Evidence map›Paper›PMID 39218752›Full record

ArticleClinical genitourinary cancer2024

Pathological Response and Outcomes in Patients With Metastatic Renal Cell Carcinoma (mRCC) Receiving Immunotherapy-Based Therapies and Undergoing Deferred Cytoreductive Nephrectomy (CN).

Damla Gunenc, Wadih Issa, Thomas Gerald, Qinhan Zhou, Song Zhang, I Chidera Ibezue, Raj Bhanvadia, Isamu Tachibana, James Brugarolas, Hans Hammers and 9 more

Abstract read
In one paragraph

Article in Clinical genitourinary cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Navigating advanced renal cell carcinoma in the era of artificial intelligence.Cancer imaging : the official publication of the International Cancer Imaging Society · 2025
    Review
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Damla GunencUniversity of Texas Southwestern, Department of Internal Medicine, Division of Hematology and Oncology, Dallas, TX.
Wadih IssaUniversity of Texas Southwestern, Department of Internal Medicine, Division of Hematology and Oncology, Dallas, TX.
Thomas GeraldUniversity of Texas Southwestern, Department of Urology, Dallas, TX.
Qinhan ZhouUniversity of Texas Southwestern, Department of Internal Medicine, Division of Hematology and Oncology, Dallas, TX.
Song ZhangPeter O'Donnell Jr. School of Public Health, University of Texas Southwestern, Dallas, TX.
I Chidera IbezueUniversity of Texas Southwestern, Department of Urology, Dallas, TX.
Raj BhanvadiaUniversity of Texas Southwestern, Department of Urology, Dallas, TX.
Isamu TachibanaUniversity of Texas Southwestern, Department of Urology, Dallas, TX.
James BrugarolasUniversity of Texas Southwestern, Department of Internal Medicine, Division of Hematology and Oncology, Dallas, TX.
Hans HammersUniversity of Texas Southwestern, Department of Internal Medicine, Division of Hematology and Oncology, Dallas, TX.
Qian QinUniversity of Texas Southwestern, Department of Internal Medicine, Division of Hematology and Oncology, Dallas, TX.
Payal KapurUniversity of Texas Southwestern, Department of Pathology, Dallas, TX.
Solomon WolduUniversity of Texas Southwestern, Department of Urology, Dallas, TX.
Kris GastonUniversity of Texas Southwestern, Department of Urology, Dallas, TX.
Yair LotanUniversity of Texas Southwestern, Department of Urology, Dallas, TX.
Jeffrey CadedduUniversity of Texas Southwestern, Department of Urology, Dallas, TX.
Andrew Z WangUniversity of Texas Southwestern, Department of Radiation Oncology, Dallas, TX.
Vitaly MargulisUniversity of Texas Southwestern, Department of Urology, Dallas, TX.
Tian ZhangUniversity of Texas Southwestern, Department of Internal Medicine, Division of Hematology and Oncology, Dallas, TX. Electronic address: tian.zhang@utsouthwestern.edu.

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
NCI NIH HHS P30 CA142543
6 · The paper itself

Abstract

In this study we evaluated outcomes of patients with metastatic renal cell carcinoma who received immunotherapy before surgery. We found that receiving immunotherapy combinations before surgery can offer patients benefits in reducing tumor size and improving disease control.

backgroundImmunotherapy (IO) has improved outcomes for patients with metastatic renal cell carcinoma (mRCC). However, the timing of surgical intervention for cytoreductive nephrectomy (CN) is still controversial for this group of patients. PATIENTS AND

methodsWe identified patients with mRCC receiving IO-based therapies and undergoing CN. Patients were divided into 2 cohorts: those who underwent upfront CN and those who underwent deferred CN. Pathologic and radiographic features along with clinical outcomes were systematically collected. Comparisons were performed using Chi-square test, paired t-Test or Mann-Whitney-U test. Progression Free survival (PFS) and Overall Survival (OS) were estimated using the Kaplan-Meier method.

resultsFifty-one patients with mRCC were included, with a median follow-up of 21 months. 38 (74.5%) patients received IO-based therapies prior to CN, while 13 (25.5%) patients underwent up-front CN. IO-based therapies reduced median tumor size from pretreatment 10 cm to 8.6 cm post-treatment when given prior to CN. IO-TKI had a trend toward higher tumor shrinkage (-2.3 vs -1.2 cm). Pathologic T downstaging occurred in 42% (n=16) of patients, 11% (n=4) of whom had pT0 disease. Thrombus downstaging occurred in 13% (n=6) of patients, all with either partial response (PR) or complete response (CR) in metastases. PFS (HR=0.7, 95% CI 0.29-1.98, p=0.58) and OS (HR 0.4, 95% CI 0.13-1.57, p=0.21) were not statistically significant between 2 cohorts.

conclusionsIO-based therapies, particularly IO-TKIs, resulted in pathologic necrosis and reductions in tumor size prior to deferred CN. PFS and OS were similar for patients who received either upfront IO-based therapy or after CN.

Indexed as

Carcinoma, Renal CellCytoreduction Surgical ProceduresKidney NeoplasmsNephrectomyAdultAgedFemaleFollow-Up StudiesHumansImmunotherapyMaleMiddle AgedProgression-Free SurvivalRetrospective StudiesTreatment OutcomeConsolidative nephrectomyImmunotherapyIVC ThrombusKidney cancerPerioperative treatment

Identifiers

PMID39218752
PMCPMC12160930

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.