Mucinous ovarian carcinoma is a rare subtype of epithelial ovarian cancer. Despite being a chemoresistant tumour type, surgical resection and chemotherapy are still the current standard for management. This narrative review aims to explore the current evidence for targeted therapies in mucinous ovarian carcinoma. A review of the literature was performed to identify clinical trials and case reports of targeted therapy in patients with mucinous ovarian carcinoma. The databases and registers (PubMed, MEDLINE, Embase, Europe PMC, Cochrane Central Register of Clinical Trials, clinicaltrials.gov) were searched for articles published between January 2009 to June 2021 using keywords specific for mucinous ovarian carcinoma and targeted therapy. Records were screened and assessed for eligibility based on inclusion and exclusion criteria. From 684 records, 21 studies met the criteria to be included in the review. A total of 11 different targeted therapies were identified, each demonstrating varying degrees of clinical evidence supporting further investigation in patients with mucinous ovarian carcinoma. Targeted therapies identified in this review that warrant further investigations are bevacizumab, trastuzumab, nintedanib, AZD1775, sunitinib, cediranib and pazopanib. Many of the therapeutic agents may be investigated further in combination with other targeted therapies or chemotherapy. More clinical trials focusing on targeted therapy specifically in patients with mucinous ovarian cancer are required to inform clinical use. Multinational efforts are likely to be required to successfully conduct trials in this rare tumor type.
- cystadenocarcinoma, mucinous
- medical oncology
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Mucinous ovarian carcinoma accounts for 3–5% of all epithelial ovarian cancers.1 Current standard therapeutic management involves surgical resection and platinum/taxane chemotherapy, similar to that employed in high-grade serous ovarian carcinoma.2 Curative outcomes may be achieved with surgical resection if diagnosis is made at an early stage. However, mucinous ovarian carcinomas, especially if recurrent, with advanced spread or high grade, are chemoresistant.3 Median survival of stage III/IV disease is less than 15 months, compared with 41 months for high-grade serous ovarian carcinoma.4 Patients with mucinous ovarian carcinoma are currently disadvantaged since many of the treatment regimens they are offered do not have the same level of evidence as for other cancers.5 Given these poor outcomes, new therapeutic strategies are needed for this chemoresistant tumor type.
Targeted therapy involves agents that target cancer-associated molecules to specifically inhibit the growth and spread of malignant cells. In contrast, chemotherapy uses cytotoxic drugs that kill both cancer cells and normal cells, hence, patients are likely to experience more toxic adverse effects.6 Gene mutations that confer alterations to cellular proteins and receptors form one of the hallmarks of carcinogenesis. Molecular alterations that occur in mucinous ovarian carcinoma include KRAS/NRAS mutations (65.8%), TP53 mutation (65.2%), ERBB2 amplification (26.7%) and BRAF mutation (8.7%).1 These gene mutations and the resulting proteins can be used to distinguish between normal cells and cancer cells and can serve as specific molecular targets for targeted therapy. Targeted therapy can also impact key molecular drivers that promote the growth, survival and spread of malignant cells such as vascular endothelial growth factor (VEGF). This targeting can be direct, as in the case of imatinib for BCR-ABL1 fusions or indirect, by targeting a pathway synergy, as in poly adenosine diphosphate-ribose polymerase (PARP) inhibitors for BRCA1/2-mutated tumors. The highly specific nature of targeted therapy suggests that these agents are likely to use mechanisms of action that evade the chemoresistant features of mucinous ovarian carcinoma cells. Examples of targeted agents include monoclonal antibodies or small molecules that target specific tumour-associated antigens, tumour-promoting molecules or against immune checkpoint proteins. Therapeutic agents targeting specific biomarkers and key molecular drivers of mucinous ovarian carcinoma such as ERBB2 and KRAS may exhibit promising results.7
This narrative review aims to evaluate the literature to identify and appraise the outcomes of clinical trials of targeted therapy that have included patients diagnosed with advanced (stage II-IV) or recurrent mucinous ovarian carcinoma. Currently, clinical trials of targeted therapy specifically for mucinous ovarian carcinoma have not been completed due to the rarity of the cancer. For instance, the rare tumor trial GOG-0241 evaluating four treatment regimens for mucinous ovarian carcinoma was terminated early due to poor accrual.5 However, patients with this disease are likely to have been included in pan-ovarian or pan-cancer clinical trials with a specific tumor biomarker determining trial entry. We performed a systematic literature and database search to identify such studies (Figure 1) and report those that included mucinous ovarian carcinoma grouped by the biological pathway targeted (Table 1). Through the evaluation of current evidence for novel therapeutic approaches, we aim for this study to contribute to offering personalized therapies to patients with mucinous ovarian carcinoma, stratified based on their tumor biomarkers.
