Efficacy of pazopanib monotherapy in patients who had been heavily pretreated for metastatic soft tissue sarcoma: a retrospective case series

Background We retrospectively reviewed outcomes of treatment with pazopanib, an oral multi-tyrosine kinase angiogenesis inhibitor, in patients with advanced soft tissue sarcoma, a rare and heterogeneous tumor group with limited treatment options. Methods Between 2009 and 2013, 43 patients with metastatic soft tissue sarcoma received pazopanib as salvage chemotherapy after one or more cytotoxic regimens. Response rate, progression-free survival, and overall survival were analyzed according to histological subtype, Eastern Cooperative Oncology Group performance status, and metastatic site. Results Common histological subtypes included leiomyosarcoma (n = 9), angiosarcoma (n = 6), malignant fibrous histiocytoma/undifferentiated pleomorphic sarcoma (MFH/UPS, n = 5), malignant peripheral nerve sheath tumor (MPNST, n = 5), and synovial sarcoma (n = 4). Nineteen patients (44.2%) received more than two chemotherapy regimens before pazopanib. At the time of analysis, 208 treatment cycles of pazopanib had been administered (median, 4.8 cycles per patient), and no treatment-related mortality occurred. The disease control rate was 61.0% (95% confidence interval [CI], 46.1–75.9%), and the overall response rate was 17.1% (partial response, n = 7; complete response, n = 0). Partial response was achieved in two patients with synovial sarcoma, two with MFH/UPS, one with MPNST, one with leiomyosarcoma, and one with angiosarcoma. The median lengths of progression-free survival and overall survival were 5.0 months (95% CI, 3.6–6.4 months) and 8.2 months (95% CI, 5.8–10.6 months), respectively. Progression-free survival was shorter in the patients with liposarcoma and rhabdomyosarcoma (1.3 and 0.9 months, respectively) than in those with leiomyosarcoma, MPNST, MFH/UPS, and synovial sarcoma (5.6, 6.5, 7.1, and 7.7 months, respectively). Conclusions Pazopanib demonstrated acceptable antitumor activity in the Asian patients who had been heavily pretreated for sarcoma, with seemingly more favorable results in the patients with leiomyosarcoma, MPNST, MFH/UPS, and synovial sarcoma than in those with liposarcoma and rhabdomyosarcoma. Electronic supplementary material The online version of this article (doi:10.1186/s12885-015-1160-x) contains supplementary material, which is available to authorized users.


Background
Soft tissue sarcomas (STS) are a rare and heterogeneous group of tumors that originate from mesenchymal cells and account for 1% of all adult malignancies [1,2]. The primary treatments of STS are surgery and radiotherapy. However, approximately 40% of patients experience tumor recurrence, and survival rate is poor, with a median overall survival (OS) of less than 12 months [3]. STS is comprised of more than 50 different histological subtypes [4] that differ greatly in terms of treatment response and prognosis [2]. Despite this heterogeneity, patients with advanced non-gastrointestinal stromal tumor STS are generally treated in the same manner. However, chemosensitivity varies according to tumor subtype, and survival is also influenced by tumor grade, patient age, and performance status [5]. For instance, angiosarcoma is responsive to paclitaxel [6][7][8][9], and uterine leiomyosarcoma generally shows a good response to high-dose gemcitabine combined with docetaxel [10].Anthracyclines and ifosfamide, either alone or in combination, are the gold standard treatments of advanced STS [3,11]. However, after failure of conventional first-line cytotoxic chemotherapy, available treatment options are severely limited because of a high risk-to-benefit ratio in terms of patient tolerability and survival. Hence, the availability of less toxic agents that can improve chances of progression-free survival (PFS) or OS is crucial. In light of this, a recent pivotal phase III trial in refractory sarcoma patients (the PALETTE trial) demonstrated a significantly prolonged median PFS associated with pazopanib treatment.
Pazopanib is a synthetic indazolylpyrimidine that functions as a multitargeted tyrosine kinase inhibitor (TKI) with a high affinity for vascular endothelial growth factor receptors and a low affinity for platelet-derived growth factor receptors, fibroblast growth factor receptors, and c-Kit [12]. Based on the results of the PALETTE trial, pazopanib is currently recommended as the gold standard treatment for patients with metastatic nonadipocytic STS after failure of standard chemotherapy. However, only strictly selected patients with specific histological subtypes such as non-adiopocytic sarcoma were included in the clinical trial, and clinical use of pazopanib in unselected patients has not yet been fully documented. Furthermore, most patients enrolled in the PALETTE study were of Caucasian ancestry and only 57 of the 247 patients in the pazopanib group (23.2%) were from Asian ancestry (by personal communication with GSK). A recent phase II pazopanib trial demonstrated that Asian patients with nasopharyngeal carcinoma tolerated the treatment well, with a similar toxicity profiles [13]. However, the efficacy and tolerability of pazopanib in Asian patients with sarcoma are scarcely reported. Hence, the efficacy and tolerability of pazopanib in Asian patients should be evaluated. Therefore, we retrospectively investigated the anti-tumor efficacy of pazopanib in heavily pretreated STS patients from two major Korean cancer centers and conducted a subgroup analysis according to histological subtype.

