Evidence map›Paper›PMID 37296915›Full record

ReviewCancers2023

Primary Ovarian Leiomyosarcoma Is a Very Rare Entity: A Narrative Review of the Literature.

Vincenzo Dario Mandato, Federica Torricelli, Valentina Mastrofilippo, Andrea Palicelli, Luigi Costagliola, Lorenzo Aguzzoli

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06749600 (Clinical Management and Outcomes of Primary Ovarian Leiomyosarcoma), which is not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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.

NCT06749600 recruitingnot on this mapstarted 2024, after this paper: background citation

Clinical Management and Outcomes of Primary Ovarian Leiomyosarcoma

TypeobservationalSponsorAzienda USL Reggio Emilia - IRCCSRan2024 to 2027Enrolled30ConditionsPrimary Ovarian Leiomyosarcoma
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Primary ovarian leiomyosarcoma: a case report.The Journal of international medical research · 2024
    Article
  6. Review
  7. Article
  8. 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

6 authors at 2 institutions in 1 country.

Vincenzo Dario MandatoUnit of Obstetrics and Oncological Gynecology, Azienda USL-IRCCS di, 42122 Reggio Emilia, Italy.ORCID 0000-0001-6537-1046
Federica TorricelliLaboratory of Translational Research, Azienda USL-IRCCS di, 42122 Reggio Emilia, Italy.
Valentina MastrofilippoUnit of Obstetrics and Oncological Gynecology, Azienda USL-IRCCS di, 42122 Reggio Emilia, Italy.
Andrea PalicelliUnit of Pathology, Azienda USL-IRCCS di, 42122 Reggio Emilia, Italy.ORCID 0000-0003-2299-5160
Luigi CostagliolaUnit of Obstetrics and Gynecology, Santa Maria delle Grazie Hospital, 80100 Naples, Italy.
Lorenzo AguzzoliUnit of Obstetrics and Oncological Gynecology, Azienda USL-IRCCS di, 42122 Reggio Emilia, Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITAzienda Sanitaria Unità Locale di Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrimary ovarian leiomyosarcoma is a very rare malignancy characterized by unclear management and poor survival. We reviewed all the cases of primary ovarian leiomyosarcoma to identify prognostic factors and the best treatment.

methodsWe collected and analyzed the articles published in the English literature regarding primary ovarian leiomyosarcoma from January 1951 to September 2022, using PubMed research. Clinical and pathological characteristics, different treatments and outcomes were analyzed.

results113 cases of primary ovarian leiomyosarcoma were included. Most patients received surgical resection, associated with lymphadenectomy in 12.5% of cases. About 40% of patients received chemotherapy. Follow-up information was available for 100/113 (88.5%) patients. Stage and mitotic count were confirmed to affect survival, and lymphadenectomy and chemotherapy were associated with a better survival rate. A total of 43.4% of patients relapsed, and their mean disease-free survival was 12.5 months.

conclusionsPrimary ovarian leiomyosarcomas are more common in women in their 50s (mean age 53 years). Most of them are at an early stage at presentation. Advanced stage and mitotic count showed a detrimental effect on survival. Surgical excision associated with lymphadenectomy and chemotherapy are associated with increased survival. An international registry could help collect clear and reliable data to standardize the diagnosis and treatment.

Indexed as

chemotherapylymphadenectomymitotic countprimary ovarian leiomyosarcomareviewstagesurvivalsymptomstreatment

Identifiers

PMID37296915
PMCPMC10252074
OpenAlexW4378619537

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.