Abstract
This study aimed to investigate the activity of arsenic trioxide (As2O3) combined with ascorbic acid, ifosfamide, and prednisone chemotherapy in patients with repeatedly relapsed and refractory multiple myeloma (MM). Here, we retrospectively analyzed medical data of 30 MM patients showing progressive disease after receiving at least two previous lines of treatment including an immunomodulatory agent (thalidomide or lenalidomide) and a proteasome inhibitor. There were 19 men and eleven women, aged 54–73 (median 65) years, in this study. The distribution of different isotypes included immunoglobulin G(IgG) (12 patients), IgA (six patients), IgD (three), and light chain (nine patients). All the patients were Durie–Salmon stage III and had relapsed at least three times; the median cycles of prior therapies was 15 (range 10–18). The patients were treated with As2O3, ascorbic acid, and CP (ifosfamide 1 g on day 1, day 3, day 5, and day 7; prednisone 30 mg taken orally for 2 weeks). As2O3 was administered as an intravenous infusion at a dose of 10 mg/d and ascorbic acid at a dose of 2 g/d for 14 days of each 4-week cycle. The results showed that after 2 cycles of therapy, there were five patients that attained partial response, 15 had minimal response, five had no change, and five had progressive disease. The overall response rate was 66.7% (20/30 cases), 50% (10/20 cases), and 40% (2/5 cases), respectively, after 2, 4, and 6 cycles of the therapy. But there were no patients that attained complete remission. The median time of overall survival and progression-free survival were 48 (29–120) and 6 (2–8) months, respectively. The most common treatment-related adverse events included neutropenia, fatigue, anemia, thrombocytopenia, and infection that could be tolerated. The results showed that As2O3 combined with ascorbic acid, ifosfamide, and prednisone chemotherapy may be a choice treatment for repeatedly relapsed and refractory MM patients.
Keywords: chemotherapy, response
Introduction
Over the past decade, increasing knowledge of multiple myeloma (MM) biology has already been contributing to a more specific drug design, and we have recently learned that in the pathogenesis of MM, as important as the malignant cells themselves is their interaction with the microenvironment. Bortezomib and lenalidomide have returned a remarkable treatment response in recent years, but MM patients have still inevitably relapsed.1 MM remains an incurable disease for now, with median survival rates of 4–6 years. Thus, newer treatments with good safety profiles are needed to improve the quality of responses, prolong progression, and increase overall survival (OS).
Arsenic trioxide (As2O3) is a promising compound to explore in MM because of its multifaceted antitumor activity.2,3 In this study, we explored the clinical activity of As2O3 combined with chemotherapy for relapsed and refractory MM after bortezomib and lenalidomide treatment. In the modern era, interest in arsenic as a chemotherapy was rekindled after it was identified as an active ingredient in traditional medicines in the People’s Republic of China.4 As2O3 affects multiple cellular functions via different molecular targets. As2O3 targets the mitochondria, decreasing the mitochondrial membrane potential (ΔΨm) via multiple specific targets, including Bcl-2 and the permeability transition pore complex.5 This change in potential results in the release of cytochrome C, which activates the caspase cascade. It also results in increased release of reactive oxygen species (ROS) from the mitochondria. ROS levels are increased further by As2O3 inhibition of the antioxidant enzyme GPx.6 As2O3 also inhibits activation of the cell-survival factor NF-κB via inhibition of IKK, the kinase responsible for releasing NF-κB that is sequestered in the cytoplasm.7
A multicenter trial confirmed the role of As2O3 in the management of relapsed or refractory MM using a higher dose and shorter schedule. Nine (43%) of 21 evaluated patients had an objective response. One patient with refractory disease had a 50% decrease in plasmacytoma size, eight patients had stable disease, and four had progressive disease (PD) at the first evaluation visit.8 So single-agent As2O3 for MM was not satisfactory. Wang and Fang9 reported that As2O3, ginseng saponin, and beta-elemene can inhibit the growth and telomerase activity of K562 cells. The inhibiting effects were enhanced when they were used in combination with cyclophosphamide. Ifosfamide is a common drug to treat MM, and arsenic is a routine drug for treating hematology diseases, especially for acute promyelocytic leukemia (APL), in the People’s Republic of China, so we attempted to treat MM with the combination of arsenic, ifosfamide, ascorbic acid, and prednisone.
