Background This phase I, dose-finding study evaluated the maximum tolerated dose (MTD), safety, pharmacokinetics, and antitumor activity of sunitinib plus S-1/cisplatin in Japanese patients with advanced/metastatic gastric cancer. Patients and methods Patients received oral sunitinib on a continuous daily dosing (CDD) or 2-weeks-on/2-weeks-off schedule (Schedule 2/2; 25 mg/day or 37.5 mg/day), plus S-1 (80–120 mg/day)/cisplatin 60 mg/m2. Results Twenty-seven patients received treatment, including 26 patients treated per protocol (sunitinib 25 mg/day CDD schedule, n = 4; sunitinib 25 mg/day Schedule 2/2, n = 16 [dose-limiting toxicity (DLT) cohort, n = 6 plus expansion cohort, n = 10]; sunitinib 37.5 mg/day Schedule 2/2, n = 6). One patient erroneously self-administered sunitinib 12.5 mg/day and was excluded from the analyses. The MTD was sunitinib 25 mg/day on Schedule 2/2. DLTs were reported for: 2/4 patients given sunitinib 25 mg/day on the CDD schedule; 1/6 patients administered sunitinib 25 mg/day on Schedule 2/2 (grade [G] 3 neutropenic infection, G4 thrombocytopenia, and S-1 dose interruption ≥5 days), and 3/6 patients given sunitinib 37.5 mg/day on Schedule 2/2. Results below are for the overall MTD cohort (n = 16). The most frequently reported G3/4 adverse events were neutropenia (93.8 %) and leukopenia (75.0 %). The objective response rate was 37.5 %; six additional patients experienced no disease progression for ≥24 weeks. Median progression-free survival was 12.5 months. No pharmacokinetic drug–drug interactions were observed between sunitinib/S-1/cisplatin and S-1/cisplatin. Conclusions The MTD of sunitinib was 25 mg/day on Schedule 2/2 combined with cisplatin/S-1 in patients with advanced/metastatic gastric cancer. This regimen had a manageable safety profile and preliminary antitumor activity.
Hinweise
Presented in part on the clinical trial registry located at ClinicalTrials.gov (identification No. NCT00553696) and at:
The European Society for Medical Oncology 35th ESMO Congress, Milan, Italy, October 8–12, 2010
The 9th Annual Meeting of the Japanese Society of Medical Oncology, Yokohama, Japan, July 21–23, 2011.
Introduction
Gastric cancer is the second most common cause of cancer-related death worldwide, with more than 730,000 deaths estimated to have occurred in 2008 [1]. Globally, the 5-year survival rate for gastric cancer is approximately 20 % [2], and most patients present with advanced, non-resectable disease [3‐5].
Despite recent advances in the treatment for gastric cancer [6], a standard chemotherapy regimen has not been established for recurrent or unresectable advanced gastric cancer; combination chemotherapy is associated with significant survival and quality of life advantages, compared with best supportive care [7, 8]. The use of a 5-fluorouracil (5-FU)-based regimen in combination with a platinum analog is the most widely accepted first-line treatment regimen, although combination therapy does have a higher associated toxicity burden compared with single-agent chemotherapy [8].
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Blockade of receptors such as vascular endothelial growth factor receptor (VEGFR) and platelet-derived growth factor receptor (PDGFR) has been shown to inhibit tumor-related angiogenesis and tumor growth [9, 10]. Not only are these receptors expressed in gastric cancers but they are known to have direct effects on the growth and metastasis of this disease [9‐14].
Sunitinib malate (SUTENT®; Pfizer Inc., New York, NY, USA) is an oral, multitargeted, tyrosine kinase inhibitor of VEGFRs 1–3, PDGFR-α and -β, and other receptors [15‐17]. Sunitinib is approved multinationally for the treatment of unresectable and/or metastatic imatinib-resistant/-intolerant gastrointestinal stromal tumor, advanced/metastatic renal cell carcinoma, and unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumors. Phase II study results in advanced gastric cancer have shown that sunitinib had activity as a single-agent; progression-free survival (PFS) was 2.3 months and overall survival was 6.8 months in the second-line setting [18].