Targeted therapy agents
The principle mechanism of action of monoclonal VEGF antibodies is via the inhibition of tumor angiogenesis. In four phase III ovarian cancer trials, including a total of 42 patients with mucinous ovarian carcinoma, the addition of bevacizumab to chemotherapy significantly improved overall progression-free survival by 2–4 months and median overall survival by 5 months.8–11 Only a subset of patients in these trials had a diagnosis of mucinous ovarian carcinoma and histological subtype-based analyses of outcomes were not reported. This limits the inferences that can be drawn regarding progression-free survival and overall survival for patients with this disease treated with bevacizumab in these trials. The rare tumor trial GOG-0241 attempted to evaluate several treatment regimens, including bevacizumab, specifically in patients with advanced mucinous ovarian carcinoma.5 There was no benefit to overall survival when comparing the arms with and without bevacizumab for all 50 patients (hazard ratio [HR] 1.04) as well as for the 18 patients with confirmed mucinous ovarian carcinoma after central pathology review (HR 1.08). No significant conclusions can be drawn from this study due to the small sample size. Two case reports of patients with heavily treated recurrent stage IIIa mucinous ovarian carcinoma commenced on bevacizumab resulting in resolution of symptoms and halted disease progression for 12 and 30 months respectively based on CA-125 levels, corresponding to stable disease based on response evaluation criteria in solid tumors (RECIST) criteria.12 13 The positive outcomes outlined on these case reports and the significant improvements in overall progression-free survival and overall survival observed in the bevacizumab trials above support further investigation of bevacizumab in a larger cohort of patients with mucinous ovarian carcinoma.
An alternative mechanism to inhibit VEGF receptors is by the small molecule inhibitor cediranib, which similarly functions by suppressing tumor angiogenesis. The phase III trial ICON6 included 4 patients with mucinous ovarian carcinoma and showed a prolongation in progression-free survival – 11 months in the group that received chemotherapy followed by maintenance cediranib, compared with 8.7 months for chemotherapy only.14 Overall survival data from this trial available at the time of publication, although immature, demonstrated no significant difference in overall survival in the randomized arms of the trial. Mucinous ovarian carcinoma-specific data was not reported.
Tyrosine kinase receptor inhibitors
Platelet derived growth factor (PDGF), similar to VEGF, plays a major role in tumor angiogenesis and tumor cell proliferation. Sunitinib targets multiple receptor tyrosine kinases including the receptors for PDGF and VEGF, thereby inhibiting tumor vascularization and promoting tumor cell apoptosis. In a phase II trial comparing continuous and non-continuous monotherapy with sunitinib in platinum resistant ovarian cancer, the non-continuous regimen demonstrated the best reported response according to RECIST criteria. The response rate (complete and partial) for the non-continuous treatment arm was 15.7%, compared with 5.4% for the continuous treatment arm.15 This trial included 3 patients with mucinous ovarian carcinoma. Histological subtype-based analysis of responses was not reported which limits the inferences that can be drawn regarding the benefit of sunitinib in mucinous ovarian carcinoma. The results of this study support further investigation of non-continuous sunitinib monotherapy in patients with mucinous ovarian carcinoma.
