- Open Access
TOP2A as marker of response to pegylated lyposomal doxorubicin (PLD) in epithelial ovarian cancers
Journal of Ovarian Research volume 12, Article number: 17 (2019)
Relapsed epithelial ovarian cancer (EOC) is frequently treated with pegylated liposomal doxorubicin (PLD). Unfortunately, most patients do not benefit from treatment. Prediction of response is crucial to optimize PLD use and avoid unnecessary toxicities. We aimed at assessing the value of topoisomerase II alpha (TOP2A) expression as predictive marker of response to PLD-based therapy in patients with relapsed EOCs.
We retrospectively analyzed Formalin Fixed Paraffin Embedded (FFPE) tissues from 101 patients with platinum resistant (PR) or partially platinum-sensitive (PPS) EOCs treated with PLD-based chemotherapy beyond second line in three referral cancer centers between January 2010 and June 2018. TOP2A expression was measured by immunohistochemistry (IHC): images of each sample were acquired by optical microscope and analyzed by using automatic counter software. Correlation between TOP2A expression and response to PLD was assessed. Since no cut-off for positivity has been validated yet, we dichotomized TOP2A expression based on a cut-off of 18% (mean value in this study).
TOP2A expression beyond cut-off was not prognostic for primary platinum-free interval in our series (p = 0.77) neither for optimal cytoreduction (p = 0.9). TOP2A > 18% was associated with a longer time to progression (TTP) following PLD-treatment, although not statistically significant (p = 0.394). No difference was observed between PR and PPS patients’ groups (p = 0.445 and p = 0.185, respectively). Not unexpectedly, patients with TOP2A expression > 18% treated with PLD monotherapy achieved a longer TTP compared with PLD-doublet therapy (p = 0.05).
Our data suggest that TOP2A status might predict activity of PLD in patients with PR/PPS EOCs.
Epithelial ovarian cancer (EOC) is the leading cause of death among women with gynecological malignancies with 22,400 estimated new cases in 2017 . Optimal cytoreduction to no residual disease followed by adjuvant chemotherapy with platinum-taxane combination is the standard of care [2, 3]. However, over 70% of patients with advanced stage diseases experience relapse after front-line treatment . Residual disease (R) at primary surgery and sensitivity to first-line platinum-based chemotherapy (PFI, platinum-free interval) still represent the major determinants of clinical outcome [5, 6]. For partially platinum-sensitive patients (PPS), defined as progressed between six and twelve months after conclusion of first line platinum-therapy, standard options include a second line platinum-based-doublet chemotherapy or pegylated liposomal doxorubicin [PLD] - trabectedin. For platinum resistant ovarian cancers (PR), defined as progressing within 6 months from last platinum therapy, limited and debatable options are available . In these patients, subsequent single-agent chemotherapies with non-platinum drugs show limited activity . The most effective drugs include paclitaxel, gemcitabine, etoposide, topotecan and PLD [9,10,11,12].
PLD is one of the preferred drugs due to its favorable toxicity profile (absence of alopecia, limited cardiac toxicity, and only moderate hematological and skin toxicity) [13, 14]. However, response rates range from 16 to 25%. Consequently, to optimize the use of PLD and avoid unnecessary toxicities, prediction of response is crucial.
TOP2A gene is located on the locus q21 of chromosome 17, close to the HER2 gene, and is responsible for coding the nuclear enzyme type 2 topoisomerase alpha (TOP2A) . TOP2A plays a key role in DNA stability and represents one of the targets of chemotherapeutic agents, such as etoposide and anthracyclines [16,17,18]. Several retrospective analyses have already suggested a correlation between TOP2A status and response to anthracyclines in breast cancer, both as neoadjuvant and adjuvant treatment [19,20,21,22,23]. Conversely, in EOCs few studies have investigated the prognostic and predictive role of TOP2A. Heterogeneous results are mainly related with the use of different detection techniques such as immunohistochemistry (IHC), Real-Time Polymerase Chain Reaction (RT-PCR) and Fluorescent-In Situ Hybridization (FISH) [24,25,26].
The aim of our study was to assess the correlation between TOP2A protein expression and clinical outcome of patients following PLD-based treatment in both platinum partially-sensitive and platinum-resistant patients.
