Neoadjuvant chemotherapy reduces the treatment-free interval after first-line treatment in patients with advanced ovarian cancer

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Standard

Neoadjuvant chemotherapy reduces the treatment-free interval after first-line treatment in patients with advanced ovarian cancer. / Ekmann-Gade, Anne Weng; Hogdall, Claus Kim; Engelholm, Svend Aage; Fago-Olsen, Carsten Lindberg.

I: Anticancer Research, Bind 40, Nr. 5, 2020, s. 2765-2770.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ekmann-Gade, AW, Hogdall, CK, Engelholm, SA & Fago-Olsen, CL 2020, 'Neoadjuvant chemotherapy reduces the treatment-free interval after first-line treatment in patients with advanced ovarian cancer', Anticancer Research, bind 40, nr. 5, s. 2765-2770. https://doi.org/10.21873/anticanres.14248

APA

Ekmann-Gade, A. W., Hogdall, C. K., Engelholm, S. A., & Fago-Olsen, C. L. (2020). Neoadjuvant chemotherapy reduces the treatment-free interval after first-line treatment in patients with advanced ovarian cancer. Anticancer Research, 40(5), 2765-2770. https://doi.org/10.21873/anticanres.14248

Vancouver

Ekmann-Gade AW, Hogdall CK, Engelholm SA, Fago-Olsen CL. Neoadjuvant chemotherapy reduces the treatment-free interval after first-line treatment in patients with advanced ovarian cancer. Anticancer Research. 2020;40(5):2765-2770. https://doi.org/10.21873/anticanres.14248

Author

Ekmann-Gade, Anne Weng ; Hogdall, Claus Kim ; Engelholm, Svend Aage ; Fago-Olsen, Carsten Lindberg. / Neoadjuvant chemotherapy reduces the treatment-free interval after first-line treatment in patients with advanced ovarian cancer. I: Anticancer Research. 2020 ; Bind 40, Nr. 5. s. 2765-2770.

Bibtex

@article{221c5959c5ed42a1bd414d8dcd16e245,
title = "Neoadjuvant chemotherapy reduces the treatment-free interval after first-line treatment in patients with advanced ovarian cancer",
abstract = "Background/Aim: The aim of the study was to compare platinum resistance and treatment-free interval (TFI) following treatment with neoadjuvant chemotherapy (NACT) and interval debulking surgery (IDS) or primary debulking surgery (PDS) in women with advanced epithelial ovarian cancer (EOC). Patients and Methods: The study included patients diagnosed with primary EOC, stage IIIC or IV, between 2005 and 2013. Patients were grouped according to first-line treatment (PDS vs. NACT-IDS). Date of second-line treatment initiation was used to evaluate platinum sensitivity. Results: The study population included 521 patients, of which 371 (71%) and 150 (29%) underwent PDS and NACT-IDS, respectively. We found no difference in platinum resistance between groups. Platinum-sensitive patients treated with NACT-IDS had a shorter median TFI (372 vs. 497 days, p=0.042). Similarly, patients with no residual tumor after IDS had a shorter median TFI (280 vs. 302 days, p=0.005). Conclusion: NACT-IDS may shorten the TFI after first-line platinum-based chemotherapy.",
keywords = "Neoadjuvant chemotherapy, Ovarian cancer, Platinum resistance, Treatmentfree interval",
author = "Ekmann-Gade, {Anne Weng} and Hogdall, {Claus Kim} and Engelholm, {Svend Aage} and Fago-Olsen, {Carsten Lindberg}",
year = "2020",
doi = "10.21873/anticanres.14248",
language = "English",
volume = "40",
pages = "2765--2770",
journal = "Anticancer Research",
issn = "0250-7005",
publisher = "International Institute of Anticancer Research",
number = "5",

}

RIS

TY - JOUR

T1 - Neoadjuvant chemotherapy reduces the treatment-free interval after first-line treatment in patients with advanced ovarian cancer

AU - Ekmann-Gade, Anne Weng

AU - Hogdall, Claus Kim

AU - Engelholm, Svend Aage

AU - Fago-Olsen, Carsten Lindberg

PY - 2020

Y1 - 2020

N2 - Background/Aim: The aim of the study was to compare platinum resistance and treatment-free interval (TFI) following treatment with neoadjuvant chemotherapy (NACT) and interval debulking surgery (IDS) or primary debulking surgery (PDS) in women with advanced epithelial ovarian cancer (EOC). Patients and Methods: The study included patients diagnosed with primary EOC, stage IIIC or IV, between 2005 and 2013. Patients were grouped according to first-line treatment (PDS vs. NACT-IDS). Date of second-line treatment initiation was used to evaluate platinum sensitivity. Results: The study population included 521 patients, of which 371 (71%) and 150 (29%) underwent PDS and NACT-IDS, respectively. We found no difference in platinum resistance between groups. Platinum-sensitive patients treated with NACT-IDS had a shorter median TFI (372 vs. 497 days, p=0.042). Similarly, patients with no residual tumor after IDS had a shorter median TFI (280 vs. 302 days, p=0.005). Conclusion: NACT-IDS may shorten the TFI after first-line platinum-based chemotherapy.

AB - Background/Aim: The aim of the study was to compare platinum resistance and treatment-free interval (TFI) following treatment with neoadjuvant chemotherapy (NACT) and interval debulking surgery (IDS) or primary debulking surgery (PDS) in women with advanced epithelial ovarian cancer (EOC). Patients and Methods: The study included patients diagnosed with primary EOC, stage IIIC or IV, between 2005 and 2013. Patients were grouped according to first-line treatment (PDS vs. NACT-IDS). Date of second-line treatment initiation was used to evaluate platinum sensitivity. Results: The study population included 521 patients, of which 371 (71%) and 150 (29%) underwent PDS and NACT-IDS, respectively. We found no difference in platinum resistance between groups. Platinum-sensitive patients treated with NACT-IDS had a shorter median TFI (372 vs. 497 days, p=0.042). Similarly, patients with no residual tumor after IDS had a shorter median TFI (280 vs. 302 days, p=0.005). Conclusion: NACT-IDS may shorten the TFI after first-line platinum-based chemotherapy.

KW - Neoadjuvant chemotherapy

KW - Ovarian cancer

KW - Platinum resistance

KW - Treatmentfree interval

U2 - 10.21873/anticanres.14248

DO - 10.21873/anticanres.14248

M3 - Journal article

C2 - 32366422

AN - SCOPUS:85084276374

VL - 40

SP - 2765

EP - 2770

JO - Anticancer Research

JF - Anticancer Research

SN - 0250-7005

IS - 5

ER -

ID: 255842380