Site-specific disease progression in patients with metastatic renal cell carcinoma treated with first-line nivolumab plus ipilimumab or axitinib-based immunotargeted combinations.
Abstract
478 Background: Data on site-specific progression patterns in metastatic renal cell carcinoma (mRCC) treated with immuno-oncology agents are limited. This study aimed to characterize sites of progression in patients receiving nivolumab plus ipilimumab (Nivo-Ipi) or axitinib-based immunotargeted combinations in the first-line setting. Methods: A retrospective, observational cohort study included patients with clear-cell mRCC who received either Nivo-Ipi (Cohort A) or pembrolizumab-axitinib and avelumab-axitinib (Cohort B) from 2018 to 2024. The primary objective was to assess the occurrence of new lesions in different organs. Secondary analysis evaluated disease progression by an increase of more than 20% in target lesion size. Results: A total of 334 patients were identified, with radiographic progression observed in 86.3% (107/124) of Cohort A and 60% (126/210) of Cohort B. In the ITT population (n=233), the median age at mRCC diagnosis was 59.7 years (range 31–84), 79% were male, 74% had undergone nephrectomy, 61% had intermediate IMDC risk, and 64% had two or more metastatic sites. Cohort B had a younger median age (60.2 vs. 65.4 years), a higher incidence of bone metastases (28.6% vs. 13.1%), and more favorable risk (15.1% vs. 0.9%) compared to Cohort A. The site-specific rate of new lesions differed between cohorts (Table). Progression due to increased target lesions occurred in 60.7% (65/107) of Cohort A and 77.8% (98/126) of Cohort B patients. Conclusions: New lesion development was more frequent with Nivo-Ipi, with lymph nodes being the most common site of new lesions of mRCC across both cohorts. Cohort An=107 Cohort Bn=126 Baseline At the time of progression Baseline At the time of progression Patients with new lesions, n (%) - 42 (39.3) - 28 (22.2) Sites of metastases, n (%) Lung 73 (68) 81 (76) 76 (60) 79 (63) Lymph node 55 (51) 94 (88) 68 (54) 81 (64) Liver 27 (25) 28 (26) 39 (31) 47 (37) Bone 14 (13) 26 (24) 36 (29) 41 (33) Adrenal gland 19 (18) 20 (19) 20 (16) 28 (22) Contralateral kidney 5 (5) 5 (5) 1 (0.8) 2 (1.6) Brain 1 (1) 2 (2) 4 (3) 4 (3) Soft tissues 4 (4) 4 (4) 1 (0.8) 1 (0.8) Pancreas 2 (2) 3 (3) 0 (0) 2 (1.6) Other* 5 (5) 7 (7) 9 (7) 9 (7) *Thyroid gland, pleura, peritoneum, ovary, breast.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (12)
Ilya Tsimafeyeu
Bureau for Cancer Research - BUCARE, Moscow office, Moscow, Russian Federation
Fuad Guliyev
National Center of Oncology, Baku, Azerbaijan
Gunel Musayeva
National Center of Oncology, Baku, Azerbaijan
Ramil Abdrakhmanov
Kazakh Institute of Oncology and Radiology, Almaty, Kazakhstan
Viacheslav Chubenko
Napalkov State Budgetary Healthcare Institution "Saint-Petersburg Clinical Scientific and Practical Center for Specialised Types of Medical Care (Oncological)", Saint-Petersburg, Russian Federation
Olga Baklanova
Irkutsk Regional Oncology Dispensary, Irkutsk, Russian Federation
Ruslan Zukov
20Krasnoyarsk Regional Oncology Dispensary, Krasnoyarsk, Russian Federation
Vladislav Petkau
Sverdlovskiy Regional Oncological Dispensary, Ekaterinburg, Russian Federation
Igor Myslevtsev
S.P. Botkin Multidisciplinary Scientific and Clinical Center, Moscow, Russian Federation
Alisher Kahharov
Tashkent State Dental Institute, Tashkent, Uzbekistan
Bakytzhan Ongarbayev
Kazakh Institute of Oncology and Radiology, Almaty, Kazakhstan
Dilyara Kaidarova