Materials and methods
Patients
We retrospective analyzed 30 cases of patients with relapsed and refractory MM from Beijing Chao-yang Hospital of Capital Medical University and the Second Artillery General Hospital from September 2007 to March 2014. All the patients were Durie–Salmon stage III and had relapsed at least three times; the median number of prior chemotherapy cycles was 15 (range, 10–18) before using As2O3. Five patients had received autologous stem cell transplantation. There were five patients at stage II and 25 patients at stage III, according to the International Staging System.10 The median time from diagnosis to receive the As2O3 with ascorbic acid, ifosfamide, and prednisone was 40 (35–69) months for the patients in this study. This study was approved by the Chinese Medical Ethics Committee, and work was undertaken in conformity with the provisions of the Declaration of Helsinki. Consents were obtained from the patients.
Combination therapy with As2O3, ascorbic acid, ifosfamide, and prednisone
All the patients treated with As2O3, ascorbic acid, and CP (ifosfamide 1 g intravenous [IV] drip on day 1, day 3, day 5, and day 7; prednisone 30 mg taken orally [PO] for 2 weeks). As2O3, was administered as an IV infusion at a dose of 10 mg/d and ascorbic acid at a dose of 2 g/d for 14 days of each 4-week cycle. The infusion was administered over 2 hours unless adverse effects occurred, in which case the infusion was given over 4 hours.
Assessment of efficacy and safety
The cutoff date for response and survival data was October 3, 2014. Patients who received at least 2 full cycles were evaluable for efficacy. Response to treatment was assessed by quantification of MM parameters (serum and urine protein electrophoresis and immunofixation, with quantification of the M-protein, Bence–Jones proteins in urine, b2-microglobulin, and C-reactive protein) at screening and at every 2 cycles during the treatment period. We used the criteria of European Group for Blood and Marrow Transplantation (EBMT) for evaluating disease response and progression in patients with MM treated by high-dose therapy and hemopoietic stem cell transplantation.11 The criteria of response include complete remission (CR), partial response (PR), minimal response (MR), no change (NC), and PD. We observed the overall response rate (ORR) (ORR = CR + PR + MR). The criteria for relapse were any one or more of the following: reappearance of serum or urine M-protein by immunofixation or electrophoresis, development of 5% plasma cells in the bone marrow, or appearance of any other sign of progression (ie, new plasmacytoma, lytic bone lesion, or hypercalcemia). Patients with relapsed and refractory MM that had at least two previous lines of treatment including an immunomodulatory agent (thalidomide or lenalidomide) and proteasome inhibitors showing PD, as defined by the International Myeloma Working Group (IMWG) criteria, were included.12
Safety was assessed during the therapy of As2O3, administration. Laboratory studies (blood counts, electrolyte panels, urinalysis, liver function tests, and serum tumor marker analysis) and physical examinations (ECGs, echocardiograms, chest X-rays, dermatologic and neurologic consults, and nerve conduction velocity tests) were performed during therapy.
Safety was assessed by a numerical tabulation of adverse events, assessed in accordance with the National Cancer Institute (NCI) Common Toxicity Criteria, version 2, eg, grade 1 neutropenia was defined as an absolute neutrophil count (ANC) of 1,500–1,900 for grade 1; 1,000–14,000 for grade 2; 500–900 for grade 3.
Statistical analysis
The Kaplan–Meier method was used to estimate the probability of progression-free survival (PFS) and OS. OS was defined as the time from registration to death or censoring of the patient data. PFS was defined as the time relapsed between the beginning of treatment with As2O3 and tumor progression or death from any cause.
Results
Basic clinical characteristics of patients
From September 2007 to March 2014, 30 cases of relapsed and refractory MM patients were involved in this study. Patient charts were retrospectively reviewed to collect the follow-up data. There were 19 men and eleven women aged 54–73 (median 65) years in this study (Table 1). The distribution of different isotypes included immunoglobulin (Ig)G (12 patients), IgA (six patients), IgD (three patients), and light chain (nine patients). The median number of cycles of prior chemotherapy was 15 (10–18). All the patients had relapsed at least three times and then received more than two lines of chemotherapy after relapse, so all the patients were refractory. The most common prior therapies (first-line chemotherapy) were VAD (vincristine, doxorubicin, and dexamethasone), TD (thalidomide and dexamethasone), M2 (melphalan, carmustine, cyclophosphamide, vincristine, and prednisone), and bortezomib and LD (lenalidomide and dexamethasone). Five patients relapsed after receiving autologous stem cell transplant, and five patients had extramedullary plasmacytomas, in this study. There were 28 patients who received therapy with bortezomib and there were 15 patients had received lenalidomide after relapse. The second-line chemotherapies were DECP (cisplatin, etoposide, cyclophosphamide, and prednisone), VAMP (vincristine, doxorubicin, and methylprednisolone), and ABVD (vincristine, doxorubicin, carmustine, and dexamethasone).
