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32MO Long-term follow-up shows improved outcomes for stage IC-IV MOGCTs in a multicentre international analysis

32MO Long-term follow-up shows improved outcomes for stage IC-IV MOGCTs in a multicentre international analysis
32MO Long-term follow-up shows improved outcomes for stage IC-IV MOGCTs in a multicentre international analysis
Background: malignant ovarian germ cell tumors (MOGCTs) are rare, aggressive malignancies predominantly affecting young women. The literature mainly consists of small studies suggesting advanced stage as an adverse prognostic factor. Few long-term follow-up data are available, showing 65% overall survival in stage IV disease. Here, we examine a large international series to define long-term prognosis.

Methods: we analysed data from 254 FIGO stage IC/M-IV MOGCT patients, requiring surgery and chemotherapy between 1971 and 2018 at Charing Cross Hospital and Mount Vernon Cancer Center (UK) and the Multicentre Italian Trials in Ovarian Cancer (MITO) centres.

Results: most patients (87.8%, n=223) received surgery as initial treatment (50.4%, n=128 fertility-sparing, 37.4%, n=95 non-sparing). Chemotherapy mainly consisted of BEP (48%, n=122) and POMB/ACE (42.5%, n=108). First-line treatment resulted in a complete response in 84.6% (n=215), partial response or stable disease in 7.9% (n=20), while 4.7% (n=12) progressed. Overall, 37 patients (14.6%) died of disease, with the last death recorded 8 years after initial diagnosis. 5-, 10-, and 20-year estimated cancer-specific survival (CSS) rates were 85.9% (95%CI, 80.6-89.8), 83.2% (95%CI, 77.3-87.7), and 83.2% (95%CI, 77.3-87.7), respectively. According to FIGO-stage, 10-year estimated CSS rates were 92.3% (95%CI, 82.1-96.8) for stage IC/M, 79.5% (95%CI, 56.2-91.3) for stage II, 79.4%, (95%CI, 69.5-86.4) for stage III and 79.4% (95%CI, 61.5-89.7) for stage IV. The 10-year estimated CSS for dysgerminoma and Grade 2/3 immature teratoma was 94.7% (95%CI, 84.4-98.3) and 97.5% (95%CI, 83.4-99.6), respectively. For other histologies, CSS was significantly lower: 77.8% (95%CI, 61.4-87.9) for mixed MOGCTs; 71.7% (95%CI, 58.4-81.4) for yolk sac tumors (YST); 50.0% (95%CI, 5.9-84.5) for choriocarcinoma; and 33.3% (95%CI, 1.0-77.4) for embryonal carcinoma, p<0.001.

Conclusions: our analysis shows (1) improved outcomes of patients with stage IC-IV MOGCTs, compared to previously published data with 80% long-term survival in stage IV disease and (2) a need for long term follow up, as late relapses can occur.
3050-4619
Bergamini, A.
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Suyanto, S.
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Savva, C.
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Maher, E.
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Kaur, B.
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Sarwar, N.
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Caldwell, R.D.
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Rustin, G.J.S.
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Ghorani, E.
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Sharma, A.
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Fotopoulou, C.
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Smith, J.R.
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Saso, S.
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Greenwood, M.
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Cormio, G.
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Fagotti, A.
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Cassani, C.
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Scarfone, G.
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Pignata, S.
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Seckl, M.J.
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Bergamini, A.
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Suyanto, S.
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Savva, C.
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Maher, E.
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Kaur, B.
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Sarwar, N.
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Caldwell, R.D.
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Rustin, G.J.S.
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Ghorani, E.
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Sharma, A.
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Fotopoulou, C.
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Smith, J.R.
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Saso, S.
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Greenwood, M.
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Cormio, G.
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Fagotti, A.
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Cassani, C.
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Scarfone, G.
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Pignata, S.
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Seckl, M.J.
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Bergamini, A., Suyanto, S., Savva, C., Maher, E., Kaur, B., Sarwar, N., Caldwell, R.D., Rustin, G.J.S., Ghorani, E., Sharma, A., Fotopoulou, C., Smith, J.R., Saso, S., Greenwood, M., Cormio, G., Fagotti, A., Cassani, C., Scarfone, G., Pignata, S. and Seckl, M.J. (2026) 32MO Long-term follow-up shows improved outcomes for stage IC-IV MOGCTs in a multicentre international analysis. ESMO Rare Cancers. (doi:10.1016/j.esmorc.2026.100239).