In preclinical tumor models, sunitinib has been shown to enhance the antitumor activity of 5-FU and cisplatin, suggesting that sunitinib might enhance the effect of chemotherapy in cancer patients [19, 20]. In the First-Line Advanced Gastric Cancer Study (FLAGS), the combination of S-1, an oral derivative of 5-FU, and cisplatin was found to be effective when administered as a 3-week on/1-week off regimen (Schedule 3/1) [21]. Therefore, this phase I, dose-finding study was conducted to determine the maximum tolerated dose (MTD) and overall safety profile of sunitinib plus S-1 and cisplatin in Japanese patients with advanced/metastatic gastric cancer. Tolerability, pharmacokinetics (PK), and antitumor activity were also evaluated.
Materials and methods
Study population
Patients (male or female) eligible for inclusion in this study were aged ≥20 years, had an Eastern Cooperative Oncology Group performance status of 0 or 1, adequate organ function, and histologically or cytologically confirmed Stage IV gastric adenocarcinoma or gastroesophageal junction adenocarcinoma not amenable to surgery or radiation. Prior adjuvant therapy was permitted with a recurrence-free interval of >3 months after the completion of adjuvant therapy. Prior chemotherapy in the advanced/metastatic setting was not permitted; one regimen of chemotherapy, such as S-1 monotherapy, without progressive disease was allowed if the duration of treatment was less than 4 weeks.
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Exclusion criteria included central nervous system (CNS) metastases, carcinomatous meningitis, or uncontrolled hypertension (blood pressure >150/100 mmHg). Patients with severe/unstable angina, myocardial infarction, coronary artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident, including transient ischemic attack, or pulmonary embolism within 12 months prior to starting study treatment were also excluded.
The study was conducted in accordance with the International Conference on Harmonization Good Clinical Practice guidelines, the declaration of Helsinki, and applicable local regulatory requirements and laws. Approval from the institutional review board or independent ethics committee with the appropriate jurisdiction was required for each participating investigator/center. Written informed consent was obtained from all patients.
Study design
This was a phase I, open-label, dose-finding study of sunitinib in combination with S-1 and cisplatin in patients with advanced/metastatic gastric cancer (NCT00553696). Patients received open-label, oral S-1 at a starting dose of 80–120 mg/day (based on body surface area) on Schedule 3/1 and a cisplatin 60 mg/m2 infusion on day 1 that was repeated every 28 days. Patients were allocated to different doses of oral sunitinib based on a 3 + 3 design. Initially, sunitinib was planned to be administered on a continuous daily dosing (CDD) schedule or on Schedule 3/1. After four patients received treatment in the CDD arm, the protocol was revised to use a 2-week-on/2-week-off schedule (Schedule 2/2), instead of Schedule 3/1, due to the pattern of adverse events (AEs). Patients received sunitinib 25 mg/day on a CDD schedule, or 25 mg/day or 37.5 mg/day on Schedule 2/2 in 4-week cycles (Fig. 1).
Fig. 1
Treatment schema. aSunitinib dose withheld on cycle 1 day 1 to enable pharmacokinetic analysis of S-1 and cisplatin. bS-1 and cisplatin dose withheld on cycle 1 day 1 to enable pharmacokinetic analysis of sunitinib. BID twice daily; Schedule 2/2 2 weeks on treatment followed by 2 weeks off treatment
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Initially, three patients were enrolled to receive sunitinib 25 mg/day on the CDD schedule in combination with S-1 and cisplatin 60 mg/m2. If no patients experienced a dose-limiting toxicity (DLT) in cycle 1 then patients would be enrolled to the next highest dose level. If no more than one of the initial three patients experienced a DLT within cycle 1, then the cohort was expanded to a total of six patients. If no more than one of these six patients experienced a DLT, then patients would be enrolled at the next highest dose level.