In a phase III trial including 37 patients with mucinous ovarian carcinoma, treatment with nintedanib in combination with carboplatin and paclitaxel across all included subtypes resulted in a progression-free survival of 17.6 months with nintedanib and 16.6 months with placebo.16 17 However, this efficacy was not translated to overall survival. On subgroup analysis, the HR for the mucinous/clear cell histological classification showed that overall survival was more favorable in the placebo arm over the nintedanib arm with an HR 1.28 (0.63–2.61).17 The overall survival results of this trial do not strongly support a role for nintedanib in mucinous ovarian carcinoma.
A third inhibitor, pazopanib, is effective in treating renal cell carcinoma. The phase III trial AGO-OVAR16 comparing pazopanib in combination with chemotherapy vs chemotherapy alone demonstrated an improvement in progression-free survival. However, this did not translate to an improvement in median overall survival.18 In a phase II trial including 1 patient with mucinous ovarian carcinoma, adding pazopanib to paclitaxel revealed no benefit to progression-free survival or overall survival, compared with paclitaxel alone.19 Based on these two trials, there is limited evidence to support future trials of pazopanib in mucinous ovarian carcinoma.
Human receptor epidermal growth factor 2 (HER2, also known as ERBB2) gene amplification is shown to drive tumor development and progression in 18–26% of patients with mucinous ovarian carcinoma.20 A case report described a patient with metastatic mucinous ovarian carcinoma treated previously with surgical resection, chemotherapy, bevacizumab and cetuximab with disease progression. The patient responded to trastuzumab monotherapy and combination therapy with Iapatinib with stable disease for approximately 9 months, evident with a downtrend in the serum marker CEA and improvement in Eastern Cooperative Oncology Group (ECOG) performance status.21 Furthermore, in a second case report of a patient with mucinous ovarian carcinoma pre-treated with chemotherapy and bevacizumab, the patient was switched to chemotherapy and trastuzumab after detecting a strong ERBB2 gene amplification. After ceasing treatment on experiencing severe adverse effects including peripheral neuropathy, radiographic progression of disease with extensive metastasis was observed 12 months after the last treatment.22 Another case report discussed two patients with recurrent mucinous ovarian carcinoma. The first patient was treated with chemotherapy and trastuzumab followed by trastuzumab monotherapy and achieved stable disease. However, disease recurred when trastuzumab was stopped and improved with recommencement. The second patient was initially treated with chemotherapy only, which resulted in disease progression. After commencing trastuzumab monotherapy the patient responded with normal tumor markers and no clinical evidence of disease. However, central nervous system recurrence occurred 1 month after stopping trastuzumab.20 All patients in the case reports above demonstrated a positive response to treatment with trastuzumab. However, it is challenging to infer progression-free survival and overall survival outcomes through case reports alone, since patients with no response are seldom reported. These findings warrant further investigation of trastuzumab in mucinous ovarian carcinoma through clinical trials or an unbiased approach such as a registry analysis.
Epidermal growth factor receptor inhibitors
Epidermal growth factor receptor (EGFR) inhibition by erlotinib blocks tumor cell growth and initiates apoptosis in EGFR-overexpressing tumor cells.23 Approximately 55% to 98% of advanced epithelial ovarian carcinomas have been found to overexpress EGFR.24 A phase III trial including 14 patients with mucinous ovarian carcinoma exhibited no overall or histological subtype-based improvement in median progression-free survival or overall survival.25 Tumor EGFR status was not a criterion for selection of patients in this trial. Immunohistochemistry and mutation analyses for EGFR were conducted for a proportion of patients. This analysis revealed that the presence of EGFR mutations or overexpression did not predict erlotinib efficacy. Furthermore, in this study it was observed that patients with positive EGFR had significantly worse progression-free survival and overall survival when compared with patients with negative EGFR. This study revealed that EGFR may have a role as a prognostic marker in ovarian cancer which was not evident in previous studies.26 Based on the outcomes of this study, further investigation of erlotinib in the treatment of mucinous ovarian carcinoma is not warranted.
