Evidence map›Paper›PMID 41912437›Full record

ArticleThe oncologist2026

Association between pathologic chemotherapy response score and pattern of recurrence in advanced high-grade serous ovarian cancer.

Francesco Mezzapesa, Antonio De Leo, Camelia Alexandra Coada, Elisabetta Pia Bilancia, Lucia Genovesi, Giulia Mantovani, Caterina Ravaioli, Daniela Turchetti, Dario De Biase, Daniela Rubino and 3 more

Abstract read
In one paragraph

Article in The oncologist, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

13 authors.

Francesco MezzapesaDivision of Oncologic Gynecology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.ORCID 0009-0007-9653-6692
Antonio De LeoDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Camelia Alexandra CoadaDepartment of Morpho-functional sciences, "Iuliu Hațieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Elisabetta Pia BilanciaDivision of Oncologic Gynecology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Lucia GenovesiDivision of Oncologic Gynecology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Giulia MantovaniDivision of Oncologic Gynecology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Caterina RavaioliDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Daniela TurchettiDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Dario De BiaseSolid Tumor Molecular Pathology Laboratory, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Daniela RubinoAddarii Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy.
Claudio ZamagniAddarii Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy.
Pierandrea De IacoDivision of Oncologic Gynecology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Anna Myriam PerroneDivision of Oncologic Gynecology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.

Funding

Italian Ministry of Health RC-2025-2795987
6 · The paper itself

Abstract

backgroundChemotherapy Response Score (CRS) is a three-tier histopathologic system evaluating response to neoadjuvant chemotherapy (NACT) in high-grade serous ovarian cancer (HGSOC).

methodsWe evaluated recurrence patterns and survival outcomes in advanced-stage HGSOC patients treated with NACT and interval debulking surgery (IDS) between 2015 and 2024.

resultsAmong 238 patients, CRS3 was most frequent (43.3%) and was associated higher complete cytoreduction (CC0) rates (93%) compared to CRS2 (81%) and CRS1 (57%) (p < 0.001). Median follow-up was 35 months (IQR 12.6-42.2). Median progression-free survival (PFS) was 40.4 months for CRS3, 23.4 for CRS2, and 21.5 for CRS1 (p = 0.001). Among 109 (45.7%) patients who relapsed, 25 (23%) presented with oligometastatic disease (≤5 lesions), more frequently in CRS3 (46%) than CRS2 (8.9%) or CRS1 (15%) (p < 0.001). Specifically, peritoneal (p = 0.002) and nodal (p = 0.05) oligorecurrences were more common in the CRS3 group. CRS3 predicted oligometastatic recurrence (OR = 4.89; p = 0.008) and was associated with increased use of locoregional therapies (surgery or radiotherapy) at relapse (p = 0.014). Median overall survival (OS) was 93.9, 37.2, and 31.7 months for CRS3, CRS2, and CRS1, respectively (p < 0.001).

conclusionsCRS3 predicts lower recurrence risk, increased rates of oligometastatic relapse, and greater use of locoregional treatments in patients with recurrent HGSOC after NACT and IDS.

Indexed as

Cystadenocarcinoma, SerousNeoplasm Recurrence, LocalOvarian NeoplasmsAgedCytoreduction Surgical ProceduresFemaleHumansMiddle AgedNeoadjuvant TherapyNeoplasm GradingCRSneoadjuvant chemotherapyoligometastasisovarian cancerPARPi

Identifiers

PMID41912437
PMCPMC13049597

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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.