Effects of kidney removal in combination with medicine in people with kidney cancer that has spread to other parts of the body

Key messages

People who have kidney removal surgery after receiving interferon immunotherapy (medicine that helps the immune system fight cancer) probably live longer than those who receive interferon immunotherapy without kidney removal surgery.
People who have immediate kidney removal surgery then receive tyrosine kinase inhibitor therapy (medicine that identifies and attacks specific types of cancer cells) may live shorter than those who receive tyrosine kinase inhibitor therapy before kidney removal surgery.
The quality of the included studies is limited, so we have little confidence in most of our findings.

What is metastatic renal cell carcinoma?

Renal cell carcinoma is a kind of cancer that starts in the kidneys. Metastatic means that the cancer has spread from the kidneys to other parts of the body.

What is cytoreductive nephrectomy?

Cytoreductive nephrectomy is a surgery to remove one of the kidneys that has cancer. 'Cyto' means cell, 'reductive' means to reduce, and 'nephrectomy' is a term for taking out a kidney. The aim of this surgery is to help get rid of some of the cancer cells and make other treatments more effective.

What did we want to find out?

Our review question was 'How effective is kidney removal in combination with medicines for people with kidney cancer that has already spread to other parts of the body (outside the kidney) compared with only medicines?' We were mainly interested in the effect of treatment on how long people lived and their quality of life.

What did we do?

We included only studies that allocated people to one of the treatment groups (cytoreductive nephrectomy plus medicine or medicine alone) at random. Most studies examined the effects of treatment on how long people lived.

What did we find?

We found four studies that answered our review question. People included in these studies had metastatic kidney cancer that could not be removed completely by surgery, but they were eligible for cytoreductive nephrectomy. We reported the evidence that is most important to doctors and patients.

We found that people who have cytoreductive nephrectomy after receiving interferon immunotherapy (medicine that helps the immune system fight cancer) probably live longer than people who receive interferon immunotherapy without cytoreductive nephrectomy. We are very uncertain about the effect of cytoreductive nephrectomy plus tyrosine kinase inhibitor (TKI) therapy (medicine that identifies and attacks specific types of cancer cells) compared with TKI therapy alone on survival. Lastly, immediate surgery followed by TKI therapy compared with delayed surgery after TKI therapy may worsen survival. We found no information on quality of life for any of these three comparisons.

We found no studies of surgery combined with newer immunotherapy medicines (called programmed death receptor 1/programmed death ligand 1 immune checkpoint inhibitors), which are now the main medicines used to treat people with metastatic renal cell carcinoma.

What are the limitations of the evidence?

We have little confidence in the evidence because the people in the studies were aware of which treatment they were getting, and because some results suggested cytoreductive nephrectomy could be either beneficial or harmful.

How up to date is this evidence?

The evidence is current to 1 March 2024.

Authors' conclusions: 

CN plus SACT in the form of interferon immunotherapy versus SACT in the form of interferon immunotherapy alone probably increases time to death from any cause. However, we are very uncertain about the effect of CN plus SACT in the form of TKI therapy versus SACT in the form of TKI therapy alone on time to death from any cause. Immediate CN versus deferred CN may decrease time to death from any cause. We found no quality of life data for any of these three comparisons. We also found no evidence to inform any other comparisons, in particular those involving newer immunotherapy agents (programmed death receptor 1 [PD-1]/programmed death ligand 1 [PD-L1] immune checkpoint inhibitors), which have become the backbone of SACT for metastatic renal cell carcinoma. There is an urgent need for RCTs that explore the role of CN in the context of contemporary forms of systemic immunotherapy.

Read the full abstract...
Background: 

Nephrectomy is the surgical removal of all or part of a kidney. When the aim of nephrectomy is to reduce tumor burden in people with established metastatic disease, the procedure is called cytoreductive nephrectomy (CN). CN is typically combined with systemic anticancer therapy (SACT). SACT can be initiated before or immediately after the operation or deferred until radiological signs of disease progression. The benefits and harms of CN are controversial.

Objectives: 

To assess the effects of cytoreductive nephrectomy combined with systemic anticancer therapy versus systemic anticancer therapy alone or watchful waiting in newly diagnosed metastatic renal cell carcinoma.

Search strategy: 

We performed a comprehensive search in the Cochrane Library, MEDLINE, Embase, Scopus, two trial registries, and other gray literature sources up to 1 March 2024. We applied no restrictions on publication language or status.

Selection criteria: 

We included randomized controlled trials (RCTs) that evaluated SACT and CN versus SACT alone or watchful waiting.

Data collection and analysis: 

Two review authors independently selected studies and extracted data. Primary outcomes were time to death from any cause and quality of life. Secondary outcomes were time to disease progression, treatment response, treatment-related mortality, discontinuation due to adverse events, and serious adverse events. We performed statistical analyses using a random-effects model. We rated the certainty of evidence using the GRADE approach.

Main results: 

Our search identified 10 records of four unique RCTs that informed two comparisons. In this abstract, we focus on the results for the two primary outcomes.

Cytoreductive nephrectomy plus systemic anticancer therapy versus systemic anticancer therapy alone

Three RCTs informed this comparison. Due to the considerable heterogeneity when pooling across these studies, we decided to present the results of the prespecified subgroup analysis by type of systemic agent.

Cytoreductive nephrectomy plus interferon immunotherapy versus interferon immunotherapy alone

CN plus interferon immunotherapy compared with interferon immunotherapy alone probably increases time to death from any cause (hazard ratio [HR] 0.68, 95% confidence interval [CI] 0.51 to 0.89; I²= 0%; 2 studies, 326 participants; moderate-certainty evidence). Assuming 820 all-cause deaths at two years' follow-up per 1000 people who receive interferon immunotherapy alone, the effect estimate corresponds to 132 fewer all-cause deaths (237 fewer to 37 fewer) per 1000 people who receive CN plus interferon immunotherapy.

We found no evidence to assess quality of life.

Cytoreductive nephrectomy plus tyrosine kinase inhibitor therapy versus tyrosine kinase inhibitor therapy alone

We are very uncertain about the effect of CN plus tyrosine kinase inhibitor (TKI) therapy compared with TKI therapy alone on time to death from any cause (HR 1.11, 95% CI 0.90 to 1.37; 1 study, 450 participants; very low-certainty evidence). Assuming 574 all-cause deaths at two years' follow-up per 1000 people who receive TKI therapy alone, the effect estimate corresponds to 38 more all-cause deaths (38 fewer to 115 more) per 1000 people who receive CN plus TKI therapy.

We found no evidence to assess quality of life.

Immediate cytoreductive nephrectomy versus deferred cytoreductive nephrectomy

One study evaluated CN followed by TKI therapy (immediate CN) versus three cycles of TKI therapy followed by CN (deferred CN). Immediate CN compared with deferred CN may decrease time to death from any cause (HR 1.63, 95% CI 1.05 to 2.53; 1 study, 99 participants; low-certainty evidence). Assuming 620 all-cause deaths at two years' follow-up per 1000 people who receive deferred CN, the effect estimate corresponds to 173 more all-cause deaths (18 more to 294 more) per 1000 people who receive immediate CN.

We found no evidence to assess quality of life.