AZD1775 is an inhibitor of WEE1, which is a tyrosine kinase that regulates cell cycle progression. Inhibiting WEE1 increases the apoptotic response to DNA damage in p53 deficient tumor cells, thereby enhancing the anti-tumor activity of chemotherapy in platinum-resistant tumors. A phase II study of chemotherapy and AZD1775 in TP53 mutated ovarian tumors demonstrated an objective response rate of about 43%.27 The trial included two patients with mucinous ovarian carcinoma, one demonstrated a partial response while the other patient had progressive disease. This study’s patient outcomes were presented with reference to individual histological subtypes and mutations. This allowed us to identify the responses of the two patients with mucinous ovarian carcinoma. The encouraging results of this agent for platinum-resistant tumors with p53 deficiency warrant further phase II and III clinical trials.
Monoclonal antibodies against tumor markers
CA-125 is expressed by a significant proportion of epithelial ovarian cancers and elevated levels are associated with platinum resistance and increased tumor invasiveness. Abagovomab is a monoclonal antibody that mimics CA-125 and has been shown to induce tumor specific immune responses in preclinical and phase I/II studies. In a phase III trial comparing abagovomab against a placebo as maintenance therapy, 9 patients with mucinous ovarian carcinoma were included. Despite having strongly supporting phase II data, this trial observed no benefit across all patients in recurrence-free survival or overall survival.28 However, as the authors discuss, targeting multiple tumor antigens simultaneously has shown promising effects in other solid tumor trials. This may be a reasonable avenue for future trials targeting tumor antigens.
Targeting SRC pathway
SRC family kinases and receptor tyrosine kinases are involved in signaling that promotes cell survival, growth, metastasis and angiogenesis.29 30 Preclinical studies have shown that SRC family kinases are overexpressed in mucinous ovarian carcinoma tumor cells and are thought to contribute to chemotherapy resistance.30 The anti-tumor effects of dasatinib through the inhibition of SRC family kinases and several receptor tyrosine kinases such as PDGF receptors results in inhibition of cell proliferation and promotion of cell death. Mouse in vivo studies revealed that combination therapy of dasatinib with oxaliplatin significantly reduced mucinous ovarian tumor weight.30 A phase II trial including one patient with mucinous ovarian carcinoma demonstrated no significant overall improvement in progression-free survival.31 Histological subtype-based analysis was not provided, therefore, specific outcomes of the patient with mucinous ovarian carcinoma cannot be deduced. The outcomes of this study provide inadequate evidence to direct further investigation of dasatinib in the mucinous histotype. However, despite the outcomes of this study on dasatinib monotherapy, it does not preclude further evaluation of combination therapy of dasatinib and chemotherapy in mucinous ovarian carcinoma given the pre-clinical evidence.
Farnesyltransferase is an enzyme involved in the functioning of Ras family proteins, which are critical oncogenes involved in cell proliferation. If a Ras protein is inappropriately activated, as in the case of KRAS mutation in mucinous ovarian carcinoma, it can result in proteins that promote uncontrolled cell growth and proliferation. The anti-tumor activity of lonafarnib, a farnesyltransferase inhibitor, is attributed to the inhibition of post-atranslational modifications that are required for Ras to function.32 A phase II trial including 5 patients with mucinous ovarian carcinoma demonstrated no benefit in adding lonafarnib to carboplatin and paclitaxel therapy, with no improvements seen in progression-free survival and overall survival compared with the chemotherapy only arm.33 Conclusions regarding the efficacy of lonafarnib in mucinous ovarian carcinoma cannot be drawn due to the absence of a histological subtype-based analysis of outcomes. However, based on the overall results of this trial, further investigation of lonafarnib in ovarian cancer is not supported.
The main limitations of the clinical trials included in this review are primarily a result of the rarity of mucinous ovarian carcinoma. There have been no completed clinical trials of targeted therapy to date that are specific to patients with this histotype, and only a single trial (GOG-0241) of this nature has been initiated to date before being terminated. Therefore, this review identified studies that have included patients with mucinous ovarian carcinoma. However, the sample size of patients with this disease within the discussed pan-ovarian clinical trials have been relatively low, with the maximum number of mucinous histotype patients in a single trial being 40, in the AGO-OVAR16 trial of pazopanib. The majority of the articles did not provide a histological subtype-based analysis of responses to therapy, limiting the inferences that can be drawn specifically regarding the efficacy of a therapeutic agent in patients with mucinous ovarian carcinoma. Second, in the future targeted therapies are likely to have the potential to be offered to patients with mucinous ovarian carcinoma based on tumor biomarker stratification. Except for trials and case reports in trastuzumab, AZD1775 and erlotinib, many of the trials discussed in this review did not have specific tumor biomarkers determining entry of patients into trials.
