Lymphocytic infiltration and Chemotherapy Response Score as prognostic markers in ovarian cancer patients treated with Neoadjuvant chemotherapy.

Bevacizumab Chemotherapy Response Score Lymphocytic infiltration Neoadjuvant chemotherapy Ovarian cancer

Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
06 2020
Historique:
received: 13 12 2019
accepted: 02 03 2020
pubmed: 17 3 2020
medline: 14 1 2021
entrez: 17 3 2020
Statut: ppublish

Résumé

Neoadjuvant Chemotherapy (NACT) followed by Interval Debulking Surgery (IDS) is an accepted frontline treatment in patients with advanced Epithelial Ovarian Cancer (EOC). Histopathologic assessment of tumor post NACT may provide a surrogate for response to treatment. The present study aims to characterize the pathological response and to examine its prognostic significance in these patients. Medical records of women with EOC treated in our institution from 2011 to 2016 were retrospectively identified. IDS specimens were reviewed by study pathologist and Chemotherapy Response Score (CRS), lymphocytic infiltration, necrosis and mitosis were assessed. 55 patients with EOC treated with NACT were identified and 48 had complete clinical and pathological data. Median age was 63 years. CRS assessed at omentum predicted PFS when adjusted for age, stage, debulking status (complete, optimal, suboptimal) and post IDS bevacizumab administration (mPFS CRS 1 vs 2 vs 3: 10.3-14-18.7 months 95% CI [7.4-15.7], [12.2-22.9], [13.5-31.3]). Presence of lymphocytic infiltration was associated with improved OS (log-rank test P = 0.015). Post IDS bevacizumab was associated with shorter PFS in patients with lymphocytic infiltration. BRCA status was known for 25 patients and presence of BRCA1/2 mutations was strongly correlated with lymphocytic infiltration (P = 0.011) but not CRS omentum (P = 0.926). Our study confirms the predictive value of CRS in EOC patients treated with NACT and IDS, but also demonstrates the prognostic significance of lymphocytic infiltration as well as its possible interaction with bevacizumab treatment.

Identifiants

pubmed: 32173048
pii: S0090-8258(20)30224-9
doi: 10.1016/j.ygyno.2020.03.008
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

599-605

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Dr. Liontos, receiving honoraria by Roche, Astra Zeneca, Astellas, MSD, Janssen, BMS and IPSEN, Dr. Koutsoukos, receiving honoraria by Roche, BMS, MSD and IPSEN, Dr. Zagouri receiving honoraria by Roche, Novartis, Eli-Lilly, Dr. Dimopoulos, receiving honoraria by Janssen, Celgene, Takeda, Amgen, Genesis Pharma and BMS, Dr. Bamias, receiving grant support from BMS, Astra Zeneca and MSD and honoraria from Roche, BMS and MSD. Dr. Sotiropoulou, Dr. Kaparelou, Mr. Tzannis(,) Dr. Tsironis, Dr. Kyriazoglou, Dr. Tsiara, Dr. Zakopoulou, Dr. Thomakos, Dr. Haidopoulos and Dr. Rodolakis declare no conflict of interest.

Auteurs

Michalis Liontos (M)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece. Electronic address: mliontos@gmail.com.

Maria Sotiropoulou (M)

Department of Pathology, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Maria Kaparelou (M)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Kimon Tzannis (K)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

George Tsironis (G)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Anastasios Kyriazoglou (A)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Anna Tsiara (A)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Roubini Zakopoulou (R)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Konstantinos Koutsoukos (K)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Flora Zagouri (F)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Nikolaos Thomakos (N)

Department of Obstetrics and Gynaecology; Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Dimitrios Haidopoulos (D)

Department of Obstetrics and Gynaecology; Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Alexandros Rodolakis (A)

Department of Obstetrics and Gynaecology; Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Meletios A Dimopoulos (MA)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

Aristotelis Bamias (A)

Department of Clinical Therapeutics, Alexandra General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

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