Materials and methods
We screened a total of 128 patients with PR/PPS EOCs treated with PLD-based chemotherapy beyond second line in three different referral centers (Candiolo Cancer Institute FPO/IRCCS, Ordine Mauriziano Hospital and Sant’Anna Hospital) between January 2010 and April 2018. Among these, 27 cases were excluded due to non-complete medical records or unavailability of tumor material for IHC analysis. For each of the 101 selected patients, the following clinico-histopathological data were recorded: i) age at diagnosis; ii) morphological features of ovarian cancer including tumor histotype, grade (according to World Health Organization Classification of Tumours of Female Reproductive Organs, 4th Edition) and stage (according to the International Federation of Gynecology and Obstetrics [FIGO]); iii) PFI (Platinum-Free Interval) to last platinum-based therapy; iv) number of previous lines before PLD; v) PLD-based treatment scheme; vi): Cancer Antigen 125 (CA-125) pre- and post-PLD treatment; vii) best radiological response according to RECIST 1.1 criteria, if available; viii) BRCA status; ix) date of death or last follow up (FU). Complete patients’ clinical data are reported in Table 1.
In Italy, the National Regulation established that retrospective studies require a notification to the local ethical committee with the tacit consent formula. We therefore notified the Candiolo Cancer Institute ethical committee about the conduct of the study on August 2016. All patients included in our retrospective study were treated according with the ethical standards of our local committee on human experimentation and with the Helsinki Declaration.
FFPE tissue blocks of the above 101 cases were obtained from the archives of the Units of Pathology at Candiolo Cancer Institute (IRCCS), A.S.O. Ordine Mauriziano Hospital and Sant’Anna Hospital at Torino. Immunohistochemistry was performed as previously described  to detect topoisomerase II alpha using a monoclonal rabbit antibody (clone D10G9 Cell Signaling Technology). At least 10 images of each sample were acquired by optical microscope (20×) connected with charge-coupled device (CCD) camera and analyzed by using automatic counter software (NIH ImageJ). Only cells with TOP2A nuclear signatures were considered as positive. TOP2A expression was calculated as the ratio between positive cells and a total of at least 500 cells in 10 different fields.
Time to progression (TTP) following PLD-based treatment was assessed as the time elapsed between PLD start and first tumor progression or death, whichever comes first. TTP was estimated by the Kaplan-Meier method and compared according to TOP2A expression using the log-rank test. Because no positivity cut-off has been validated, similar to other studies we dichotomized TOP2A expression based on the mean value of our cohort (18%). A p < 0.05 was considered statistically significant. All analyses were performed using the SPSS statistical software program, version 22.0 (IBM SPSS Inc., Chicago, IL, United States of America).
In our series, more than 75% were serous high grade, G3, advanced stage (IIIC-IV) EOCs. PFI showed that almost 65% of the patients were platinum-resistant. Eighty-seven per cent of the patients received PLD as second-line therapy and more than 50% as single-agent.
All 101 cases analyzed showed nuclear TOP2A expression, which ranged from 2 to 48% of nuclear cell signature with a mean of 18% (Fig. 1).
No statistically significant association between TOP2A expression and tumor histotype, grading or PFI were found. TOP2A expression beyond cut-off was not prognostic for primary platinum-free interval in our series (p = 0.77) neither for optimal cytoreduction (p = 0.9).
Median time to progression from PLD-based treatment was 5, 1 months (range 1–24 months). Cancer Antigen 125 (CA-125) was above normal range in the 93% of cases before PLD treatment (median value 1142 UI/dL) and in the 78, 3% post-treatment (median value 1493 UI/dL), but not statistical correlation was found between serological response and TOP2A status (p = 0.285). TOP2A expression beyond cut-off was associated with a higher probability of response to PLD in terms of TTP, although not statistically significant (p = 0.0394, Fig. 2a). No difference was observed between PR and PPS groups (p = 0.445 and p = 0.185, respectively). Among the 67 patients with available radiological assessments, no difference could be observed in term of response: 31 patients obtained a disease control (partial response [PR] + stable disease [SD]) and 36 progressed. Patients with TOP2A higher expression treated with PLD monotherapy achieved a longer TTP compared with PLD-doublet therapy (5, 8 vs 3, 4 months, p = 0.035, Fig. 2b). Complete results are summarized in Table 2.
BRCA germline-status was known in 29 patients. Among the eleven mutated patients, 7 carried a BRCA1 and 4 a BRCA2 mutations; twelve patients were wild-type and other six patients showed a variant of unknown significance (VUS). As expected, patients with BRCA mutations achieved a longer TTP (median 11 months, range 3–22, data not shown) compared with the median of our study population, although statistical analysis could not be performed due to the small numbers of cases.
