Adjuvant therapy with tyrosine kinase inhibitors for localized and locally advanced renal cell carcinoma: an updated systematic review and meta-analysis

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Adjuvant therapy with tyrosine kinase inhibitors for localized and locally advanced renal cell carcinoma: an updated systematic review and meta-analysis. / Laukhtina, Ekaterina; Quhal, Fahad; Mori, Keiichiro; Sari Motlagh, Reza; Pradere, Benjamin; Schuettfort, Victor M; Mostafaei, Hadi; Katayama, Satoshi; Grossmann, Nico С; Rajwa, Pawel; Resch, Irene; Enikeev, Dmitry; Karakiewicz, Pierre I; Shariat, Shahrokh F; Schmidinger, Manuela.

In: UROL ONCOL-SEMIN ORI, Vol. 39, No. 11, 11.2021, p. 764-773.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Laukhtina, E, Quhal, F, Mori, K, Sari Motlagh, R, Pradere, B, Schuettfort, VM, Mostafaei, H, Katayama, S, Grossmann, NС, Rajwa, P, Resch, I, Enikeev, D, Karakiewicz, PI, Shariat, SF & Schmidinger, M 2021, 'Adjuvant therapy with tyrosine kinase inhibitors for localized and locally advanced renal cell carcinoma: an updated systematic review and meta-analysis', UROL ONCOL-SEMIN ORI, vol. 39, no. 11, pp. 764-773. https://doi.org/10.1016/j.urolonc.2021.07.022

APA

Laukhtina, E., Quhal, F., Mori, K., Sari Motlagh, R., Pradere, B., Schuettfort, V. M., Mostafaei, H., Katayama, S., Grossmann, N. С., Rajwa, P., Resch, I., Enikeev, D., Karakiewicz, P. I., Shariat, S. F., & Schmidinger, M. (2021). Adjuvant therapy with tyrosine kinase inhibitors for localized and locally advanced renal cell carcinoma: an updated systematic review and meta-analysis. UROL ONCOL-SEMIN ORI, 39(11), 764-773. https://doi.org/10.1016/j.urolonc.2021.07.022

Vancouver

Bibtex

@article{7d2db5af29734efa8c2e8cd8d43cc369,
title = "Adjuvant therapy with tyrosine kinase inhibitors for localized and locally advanced renal cell carcinoma: an updated systematic review and meta-analysis",
abstract = "PURPOSE: Tyrosine kinase inhibitors (TKIs) have been widely used in the management of patients with metastatic renal cell carcinoma (RCC). However, the use of systemic therapies in the adjuvant setting of localized and locally advanced RCC has shown conflicting results across the literature. Therefore, we aimed to conduct an updated systematic review and meta-analysis comparing the efficacy and safety of TKIs in the adjuvant setting for patients with localized and locally advanced RCC.MATERIALS AND METHODS: The MEDLINE and EMBASE databases were searched in December 2020 to identify phase III randomized controlled trials of patients receiving adjuvant therapies with TKI for RCC. Disease-free survival (DFS) and overall survival (OS) were the primary endpoints. The secondary endpoints included treatment-related adverse events (TRAEs) of high and any grade.RESULTS: Five trials (S-TRAC, ASSURE, PROTECT, ATLAS, and SORCE) were included in our meta-analysis comprising 6,531 patients. The forest plot revealed that TKI therapy was associated with a significantly longer DFS compared to placebo (pooled HR: 0.88, 95% CI: 0.81-0.96, P= 0.004). The Cochrane's Q test (P = 0.51) and I2 test (I2 = 0%) revealed no significant heterogeneity. Adjuvant TKI was not associated with improved OS compared to placebo (pooled HR: 0.93, 95% CI: 0.83-1.04, P= 0.23). The Cochrane's Q test (P = 0.74) and I2 test (I2 = 0%) revealed no significant heterogeneity. The forest plot revealed that TKI therapy, compared to placebo, was associated with higher rates of high grade TRAEs (OR: 5.20, 95% CI: 4.10-6.59, P< 0.00001) as well as any grade TRAEs (OR: 3.85, 95% CI: 1.22-12.17, P= 0.02). The Cochrane's Q tests (P < 0.0001 and P < 0.00001, respectively) and I2 tests (I2 = 79% and I2 = 90%, respectively) revealed significant heterogeneity.CONCLUSIONS: The findings of our analyses suggest an improved DFS in patients with localized and locally advanced RCC receiving adjuvant TKI as compared to placebo; however, this did not translate into any significant OS benefit. Additionally, TKI therapy led to significant toxicity. Adjuvant TKI does not seem to offer a satisfactory risk and/orbenefit balance for all patients. Select patients with very poor prognosis may be considered in a shared decision-making process with the patient. With the successful arrival of immune-based therapies in RCC, these may allow a more favorable risk/benefit profile.",
keywords = "Carcinoma, Renal Cell/drug therapy, Chemotherapy, Adjuvant/methods, Disease-Free Survival, Female, Humans, Kidney Neoplasms/drug therapy, Male, Protein Kinase Inhibitors/pharmacology",
author = "Ekaterina Laukhtina and Fahad Quhal and Keiichiro Mori and {Sari Motlagh}, Reza and Benjamin Pradere and Schuettfort, {Victor M} and Hadi Mostafaei and Satoshi Katayama and Grossmann, {Nico С} and Pawel Rajwa and Irene Resch and Dmitry Enikeev and Karakiewicz, {Pierre I} and Shariat, {Shahrokh F} and Manuela Schmidinger",
note = "Copyright {\textcopyright} 2021 The Author(s). Published by Elsevier Inc. All rights reserved.",
year = "2021",
month = nov,
doi = "10.1016/j.urolonc.2021.07.022",
language = "English",
volume = "39",
pages = "764--773",
journal = "UROL ONCOL-SEMIN ORI",
issn = "1078-1439",
publisher = "Elsevier Inc.",
number = "11",