Patients and treatment
We retrospectively reviewed the medical records of patients with advanced STS who were treated with pazopanib between May 2009 and November 2013 at Samsung Medical Center and Yonsei University College of Medicine, South Korea. The inclusion criteria were as follows: (1) pathologically confirmed STS and (2) availability of complete clinical information, including patient demographic characteristics, primary tumor site, tumor stage, and treatment record. The following clinicopathological variables were collected: age, sex, histological type, extent of metastasis, Eastern Cooperative Oncology Group (ECOG) performance status, and treatment history. The study was reviewed and approved by the Institutional Review Board of Samsung Medical Center and Yonsei University College of Medicine.

Treatment
Pazopanib was administered orally at a dose of 800 mg once daily. The dose was reduced to 600, 400, or 200 mg for the management of adverse events at the discretion of the physician. Treatment was repeated every 4 weeks and continued until disease progression, unacceptable toxicity, or patient refusal. Evaluation of tumor response was performed every 2 months based on computed tomographic or magnetic resonance imaging findings. Responses were assessed according to the Response Evaluation Criteria in Solid Tumors, version 1.1 [14].

Statistical analysis
Standard descriptive and analytical methods were used to describe the patient population and their baseline characteristics. OS was defined as the time from the initiation of pazopanib treatment to the date of death or last follow-up. PFS was defined as the time from initiation of the pazopanib treatment to the date of documented disease progression or death from any cause. Kaplan-Meier estimates were used to analyze time-toevent variables, and 95% confidence intervals (CIs) were computed for time-to-event medians. Survival comparisons were performed using univariate log-rank tests. The Cox proportional hazards model was used for multivariate analyses. Two-tailed P < 0.05 was considered statistically significant. Statistical analysis was performed using the SPSS version 18 software (SPSS Inc., Chicago, IL, USA).
All of the patients had previously received at least one cytotoxic chemotherapy regimen before pazopanib treatment, and most of the patients had been heavily pretreated with at least two previous cytotoxic regimens. Fifteen patients (34.9%) had received two prior regimens, and 19 patients (44.2%) had received three or more prior regimens. In the study cohort, the following patients had received prior regimens: 69.8% (n = 30), doxorubicin-based chemotherapy; 90.7% (n = 39), ifosfamide-based chemotherapy; 74.4% (n = 32), taxane-based chemotherapy; and 65.1% (n = 28), gemcitabine-based chemotherapy.
Pazopanib therapy was administered in 208 treatment cycles, with a median of 4.8 cycles per patient (range, 1-17 cycles). At the time of analysis, 6 patients were still receiving pazopanib treatment, and the remaining 37 patients had stopped treatment because of progression (n = 30), patient refusal (n = 1), toxicity (n = 1), or other reasons (n = 5).

Survival outcomes
At a median follow-up of 12.0 months (95% CI, 5.7-18.3 months), the median PFS was 5.0 months (95% CI, 3.6-6.4 months), and the median OS was 8.2 months (95% CI, 5.8-10.6 months). We analyzed PFS and OS in patients with different histological subtypes (Table 2). Patients with liposarcoma or rhabdomyosarcoma had significantly poorer survival when compared with patients with non-liposarcoma or non-RMS cases (P < .001, Additional file 1: Figure S1A). Accordingly, the patients with liposarcoma (n = 2) had poorer survival after pazopanib treatment than those with other types of sarcoma (Additional file 1: Figure S2A). Of note, the patients with RMS progressed to pazopanib rapidly, but were all alive at the time of this writing. Age (>50 years vs ≤50 years, P = 0.079), number of prior chemotherapy regimens (≥2 vs 0-1, P = 0.162), primary site (truck/retroperitoneum vs extremity, P > 0.05), and existence of liver and lung metastases (presence vs absence, P = 0.756) were not significantly correlated with PFS at univariate level. However, performance status (ECOG 2 vs. 0 or 1, P = 0.034) and prior response to doxorubicin (stale response or progression vs partial response, P = 0.05) at the time of pazopanib treatment were significant adverse factors of pazopanib treatment in terms of PFS.