Table 1.
Patient characteristics (n=30)
| Characteristic | Number of patients, n=30 |
|---|---|
| Age, yrs | 65 (54–73) |
| Male/female | 19/11 |
| WBC count (×109/L) | 4.7 (1.0–11.6) |
| Platelets (×109/L) | 159 (47–362) |
| Hemoglobin (g/dL) | 98 (62–125) |
| B2-MG (mg/L) | 7.25 (1.75–38.15) |
| ESR (mm/h) | 70 (30–135) |
| Plasma cell aspirate (%) of bone marrow | 49 (32–85) |
| Number of previous therapies | 15 (10–18) |
| Type of diseases | |
| IgG/κ | 8 |
| IgG/λ | 4 |
| IgA/κ | 6 |
| IgD/λ | 3 |
| λ light chain | 6 |
| κ light chain | 3 |
| Durie–Salmon stage | |
| III A | 28 |
| II B | 2 |
| ISS stage | |
| II | 5 |
| III | 25 |
| Number of previous therapies before arsenic trioxide treatment, as first-line therapy | |
| VAD | 26 (86.7) |
| M2 | 19 (63.3) |
| TD | 30 (100) |
| Bortezomib | 28 (96.7) |
| LD | 15 (50) |
| Autologous stem cell transplantation | 5 (16.7) |
| Number of previous therapies before arsenic trioxide treatment as second-line therapy | |
| DECP | 25 (83.3) |
| VAMP | 15 (50) |
| ABVD | 6 (20) |
Notes: Values are expressed as median (range or percent). VAD, vincristine, doxorubicin, and dexamethasone; M2, melphalan, carmustine, cyclophosphamide, vincristine, and prednisone; TD, thalidomide and dexamethasone; LD, lenalidomide and dexamethasone; DECP, cisplatin, etoposide, cyclophosphamide, and prednisone; VAMP, vincristine, doxorubicin, and methylprednisolone; and ABVD, vincristine, doxorubicin, carmustine, and dexamethasone.
Abbreviations: B2-MG, b2-microglobulin; ESR, estimated sedimentation rate; Ig, immunoglobulin; ISS, International Staging System; WBC, white blood cells; yrs, years.
Patient disposition and efficacy
A total of 30 patients completed at least 2 cycles of As2O3 combined with ascorbic acid, ifosfamide, and prednisone chemotherapy. After 2 cycles of therapy, there were five patients who attained PR, 15 that had MR, five that had NC, and five that had PD. The ten patients with NC and PD changed to another treatment scheme. Thus, 20 patients completed 4 cycles of As2O3 combined with ascorbic acid, ifosfamide, and prednisone chemotherapy. Of these, five patients achieved PR, five had MR, seven had NC, and three had PD. Only five PR patients completed 6 cycles of therapy, while the seven NC, three PD, and five MR patients changed to another scheme, with one patient attaining PR, one having MR, one having NC, and two having PD (Table 2). The ORR was 66.7% (20/30 cases), 50% (10/20 cases), and 40% (2/5 cases), respectively, after 2, 4, and 6 cycles of the therapy. But there were no patients who attained CR. The ten patients with PD died, all from PD.
Table 2.
Response of MM patients of relapsed and refractory to As2O3 combined with ascorbic acid, ifosfamide, and prednisone (%)
| N | ORR (%) | CR (%) | PR (%) | MR (%) | NC (%) | PD (%) | |
|---|---|---|---|---|---|---|---|
| 2 cycles | 30 | 20 (66.7%) | 0 | 5 (16.7) | 15 (50) | 5 (16.7) | 5 (16.7) |
| 4 cycles | 20 | 10 (50%) | 0 | 5 (25) | 5 (25) | 7 (35) | 3 (15) |
| 6 cycles | 5 | 2 (40%) | 0 | 1 (20) | 1 (20) | 1 (20) | 2 (40) |
Abbreviations: As2O3, arsenic trioxide; CR, complete remission; MM, multiple myeloma; MR, minimal response; NC, no change; ORR, overall response rate; PD, progressive disease; PR, partial response.