The MTD was defined as the highest dose cohort where 0/3 or ≤1/6 patients experienced a DLT, with the next highest dose having at least 2/3 or 2/6 patients who experienced a DLT. DLTs are defined in Table 1. In this study, the MTD level was confirmed by expanding enrollment to include up to 10 additional patients with advanced/metastatic disease in order to obtain additional safety data for the combination treatment. It was anticipated that a total of approximately 30 patients would be enrolled in this study.
Table 1
Definition of DLT
Category
DLT criteria
Hematologic
Grade 4 neutropenia lasting ≥7 days
Grade ≥3 febrile neutropenia
Grade ≥3 neutropenic infection
Grade 4 thrombocytopenia or grade 3 thrombocytopenia with bleeding
Non-hematologica
Grade 3 toxicities lasting ≥7 days
Grade 4 non-hematologic toxicity
Grade 3/4 nausea, vomiting or diarrhea persisting despite maximum supportive therapy
Missed/delayed dose due to toxicity
Break from sunitinib dose ≥6/28 days on the CDD schedule or ≥3/14 days on Schedule 2/2
Break from S-1 dose ≥5/21 days per cycle
Delay of >3 weeks in starting the second treatment cycle
CDD continuous daily dosing; DLT dose-limiting toxicity; Schedule 2/2 2 weeks on treatment followed by 2 weeks off treatment
aExceptions: hyperamylasemia or hyperlipasemia without other clinical evidence of pancreatitis and asymptomatic hyperuricemia; asymptomatic hypertension with adequately controlled blood pressure
Dose modifications of sunitinib were not allowed until a DLT was reached. Once dose reduction occurred due to study drug-related toxicity, the dose was not re-escalated. Patients could undergo a maximum of two dose reductions of either S-1 and/or cisplatin. However, patients requiring more than two dose reductions of S-1 or sunitinib were withdrawn from the study. Additionally, patients with >1 missed cisplatin dose were withdrawn. Treatment was continued for 8 cycles or until disease progression, unacceptable toxicity, or withdrawal of patient consent.
The primary endpoint was the assessment of first-cycle DLTs for sunitinib plus S-1 and cisplatin. Secondary endpoints included overall safety, tumor response, PFS, and PK.
Assessments
Patients were evaluable for DLT assessment if they received all day 1 chemotherapy and ≥80 % of their sunitinib doses and S-1 doses. Those who could not receive ≥80 % of their doses for reasons other than a DLT were excluded from the DLT evaluation. Tumor assessment was performed at baseline, on day 22 of cycle 1, and every 4 weeks thereafter until radiographic-confirmed disease progression or end of treatment scan. Objective tumor response in patients with at least one target lesion was measured using the Response Evaluation Criteria in Solid Tumors (RECIST) guidelines [22] and confirmed no sooner than 4 weeks after the initial documentation of response.
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Safety was assessed at regular intervals (during cycle 1 on days 1, 2, 8, 15, and 22; during cycles 2–8 on days 1, 2, and 21; and during cycles ≥9 on days 1 and 21). AEs were monitored during the study and graded using the National Cancer Institute Common Terminology for Adverse Events version 3.0 clinical assessments, including laboratory testing for blood hematology and serum chemistry.
To investigate PK drug–drug interactions, full PK profiles of sunitinib, its active metabolite SU12662, S-1 (5-FU, tegafur) and cisplatin (total and free) were assessed in all cohorts comprising the 3 + 3 design, and in the MTD expansion cohort. Blood samples for analyses of cisplatin and S-1 were collected on cycle 1 days 1–2 (S-1 and cisplatin), before starting sunitinib dosing on day 2, and on cycle 2 days 1–2 (in combination with sunitinib) in the MTD cohort. In the expansion cohort, blood samples for the analyses of sunitinib and SU12662 were collected on cycle 1 days 1–2 (sunitinib alone), prior to administration of S-1 and cisplatin on day 2, and cycle 2 days 1–2 (in combination with S-1 and cisplatin). PK parameters were calculated using non-compartmental methods.
