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Hyperthermic Intraperitoneal Chemotherapy After Interval Cytoreductive Surgery for Patients With Advanced-Stage Ovarian Cancer Who Had Received Neoadjuvant Chemotherapy

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dc.contributor.authorLee, JY-
dc.contributor.authorLee, YJ-
dc.contributor.authorSon, JH-
dc.contributor.authorKim, S-
dc.contributor.authorChoi, MC-
dc.contributor.authorSuh, DH-
dc.contributor.authorSong, JY-
dc.contributor.authorHong, DG-
dc.contributor.authorKim, MK-
dc.contributor.authorKim, JH-
dc.contributor.authorChang, SJ-
dc.date.accessioned2023-12-11T05:42:25Z-
dc.date.available2023-12-11T05:42:25Z-
dc.date.issued2023-
dc.identifier.issn2168-6254-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/31988-
dc.description.abstractImportance: Hyperthermic intraperitoneal chemotherapy (HIPEC) followed by interval cytoreductive surgery (ICS) has shown survival benefits for patients with advanced-stage ovarian cancer. However, there is still a lack of consensus regarding the integration of HIPEC into clinical practice.

Objective: To evaluate the safety and effectiveness of ICS with HIPEC compared with ICS alone in clinical practice for patients with advanced-stage ovarian cancer.

Design, setting, and participants: This prospective, multicenter, comparative effectiveness cohort study enrolled 205 patients with stage III or IV ovarian cancer who had received at least 3 cycles of neoadjuvant chemotherapy followed by ICS with HIPEC or ICS without HIPEC at 7 Korean Gynecologic Oncology Group institutions between September 1, 2017, and April 22, 2022. Nine patients were excluded because they did not meet the inclusion criteria.

Exposures: Neoadjuvant chemotherapy followed by ICS with HIPEC or ICS without HIPEC.

Main outcomes and measures: The primary end point was progression-free survival (PFS). Overall survival (OS) and the safety profile were the key secondary end points.

Results: This study included 196 patients (median age, 58.0 years [range, 38-82 years]), of whom 109 underwent ICS with HIPEC and 87 underwent ICS without HIPEC. The median duration of follow-up was 28.2 months (range, 3.5-58.6 months). Disease recurrence occurred in 128 patients (65.3%), and 30 patients (15.3%) died. Interval cytoreductive surgery with HIPEC was associated with a significant improvement in median PFS compared with ICS without HIPEC (22.9 months [95% CI, 3.5-58.6 months] vs 14.2 months [95% CI, 4.0-56.2 months]; P = .005) and median OS (not reached [95% CI, 3.5 months to not reached] vs 53.0 [95% CI, 4.6-56.2 months]; P = .002). The frequency of grade 3 or 4 postoperative complications was similar in both groups (ICS with HIPEC, 3 of 109 [2.8%] vs ICS without HIPEC, 3 of 87 [3.4%]; P > .99). Among patients with recurrence, the frequency of peritoneal recurrence was lower in the ICS with HIPEC group than in the ICS without HIPEC group (21 of 64 [32.8%] vs 41 of 64 [64.1%]; P = .001).

Conclusions and relevance: This study suggests that ICS in conjunction with HIPEC was associated with longer PFS and OS than ICS without HIPEC for patients with advanced-stage ovarian cancer and was not associated with higher rates of postoperative complications. The lower rate of peritoneal recurrence after HIPEC may be associated with improved OS.
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dc.language.isoen-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols-
dc.subject.MESHCarcinoma, Ovarian Epithelial-
dc.subject.MESHCohort Studies-
dc.subject.MESHCombined Modality Therapy-
dc.subject.MESHCytoreduction Surgical Procedures-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHHyperthermia, Induced-
dc.subject.MESHHyperthermic Intraperitoneal Chemotherapy-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoadjuvant Therapy-
dc.subject.MESHNeoplasm Recurrence, Local-
dc.subject.MESHOvarian Neoplasms-
dc.subject.MESHPeritoneal Neoplasms-
dc.subject.MESHPostoperative Complications-
dc.subject.MESHProspective Studies-
dc.subject.MESHSurvival Rate-
dc.titleHyperthermic Intraperitoneal Chemotherapy After Interval Cytoreductive Surgery for Patients With Advanced-Stage Ovarian Cancer Who Had Received Neoadjuvant Chemotherapy-
dc.typeArticle-
dc.identifier.pmid37672264-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10483378-
dc.contributor.affiliatedAuthorChang, SJ-
dc.type.localJournal Papers-
dc.identifier.doi10.1001/jamasurg.2023.3944-
dc.citation.titleJAMA surgery-
dc.citation.volume158-
dc.citation.number11-
dc.citation.date2023-
dc.citation.startPage1133-
dc.citation.endPage1140-
dc.identifier.bibliographicCitationJAMA surgery, 158(11). : 1133-1140, 2023-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.identifier.eissn2168-6262-
dc.relation.journalidJ021686254-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Obstetrics & Gynecology
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