There were 12 IgG-subtype MM patients who finished 2 cycles of chemotherapy, and three patients attained PR, five had MR, two had NC, and two had PD. Ten IgG-subtype MM patients finished 4 cycles of chemotherapy: two attained PR, two had MR, four had NC, and two had PD. There were two IgG-subtype patients that finished 6 cycles of chemotherapy: one attained PR and one had NC. There were six IgA-subtype MM patients that finished 2 cycles of chemotherapy: one attained PR, two had MR, two had NC, and one had PD. There were six IgA-subtype patients that finished 4 cycles of chemotherapy: two attained PR, two had MR, one had NC, and one had PD. Only one IgA-subtype patient finished 6 cycles of chemotherapy and attained MR. Three IgD-subtype MM patients finished 2 cycles of chemotherapy: two patients attained MR and one had PD. Only one IgD-subtype patient finished 4 cycles of chemotherapy and attained NC. Nine light chain MM patients finished 2 cycles of chemotherapy: one patient attained PR, six had MR, one had NC, and one had PD. Three light chain MM patients finished 4 cycles of chemotherapy: one attained PR, one had MR, and one had NC. Two light chain patients finished 6 cycles of chemotherapy and attained PD. The median time of OS and PFS were 48 (29–120) and 6 (2–8) months, respectively (Figures 1 and 2).
Figure 1.
The time of OS for the relapse and refractory MM patients treated with arsenic trioxide, ascorbic acid, ifosfamide, and prednisone.
Abbreviations: MM, multiple myeloma; OS, overall survival.
Figure 2.
The time of PFS for the relapse and refractory MM patients treated with arsenic trioxide, ascorbic acid, ifosfamide, and prednisone.
Abbreviations: MM, multiple myeloma; PFS, progression-free survival.
Adverse events
In all, 25 patients developed neutropenia (1–2 grade), with 16 of these patients experiencing thrombocytopenia and 21 patients developing anemia. Only five patients felt nausea, but 22 patients reported fatigue. Eight patients developed infections (three had pneumonia, four had acute upper respiratory tract infection, and one had urinary tract inflammation). Seven patients had elevated transaminase during therapy, which was controlled using tiopronin injection to protect the liver. Arrhythmia was observed in four patients after therapy and needed drugs for control (Table 3).
Table 3.
Treatment-related adverse events
| Event | Number of patients (%) |
|---|---|
| Neutropenia (grade 1–2) | 25 (83.3) |
| Fatigue (grade 1–2) | 22 (73.3) |
| Anemia | 21 (70) |
| Thrombocytopenia | 16 (53.3) |
| Infection | 8 (26.7) |
| Liver function profiles increased | 7 (23.3) |
| Nausea/vomiting | 5 (16.7) |
| Arrhythmia | 4 (13.3) |
Discussion
MM is characterized by clonal proliferation of malignant plasma cells in the bone marrow associated, in most patients, with the production of monoclonal Igs. Despite several recent therapeutic advances, including the bortezomib and lenalidomide treatments for MM, MM remains incurable; almost all patients eventually relapse and develop drug resistance. And there are few effective salvage regimens available for patients with disease resistant to the newer agents. Therefore, there is a clear need for improved salvage regimens in MM. As2O3 is the essential component of the Chinese medicine arsenic.13 The use of As2O3 as a medicinal agent dates back 2,000 years. As2O3 has demonstrated clinical activity in patients with newly diagnosed APL, producing CR in 83%–86% of patients and 3-year OS rates of 79%–86%. As2O3 has also recently emerged as an effective treatment for patients with relapsed or refractory APL.14,15
As2O3 has demonstrated remarkable efficacy in APL.16–19 Recently some reports have led to a renewed interest in As2O3 in the management of malignancies,20,21 especially those of hematologic origin, such as MM.
In a Phase II trial at the University of Arkansas, the activity of As2O3 was evaluated in 14 patients with relapsed MM refractory to conventional salvage therapy. As2O3 was administered at a dose of 0.15 mg/kg daily for 60 days. Responses were noted in three patients: one achieved 75% reduction in the monoclonal protein, and the other two achieved 50% and 25%, respectively. Stable disease was observed in eight patients.22 So the therapy response to single-agent As2O3 for MM was not satisfactory.
