Evidence map›Paper›PMID 35581611›Full record

ArticleJournal of medical case reports2022

Complete response to combination therapy using nivolumab and ipilimumab for metastatic, sarcomatoid collecting duct carcinoma presenting with high expression of programmed death-ligand 1: a case report.

Takayoshi Fuu, Kazuyoshi Iijima, Yukiko Kusama, Toshiaki Otsuki, Haruaki Kato

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% of its field
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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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

5 authors at 2 institutions in 1 country.

Takayoshi FuuDepartment of Urology, Nagano Municipal Hospital, 1333-1, Tomitake, Nagano, Nagano, Japan. gjerryfuu@gmail.com.ORCID http://orcid.org/0000-0002-6199-1608
Kazuyoshi IijimaDepartment of Urology, Nagano Municipal Hospital, 1333-1, Tomitake, Nagano, Nagano, Japan.
Yukiko KusamaDepartment of Pathology, Nagano Municipal Hospital, 1333-1, Tomitake, Nagano, Nagano, Japan.
Toshiaki OtsukiDepartment of Pathology, Shinshu University Hospital, 3-1-1, Asahi, Matsumoto, Nagano, Japan.
Haruaki KatoDepartment of Urology, Nagano Municipal Hospital, 1333-1, Tomitake, Nagano, Nagano, Japan.
Nagano Municipal Hospital · JPShinshu University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCollecting duct carcinoma and sarcomatoid renal cell carcinoma are tumors with poor prognosis. Immune checkpoint inhibitors have been established as the standard treatment for advanced renal cell carcinoma. Some cases of remission of collecting duct carcinoma and sarcomatoid renal cell carcinoma have been reported using immune checkpoint inhibitor interventions. Specifically, sarcomatoid renal cell carcinoma expresses high levels of programmed death-ligand 1, an immune checkpoint protein, and immune checkpoint inhibitors have been reported to be highly effective for treating sarcomatoid renal cell carcinoma. CASE PRESENTATION: We describe the case of a 70-year-old Japanese male who underwent radical right nephrectomy for a right renal mass identified on computed tomography. The pathological examination demonstrated that the renal mass was urothelial carcinoma and collecting duct carcinoma with sarcomatoid changes, and programmed death-ligand 1 was highly expressed with a tumor proportion score of more than 10%. There was no evident submucosal connective tissue invasion in the urothelial carcinoma component, and collecting duct carcinoma was diagnosed as primary cancer. The tumor-node-metastasis classification was pT3aN0, venous invasion 1, lymphovascular invasion 0, and Fuhrman nuclear grade 4. Two months after the nephrectomy, multiple metastases were observed in both lungs, the right hilar lymph node, and the S6 segment of the right liver lobe. We initiated first-line combination therapy with nivolumab (240 mg, fixed dose) and ipilimumab (1 mg/kg). One day after administration, the patient developed drug-induced interstitial pneumonia, thus we applied steroid injections. After one administration of immunotherapy, the metastatic lesion showed complete response within 6 months, which was maintained after 3 years.

conclusionWe report the first case of complete response to a single dose of combination therapy with nivolumab and ipilimumab for metastatic collecting duct carcinoma with sarcomatoid changes and high expression of programmed death-ligand 1. This case suggests high expectations for immune checkpoint inhibitors as treatment for sarcomatoid-transformed renal carcinoma tumors that express high levels of programmed death-ligand 1.

Indexed as

Carcinoma, Renal CellCarcinoma, Transitional CellKidney NeoplasmsNeoplasms, Second PrimarySarcomaSoft Tissue NeoplasmsUrinary Bladder NeoplasmsAgedB7-H1 AntigenHumansImmune Checkpoint InhibitorsIpilimumabMaleNivolumabB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsIpilimumabNivolumabCase reportCollecting duct carcinomaImmune checkpoint inhibitorsImmune-related adverse eventsProgrammed death-ligand 1Sarcomatoid renal cell carcinoma

Identifiers

PMID35581611
PMCPMC9116048
OpenAlexW4280536243

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.