Efficacy of vinorelbine combined with low-dose methotrexate for treatment of inoperable desmoid tumor and prognostic factor analysis

Shu Li, Zhengfu Fan, Zhiwei Fang, Jiayong Liu, Chujie Bai, Ruifeng Xue, Lu Zhang, Tian Gao

Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Bone and Soft Tissue Tumors,Peking University Cancer Hospital amp; Institute, Beijing 100142, China

＊These authors contributed equally to this work.

Correspondence to: Zhengfu Fan. Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Bone and Soft Tissue Tumors, Peking University Cancer Hospital amp; Institute, Beijing 100142, China. Email: zhengfufan@126.com.

Efficacy of vinorelbine combined with low-dose methotrexate for treatment of inoperable desmoid tumor and prognostic factor analysis

Shu Li＊, Zhengfu Fan＊, Zhiwei Fang, Jiayong Liu, Chujie Bai, Ruifeng Xue, Lu Zhang, Tian Gao

Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Bone and Soft Tissue Tumors,Peking University Cancer Hospital amp; Institute, Beijing 100142, China

＊These authors contributed equally to this work.

Correspondence to: Zhengfu Fan. Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Bone and Soft Tissue Tumors, Peking University Cancer Hospital amp; Institute, Beijing 100142, China. Email: zhengfufan@126.com.

Objective:To assess the efficacy of conservative chemotherapy for inoperable desmoid tumor (DT) and analyze the prognostic factors.Methods:From November 2008 to April 2016, 71 patients of inoperable DT were treated with vinorelbine and low-dose methotrexate in the Department of Bone and Soft Tissue Tumors, Peking University Cancer Hospital amp;Institute, and enrolled in this retrospective study. The chemotherapy duration is one year. The efficacy of chemotherapy and the prognosis were observed.Results:Of the 71 patients, 55% were female. Age of onset varied from 1 to 47 years, and the median age was 14 years. Only 11 (15.5%) cases suffered primary tumor. The distribution of the site of tumors was: 31 (43.7%) in the trunk, 36 (50.7%) in the limbs, and 4 (5.6%) in the peritoneal and pelvic cavity. The size of tumor (the maximum diameter) differed from 2 to 37 cm with a mean of 9.3 cm. The median follow-up duration was 28 (range, 6—87)months. Common side effects included: nausea and vomiting, liver injury, bone marrow suppression and oral ulcers.When the chemotherapy finished, 1 (1.4%) case achieved complete response, 24 (33.8%) achieved partial response,37 (52.1%) achieved stable disease and 9 (12.7%) had progressive disease. The overall response rate was 87.3%.The progression-free survival (PFS) of the participants were from 6 to 87 months, and the 2-, 3- and 5-year PFS was 79.9%, 68.4% and 36.3%, respectively. No significant difference was identified in PFS in subgroups of gender,age of onset, age of chemotherapy, tumor site and tumor size.Conclusions:For recurrent, inoperable and progressive DT, enough course of chemotherapy with vinorelbine combined with low-dose methotrexate was an optional choice for local control.

Desmoid tumor; aggressive fibromatosis; chemotherapy

Introduction

Desmoid tumor (DT) is also known as aggressive fibromatosis (AF) and desmoid type fibromatosis. It is a rare, fibroblast-origin, benign tumor, and accounts for 0.03% of all neoplasms, with the annual incidence of 2—4 cases per million (1). DT could occur all over the body.The most common areas are limbs and trunk (2). It tends to occur in female adults with a male/female ratio of approximately 1:3, and the average age and median age of patients were 31 years and 29 years respectively (1). DT could be stable, aggressive, or have spontaneous remission(3), and will not metastasize to lymph node and distant areas. But it is easy to recur locally due to its local invasive growth, rather than the satellite lesions and skip metastasis.Most local recurrences occur within the first two years after operation, but sometimes it may recur in the 12th year after operation (4).

The high recurrent rate of DT after resection makes it very difficult to treat. Penget al. (5) reported 211 patients with DT and the 5-year recurrent rate is about 50% after surgery. Radiation therapy could improve local control of patients with positive margin, but its clinical application was restricted by the complications such as limb contracture, growth disorder, pathological fracture and sarcoma after radiation. Thus, radiotherapy is not suitable for young patients. Shinet al. (6) found that adjuvant radiotherapy may delay the recurrence of the tumor,although it seems to have no effect on the final relapse rate.For these patients who are not suitable for surgery and radiotherapy, systemic treatment is necessary. But the clinical data of systemic treatment of DT are still limited.

In the current study, we summarized the clinical manifestation, treatment effect and prognostic data of patients with inoperable and progressive DT, who were treated in the Department of Bone and Soft Tissue Tumors, Peking University Cancer Hospital amp; Institute.

