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Poster display session

211P - Adjuvant axitinib in Asian vs non-Asian patients with metastatic renal cell carcinoma (mRCC): ATLAS trial subgroup analysis

Date

23 Nov 2019

Session

Poster display session

Topics

Tumour Site

Renal Cell Cancer

Presenters

Chi Fai Ng

Citation

Annals of Oncology (2019) 30 (suppl_9): ix71-ix76. 10.1093/annonc/mdz425

Authors

C.F. Ng1, T.G. Kwon2, M. Eto3, H. Miyake4, S.I. Seo5, S. Byun6, J..L. Lee7, B. Rosbrook8, E. Grande9, M. Gross-Goupil10, D.I. Quinn11

Author affiliations

  • 1 Division Of Oncology, Depatment Of Surgery, The Chinese University of Hong Kong, N/A - Hong Kong/HK
  • 2 Department Of Urology, School of Medicine, Kyungpook National University, Daegu/KR
  • 3 Department Of Urology, Kyushu University, Fukuoka/JP
  • 4 Department Of Urology, Hamamatsu University School of Medicine, 431-3192 - Hamamatsu/JP
  • 5 Department Of Urology, Sungkyunkwan University, Seoul/KR
  • 6 Department Of Urology, Seoul National University Bundang Hospital, Seongnam/KR
  • 7 Department Of Urology, Asan Medical Center, University of Ulsan College of Medicine, 138-931 - Seoul/KR
  • 8 Clinical Statistics, Pfizer Oncology, San Diego/US
  • 9 Head Of Medical Oncology Department, MD Anderson Cancer Center Madrid, 28033 - Madrid/ES
  • 10 Department Of Medical Oncology, CHU Bordeaux Hopital St. André, 33000 - Bordeaux/FR
  • 11 Translation And Clinical Science Program / Oncology, University of Southern California Norris Comprehensive Cancer Center, 90033 - Los Angeles/US

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Abstract 211P

Background

The ATLAS trial compared axitinib (AXI) vs placebo in patients (pts) with locoregional renal cell carcinoma at risk of recurrence after nephrectomy. ATLAS was stopped due to futility at a pre-planned interim analysis. A subgroup analysis was performed to describe differences between Asian vs Non-Asian pts and different Asian groups by geography in baseline characteristics and safety.

Methods

The exploratory subgroup analysis population included 363 pts randomized to receive AXI and 361 randomized to placebo. The primary endpoint was disease-free survival (DFS).

Results

DFS had the largest treatment effect in highest risk pts for Asian and Non-Asian pts: Hazard ratio = 0.731 (Asians) vs. 0.755 (Non-Asians). A similar trend was noted for Fuhrman Grade 3-4. Additional key results from the analysis are presented in the table.

Table: 211P Summary of key findings

Axitinib N = 363Placebo N = 361
Asian N = 262Non- Asian N = 101Asian N = 264Non- Asian N = 97
Key Pts Characteristics
Pts in Highest Risk Group, %51.972.351.566.0
Median time since diagnosis, wk8.710.38.610.0
Drug Treatment Differences
Completed 3y Treatment, %31.515.031.115.6
Median Treatment Duration, mo25.315.627.022.9
Median Daily Dose, mg6.68.69.910.0
Pts Safety Experience
Frequency of Dose Reduction, %68.550.011.77.3
AE Leading to Dose Reduction, %58.846.07.610.4
AE Leading to Discontinuation, %27.315.012.110.4

AE=adverse events Asian pts on AXI had higher frequencies of proteinuria, hypothyroidism, and nasopharyngitis and lower frequencies of fatigue and asthenia compared to Non-Asian pts on AXI. Within major Asian groups, proteinuria, hypothyroidism, nasopharyngitis and hypertension were more common in Japanese > Korean > Chinese pts.

Conclusions

DFS did not vary based on ethnicity. Asian pts had a lower median daily dose, and more frequent dose reduction vs non-Asian pts. More Asian pts had AEs leading to dose reductions of AXI and study withdrawals vs non-Asian pts. There were notable differences in AEs between Asian and Non-Asian pts and between Japanese, Korean and Chinese pts.

Clinical trial identification

NCT01599754.

Editorial acknowledgement

The study is sponsored by Pfizer. Medical writing support was provided by Charles Cheng, MS, of Engage Scientific Solutions, and funded by Pfizer.

Legal entity responsible for the study

This study was sponsored by Pfizer Inc and SFJ Pharmaceuticals.

Funding

This study was sponsored by Pfizer Inc and SFJ Pharmaceuticals.

Disclosure

C.F. Ng: Advisory / Consultancy, Speaker Bureau / Expert testimony: Boston Scientific; Advisory / Consultancy, Speaker Bureau / Expert testimony, Research grant / Funding (institution): Janssen; Advisory / Consultancy, Speaker Bureau / Expert testimony, Research grant / Funding (institution): Astellas; Speaker Bureau / Expert testimony, Research grant / Funding (institution): Ferring; Speaker Bureau / Expert testimony: Amgen; Research grant / Funding (institution): Olympus. T.G. Kwon: Research grant / Funding (institution): Kyungpook National University Chilgok Hospital. M. Eto: Advisory / Consultancy, Speaker Bureau / Expert testimony, Research grant / Funding (self): ONO; Advisory / Consultancy, Speaker Bureau / Expert testimony: Bristol-Myers Squibb; Advisory / Consultancy, Speaker Bureau / Expert testimony, Research grant / Funding (self): Pfizer; Advisory / Consultancy, Speaker Bureau / Expert testimony: Novartis; Speaker Bureau / Expert testimony: Bayer. S.I. Seo: Honoraria (self): Ipsen; Honoraria (self): Pfizer; Research grant / Funding (self): Alvogen. B. Rosbrook: Shareholder / Stockholder / Stock options, Full / Part-time employment: Pfizer. E. Grande: Honoraria (self), Research grant / Funding (self): Pfizer; Honoraria (self): Bristol-Myers Squibb; Honoraria (self), Research grant / Funding (self): IPSEN; Honoraria (self), Research grant / Funding (self): Roche; Honoraria (self): Eisai; Honoraria (self): Eusa Pharma; Honoraria (self): MSD; Honoraria (self): Sanofi-Genzyme; Honoraria (self): Adacap; Honoraria (self): Novartis; Honoraria (self): Pierre Fabre; Honoraria (self), Research grant / Funding (self): Lexicon; Honoraria (self): Celgene; Research grant / Funding (self): AstraZeneca; Research grant / Funding (self): MTEM/Threshold. M. Gross-Goupil: Advisory / Consultancy, Research grant / Funding (self), Travel / Accommodation / Expenses: Pfizer; Advisory / Consultancy, Research grant / Funding (self), Travel / Accommodation / Expenses: BMS; Advisory / Consultancy, Research grant / Funding (self), Travel / Accommodation / Expenses: MSD; Advisory / Consultancy, Research grant / Funding (self): Ipsen; Advisory / Consultancy, Travel / Accommodation / Expenses: Roche; Travel / Accommodation / Expenses: Amgen. D.I. Quinn: Advisory / Consultancy: Pfizer; Advisory / Consultancy: Bayer; Advisory / Consultancy: Novartis; Advisory / Consultancy: Bristol-Myers Squibb; Advisory / Consultancy: Merck; Advisory / Consultancy: Exelixis; Advisory / Consultancy: Genentech; Advisory / Consultancy: Roche; Advisory / Consultancy: AstraZeneca; Advisory / Consultancy: Astellas. All other authors have declared no conflicts of interest.

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