Discussion
We demonstrated that pazopanib is a feasible treatment option with acceptable antitumor activity in patients who had been heavily pretreated for metastatic STS.
Considering that a few patients in the previous clinical trials were of Asian ethnicity [15][16][17], our study also shows that pazopanib is well tolerated in Asian STS patients. Beyond standard systemic treatment with doxorubicin and ifosfamide, newer agents such as gemcitabine, trabectedin, and pazopanib have been assessed for subsequent treatment of STS. In a phase III trial, pazopanib treatment significantly improved PFS compared with placebo, with a median prolongation of 3 months [16]. These results led to the approval of pazopanib for STS, making it the first anti-angiogenic drug approved for STS. In terms of efficacy, our study shows similar outcomes (PFS, 5.0 months and OS, 8.2 months) as those of the PALETTE trial. However, our observation of shorter OS compared with that in the PALETTE trial might be because most of our patients had been heavily pretreated with at least two prior chemotherapy regimens. Regarding toxicity profile, despite the retrospective nature of our study, we used the same dosage and dose modification protocol as those used in the PALETTE trial. Similar frequency of dose reduction (48% in our cohort vs 39% in the PALLETE trial) and treatment duration (median, 19 weeks vs 16.4 weeks) were observed.Given the diverse histological subtypes of STS with different biological and clinical behaviors, an exploratory subgroup analysis according to histological subtype was performed in previous trials [15,16]. In the EORTC 63043 study, 142 patients were recruited into four different strata as follows: adipocytic STS, leiomyosarcoma, synovial sarcoma, and other STS types. Among the strata, the adipocytic sarcoma stratum was closed due to poor PFS rate at 12 weeks. Based on this phase II trial, adipocytic STS was excluded from the PALETTE trial. In a recent subgroup analysis of longterm responders to pazopanib [17], patients with leiomyosarcomas and synovial sarcomas, vascular tumors, alveolar soft part sarcoma, solitary fibrous tumors, and desmoplastic small round cell tumors were the main long-term responders and survivors. In line with these results, we also observed better anti-tumor activity of pazopanib in patients with non-adipocytic sarcoma such as leiomyosarcoma, MPNST, MFH/UPS, or synovial sarcoma but less activity in patients with adipocytic sarcoma or rhabdomyosarcoma.
With regard to treatment response to angiogenesis inhibitors such as pazopanib among patients with adipocytic sarcoma, several trials have reported varying results from subgroup analyses [16,18,19]. Similar to the PALETTE trial, a phase II trial demonstrated that patients with liposarcoma were poor responders to sorafenib [18]. By contrast, patients with liposarcoma showed a promising treatment response to sunitinib in a single-institution study, with 3.9 months of PFS and 18.6 months of OS [19]. Currently, the underlying biological mechanism of poor response to pazopanib in adiopocytic sarcoma has not been defined, but it may depend on the heterogeneity of adipocytic sarcoma subtypes (i.e., dedifferentiated, myxoid, round cell, and pleomorphic). In our previous work, we showed a distinct prognosis and the clinical features of dedifferentiated liposarcoma among other adipocytic sarcomas [20]. However, as all but two liposarcoma patients included in this analysis had myxoid liposarcoma, we cannot draw definitive conclusions regarding treatment response to pazopanib according to different subtypes.
In terms of pediatric sarcomas, clinical activity with pazopanib was demonstrated for desmoplastic small round cell tumors and alveolar rhabdomyosarcoma in a phase I study [21]. In our case series, poor responders were patients with embryonal and spindle cell rhabdomyosarcoma who had failed to respond to four previous cytotoxic regimens. Because these patients already had refractory sarcoma at the time of pazopanib therapy, it is difficult to define the anti-tumor activity of pazopanib in this subset. However, these patients failed to respond to pazopanib within 2 months of therapy initiation, which suggests that pazopanib is not an optimal treatment option for this subtype. Nevertheless, because of our small sample size, further observations are required regarding the effect of pazopanib in adult-onset pediatric type sarcoma. Some limitations of this study include its retrospective nature and small sample size, especially for the histological subgroup analyses. However, to date, no study reports the efficacy of pazopanib specifically in an Asian population. Furthermore, unlike well-controlled clinical trials [15,16], our patient cohort was mostly composed of individuals with poor performance status who had been heavily pretreated.

Conclusion
In summary, we demonstrated that pazopanib is a feasible option for the patients who had been heavily pretreated for metastatic sarcoma, with a small subset of patients achieving long-term responses. To gain insight into the subgroup of patients who could benefit most from pazopanib, an expansion of the patient pool through a large multicenter cohort study is needed.

Additional file
Additional file 1: Figure S1. Survival according to histological subtype. A) Progression-free survival (PFS) and B) overall survival (OS).