Treatment of patients affected by relapsed PR or PPS EOCs is still a major challenge for gynecologic oncologists and medical oncologists. To personalize the use of PLD and avoid unnecessary toxicities, prediction of response is of crucial importance. We have already demonstrated that TOP2A gene copy number is associated with protein overexpression and correlates with the activity of PLD in a small series of 38 PR EOCs and patients-derived xenografts (PDXs) . Considering the concordance between TOP2A gene copy number and TOP2A protein expression, we aimed at developing a cost-effective and reproducible method (IHC) to assess the correlation between TOP2A and PLD activity. In our study we found that the prevalence of TOP2A expression is consistent with that observed by van der Zee at al . and Faggad et al.  in their retrospective series. Moreover, we report here that TOP2A expression above 18% is associated with a higher probability of response to PLD in patients with PR/PPS EOCs. Finally, we showed that, regardless platinum-free interval, patients with TOP2A expression above cut-off, achieved a longer time to progression if treated with PLD monotherapy compared with PLD-doublet therapy (p = 0.035). These data may be explained by the known detrimental effect of poly-chemotherapy in pretreated patients [30, 31].
To our knowledge this is the biggest study investigating the role of TOP2A in predicting PLD activity in ovarian cancers.
However, our study has several limits. First of all the absence of a validated cut-off for TOP2A positivity at IHC impairs the reproducibility of the test. Moreover, assessment of TOP2A expression mainly at diagnosis may be discordant with TOP2A status at relapse, considering tumor heterogeneity and clonal evolution during progression. Finally our patient population was heterogeneous in terms of PFIs and PLD combinations.
Other predictors of sensitivity to anthracyclines have been studied. Among these, chromosome 17 polysomy, HER2, TIMP-1 , stroma-related genes and the immune response  have been already investigated with controversial results. More recently, defects in the homologous recombination system, such as BRCA1 and BRCA2 mutations have been associated with higher rates of response to platinum-based and anthracyclines regimens both in triple negative breast cancers (TNBCs) and EOCs .
In conclusion, although we believe that these results should be regarded as an hypothesis-generating attempt to identify a biomarker of response, only a multifactorial panel could be predictive of response to PLD in ovarian cancer .
Cancer Antigen 125
Eastern Cooperative Oncology Group (ECOG)
Epithelial ovarian cancer
Formalin Fixed Paraffin Embedded
International Federation of Gynecology and Obstetric
Fluorescent-In Situ Hybridization
Pegylated liposomal doxorubicin
Real-Time Polymerase Chain Reaction
Triple negative breast cancers
Topoisomerase II alpha
Time to progression
Variant of unknown significance
Miller KD, Siegel RL, Lin CC, Mariotto AB, Kramer JL, Rowland JH, et al. Cancer treatment and survivorship statistics, 2016. CA Cancer J Clin. 2016;66(4):271–89.
Ledermann JA, Raja FA, Fotopoulou C, Gonzalez-Martin A, Colombo N, Sessa C, et al. Newly diagnosed and relapsed epithelial ovarian carcinoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2013;24(Suppl 6):vi24–32.
Oza AM, Cook AD, Pfisterer J, Embleton A, Ledermann JA, Pujade-Lauraine E, et al. Standard chemotherapy with or without bevacizumab for women with newly diagnosed ovarian cancer (ICON7): overall survival results of a phase 3 randomised trial. Lancet Oncol. 2015;16(8):928–36.
Colombo N, Lorusso D, Scollo P. Impact of recurrence of ovarian Cancer on quality of life and outlook for the future. Int J Gynecol Cancer. 2017;27(6):1134–40.
du Bois A, Reuss A, Pujade-Lauraine E, Harter P, Ray-Coquard I, Pfisterer J. Role of surgical outcome as prognostic factor in advanced epithelial ovarian cancer: a combined exploratory analysis of 3 prospectively randomized phase 3 multicenter trials: by the Arbeitsgemeinschaft Gynaekologische Onkologie Studiengruppe Ovarialkarzinom (AGO-OVAR) and the Groupe d'Investigateurs Nationaux pour les etudes des cancers de l'Ovaire (GINECO). Cancer. 2009;115(6):1234–44.
Karam A, Ledermann JA, Kim JW, Sehouli J, Lu K, Gourley C, et al. Fifth ovarian Cancer consensus conference of the gynecologic Cancer InterGroup: first-line interventions. Ann Oncol. 2017;28(4):711–7.
