<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu YL</submitter><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><pagination>1915-1921</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8407101</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(12)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Although trials of neoadjuvant chemotherapy in ovarian cancer use 3 neoadjuvant cycles, real-world practice varies. We sought to evaluate the influence of increasing pre-operative cycles on survival, accounting for surgical outcomes.&lt;h4>Methods&lt;/h4>We identified 199 women with newly diagnosed ovarian cancer recommended for neoadjuvant chemotherapy who underwent interval debulking surgery from July 2015 to December 2018. Non-parametric tests were used to compare clinical characteristics by neoadjuvant cycles. The Kaplan-Meier method was used to estimate differences in progression-free and overall survival. The log-rank test was used to assess the relationship of covariates to outcome.&lt;h4>Results&lt;/h4>The median number of neoadjuvant cycles was 4 (range 3-8), with 56 (28%) women receiving ≥5 cycles. Compared with those receiving 3 or 4, women with ≥5 neoadjuvant cycles received fewer or no post-operative cycles (p&lt;0.001) but had no other differences in clinical factors (p>0.05). Complete gross resection rates were similar among those receiving 3, 4, and ≥5 neoadjuvant cycles (68.5%, 70%, and 71.4%, respectively, p=0.96). There were no significant differences in progression-free or overall survival when comparing 3 versus 4 neoadjuvant cycles. However, more cycles (≥5 vs 4) were associated with worse progression-free survival, even after adjustment for &lt;i>BRCA&lt;/i> status and complete gross resection (HR 2.20, 95% CI 1.45 to 3.33, p&lt;0.001), and worse overall survival, even after adjustment for histology, response on imaging, and complete gross resection rates (HR 2.78, 95% CI 1.37 to 5.63, p=0.016). The most common reason for receiving ≥5 cycles was extent of disease requiring more neoadjuvant chemotherapy.&lt;h4>Conclusions&lt;/h4>Despite maximal cytoreduction, patients receiving ≥&lt;u>5&lt;/u> neoadjuvant cycles have a poorer prognosis than those receiving 3-4 cycles. Future studies should focus on reducing surgical morbidity and optimizing novel therapies in this high-risk group.</pubmed_abstract><journal>International journal of gynecological cancer : official journal of the International Gynecological Cancer Society</journal><pubmed_title>Pre-operative neoadjuvant chemotherapy cycles and survival in newly diagnosed ovarian cancer: what is the optimal number? A Memorial Sloan Kettering Cancer Center Team Ovary study.</pubmed_title><pmcid>PMC8407101</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><pubmed_authors>Grisham R</pubmed_authors><pubmed_authors>Gardner G</pubmed_authors><pubmed_authors>O'Cearbhaill R</pubmed_authors><pubmed_authors>Zhou QC</pubmed_authors><pubmed_authors>Abu-Rustum NR</pubmed_authors><pubmed_authors>Sonoda Y</pubmed_authors><pubmed_authors>Aghajanian CA</pubmed_authors><pubmed_authors>Zivanovic O</pubmed_authors><pubmed_authors>Iasonos A</pubmed_authors><pubmed_authors>Tew W</pubmed_authors><pubmed_authors>Konner JA</pubmed_authors><pubmed_authors>Chi DS</pubmed_authors><pubmed_authors>Liu YL</pubmed_authors><pubmed_authors>Long Roche K</pubmed_authors><pubmed_authors>Broach V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pre-operative neoadjuvant chemotherapy cycles and survival in newly diagnosed ovarian cancer: what is the optimal number? A Memorial Sloan Kettering Cancer Center Team Ovary study.</name><description>&lt;h4>Objective&lt;/h4>Although trials of neoadjuvant chemotherapy in ovarian cancer use 3 neoadjuvant cycles, real-world practice varies. We sought to evaluate the influence of increasing pre-operative cycles on survival, accounting for surgical outcomes.&lt;h4>Methods&lt;/h4>We identified 199 women with newly diagnosed ovarian cancer recommended for neoadjuvant chemotherapy who underwent interval debulking surgery from July 2015 to December 2018. Non-parametric tests were used to compare clinical characteristics by neoadjuvant cycles. The Kaplan-Meier method was used to estimate differences in progression-free and overall survival. The log-rank test was used to assess the relationship of covariates to outcome.&lt;h4>Results&lt;/h4>The median number of neoadjuvant cycles was 4 (range 3-8), with 56 (28%) women receiving ≥5 cycles. Compared with those receiving 3 or 4, women with ≥5 neoadjuvant cycles received fewer or no post-operative cycles (p&lt;0.001) but had no other differences in clinical factors (p>0.05). Complete gross resection rates were similar among those receiving 3, 4, and ≥5 neoadjuvant cycles (68.5%, 70%, and 71.4%, respectively, p=0.96). There were no significant differences in progression-free or overall survival when comparing 3 versus 4 neoadjuvant cycles. However, more cycles (≥5 vs 4) were associated with worse progression-free survival, even after adjustment for &lt;i>BRCA&lt;/i> status and complete gross resection (HR 2.20, 95% CI 1.45 to 3.33, p&lt;0.001), and worse overall survival, even after adjustment for histology, response on imaging, and complete gross resection rates (HR 2.78, 95% CI 1.37 to 5.63, p=0.016). The most common reason for receiving ≥5 cycles was extent of disease requiring more neoadjuvant chemotherapy.&lt;h4>Conclusions&lt;/h4>Despite maximal cytoreduction, patients receiving ≥&lt;u>5&lt;/u> neoadjuvant cycles have a poorer prognosis than those receiving 3-4 cycles. Future studies should focus on reducing surgical morbidity and optimizing novel therapies in this high-risk group.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2024-11-12T21:27:42.622Z</modification><creation>2022-02-11T13:22:00.288Z</creation></dates><accession>S-EPMC8407101</accession><cross_references><pubmed>33106271</pubmed><doi>10.1136/ijgc-2020-001641</doi></cross_references></HashMap>