of Urology – Young Academic Urologists (EAU-YAU), Urothelial Carcinoma Working Group

N1 - Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

PY - 2021/8

Y1 - 2021/8

N2 - PURPOSE: The present systematic review aimed to identify prognostic values of blood-based biomarkers in patients treated with neoadjuvant chemotherapy (NAC) for urothelial carcinoma of the bladder (UCB).MATERIAL AND METHODS: The PubMed, Web of Science, and Scopus databases were searched in August 2020 according to the PRISMA statement. Studies were deemed eligible if they compared oncological outcomes in patients treated with NAC for UCB with and without pretreatment laboratory abnormalities.RESULTS: Overall, ten studies, including 966 patients who underwent NAC, met our eligibility criteria. Six studies provided data on pretreatment neutrophil to lymphocyte ratio (NLR) with contradicting results on its association with pathologic response (PR) and complete pathologic response (pCR); some studies reported a strong association between a high level of pretreatment NLR and worse survival outcomes. Two studies reported that higher pretreatment platelet-lymphocyte ratio (PLR) is associated with a lower likelihood of achieving PR and/or pCR, while lymphocyte count alone had the opposite association. One study reported a negative association between pretreatment blood-based myeloid-derived suppressors cells and pCR. Patients who experienced a remission have been reported to have higher level of lymphocyte subsets (CD3+, CD4+, CD57+ cells, the ratio of CD4+/CD8+) compared to those who had progression. One study found that low pretreatment blood-based human chorionic gonadotrophin b subunit (hCGβ) was associated with improved overall survival (OS). High levels of epithelial tumor markers (CA-125, CA 19-9) were also associated with worse OS and recurrence-free survival in the NAC setting.CONCLUSION: Current evidence suggests that several readily available, easy measurable blood-based biomarkers hold promise to improve our selection of UCB patients who are likely benefit from NAC. However, their role as an adjunct to established histopathologic characteristics for clinical decision-making requires further validation along the biomarker phased approach.

AB - PURPOSE: The present systematic review aimed to identify prognostic values of blood-based biomarkers in patients treated with neoadjuvant chemotherapy (NAC) for urothelial carcinoma of the bladder (UCB).MATERIAL AND METHODS: The PubMed, Web of Science, and Scopus databases were searched in August 2020 according to the PRISMA statement. Studies were deemed eligible if they compared oncological outcomes in patients treated with NAC for UCB with and without pretreatment laboratory abnormalities.RESULTS: Overall, ten studies, including 966 patients who underwent NAC, met our eligibility criteria. Six studies provided data on pretreatment neutrophil to lymphocyte ratio (NLR) with contradicting results on its association with pathologic response (PR) and complete pathologic response (pCR); some studies reported a strong association between a high level of pretreatment NLR and worse survival outcomes. Two studies reported that higher pretreatment platelet-lymphocyte ratio (PLR) is associated with a lower likelihood of achieving PR and/or pCR, while lymphocyte count alone had the opposite association. One study reported a negative association between pretreatment blood-based myeloid-derived suppressors cells and pCR. Patients who experienced a remission have been reported to have higher level of lymphocyte subsets (CD3+, CD4+, CD57+ cells, the ratio of CD4+/CD8+) compared to those who had progression. One study found that low pretreatment blood-based human chorionic gonadotrophin b subunit (hCGβ) was associated with improved overall survival (OS). High levels of epithelial tumor markers (CA-125, CA 19-9) were also associated with worse OS and recurrence-free survival in the NAC setting.CONCLUSION: Current evidence suggests that several readily available, easy measurable blood-based biomarkers hold promise to improve our selection of UCB patients who are likely benefit from NAC. However, their role as an adjunct to established histopathologic characteristics for clinical decision-making requires further validation along the biomarker phased approach.

KW - Antineoplastic Agents/therapeutic use

KW - Biomarkers, Tumor/blood

KW - Humans

KW - Male

KW - Neoadjuvant Therapy/methods

KW - Prognosis

KW - Urinary Bladder Neoplasms/blood

U2 - 10.1016/j.urolonc.2021.03.005

DO - 10.1016/j.urolonc.2021.03.005

M3 - SCORING: Review article

C2 - 33888424

VL - 39

SP - 471

EP - 479

JO - UROL ONCOL-SEMIN ORI

JF - UROL ONCOL-SEMIN ORI

SN - 1078-1439

IS - 8

ER -