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. 2024 Nov;18(11):E371–E386. doi: 10.5489/cuaj.9041

Table 1.

Consensus topic statements and results as voted at the CKCF Meeting on February 10, 2024

Statement Consensus
1. nccRCC tumors should be classified according to the WHO Classification of Tumors, 5th Edition. Achieved: 100%
2. Patients diagnosed with nccRCC following renal mass biopsy should receive similar preoperative investigations and staging as those with ccRCC. Achieved: 97%
3. For patients diagnosed with a ≤2 cm in diameter localized papillary or chromophobe RCC following renal mass biopsy, active surveillance is considered the preferred management option. Achieved: 94%
4. For patients diagnosed with a 2–4 cm in diameter localized papillary or chromophobe RCC following renal mass biopsy, active surveillance or definitive treatment are considered the preferred management options. Achieved: 97%
5. For patients diagnosed with >4 cm in diameter localized papillary or chromophobe RCC following renal mass biopsy, surgery (radical or partial nephrectomy, when feasible) is considered the preferred management option. Achieved: 97%
6. In patients receiving definitive therapy for localized papillary or chromophobe RCC, postoperative surveillance should be similar to ccRCC. Achieved: 94%
7. Patients with resected nccRCC should not be offered adjuvant systemic therapy, unless as part of a clinical trial. Achieved: 100%
8. Most patients diagnosed with nccRCC should be offered germline genetic testing and/or counseling. Achieved: 83%
9. Patients diagnosed with metastatic papillary or chromophobe RCC should be counseled and managed according to the IMDC prognostic model. Achieved: 100%
10. Patients diagnosed with metastatic nccRCC should be offered the opportunity to participate in a clinical trial when available. Achieved: 100%
11. In select patients with de novo metastatic papillary or chromophobe RCC, upfront cytoreductive nephrectomy may be considered after multidisciplinary discussion. Achieved: 100%
12. Patients with de novo metastatic papillary or chromophobe RCC may be considered for deferred cytoreductive nephrectomy depending on the response to initial systemic therapy and after multidisciplinary discussion. Achieved: 100%
13. For patients with oligometastatic papillary or chromophobe RCC, MDT may be considered. Achieved: 100%
14. In patients with metastatic papillary or chromophobe RCC with favorable/intermediaterisk disease and low volume/asymptomatic or minimally symptomatic disease, active surveillance may be considered. Achieved: 100%
15. Patients with metastatic papillary RCC who are not eligible for clinical trials and require systemic therapy should be offered ICI-based combination therapy or monotherapy with cabozantinib. Achieved: 100%
16. In patients with metastatic chromophobe RCC who require systemic therapy, there is currently no standard of care, and these patients should be offered clinical trial enrollment when available. Achieved: 100%
17. Patients with metastatic nccRCC (excluding SMARCB1-deficient renal medullary carcinoma and collecting duct RCC) with sarcomatoid or rhabdoid dedifferentiation should be offered combination ICI-based therapy. Achieved: 100%

ICI: immune checkpoint inhibitor; IMDC: International Metastatic RCC Database Consortium; MDT: metastasis-directed therapy; nccRCC: non-clear cell renal cell carcinoma; WHO: World Health Organization.