The main limitations of the review methodology includes the inability to search the full-text or supplementary files for keywords in the databases and registers searched for this review to increase the specificity of the search. This made it quite laborious to look through the baseline characteristics table of trials when screening records. This limitation also makes it likely that trials were potentially missed by the search process utilized in this review – trials that included patients with mucinous ovarian carcinoma but only mentioned this elsewhere in the full-text or in the supplementary materials. Unfortunately, performing such a search using a full-text searching tool such as Google Scholar results in tens of thousands of results, which is unfeasible to screen. Utilizing natural language processing systems may be an avenue for improving search efficacy and specificity in future reviews.34 An extension of this review could involve gathering histological subtype-based data and outcomes for the subset of patients with mucinous ovarian carcinoma in trials, by contacting the conducting team of individual trials. This step could allow inferences to be made regarding the efficacy of the targeted agents discussed.
The aim of this review was to identify and evaluate the current evidence for targeted therapy in patients with mucinous ovarian carcinoma to inform directions for further investigation of therapeutic agents, thereby contributing to the development of personalized treatment and perhaps potential integration into standard treatment for this disease (Table 2). Despite the limitations, it is evident that the targeted therapies outlined in this review have varying degrees of evidence for further investigation in patients with mucinous ovarian carcinoma. The molecular targets that have been explored in the above trials are VEGF, HER2, WEE1 tyrosine kinase, multiple tyrosine kinase receptors, CA-125, PDGFR, FGFR, EGFR, farnesyltransferase and SRC family kinases. Based on the clinical trials and case reports evaluated, further investigation is warranted for bevacizumab, trastuzumab, AZD1775 and cediranib. Many of the agents, even those that showed no efficacy as monotherapies, may be investigated further in combination with other targeted therapies or chemotherapeutic agents. Due to the small sample sizes within the mucinous ovarian carcinoma subsets, observed differences in progression-free survival and overall survival may not meet the threshold for significance. Therefore, it is likely that outcomes based on RECIST criteria, ECOG performance status and tumor marker trends will be more useful in this context.
Suggestions for future trials investigating the agents that show promising patient outcomes include aims to optimize timing and duration of treatment and identify potential patient/tumor factors that may predict treatment efficacy. It is likely that multinational efforts will be required to successfully conduct these rare tumor trials in mucinous ovarian carcinoma. However, given the phase III GOG-0241 trial that was terminated due to poor accrual, such trials may never be undertaken. In which case, evaluating outcomes of pan-ovarian or pan-cancer trials in reviews like this may help clinicians make informed choices regarding off-label treatment in mucinous ovarian carcinoma. In the future, prospective registry trials, adaptive trials and basket trials such as Bouquet-ENGOT-gyn2, as well as non-trial options such as multi-institutional series or regional/national databases, could play a role in gathering therapeutic evidence for such rare tumors. Analysis of existing data is challenging given variable reporting mechanisms, missing data and uncontrolled confounders, but could provide stimulus to pursue a promising therapy in a more controlled fashion.
Patient consent for publication
KLG is funded by the Peter MacCallum Cancer Foundation, the Australian National Health and Medical Research Council (NHMRC) and the US Dept of Defense.
Contributors DN undertook literature review and analysis and drafted the manuscript. KLG conceptualized the study, provided input on design, supervised the conduct of the study and contributed to drafting the manuscript. Both authors approved the final version.
Funding This study was supported by National Health and Medical Research Council (2002943), Peter MacCallum Foundation, Congressionally Directed Medical Research Programs (OC200056).
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.