TOP2A as marker of response to pegylated lyposomal doxorubicin (PLD) in epithelial ovarian cancers

Epithelial ovarian cancer (EOC) is the leading cause of death among women with gynecological malignancies with 22,400 estimated new cases in 2017 [1]. 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 [4]. 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 [7]. In these patients, subsequent single-agent chemotherapies with non-platinum drugs show limited activity [8]. The most effective drugs include paclitaxel, gemcitabine, etoposide, topotecan and PLD [9‐12].

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) [15]. TOP2A plays a key role in DNA stability and represents one of the targets of chemotherapeutic agents, such as etoposide and anthracyclines [16‐18]. Several retrospective analyses have already suggested a correlation between TOP2A status and response to anthracyclines in breast cancer, both as neoadjuvant and adjuvant treatment [19‐23]. 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) [24‐26].

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.

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) [28]. 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 [29]. and Faggad et al. [26] 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 [32], stroma-related genes and the immune response [33] 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 [34].

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 [35].