}

RIS

TY - JOUR

T1 - Adjuvant therapy with tyrosine kinase inhibitors for localized and locally advanced renal cell carcinoma: an updated systematic review and meta-analysis

AU - Laukhtina, Ekaterina

AU - Quhal, Fahad

AU - Mori, Keiichiro

AU - Sari Motlagh, Reza

AU - Pradere, Benjamin

AU - Schuettfort, Victor M

AU - Mostafaei, Hadi

AU - Katayama, Satoshi

AU - Grossmann, Nico С

AU - Rajwa, Pawel

AU - Resch, Irene

AU - Enikeev, Dmitry

AU - Karakiewicz, Pierre I

AU - Shariat, Shahrokh F

AU - Schmidinger, Manuela

N1 - Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.

PY - 2021/11

Y1 - 2021/11

N2 - PURPOSE: Tyrosine kinase inhibitors (TKIs) have been widely used in the management of patients with metastatic renal cell carcinoma (RCC). However, the use of systemic therapies in the adjuvant setting of localized and locally advanced RCC has shown conflicting results across the literature. Therefore, we aimed to conduct an updated systematic review and meta-analysis comparing the efficacy and safety of TKIs in the adjuvant setting for patients with localized and locally advanced RCC.MATERIALS AND METHODS: The MEDLINE and EMBASE databases were searched in December 2020 to identify phase III randomized controlled trials of patients receiving adjuvant therapies with TKI for RCC. Disease-free survival (DFS) and overall survival (OS) were the primary endpoints. The secondary endpoints included treatment-related adverse events (TRAEs) of high and any grade.RESULTS: Five trials (S-TRAC, ASSURE, PROTECT, ATLAS, and SORCE) were included in our meta-analysis comprising 6,531 patients. The forest plot revealed that TKI therapy was associated with a significantly longer DFS compared to placebo (pooled HR: 0.88, 95% CI: 0.81-0.96, P= 0.004). The Cochrane's Q test (P = 0.51) and I2 test (I2 = 0%) revealed no significant heterogeneity. Adjuvant TKI was not associated with improved OS compared to placebo (pooled HR: 0.93, 95% CI: 0.83-1.04, P= 0.23). The Cochrane's Q test (P = 0.74) and I2 test (I2 = 0%) revealed no significant heterogeneity. The forest plot revealed that TKI therapy, compared to placebo, was associated with higher rates of high grade TRAEs (OR: 5.20, 95% CI: 4.10-6.59, P< 0.00001) as well as any grade TRAEs (OR: 3.85, 95% CI: 1.22-12.17, P= 0.02). The Cochrane's Q tests (P < 0.0001 and P < 0.00001, respectively) and I2 tests (I2 = 79% and I2 = 90%, respectively) revealed significant heterogeneity.CONCLUSIONS: The findings of our analyses suggest an improved DFS in patients with localized and locally advanced RCC receiving adjuvant TKI as compared to placebo; however, this did not translate into any significant OS benefit. Additionally, TKI therapy led to significant toxicity. Adjuvant TKI does not seem to offer a satisfactory risk and/orbenefit balance for all patients. Select patients with very poor prognosis may be considered in a shared decision-making process with the patient. With the successful arrival of immune-based therapies in RCC, these may allow a more favorable risk/benefit profile.