Materials and methods

Patients

From November 2008 to April 2016, 71 patients with inoperable and progressive DT were treated in the Department of Bone and Soft Tissue Tumors, Peking University Cancer Hospital amp; Institute, and all the cases were pathologically diagnosed by experienced pathologists through core biopsy for primary cases and pathology consultation for recurrent cases. The clinical characteristics are described inTable 1. This study was approved by the Ethic Committee of Peking University Cancer Hospital and carried out in accordance with the approved guidelines.

Procedure and treatment

All the cases were evaluated by magnetic resonance imaging (MRI) or computed tomography (CT) scan before receiving chemotherapy to assess the possibility of radical resection and measure the tumor size by experienced radiologists. Patients with inoperable DT were enrolled in the study. The criteria for inoperable cases include: 1) the radical resection will cause massive defect of soft tissue and result in loss of limb function and huge change of appearance; 2) the radical resection will implicate the main nerves and vessels; 3) the tumor is invasive to the bone; 4)the patients refuse surgery; and 5) amputation is not considered. The exclusion criteria were: 1) the patients were with contraindications for chemotherapy; or 2) the patients refused chemotherapy.

Table 1 Clinical characteristics and effect of chemotherapy(N=71)

The patients were followed up through outpatient and telephone by the same doctor (Li S), and the effect of chemotherapy was evaluated by MRI or CT scan to measure the tumor size. The assessment for response was taken before the chemotherapy, 6 and 12 months after initial chemotherapy and every 6 months after chemotherapy cessation. All patients were told to try to take all the reexaminations in Peking University Cancer Hospital. The tumor change was evaluated with Response Evaluation Criteria in Solid Tumors (RECIST) guidelines(version 1.1) (7).

Statistical analysis

The tumor response to chemotherapy was observed according to RECIST guidelines. Kaplan-Meier method was used to calculate the relationship between survival data and the potential influencing factors, such as gender, age of onset, age of chemotherapy, tumor site and tumor size.Progression-free survival (PFS) analyses were performed by SPSS software (Version 16.0; SPSS Inc., Chicago, IL,USA) with a two-sided test at a 5% level of significance.

Results

The female/male ratio of the enrolled patients was about 1.2:1. Age of onset varied from 1 to 47 years, the median age was 14 years, and the ratio of adolescent and children to adult is about 1.2:1. Most patients (84.5%) suffered tumor recurrence. In 36 (50.7%) cases, tumors were in the limbs, and 45.1% suffered the dysfunction of limb movement, which is the main symptom for DT patients.The size of tumor (the maximum diameter) differed from 2 to 37 cm with a mean diameter of 9.3 cm. In 78.9% of cases, the tumor was more than 5 cm in diameter. The main cause was repeated resection and recurrence. The age when chemotherapy started varies from 3 to 52 years. The median age was 20 years, and 34 of 71 cases started chemotherapy when they were under 18 years. The median follow-up duration was 28 (range, 6—87) months.

The chemotherapy duration of 14 cases was less than 1 year. The rest 57 patients completed at least 12 months of chemotherapy. When the chemotherapy finished, 1 case achieved complete response (CR), 24 achieved partial response (PR), 37 achieved stable disease (SD), and 9 had progressive disease (PD). The overall response rate (ORR)was 87.3% (Table 1). The PFS of the participants was from 6 to 87 months, and the 2-, 3- and 5-year PFS was 79.9%,68.4% and 36.3%, respectively (Figure 1).

The common side effects included: nausea and vomiting,liver injury, bone marrow suppression and oral ulcers.Patients with elevation in hepatic transaminases (Grade 1 or more) were administered with reduced glutathione sodium (ivgtt) and bicyclol tablets (po). Patients with bone marrow suppression (Grade 2 or more) were administered with granulocyte stimulating factor. The antiemetics such as metoclopramide tablets were administered together with MTX. Patients with oral ulcers were treated with calcium folinate gargling and rinsing. The complication for most patients was tolerable.

No significant difference was identified in PFS in subgroups of gender, age of onset, age of chemotherapy,tumor site and tumor size. PFS curves of different subgroups are showed inFigure 2and the clinical characteristics of different subgroups are showed in theTable 2.

Discussion

Surgery

Figure 1 Kaplan-Meier curve of progression-free survival (PFS).