Wilson MK, Pujade-Lauraine E, Aoki D, Mirza MR, Lorusso D, Oza AM, et al. Fifth ovarian Cancer consensus conference of the gynecologic Cancer InterGroup: recurrent disease. Ann Oncol. 2017;28(4):727–32.
Edwards SJ, Barton S, Thurgar E, Trevor N. Topotecan, pegylated liposomal doxorubicin hydrochloride, paclitaxel, trabectedin and gemcitabine for advanced recurrent or refractory ovarian cancer: a systematic review and economic evaluation. Health Technol Assess. 2015;19(7):1–480.
Lawrie TA, Bryant A, Cameron A, Gray E, Morrison J. Pegylated liposomal doxorubicin for relapsed epithelial ovarian cancer. Cochrane Database Syst Rev. 2013;7:CD006910.
Monk BJ, Herzog TJ, Kaye SB, Krasner CN, Vermorken JB, Muggia FM, et al. Trabectedin plus pegylated liposomal doxorubicin (PLD) versus PLD in recurrent ovarian cancer: overall survival analysis. Eur J Cancer. 2012;48(15):2361–8.
Bozkaya Y, Doğan M, Umut Erdem G, Tulunay G, Uncu H, Arık Z, et al. Effectiveness of low-dose oral etoposide treatment in patients with recurrent and platinum-resistant epithelial ovarian cancer. J Obstet Gynaecol. 2017;37(5):649–54.
Ferrandina G, Ludovisi M, Lorusso D, Pignata S, Breda E, Savarese A, et al. Phase III trial of gemcitabine compared with pegylated liposomal doxorubicin in progressive or recurrent ovarian cancer. J Clin Oncol. 2008;26(6):890–6.
Krasner CN, Poveda A, Herzog TJ, Vermorken JB, Kaye SB, Nieto A, et al. Patient-reported outcomes in relapsed ovarian cancer: results from a randomized phase III study of trabectedin with pegylated liposomal doxorubicin (PLD) versus PLD alone. Gynecol Oncol. 2012;127(1):161–7.
Ferrandina G, Amadio G, Paris I, Distefano M, Palluzzi E, de Vincenzo R, et al. Real-world Management of Trabectedin/Pegylated liposomal doxorubicin in platinum-sensitive recurrent ovarian Cancer patients: a National Survey. Int J Gynecol Cancer. 2017;27(6):1141–8.
Nikolaou C, Bermúdez I, Manichanh C, García-Martinez J, Guigó R, Pérez-Ortín JE, et al. Topoisomerase II regulates yeast genes with singular chromatin architectures. Nucleic Acids Res. 2013;41(20):9243–56.
Roca J. Topoisomerase II: a fitted mechanism for the chromatin landscape. Nucleic Acids Res. 2009;37(3):721–30.
Li D, Yuan Z, Chen S, Zhang C, Song L, Gao C, et al. Synthesis and biological research of novel azaacridine derivatives as potent DNA-binding ligands and topoisomerase II inhibitors. Bioorg Med Chem. 2017;25(13):3437–46.
Nitiss JL. Targeting DNA topoisomerase II in cancer chemotherapy. Nat Rev Cancer. 2009;9(5):338–50.
Petit T, Wilt M, Velten M, Millon R, Rodier JF, Borel C, et al. Comparative value of tumour grade, hormonal receptors, Ki-67, HER-2 and topoisomerase II alpha status as predictive markers in breast cancer patients treated with neoadjuvant anthracycline-based chemotherapy. Eur J Cancer. 2004;40(2):205–11.
Durbecq V, Paesmans M, Cardoso F, Desmedt C, Di Leo A, Chan S, et al. Topoisomerase-II alpha expression as a predictive marker in a population of advanced breast cancer patients randomly treated either with single-agent doxorubicin or single-agent docetaxel. Mol Cancer Ther. 2004;3(10):1207–14.
Di Leo A, Biganzoli L, Claudino W, Licitra S, Pestrin M, Larsimont D. Topoisomerase II alpha as a marker predicting anthracyclines’ activity in early breast cancer patients: ready for the primetime? Eur J Cancer. 2008;44(18):2791–8.
Cardoso F, Di Leo A, Larsimont D, Gancberg D, Rouas G, Dolci S, et al. Evaluation of HER2, p53, bcl-2, topoisomerase II-alpha, heat shock proteins 27 and 70 in primary breast cancer and metastatic ipsilateral axillary lymph nodes. Ann Oncol. 2001;12(5):615–20.
