Anlotinib + Benmelstobart vs Surgery for Patients With Localized Renal Cell Carcinoma Scheduled to Undergo Partial Nephrectomy

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorTianjin Medical University Cancer Institute and Hospital

About this trial

Evaluation of long-term renal function improvement, surgical safety, as well as efficacy and safety of preoperative anlotinib hydrochloride capsules combined with benmelstobart injection versus surgery in patients with localized renal cell carcinoma undergoing partial nephrectomy

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged between 18 and 75 years, inclusive.

Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

Subjects with newly diagnosed cT1bN0M0 renal cell carcinoma (RCC) scheduled to undergo partial nephrectomy.

Have at least one measurable lesion as defined by the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.

Disqualifiers

Subjects with a solitary kidney tumor.

Subjects with bilateral renal tumors or unilateral multiple renal tumors (n ≥ 2).

Subjects with hereditary or familial renal tumors (e.g., von Hippel-Lindau [VHL] disease).

Subjects with a prior history of renal transplantation.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Anlotinib hydrochloride + Benmelstobart + Partial nephrectomy

    Drug

    Patients receive neoadjuvant therapy with oral anlotinib hydrochloride capsules and intravenous benmelstobart injection, followed by partial nephrectomy for localized renal cell carcinoma.

  • Partial nephrectomy

    Procedure/Surgery

    Patients receive upfront partial nephrectomy without neoadjuvant therapy, as the standard treatment for localized renal cell carcinoma.

Treatment groups

144 Participants
are divided into 2 treatment groups
Group A: Anlotinib + BenmelstobartExperimental treatment 1 intervention
Group B: Upfront partial nephrectomy (standard care)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pentafecta Achievement

It includes: negative surgical margin, warm ischemia time (WIT) ≤ 25 minutes, no perioperative complications, estimated glomerular filtration rate (eGFR) preservation ≥ 90% at 9-12 months postoperatively, and no increase in chronic kidney disease (CKD) stage at 9-12 months postoperatively. The eGFR preservation rate is calculated as the percentage of the postoperative eGFR relative to the preoperative baseline eGFR. An increase in CKD stage is defined as progression to Stage III, IV, or V; progression from Stage I to Stage II is not considered an increase in CKD stage.

Time frame
Through study completion, an average of 1 year

Secondary outcomes

1

Primary tumor partial response (PR) rate in the experimental arm

Time frame
Through study completion, an average of 1 year
2

Safety

Number of participants with treatment-related adverse events as assessed by CTCAE 6.0 To further describe safety and assess toxicities encountered with the use of the proposed treatment regimen in participants

Time frame
Through study completion, an average of 2 years
3

2-year DFS Rate

2-year Disease-Free Survival Rate

Time frame
2-years
4

R.E.N.A.L. score changes in the experimental group

The R.E.N.A.L. Nephrometry Score is a 4-12 point anatomical classification system for renal tumors, with each letter representing a key feature scored as 1, 2, or 3 points, as follows: (R) Radius (Maximum tumor diameter, cm); (E) Exophytic/endophytic properties (Tumor growth pattern); (N) Nearness to the collecting system or renal sinus (Tumor distance to collecting system/renal sinus, mm); (A) Anterior/posterior location; (L) Location relative to the polar line (Relationship to renal polar line; suffix (h) is added if the tumor is adjacent to major renal artery or vein)

Time frame
Through study completion, an average of 1 year

Other outcomes

Sponsors and contacts

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