Evidence map›Paper›PMID 41316348›Full record

ArticleWorld journal of surgical oncology2025

Pathological complete response to pembrolizumab in recurrent retroperitoneal dedifferentiated liposarcoma with high tumor mutational burden: a case report.

Shun Abe, Qiliang Zhou, Takashi Ariizumi, Mika Sugai, Yusuke Kawachi, Takuya Ando, Yuki Hirose, Hirosuke Ishikawa, Kohei Miura, Hiroshi Ichikawa and 6 more

Abstract readCase Reports
In one paragraph

Article in World journal of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Shun AbeDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan. s-abe@med.niigata-u.ac.jp.
Qiliang ZhouDivision of Medical Oncology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Takashi AriizumiDivision of Orthopedic Surgery, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Mika SugaiDivision of Medical Technology, Niigata University Graduate School of Health Sciences, Niigata, Japan.
Yusuke KawachiDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Takuya AndoDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Yuki HiroseDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Hirosuke IshikawaDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Kohei MiuraDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Hiroshi IchikawaDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Kazuyasu TakizawaDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Yoshifumi ShimadaDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Jun SakataDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Takashi KobayashiDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.
Hiroyuki KawashimaDivision of Orthopedic Surgery, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Toshifumi WakaiDivision of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDedifferentiated liposarcoma (DDLPS), a common subtype of retroperitoneal soft tissue sarcoma, generally shows a limited response to conventional chemotherapy. Recently, immune checkpoint inhibitors (ICIs) have demonstrated promising activity against DDLPS. However, predictive biomarkers for response remain unclear. We present a case of recurrent retroperitoneal DDLPS with a high tumor mutational burden (TMB), demonstrating a pathological complete response (pCR) to pembrolizumab. We also explore the association between the response to ICIs and the tumor microenvironment, including programmed death-ligand 1 (PD-L1), tumor-infiltrating lymphocytes (TILs), and tumor-associated macrophages (TAMs). CASE PRESENTATION: A 73-year-old man undergoing hormone therapy for metastatic prostate cancer was incidentally found to have a multilobulated retroperitoneal tumor in the right iliac fossa during routine follow-up imaging. He underwent macroscopically complete removal of the tumor, which was histologically diagnosed as DDLPS. Eight months later, recurrence with peritoneal dissemination was detected. He received doxorubicin (6 cycles) followed by pazopanib (13 weeks) and eribulin (3 cycles). The response to all these treatments was progressive disease. Comprehensive genomic profiling of the primary tumor revealed high TMB (13 mutations/megabase). Pembrolizumab 400 mg was administered every 6 weeks. After 11 cycles, imaging revealed a partial response with a 56.7% decrease in target lesions. However, discontinuation of pembrolizumab was required due to ICI-induced inflammatory arthritis. In a second radical surgery, 9 disseminated lesions were excised. Histological examination showed extensive hyalinization and necrosis with no residual viable tumor cells, indicating pCR. He remains alive and well without disease 15 months after the second surgery. Immunohistochemistry of the primary tumor revealed negative PD-L1 expression, low TIL density, and markedly high TAM density.

conclusionsThis is the first reported case of recurrent retroperitoneal DDLPS with high TMB achieving pCR to pembrolizumab. High TMB and high TAM density in the tumor microenvironment may be predictive biomarkers for the response to ICIs in DDLPS.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalLiposarcomaNeoplasm Recurrence, LocalRetroperitoneal NeoplasmsAgedB7-H1 AntigenBiomarkers, TumorHumansMaleMutationPrognosisTumor MicroenvironmentAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenBiomarkers, TumorpembrolizumabDedifferentiated liposarcomaPathological complete responsePembrolizumabProgrammed death-ligand 1Tumor-associated macrophageTumor-infiltrating lymphocyteTumor microenvironmentTumor mutational burden

Identifiers

PMID41316348
PMCPMC12664158

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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.