AB - PURPOSE: Tyrosine kinase inhibitors (TKIs) have been widely used in the management of patients with metastatic renal cell carcinoma (RCC). However, the use of systemic therapies in the adjuvant setting of localized and locally advanced RCC has shown conflicting results across the literature. Therefore, we aimed to conduct an updated systematic review and meta-analysis comparing the efficacy and safety of TKIs in the adjuvant setting for patients with localized and locally advanced RCC.MATERIALS AND METHODS: The MEDLINE and EMBASE databases were searched in December 2020 to identify phase III randomized controlled trials of patients receiving adjuvant therapies with TKI for RCC. Disease-free survival (DFS) and overall survival (OS) were the primary endpoints. The secondary endpoints included treatment-related adverse events (TRAEs) of high and any grade.RESULTS: Five trials (S-TRAC, ASSURE, PROTECT, ATLAS, and SORCE) were included in our meta-analysis comprising 6,531 patients. The forest plot revealed that TKI therapy was associated with a significantly longer DFS compared to placebo (pooled HR: 0.88, 95% CI: 0.81-0.96, P= 0.004). The Cochrane's Q test (P = 0.51) and I2 test (I2 = 0%) revealed no significant heterogeneity. Adjuvant TKI was not associated with improved OS compared to placebo (pooled HR: 0.93, 95% CI: 0.83-1.04, P= 0.23). The Cochrane's Q test (P = 0.74) and I2 test (I2 = 0%) revealed no significant heterogeneity. The forest plot revealed that TKI therapy, compared to placebo, was associated with higher rates of high grade TRAEs (OR: 5.20, 95% CI: 4.10-6.59, P< 0.00001) as well as any grade TRAEs (OR: 3.85, 95% CI: 1.22-12.17, P= 0.02). The Cochrane's Q tests (P < 0.0001 and P < 0.00001, respectively) and I2 tests (I2 = 79% and I2 = 90%, respectively) revealed significant heterogeneity.CONCLUSIONS: The findings of our analyses suggest an improved DFS in patients with localized and locally advanced RCC receiving adjuvant TKI as compared to placebo; however, this did not translate into any significant OS benefit. Additionally, TKI therapy led to significant toxicity. Adjuvant TKI does not seem to offer a satisfactory risk and/orbenefit balance for all patients. Select patients with very poor prognosis may be considered in a shared decision-making process with the patient. With the successful arrival of immune-based therapies in RCC, these may allow a more favorable risk/benefit profile.

KW - Carcinoma, Renal Cell/drug therapy

KW - Chemotherapy, Adjuvant/methods

KW - Disease-Free Survival

KW - Female

KW - Humans

KW - Kidney Neoplasms/drug therapy

KW - Male

KW - Protein Kinase Inhibitors/pharmacology

U2 - 10.1016/j.urolonc.2021.07.022

DO - 10.1016/j.urolonc.2021.07.022

M3 - SCORING: Journal article

C2 - 34400065

VL - 39

SP - 764

EP - 773

JO - UROL ONCOL-SEMIN ORI

JF - UROL ONCOL-SEMIN ORI

SN - 1078-1439

IS - 11

ER -