Trough plasma concentrations of sunitinib and SU12662 were obtained at steady state on cycles 1–3 days 21–22 for the CDD schedule, and cycles 1–3 days 14–15 for Schedule 2/2. Blood samples were obtained before the administration of sunitinib and S-1.
On the day of cisplatin PK sampling, blood was drawn pre-dose (before administration of cisplatin, S-1 or sunitinib) and at 0.5, 1, 2, 8, and 22 h after completing infusion. Samples for evaluation of sunitinib, SU12662, and S-1 PK were obtained pre-dose (before administration of either S-1 or sunitinib) and at 1, 2, 4, 6, 8, and 10 h post-dose (before dosing of S-1). For sunitinib and SU12662, a sample was also obtained 24 h post-dose.
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Plasma samples were analyzed for sunitinib and SU12662 concentrations by Bioanalytical Systems Inc. (USA) using a validated high-performance liquid chromatography tandem mass spectrometric (HPLC-MS/MS) method. Tegafur and 5-FU plasma concentrations were also determined using a validated HPLC-MS/MS method by Tandem Labs (USA). Cisplatin concentrations were determined in both plasma and plasma ultra filtrate samples by Covance Laboratories Inc. (USA) using a validated Inductively Coupled Plasma–Mass Spectrometric (ICP/MS) method.
Statistical analysis
The sample size was determined on an empirical rather than statistical basis. Assessment of 3–6 patients for each cohort was considered adequate to characterize the safety of a treatment regimen prior to investigation in phase II clinical trials. It was anticipated that up to 30 patients would be enrolled in this study.
Efficacy analyses included all patients who received at least one protocol-specified dose of sunitinib. Descriptive statistics were used to summarize all patient characteristics, treatment administration/compliance, antitumor activity, and safety; PFS was summarized using the Kaplan–Meier method. In an unplanned exploratory analysis, clinical benefit rate (CBR; percentage of patients with a complete response, partial response, and stable disease ≥24 weeks) and PFS were calculated in patients with scirrhous-type disease of primary tumors.
Results
Patient characteristics
In total, 27 patients received treatment, including 26 patients treated per protocol (sunitinib 25 mg/day on the CDD schedule, 4; sunitinib 25 mg/day on Schedule 2/2, 16 [DLT cohort, 6 plus expansion cohort, 10]; sunitinib 37.5 mg/day on Schedule 2/2, 6), and one patient who was assigned to sunitinib 25 mg/day on Schedule 2/2 and erroneously self-administered sunitinib 12.5 mg/day throughout the study. The latter patient was excluded from the efficacy analyses. One patient remained on study as of April 2012. Demographic and baseline disease characteristics are shown in Table 2. Overall, eight patients had scirrhous-type disease (seven patients in the MTD cohort).