It is widely considered that surgery is the first choice for DT. Local control rate of patients with negative margin was better than those with positive margin (8). Zenget al.(9) reported that tumor larger than 5 cm, extra-abdominal tumor and R1 resection status were associated with worse recurrence-free survival. The only factor associated with low recurrence is negative margin (10). But we cannot simply pursue negative margin under the risk of limb appearance and function impairment, because patients with positive margin still have chance for secondary radical surgery and radiotherapy. DT is not a lethal malignancy.The amputation is not a suitable choice for patients with unresectable DT. Some scholars pointed out that the indication of amputation including function-loss, severe pain, and invasion to main nerve, vessel and/or bone (11).In the current study, DT recurred in stump of some cases suffering amputation in other hospitals, and was well controlled after chemotherapy in authors’ hospital(Figure 3). Further, Gronchiet al. (2) investigated 203 patients of DT, and found the disease-free survival rate of primary patients is better than recurrent patients (10-year disease-free survival rate: 76% to 59%). Huanget al. (12)found admission status (primary or recurrent) had significant impacts on event-free survival. In this study,most patients with DT were recurrent cases when admitted in Peking University Cancer Hospital.

Recently, some researchers got the opposite conclusion about surgical margin after summarizing their clinical data.Woltscheet al. (13) and Soto-Mirandaet al. (14) found the condition of the resection margin does not impact the local control rate of surgery, which indicated that DT has unique biological behavior, challenges the effectiveness of radical resection and highlights the need of adjuvant therapy like chemotherapy.

Radiotherapy

Figure 2 Progression-free survival (PFS) curves of subgroup analysis. (A) Gender (P=0.136); (B) Age of onset (P=0.784); (C) Tumor site(P=0.669); (D) Tumor size (P=0.941); (E) Age of chemotherapy (P=0.349).

Table 2 Clinical characteristics of different subgroups

Radiotherapy is the second choice for DT. For patients with unresectable tumor and for whom the resection will cause severe functional impairment, radiotherapy could be considered. Krizet al. (15) reported 37 patients received postoperative radiotherapy. The local control rate was 79%. However, many patients with DT were children and young people. For these young patients, radiotherapy may cause late and long-term complications, such as limb contracture, growth failure and secondary malignancy.Rutenberget al. (16) reported 30 patients with DT (all ＜30 years old) treated with radiotherapy. Local-regional control rate in patients ＜18 years old at the time of radiotherapy was only 20%, while 63% in patients of 18—30 years old.Thus, for young patients with unresectable tumors, radical surgery and radiotherapy were inapplicable. The median age of onset of the patients in the current study was 14 years old, so radiotherapy was not selected for treating these patients.

Traditional pharmacotherapy

Besides resection and radiotherapy, pharmacotherapy is considered as third-line treatment of DT. Patients of DT who cannot receive radical surgery and radiotherapy should receive pharmacotherapy. Sulindac, non-steroidal antiinflammatory drugs (NSAIDs), tamoxifen, toremifene,MTX and vinblastine (VBL), low-dose interferon,doxorubicin (DOX)-based regimens and imatinib were common used systemic therapy agents and recommended by National Comprehensive Cancer Network (NCCN)(17). Skapeket al. (18) reported 59 patients with measurable DT received tamoxifen and sulindac. Only 10 patients completed therapy. The estimated 2-year PFS was 36%. They thought such combination therapy showed relatively low activity as measured by response and PFS rates. In Hamada’s study (19), among 31 patients with extra-abdominal DT treated with meloxicam, 1 achieved CR, 7 achieved PR, 12 achieved SD, and 11 suffered PD.The authors found higher nuclear expression of β-catenin was significantly associated with poorer response. Penelet al. (20) reported 40 patients with unresectable and progressive symptomatic AF/DT treated with imatinib(400 mg/d for 1 year). The non-progression rates at 3, 6 and 12 months were 91%, 80% and 67%, respectively. The 2-year progression-free rate and overall survival rate were 55% and 95%. Nishidaet al. (21) reported 15 patients with inoperable tumors who were resistant to meloxicam treatment were treated with MTX and VBL every other week. Six patients showed PR, and only 1 patient presented disease progression. Yoonet al. (22) reported 11 patients with AF treated with oral methotrexate (10 mg once per week). All of the patients had remission.

In Garbay’s study (23), combined chemotherapy was delivered in 44 (71%) cases, monotherapy in 18 (29%)patients, and 13 (21%) patients received an anthracyclinecontaining regimen. The most common nonanthracycline regimen was MTX-VBL combination (n=27). CR, PR, SD and PD were observed in 1 (1.6%), 12 (19.4%), 37 (59.6%)and 12 (19.4%) patients, respectively. Anthracyclinecontaining regimens appeared to be associated with higher response rate.

Yamamotoet al. (24) reported 3 patients with intraabdominal DT who received low-dose dacarbazine(DTIC)-doxorubicin (DOX) (D-D) chemotherapy. Two of these patients achieved CR, and 1 patient achieved PR.Their study indicated that low-dose D-D chemotherapy was safe and effective for patients with intra-abdominal DTs. Ananthet al. (25) reported that in 5 children with progressive DF treated with liposomal doxorubicin, there was an average 4.5% reduction in tumor size.

