Pazopanib in patients with metastatic renal cell carcinoma: a single-center, real-world, retrospective Chinese study.

Metastatic renal cell carcinoma (mRCC) pazopanib real-world the International Metastatic Renal Cell Carcinoma Database Consortium risk model (IMDC risk model)

Journal

Translational andrology and urology
ISSN: 2223-4691
Titre abrégé: Transl Androl Urol
Pays: China
ID NLM: 101581119

Informations de publication

Date de publication:
Mar 2021
Historique:
entrez: 14 4 2021
pubmed: 15 4 2021
medline: 15 4 2021
Statut: ppublish

Résumé

The efficacy and safety of pazopanib in patients diagnosed with metastatic renal cell carcinoma (mRCC) have been demonstrated by a Chinese subgroup analysis of the COMPARZ (Pazopanib Versus Sunitinib in the Treatment of Locally Advanced and/or Metastatic Renal Cell Carcinoma) trial. However, the real-world data are still unknown. This single-center, retrospective study was designed to verify the real-world effects of pazopanib in Chinese patients with mRCC. Patients with mRCC and a clinical decision to initiate pazopanib as first-line therapy were eligible. The primary endpoint was progression-free survival (PFS), with overall survival (OS), objective response rate (ORR), and safety being evaluated as secondary endpoints. The effectiveness according to the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk model, number of risk factors in the intermediate risk group, age, Eastern Cooperative Oncology Group (ECOG) performance status (PS), and the number and site of organ metastasis were also assessed. A total of 32 patients were enrolled, including 23 (71.9%) males and 9 (28.1%) females. The median age was 57 years (range 29-75 years). With a median follow-up time of 23.8 months, a median PFS of 18.3 months, and an ORR of 37.5%. Median OS was not reached, and the 1-, 2-, and 3-year overall survival rates were 90.6%, 78.1, and 65.6%, respectively. According to IMDC risk model, 37.5% were placed in the favorable risk (FR) subgroup, 56.2% (the majority) were placed in the intermediate risk (IR) subgroup, and 6.3% were placed in the poor risk (PR) subgroup. Compared with the IR and PR groups, the FR group achieved the best ORR (58.3%) and median PFS (22.1 months). Having 1 risk factor, ECOG PS <2, 1 organ metastasis site, and only lung metastasis associated with a higher ORR and better median PFS. The IMDC risk model and number of metastases were associated with PFS. The most common adverse events were change in hair color (69.0%), diarrhea (63%), and hypertension (50%). Pazopanib showed efficacy and safety in real-world Chinese mRCC patients.

Sections du résumé

BACKGROUND BACKGROUND
The efficacy and safety of pazopanib in patients diagnosed with metastatic renal cell carcinoma (mRCC) have been demonstrated by a Chinese subgroup analysis of the COMPARZ (Pazopanib Versus Sunitinib in the Treatment of Locally Advanced and/or Metastatic Renal Cell Carcinoma) trial. However, the real-world data are still unknown. This single-center, retrospective study was designed to verify the real-world effects of pazopanib in Chinese patients with mRCC.
METHODS METHODS
Patients with mRCC and a clinical decision to initiate pazopanib as first-line therapy were eligible. The primary endpoint was progression-free survival (PFS), with overall survival (OS), objective response rate (ORR), and safety being evaluated as secondary endpoints. The effectiveness according to the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk model, number of risk factors in the intermediate risk group, age, Eastern Cooperative Oncology Group (ECOG) performance status (PS), and the number and site of organ metastasis were also assessed.
RESULTS RESULTS
A total of 32 patients were enrolled, including 23 (71.9%) males and 9 (28.1%) females. The median age was 57 years (range 29-75 years). With a median follow-up time of 23.8 months, a median PFS of 18.3 months, and an ORR of 37.5%. Median OS was not reached, and the 1-, 2-, and 3-year overall survival rates were 90.6%, 78.1, and 65.6%, respectively. According to IMDC risk model, 37.5% were placed in the favorable risk (FR) subgroup, 56.2% (the majority) were placed in the intermediate risk (IR) subgroup, and 6.3% were placed in the poor risk (PR) subgroup. Compared with the IR and PR groups, the FR group achieved the best ORR (58.3%) and median PFS (22.1 months). Having 1 risk factor, ECOG PS <2, 1 organ metastasis site, and only lung metastasis associated with a higher ORR and better median PFS. The IMDC risk model and number of metastases were associated with PFS. The most common adverse events were change in hair color (69.0%), diarrhea (63%), and hypertension (50%).
CONCLUSIONS CONCLUSIONS
Pazopanib showed efficacy and safety in real-world Chinese mRCC patients.

Identifiants

pubmed: 33850766
doi: 10.21037/tau-21-111
pii: tau-10-03-1321
pmc: PMC8039632
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1321-1331

Informations de copyright

2021 Translational Andrology and Urology. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tau-21-111). The authors have no conflicts of interest to declare.

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Auteurs

Jianhui Chen (J)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Wen Ye (W)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Wei Jiang (W)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Xiaofan Li (X)

Department of Hematology, Fujian Institute of Hematology, Union Hospital, Fujian Medical University, Fuzhou, China.
Fujian Provincial Key Laboratory on Hematology, Fujian Medical University, Fuzhou, China.

Rong Liu (R)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Bijuan Lin (B)

Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, China.

Jingnan Xiang (J)

Department of Emergency, Union Hospital, Fujian Medical University, Fuzhou, China.

Wei Tian (W)

Department of Dermatology, Fujian Medical University Union Hospital, Fuzhou, China.

Junjie Bai (J)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Teng Zuo (T)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Bingxin Lin (B)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Yinan Guo (Y)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Song Zheng (S)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Classifications MeSH