Table 2
Baseline patient characteristics
CDD schedule sunitinib 25 mg/day
Schedule 2/2 sunitinib 25 mg/day
Schedule 2/2 sunitinib 37.5 mg/day
All patients (n = 4)a
All patients (n = 16)b,c
Patients with scirrhous-type disease (n = 7)
All patients (n = 6)d
Gender, male, n (%)
2 (50.0)
13 (81.3)
6 (85.7)
4 (66.7)
Age, years
Median
63.0
60.0
57.0
60.5
Range
44–73
31–71
31–67
28–71
ECOG performance status, n (%)
0
1 (25.0)
7 (43.8)
2 (28.6)
3 (50.0)
1
3 (75.0)
9 (56.3)
5 (71.4)
3 (50.0)
Measurable disease, n (%)
3 (75.0)
11 (68.8)
5 (71.4)
4 (66.7)
Histology, n (%)
Diffuse
2 (50.0)
9 (56.2)
6 (85.7)
2 (33.3)
Intestinal
2 (50.0)
7 (43.8)
1 (14.3)
3 (50.0)
Other
0 (0)
0 (0)
0 (0)
1e (16.7)
Prior surgery, n (%)
1 (25.0)
5 (31.3)
1 (14.3)
2 (33.3)
Prior systemic therapy, n (%)
0
2 (50.0)
16 (100.0)
7 (100.0)
5 (83.3)
1
2 (50.0)
0 (0)
0 (0)
1 (16.7)
≥2
0 (0)
0 (0)
0 (0)
0 (0)
CDD continuous daily dosing; ECOG Eastern Cooperative Oncology Group; Schedule 2/2 2 weeks on treatment followed by 2 weeks off treatment
aIncludes one patient with scirrhous-type disease
bIncludes 10 patients from the expansion cohort
cThe subject assigned to sunitinib 25 mg/day on Schedule 2/2 who mistakenly received sunitinib 12.5 mg/day was excluded from the efficacy analyses. At baseline, this patient had an ECOG performance status of 0, stage IV measurable intestinal disease, with 2 involved tumor sites (liver and lymph node) and no prior surgery or systemic therapy
dNo patients had scirrhous-type disease in this cohort
eThis patient had mucinous histology
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Safety and drug exposure
Twenty-seven patients were evaluable for safety. The MTD was determined to be sunitinib 25 mg/day on Schedule 2/2 plus cisplatin and S-1, and a further 10 patients were allocated to this cohort. Of the four patients who received sunitinib 25 mg/day on the CDD schedule, two DLTs were reported: grade 4 thrombocytopenia (n = 1), and grade 4 thrombocytopenia plus grade 3 febrile neutropenia (n = 1). Subsequently, the treatment frequency was reduced to sunitinib 25 mg/day on Schedule 2/2. In the second cohort, one of six patients reported a DLT: grade 3 neutropenic infection plus grade 4 thrombocytopenia and S-1 dose interruption of ≥5 days. As defined in the protocol, the sunitinib dose was then increased to 37.5 mg/day on Schedule 2/2, where three of six patients experienced a DLT: grade 3 febrile neutropenia plus S-1 dose interruption of ≥5 days (n = 1), grade 4 thrombocytopenia (n = 1), and grade 4 neutropenia of ≥7 days (n = 1).
All patients experienced at least one AE. No grade 5 AEs occurred. Serious AEs (SAEs) were reported in 13 patients overall (48.1 %). Dose reductions due to AEs occurred for all three drugs: sunitinib: n = 8; S-1: n = 7; cisplatin: n = 8. At the MTD, the median relative dose intensity (% actual/intended dose intensity) was 80.6 % (range, 32.4–100.0) for sunitinib (25 mg/day, Schedule 2/2), 68.2 % (35.7–85.7) for S-1, and 73.8 % (27.1–98.9) for cisplatin. Overall, seven patients discontinued the study treatment due to AEs, including four patients in the MTD cohort.
In the MTD cohort (sunitinib 25 mg/day, Schedule 2/2; n = 16), the frequencies of common AEs of any grade are presented in Table 3. Neutropenia was the most frequently reported grade 3 or 4 AE, occurring in 15 patients (93.8 %). In total, 75.0 % of patients in the MTD cohort experienced grade 3 or 4 leukopenia. Fatigue, decreased appetite, nausea, constipation, thrombocytopenia, and stomatitis were the most common grade 1 or 2 AEs reported. In this cohort, SAEs occurred in eight patients (50.0 %); the most frequent SAEs were febrile neutropenia (n = 3, 18.8 %) and platelet count decreased (n = 2, 12.5 %).