Then what is the chemotherapy response for the combination of As2O3? The combination of As2O3 and bortezomib (As2O3 + bortezomib) has been recently shown to enhance antimyeloma activity. Both bortezomib and As2O3 were shown to activate the p38 MAPK pathway. As2O3 combination with bortezomib could enhance the activating of the p38 MAPK pathways.23 One Phase I study assessed the feasibility of concomitant As2O3, ascorbic acid, and bortezomib for patients with relapsed/refractory MM. As2O3 (0.25 mg/kg) and ascorbic acid (1 g) were given with an escalating dose of bortezomib (1 mg/m2 or 1.3 mg/m2 IV bolus on days 1 and 8 of a 21-day cycle). The results showed that four (40%) patients achieved clinical benefit, with one patient achieving a durable PR. No formal dose-limiting toxicities were encountered.24 Berenson et al assessed the safety and efficacy of MAC (melphalan, As2O3, and ascorbic acid) combination therapy for MM patients who failed more than two different prior regimens. Patients received melphalan (0.1 mg/kg PO), As2O3 (0.25 mg/kg IV), and ascorbic acid (1 g IV) on days 1–4 of week 1, As2O3 and ascorbic acid twice weekly during weeks 2–5, and no treatment during week 6 of cycle 1; during cycles 2–6, the schedule remained the same except As2O3 and ascorbic acid were given twice weekly in week 1. Objective responses occurred in 31 of 65 (48%) patients, including two CR, 15 PR, and 14 MR.25 The above study showed that As2O3 combined with other drugs could improve the response over the single As2O3.
In this study, we retrospectively analyzed clinical data of 30 relapsed and refractory MM patients treated by As2O3 combined with ascorbic acid, ifosfamide, and prednisone. These patients had received bortezomib and lenalidomide before and relapsed more than three times. There were 28/30 patients who had received bortezomib and 15/30 patients who received lenalidomide treatment before treatment by As2O3. These patients had received more than 10 chemotherapy cycles, and treatment selection was difficult for these patients. The results showed that the ORR was 66.7% (20/30 cases, with PR in five cases), 50% (10/20 cases, with PR in five cases), and 40% (2/5 cases, with PR in one case), respectively, after 2, 4, and 6 cycles of the therapy. This result was better than the reports from the aforementioned clinical trial of As2O3 as a single agent. It was difficult to receive a curative effect for these relapsed and refractory MM patients, so the ORR in this study included MR. The majority of patients attained MR when treated with As2O3 combined with ascorbic acid, ifosfamide, and prednisone in this study and an increased PR rate with the longer the course of treatment. This result further confirmed that As2O3 is an effective agent for relapsed patients and that response could be increased by combination with other chemotherapy drugs.
Arsenic is well-known as a toxic agent.26 Chronic exposure to low levels of environmental arsenic has been reported to increase the incidence of skin, liver, bladder, and lung cancers. Other commonly observed potential signs of arsenic poisoning include cardiomyopathy, renal failure, leukocytosis, gastrointestinal disorders (eg, nausea, vomiting, and diarrhea), fatigue, fever, headache, and cough. Despite its reputation as a poison, as a therapeutic entity, As2O3 has been generally well-tolerated. In this study, we observed that neutropenia (83.3%), anemia (70%), and thrombocytopenia (53.3%) occurred in more than half of the patients, who required growth factor and blood infusion support. Fatigue was more common in this study, which was untreated. Eight patients developed infections (three had pneumonia, four had acute upper respiratory tract infection, and one had urinary tract inflammation) and required antibiotic. QT prolongation, a known side effect of As2O3 therapy, was uncommon in this study, occurring in only four patients, but required drug intervention.
As2O3 combined with ascorbic acid, ifosfamide and prednisone could be selected as a salvage therapy to treat relapsed and refractory MM patients before using new agents, such as bortezomib and lenalidomide. Patients achieving MR could attain a better response by increasing the course of As2O3. And the regimen of As2O3 combined with ascorbic acid, ifosfamide, and prednisone was better tolerated by MM patients. It may be a promising choice for MM patients in early relapsed phase, to achieve a much better response.
Footnotes
Author contributions
Sun Wan-Jun collected and assembled the data, analyzed data, drafted the article, and gave final approval. Li Xin contributed to the concept, design, interpretation of the data, critical revision, and gave final approval.
Disclosure
The authors report no conflicts of interest in this work.
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