Record type: Meeting abstract

Abstract

Background: malignant ovarian germ cell tumors (MOGCTs) are rare, aggressive malignancies predominantly affecting young women. The literature mainly consists of small studies suggesting advanced stage as an adverse prognostic factor. Few long-term follow-up data are available, showing 65% overall survival in stage IV disease. Here, we examine a large international series to define long-term prognosis.

Methods: we analysed data from 254 FIGO stage IC/M-IV MOGCT patients, requiring surgery and chemotherapy between 1971 and 2018 at Charing Cross Hospital and Mount Vernon Cancer Center (UK) and the Multicentre Italian Trials in Ovarian Cancer (MITO) centres.

Results: most patients (87.8%, n=223) received surgery as initial treatment (50.4%, n=128 fertility-sparing, 37.4%, n=95 non-sparing). Chemotherapy mainly consisted of BEP (48%, n=122) and POMB/ACE (42.5%, n=108). First-line treatment resulted in a complete response in 84.6% (n=215), partial response or stable disease in 7.9% (n=20), while 4.7% (n=12) progressed. Overall, 37 patients (14.6%) died of disease, with the last death recorded 8 years after initial diagnosis. 5-, 10-, and 20-year estimated cancer-specific survival (CSS) rates were 85.9% (95%CI, 80.6-89.8), 83.2% (95%CI, 77.3-87.7), and 83.2% (95%CI, 77.3-87.7), respectively. According to FIGO-stage, 10-year estimated CSS rates were 92.3% (95%CI, 82.1-96.8) for stage IC/M, 79.5% (95%CI, 56.2-91.3) for stage II, 79.4%, (95%CI, 69.5-86.4) for stage III and 79.4% (95%CI, 61.5-89.7) for stage IV. The 10-year estimated CSS for dysgerminoma and Grade 2/3 immature teratoma was 94.7% (95%CI, 84.4-98.3) and 97.5% (95%CI, 83.4-99.6), respectively. For other histologies, CSS was significantly lower: 77.8% (95%CI, 61.4-87.9) for mixed MOGCTs; 71.7% (95%CI, 58.4-81.4) for yolk sac tumors (YST); 50.0% (95%CI, 5.9-84.5) for choriocarcinoma; and 33.3% (95%CI, 1.0-77.4) for embryonal carcinoma, p<0.001.

Conclusions: our analysis shows (1) improved outcomes of patients with stage IC-IV MOGCTs, compared to previously published data with 80% long-term survival in stage IV disease and (2) a need for long term follow up, as late relapses can occur.

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e-pub ahead of print date: 9 March 2026
Published date: 14 March 2026

Identifiers

Local EPrints ID: 510919
URI: http://eprints.soton.ac.uk/id/eprint/510919
ISSN: 3050-4619
PURE UUID: 6dd5ae73-2b7c-40cb-9a8e-f322d07a0c70
ORCID for C. Savva: ORCID iD orcid.org/0000-0003-0805-4719

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Date deposited: 27 Apr 2026 16:34
Last modified: 01 May 2026 16:49

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Contributors

Author: A. Bergamini
Author: S. Suyanto
Author: C. Savva ORCID iD
Author: E. Maher
Author: B. Kaur
Author: N. Sarwar
Author: R.D. Caldwell
Author: G.J.S. Rustin
Author: E. Ghorani
Author: A. Sharma
Author: C. Fotopoulou
Author: J.R. Smith
Author: S. Saso
Author: M. Greenwood
Author: G. Cormio
Author: A. Fagotti
Author: C. Cassani
Author: G. Scarfone
Author: S. Pignata
Author: M.J. Seckl

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