Table 3
Treatment-emergent (all-causality) adverse events in ≥30 % of patients in the maximum tolerated dose cohort (sunitinib 25 mg/day on Schedule 2/2 + cisplatin + S-1; n = 16)
Adverse event, n (%)
Grade 1/2
Grade 3/4
All grades
Leukopenia
4 (25.0)
12 (75.0)
16 (100.0)
Neutropenia
1 (6.3)
15 (93.8)
16 (100.0)
Anemia
6 (37.5)
9 (56.3)
15 (93.8)
Decreased appetite
14 (87.5)
1 (6.3)
15 (93.8)
Thrombocytopenia
9 (56.3)
6 (37.5)
15 (93.8)
Fatigue
14 (87.5)
0
14 (87.5)
Nausea
14 (87.5)
0
14 (87.5)
Constipation
12 (75.0)
0
12 (75.0)
Stomatitis
9 (56.3)
0
9 (56.3)
Diarrhea
7 (43.8)
1 (6.3)
8 (50.0)
Dysgeusia
7 (43.8)
0
7 (43.8)
Pyrexia
7 (43.8)
0
7 (43.8)
Hiccups
6 (37.5)
0
6 (37.5)
Rash
5 (31.3)
0
5 (31.3)
Vomiting
5 (31.3)
0
5 (31.3)
Schedule 2/2 2 weeks on treatment followed by 2 weeks off treatment
Pharmacokinetics
The MTD combination of sunitinib (25 mg/day, Schedule 2/2) with S-1 plus cisplatin demonstrated no changes in the PK of sunitinib or its active metabolite (SU12662). In addition, combination treatment had no impact on the PK of cisplatin, tegafur, 5-FU, or S-1, compared with S-1 plus cisplatin alone (Table 4).
Table 4
Pharmacokinetics in the maximum tolerated dose cohort (sunitinib 25 mg/day on Schedule 2/2 + cisplatin + S-1)
Treatment
Analyte
n
Mean Cmax ng/mL (CV%)
Mean AUClast ng · h/mL (CV%)
Sunitinib alone or SP
Combined
Sunitinib alone or SP
Combined
Sunitinib
Sunitinib
7
15.8 (32.2)
16.2 (44.6)
234 (25.3)
244 (38.6)
SU12662
7
2.9 (43.6)
2.8 (49.3)
46.0 (34.2)
50.5 (50.7)
Total drug
7
18.5 (33.0)
19.0 (42.3)
280 (25.0)
294 (37.2)
S-1
Tegafur
5
1,500 (9.8)
1,688 (26.9)
8,290 (10.5)
9,163 (12.7)
5-FU
5
144 (23.5)
114 (16.5)
582 (19.3)
522 (28.0)
Cisplatin
Total
5
1,794 (7.8)
1,984 (3.6)
27,478 (7.1)
31,574 (5.4)
Free
5
178 (68.3)
187 (74.6)
790 (25.8)
973 (28.3)
AUClast area under the plasma concentration–time curve from time zero until last quantifiable observation; Cmax maximum concentration; CV coefficient of variation; 5-FU 5-fluorouracil; Schedule 2/2 2 weeks on treatment followed by 2 weeks off treatment; SP cisplatin 60 mg/m2 every 28 days + S-1 40 mg/m2 twice daily every 3/1 weeks; SU12662 sunitinib active metabolite
The mean trough plasma concentrations (Ctrough) of sunitinib, SU12662, and total drug were 33.5 ng/mL, 13.9 ng/mL, and 47.5 ng/mL, respectively, for sunitinib 25 mg/day, and 69.9 ng/mL, 24.0 ng/mL, and 93.4 ng/mL, respectively, for sunitinib 37.5 mg/day. These Ctrough values suggested that plasma concentrations of sunitinib increased in a dose-dependent manner.
