Evidence map›Paper›PMID 41341318›Full record

ArticleCureus2025

Oncological Outcomes of Immature Ovarian Teratoma: A 15-Year Report From a Cancer Center.

Maria Habib, Kheyal Khalil, Zain Tayyab, Hafsa Atiq, Muhammad Usman, Shahid Khattak, Aamir Syed

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Article in Cureus, 2025. 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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1 · What the graph read from it

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Maria HabibObstetrics and Gynaecology, Ashford and St Peter's Hospitals NHS Foundation Trust, Surrey, GBR.
Kheyal KhalilSurgical Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, PAK.
Zain TayyabSurgical Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, PAK.
Hafsa AtiqSurgical Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, PAK.
Muhammad UsmanGynae-Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, PAK.
Shahid KhattakSurgical Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, PAK.
Aamir SyedSurgical Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, PAK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmature ovarian teratomas (IOTs) are a rare ovarian tumor, with recurrence rates varying widely depending on age and grade. Thus far, debate exists regarding the management of IOTs, especially of their recurrences.

objectiveTo review clinical characteristics and oncological outcomes of immature ovarian teratoma following primary and secondary surgery. METHODOLOGY: This retrospective cohort study was conducted in the department of surgical oncology, Shaukat Khanum Memorial Cancer Hospital & Research Centre, Lahore, Pakistan, between July 2008 and June 2023 (15 years). All patients with pathological confirmation of IOTs were included in the study. Women were excluded if (1) details of baseline characteristics or primary treatment were unavailable, and (2) if there was no follow-up data. Non-probability consecutive sampling technique was used for the recruitment of patients. Patient demographics and disease characteristics were summarized using descriptive statistics. Progression-free survival time and overall survival were calculated from the time of surgery to the date of recurrence or the date of death. The Kaplan-Meier method was used for survival curves. Statistical analysis was performed using Statistical Product and Service Solutions (SPSS, version 23; IBM SPSS Statistics for Windows, Armonk, NY).

resultsOf 37 women, most of the patients belonged to an age group of 21-30 years (N-16, 43.2%). Stage 1a (N-18, 48.6%) and grade III disease (N-12, 32.4%). Laparotomy was performed in 91.9% (N-34) of the patients. The majority of the patients underwent unilateral salpingo-oophorectomy (N-27, 73%). Twenty-seven patients received adjuvant chemotherapy (73%). Relapse occurred in 31.5% (N-13) of the patients. However, the most common site of relapse was the liver (N-5, 13.5%). Secondary cytoreductive surgery was done in eight (61.5%) patients, while the rest of the cohort received adjuvant chemotherapy. Overall survival after a mean follow-up of 43 months was 81%.

conclusionIOT occurs most commonly in young women. The most common presentation is early stage but high grade, and fertility-sparing surgery has good oncological outcomes. With secondary cytoreductive surgery and platinum-based chemotherapy, it is possible to salvage most recurrences.

Indexed as

adjuvant chemotherapycytoreductive surgery (crs)immature ovarian teratomasoncological outcomesprimary debulking surgery

Identifiers

PMID41341318
PMCPMC12670979

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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.