Evidence map›Paper›PMID 42147549›Full record

ArticleCureus2026

Spontaneous Regression of Soft Tissue Sarcoma Following Biopsy: A Case Report and Systematic Review of the Literature.

Megan C Gannon, Rachel M Gabor, Anushka Gupta, Cheshta Gupta, Ruhi M Shah, Rohit Sharma

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. 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

6 authors.

Megan C GannonDepartment of Surgery, Marshfield Clinic Health System, Marshfield, USA.
Rachel M GaborCenter for Clinical Epidemiology and Population Health, Marshfield Clinic Research Institute, Marshfield Clinic Health System, Marshfield, USA.
Anushka GuptaDepartment of Physiology and Medical Cell Biology, Western University, London, CAN.
Cheshta GuptaDepartment of Physiology and Medical Cell Biology, Western University, London, CAN.
Ruhi M ShahDepartment of Physiology and Medical Cell Biology, Western University, London, CAN.
Rohit SharmaDepartment of Surgery, Marshfield Clinic Health System, Marshfield, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spontaneous regression (SR) of malignancy is a rare phenomenon offering unique insights into tumor-host immunology. In sarcomas, the incidence, triggers, and clinical implications of SR are poorly characterized. We aim to synthesize the published literature on SR in sarcoma and report a novel case from our institution where diagnostic biopsy triggered a complete pathological response (pCR). We retrospectively reviewed one institutional case: a 59-year-old female with myxofibrosarcoma (MFS) who demonstrated significant regression following core needle biopsy. We subsequently conducted a descriptive systematic review in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, rather than a formal meta-analysis. PubMed, Embase, and Scopus were searched from inception to July 2025 for reports of SR in pathologically confirmed sarcomas without prior cytotoxic therapy. In our institutional experience, the patient (59-year-old female, MFS) achieved complete clinical resolution within weeks of biopsy. Definitive wide excision revealed no viable tumor cells, confirming pCR. The systematic review identified 32 published studies describing 32 unique cases of SR in sarcoma. Diagnostic biopsy was the leading identified trigger (25%). Biopsy-associated regressions occurred more rapidly (median 0.9 months) compared to infection-associated (median five months) or spontaneous cases. Despite clinical regression, 75% of patients in the biopsy-triggered group underwent definitive surgical resection. SR in sarcoma is frequently preceded by an immune-stimulating event, most notably biopsy. While SR provides in vivo evidence of host anti-tumor immunity, the potential for incomplete or transient response underscores that SR should not preclude definitive oncologic management. Ultimately, SR can be conceptualized as a "neoadjuvant immune boost" rather than a definitive cure. Wide surgical resection based on pre-regression tumor fields remains the standard of care to eradicate microscopic disease and ensure oncologic safety.

Indexed as

low-grade myxofibrosarcomasoft-tissue sarcomaspontaneous tumor regressionsystematic review and meta analysisupper extremity sarcoma

Identifiers

PMID42147549
PMCPMC13179007

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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.