Antitumor activity
All patients were evaluable for efficacy. In the MTD group (sunitinib 25 mg/day, Schedule 2/2), 11/16 patients had measurable disease. No patients had a complete response, and partial responses occurred in 6/11 patients (54.5 %) with measurable disease, resulting in an overall objective response rate (ORR) of 37.5 % (95 % confidence interval [CI], 15.2–64.6) in 16 evaluable patients. A further six patients experienced no disease progression for ≥24 weeks, producing a CBR of 75.0 % (95 % CI, 47.6–92.7) among the 16 patients. Maximum percentage reduction in target lesion size in the 11 patients with measurable disease is shown in Fig. 2. The CBR for patients treated at the MTD with scirrhous-type disease was 57.1 % (95 % CI, 18.4–90.1; 4/7 patients). Tumor response in one patient with scirrhous-type disease is shown in Fig. 3. At the MTD, median PFS was 12.5 months (95 % CI, 6.4–16.5) and 6-month survival was 78.3 % (95 % CI, 56.5–100.0; Table 5; Fig. 4). Among the seven patients with scirrhous-type disease, four of five patients who had measurable lesion had a partial response, and median PFS was 12.5 months (95 % CI, 10.1–13.3).
Fig. 2
Maximum percentage change in target lesion size in the maximum tolerated dose (MTD) cohort (sunitinib 25 mg/day on Schedule 2/2 + cisplatin + S-1).aSchedule 2/2 2 weeks on treatment followed by 2 weeks off treatment. aFive of 16 patients receiving the MTD did not have measurable disease
Fig. 3
Tumor response in a patient with scirrhous gastric cancer who received the maximum tolerated dose of sunitinib (25 mg/day on Schedule 2/2) combined with cisplatin and S-1. Blue arrowheads: primary lesion; orange arrowheads: peritoneal metastasis; green arrowheads: lymph node metastasis; Schedule 2/2 2 weeks on treatment followed by 2 weeks off treatment
Table 5
Summary of progression-free survival
CDD schedule
Schedule 2/2
Sunitinib 25 mg/day (n = 4)
Sunitinib 25 mg/day (n = 16)a
Sunitinib 37.5 mg/day (n = 6)
Patients with events, n (%)
2 (50.0)
9 (56.3)
4 (66.7)
Progression-free survival, monthsb
Median
7.1
12.5
5.8
95 % CI
6.7–7.5
6.4–16.5
4.4–7.9
Probability of being event-free at month 6c
Percentage
100.0
78.3
50.0
95 % CId
100.0–100.0
56.5–100.0
1.0–99.0
Exploratory analysis: scirrhous-type disease
Schedule 2/2
Sunitinib 25 mg/day (n = 7)a
Patients with events, n (%)
4 (57.1)
Progression-free survival, monthsb
Median
12.5
95 % CI
10.1–13.3
CDD continuous daily dosing; CI confidence interval; Schedule 2/2 2 weeks on treatment followed by 2 weeks off treatment
aMaximum tolerated dose
bBased on the Brookmeyer and Crowley Method
cEstimated from the Kaplan–Meier curve
dCalculated from the product-limit method
Fig. 4
Kaplan-Meier estimate of progression-free survival in the maximum tolerated dose cohort (sunitinib 25 mg/day on Schedule 2/2 + cisplatin + S-1). CI confidence interval; Schedule 2/2 2 weeks on treatment followed by 2 weeks off treatment
×
×
×
Discussion
In this study, the MTD of sunitinib in combination with S-1 (80–120 mg) plus cisplatin 60 mg/m2 was established as 25 mg/day on Schedule 2/2 in patients with advanced or metastatic gastric cancer for whom curative therapy was not an option. Other tested combinations included sunitinib 25 mg/day on a CDD schedule and a dose-increment from the MTD cohort to 37.5 mg; both cohorts were discontinued after DLTs were experienced. An additional 10 patients were then enrolled in the MTD cohort and followed for safety, antitumor activity, and PK parameters.