New strategy of drug therapy

Figure 3 Magnetic resonance imaging (MRI) of desmoid tumor(DT) before and after chemotherapy. (A) DT in left thigh before chemotherapy; (B) DT in left thigh after chemotherapy; (C)Recurrent DT in the stump and armpit after amputation; (D) DT in the stump and armpit after chemotherapy. The tumor shrunk obviously after 1 year’s chemotherapy.

Joet al. (26) evaluated the efficacy and safety of sunitinib in patients with advanced AF. Nineteen patients with pathologically proven AF were treated with sunitinib (37.5 mg/d) for 4 continuous weeks. Five patients achieved PR and 8 had SD. The 2-year PFS was 74.7% and OS was 94.4%. The main adverse events were neutropenia,diarrhea, and hand-foot syndrome. In 3 of 12 patients with mesenteric AF, mesenteric mass bleeding, bowel perforation and bowel fistula with tumor mass necrosis were observed. The author thought sunitinib showed potential anti-tumor activity and may be useful for the management of non-mesenteric AF.

Martin-Liberalet al. (27) first reported the outcome of two patients suffered progressive DT/AF and treated with pazopanib. Both patients achieved dramatic improvement in their symptoms and radiological signs of response. The clinical benefit lasted for more than 1 year. Then, Szucset al. (28) reported 8 patients with DT treated with pazopanib, 3 of whom achieved PR and 5 achieved SD, and 6 patients derived clinical benefit from treatment in terms of improved function and/or pain reduction.

In a phase I study (29), 7 patients with DT were enrolled and treated with an oral gamma secretase inhibitor, PF-03084014, and 5 patients achieved PR.

Summary

Azzarelliet al. first reported 30 patients with DT who were treated with MTX and VBL. The response rate was 40%,and 10-year survival rate was 67% (30). However, it was found that peripheral neuropathy occurred in about 10% of patients treated with VBL. Neurotoxicity of NVB is less than that of VBL, and the therapeutic effect is the same(31). MTX+VBL therapy was used in 27 cases in Garbay’s study (23). The median chemotherapy duration lasted for 18 weeks, 4 patients achieved PR (15%), 14 achieved SD(52%), and 9 suffered PD (33%).

In our study, better outcomes were obtained (1 CR, 24 PR, 37 SD and 9 PD; ORR 87.3%), which might be the result of longer duration of chemotherapy (1 yearvs. 18 weeks). Our chemotherapy protocol had less acute and long-term chemotherapy toxicity and was convenient for outpatients. There had been no common consensus on chemotherapy duration till now. But some scholars suggested that the chemotherapy should last for at least one year even without the radiological evidence of tumor response, unless tumor progressed and severe chemotherapy toxicity occurred (32). According to our experience and follow-up data, we thought that chemotherapy should last for at least 12 months and could be prolonged to 18 months regarding the status of patients(effects and side effects of chemotherapy).

Compared to other studies (Table 3), the chemotherapy of MTX and NVB seemed to have better ORR and PFS for inoperable DT. But the limitation of the result is that the study is a single-arm retrospective study. Further controlled studies comparing this regimen with others are eagerly awaited, and multiple-center cooperation is recommended for conducting large-scale controlled studies.

Table 3 Comparison of curative effect among different therapeutic regimens

Conclusions

For recurrent, unresectable and progressive DT, enough course of chemotherapy with vinorelbine combined with low-dose methotrexate was an optional choice for local control, especially for young patients who were not suitable for radiotherapy.

Acknowledgements

None.

Footnote

Conflicts of Interest: Th e authors have no conflicts of interest to declare.

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Cite this article as: Li S, Fan Z, Fang Z, Liu J, Bai C, Xue R,Zhang L, Gao T. Efficacy of vinorelbine combined with lowdose methotrexate for treatment of inoperable desmoid tumor and prognostic factor analysis. Chin J Cancer Res 2017;29(5):455-462. doi: 10.21147/j.issn.1000-9604.2017.05.10

Submitted Sep 05, 2017. Accepted for publication Oct 12, 2017.

10.21147/j.issn.1000-9604.2017.05.10

View this article at: https://doi.org/10.21147/j.issn.1000-9604.2017.05.10

the chemotherapy of vinorelbine (NVB, 6—10 mg/m2, ivgtt, per week)combined with low-dose methotrexate (MTX, 30 mg/m2,po, per week; the total dose was divided into 5 pieces from the 1st day to the 5th day in a week). The planned whole chemotherapy period was 12 months.