Di Leo A, Desmedt C, Bartlett JM, Piette F, Ejlertsen B, Pritchard KI, et al. HER2 and TOP2A as predictive markers for anthracycline-containing chemotherapy regimens as adjuvant treatment of breast cancer: a meta-analysis of individual patient data. Lancet Oncol. 2011;12(12):1134–42.
Slamon DJ. Studies of the HER-2/neu proto-oncogene in human breast cancer. Cancer Investig. 1990;8(2):253.
Koshiyama M, Fujii H, Kinezaki M, Morita Y, Nanno H, Yoshida M. Immunohistochemical expression of topoisomerase IIalpha (topo IIalpha) and multidrug resistance-associated protein (MRP), plus chemosensitivity testing, as chemotherapeutic indices of ovarian and endometrial carcinomas. Anticancer Res. 2001;21(4B):2925–32.
Faggad A, Darb-Esfahani S, Wirtz R, Sinn B, Sehouli J, Könsgen D, et al. Topoisomerase IIalpha mRNA and protein expression in ovarian carcinoma: correlation with clinicopathological factors and prognosis. Mod Pathol. 2009;22(4):579–88.
Annaratone L, Marchiò C, Russo R, Ciardo L, Rondon-Lagos SM, Goia M, et al. A collection of primary tissue cultures of tumors from vacuum packed and cooled surgical specimens: a feasibility study. PLoS One. 2013;8(9):e75193.
Erriquez J, Becco P, Olivero M, Ponzone R, Maggiorotto F, Ferrero A, et al. TOP2A gene copy gain predicts response of epithelial ovarian cancers to pegylated liposomal doxorubicin: TOP2A as marker of response to PLD in ovarian cancer. Gynecol Oncol. 2015;138(3):627–33.
van der Zee AG, de Vries EG, Hollema H, Kaye SB, Brown R, Keith WN. Molecular analysis of the topoisomerase II alpha gene and its expression in human ovarian cancer. Ann Oncol. 1994;5(1):75–81.
Pujade-Lauraine E, Alexandre J. Update of randomized trials in recurrent disease. Ann Oncol. 2011;22(Suppl 8):viii61–viii4.
Previs RA, Bevis KS, Huh W, Tillmanns T, Perry L, Moore K, et al. A prognostic nomogram to predict overall survival in women with recurrent ovarian cancer treated with bevacizumab and chemotherapy. Gynecol Oncol. 2014;132(3):531–6.
Ejlertsen B, Jensen MB, Nielsen KV, Balslev E, Rasmussen BB, Willemoe GL, et al. HER2, TOP2A, and TIMP-1 and responsiveness to adjuvant anthracycline-containing chemotherapy in high-risk breast cancer patients. J Clin Oncol. 2010;28(6):984–90.
Farmer P, Bonnefoi H, Anderle P, Cameron D, Wirapati P, Becette V, et al. A stroma-related gene signature predicts resistance to neoadjuvant chemotherapy in breast cancer. Nat Med. 2009;15(1):68–74.
Durbecq V, Desmed C, Paesmans M, Cardoso F, Di Leo A, Mano M, et al. Correlation between topoisomerase-IIalpha gene amplification and protein expression in HER-2 amplified breast cancer. Int J Oncol. 2004;25(5):1473–9.
Desmedt C, Di Leo A, de Azambuja E, Larsimont D, Haibe-Kains B, Selleslags J, et al. Multifactorial approach to predicting resistance to anthracyclines. J Clin Oncol. 2011;29(12):1578–86.
This work has been supported by the following grant to GV: VALG_RIC_ LOC_14_01: Rete OncologicaPiemonte e Valle d’Aosta and Ministry of the University (ex 60%, 2015) and to MFD IG#16473 of the Italian Association for Cancer Research (AIRC).
Availability of data and materials
All data are available in the manuscript.
Ethics approval and consent to participate
Due to the retrospective nature of the study, informed consent was waived by the Medical Ethics Committee of Candiolo Cancer Institute, FPO/IRCCS Candiolo.
Consent for publication
Written informed consents for the publication of related Tables and figures had been obtained from the individuals.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Ghisoni, E., Maggiorotto, F., Borella, F. et al. TOP2A as marker of response to pegylated lyposomal doxorubicin (PLD) in epithelial ovarian cancers. J Ovarian Res 12, 17 (2019) doi:10.1186/s13048-019-0492-6
- Ovarian cancer
- Topoisomerase 2 alpha
- Pegylated liposomal doxorubicin