The MTD combination regimen demonstrated a manageable safety profile, with neutropenia and leukopenia as the most frequently reported grade 3 or 4 AEs: 93.8 % and 75.0 %, respectively. This safety profile was also consistent with a similar phase I dose-escalation study conducted in Western patients with advanced gastric cancer [23]. In general, the type of AEs was consistent with those previously reported when 5-FU and cisplatin were administered in patients with gastric cancer [24], although the frequency of events, particularly hematologic AEs, was greater than expected from previous studies of sunitinib in other tumor types [18, 25‐28]. Previously reported mild skin reactions associated with sunitinib, such as yellowing skin/discoloration [29], were not observed in this study. There were no grade 3 or 4 non-hematologic events reported in ≥30 % of patients within the MTD cohort. No new safety signals were observed for sunitinib.
Although tumor evaluation was not the primary objective of this study, the ORR for the MTD cohort was 37.5 % (95 % CI, 15.2–64.6) and included responses in patients with scirrhous-type disease. Since five of 16 patients treated at the MTD did not have measurable disease and were assessed as non-responders in the ORR calculation, tumor response rates may be underestimated in our study. The ORR at the MTD among the 11 patients with measurable disease was 54.5 %. Median PFS was 12.5 months (95 % CI, 6.4–16.5) in the overall MTD cohort. These results demonstrate promising preliminary antitumor activity, compared with that observed for sunitinib as a single-agent modality in advanced gastric cancer, [18] and with the median PFS of 6 months reported for S-1 plus cisplatin [30]. However, our results must be interpreted with caution given the limited sample size studied.
A multitargeted tyrosine kinase inhibitor like sunitinib may be a promising drug for scirrhous gastric cancer. Our preliminary results suggest that sunitinib in combination with S-1 and cisplatin might have antitumor activity in patients with this disease type. However, as only seven of 16 patients at the MTD had scirrhous-type disease, caution should be used when interpreting these results. Despite this caveat, these data are encouraging, as scirrhous gastric cancer carries a worse prognosis than the non-scirrhous-type [31, 32], as it is characterized by rapid cancer cell infiltration and proliferation accompanied by extensive stromal fibrosis [32]. The proliferative and invasive ability of scirrhous gastric cancer cells have been shown to be closely associated with the growth factors produced by organ-specific fibroblasts and other stromal cells [32]. Therefore, targeting this cancer–stroma interaction using a multitargeted tyrosine kinase inhibitor such as sunitinib could be a reasonable treatment option for patients with scirrhous gastric cancer. However, large randomized studies would be required to confirm this hypothesis.
The combination of sunitinib with cisplatin plus S-1 demonstrated no PK drug–drug interactions, consistent with the different pathways of metabolism and elimination for these drugs. These findings are consistent with those from the phase I study with cisplatin plus 5-FU in Western patients [23]. The mean observed Ctrough plasma concentration of 47.5 ng/mL, for total drug (sunitinib plus SU12662) at steady-state with sunitinib 25 mg/day dosing, in the present study suggests that optimal sunitinib exposure was almost achieved, in terms of the required concentration for target inhibition of ≥50 ng/mL [16].
In summary, the MTD of sunitinib was 25 mg/day on Schedule 2/2 in combination with cisplatin and S-1 when administered as a first-line therapy in patients with advanced or metastatic gastric cancer. This combination had a manageable safety profile and showed preliminary evidence of antitumor activity.
Acknowledgments
We thank the participating patients and their families, as well as the investigators, research nurses, study coordinators, and operations staff. Medical writing support was provided by Nicola Crofts and Molly Heitz (ACUMED®, Tytherington, UK) with funding from Pfizer Inc.
Conflict of interest
Narikazu Boku, Nozomu Machida, Kei Muro, and Yoshinori Miyata have nothing to disclose.
Mariajose Lechuga and Nobuyuki Kimura are Pfizer Inc. employees and hold Pfizer Inc. stock.
Satoshi Hashigaki and Mie Suzuki are Pfizer Inc. employees.
Funding source
This study was sponsored by Pfizer Inc.
Quantity of supporting information
None
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