Abstract
Purpose
A phase III trial assessed the efficacy of palonosetron plus dexamethasone given once in preventing acute and delayed chemotherapy-induced nausea and vomiting (CINV) following a broad range of moderately emetogenic chemotherapy (MEC) regimens.
Methods
This multicentre, randomized, open-label, non-inferiority trial evaluated two different treatment groups. One group received palonosetron (0.25 mg intravenously) and dexamethasone (8 mg intravenously) before chemotherapy, while the other was administered the same regimen on day 1 followed by dexamethasone 8 mg orally on days 2 and 3. The primary endpoint was complete response (CR; defined as no emetic episodes and no rescue medication) during the overall phase (days 1–5 after chemotherapy initiation). The non-inferiority margin was predefined as a 15% difference between groups in the primary endpoint.
Results
Of 332 chemotherapy-naïve patients included in the intention-to-treat analysis, 65.1% were female, and 35.2% received anthracycline plus cyclophosphamide (AC)-based regimens. Overall CR rates were 67.5% for those administered dexamethasone only on day 1 (n = 166), and 71.1% for those also administered dexamethasone on days 2 and 3 (n = 166; difference −3.6% (95% confidence interval, −13.5 to 6.3)). CR rates were not significantly different between groups during the acute (0–24 h post-chemotherapy; 88.6% versus 84.3%; P = 0.262) and delayed phases (days 2–5; 68.7% versus 77.7%; P = 0.116).
Conclusions
Palonosetron plus single-dose dexamethasone administered before common MEC regimens provide protection against acute and delayed CINV which is non-inferior to that of palonosetron plus dexamethasone for 3 days. However, the major benefit of the single-day regimen occurs in patients receiving non-AC MEC regimens.
Keywords: Palonosetron, Serotonin antagonists, Dexamethasone, Moderately emetogenic chemotherapy, Nausea, Vomiting
Introduction
Chemotherapy-induced nausea and vomiting (CINV) can severely impact performance status and quality of life [1]. CINV has been traditionally categorized as acute or delayed: acute CINV is that occurring within 24 h after initiation of chemotherapy, whereas delayed emesis is that occurring between days 2 and 5 [2]. The risk of CINV depends on several factors, although the emetogenic potential of the chemotherapeutic agent is the most predictive factor [3]. Intravenously administered cytotoxic agents were initially assigned to five levels of emetogenicity that was subsequently divided into four emetic risk categories (high, moderate, low, and minimal) [4, 5]. A critical factor in guiding anti-emetic treatment is the ability of chemotherapy to induce a substantial risk of delayed emesis. There is limited knowledge of the potential for delayed emesis of many moderately emetogenic agents, but recent guidelines support the use of a serotonin (5-HT3)-receptor antagonist plus dexamethasone before moderately emetogenic chemotherapy (MEC), with either agent given alone on days 2 and 3 [6]. A meta-analysis of results from 32 trials that included 5,613 patients who received highly emetogenic chemotherapy or MEC indicated that dexamethasone is superior to placebo or no treatment for complete protection against both acute and delayed CINV [7]. Most clinical trials also found that the addition of dexamethasone is more effective than a 5-HT3-receptor antagonist alone for control of acute and delayed emesis [2]. However, dexamethasone for prophylaxis of delayed emesis after MEC induces moderate-to-severe adverse effects that may have substantial impact on the quality of life [8]. In addition, the first-generation 5-HT3-receptor antagonists have only modest efficacy in prevention of delayed emesis induced by MEC [9].
Palonosetron is a second-generation 5-HT3-receptor antagonist that has a greater binding affinity and a prolonged half-life (∼40 h) compared with first-generation agents [10]. In two randomized, double-blind, controlled, phase III, non-inferiority trials involving patients receiving MEC, single-dose palonosetron (0.25 mg intravenously) produced a statistically significant increase in the complete response (CR) rate compared with single-dose ondansetron or dolasetron for CINV during the delayed and overall phases [11, 12]. Pooled analysis of these trials showed that palonosetron also induces a statistically significant improvement in the CR rate during the acute phase compared with pooled data from patients who received ondansetron or dolasetron (72% versus 61%, respectively) [13]. Significantly more patients receiving palonosetron achieved complete protection from delayed CINV compared with those who received either ondansetron or dolasetron (64% versus 47%, respectively). It is well known that the addition of dexamethasone to a 5-HT3-receptor antagonist improves the anti-emetic efficacy during the acute phase, control of which is the strongest prognostic factor for successful prevention of delayed CINV [2, 14]. In a recent open-label, phase II study evaluating the combination of palonosetron and dexamethasone (8 mg) administered intravenously on day 1 in patients receiving MEC, CR was seen in 84% of patients during the acute phase [15].
Based on this data, palonosetron plus a single dose of dexamethasone administered before chemotherapy might provide a more convenient regimen for the prevention of acute and delayed CINV following MEC regimens. Accordingly, the present phase III trial was designed to test the hypothesis that the efficacy of a single-day two-drug regimen against CINV is non-inferior to that of the same regimen with additional dexamethasone doses on days 2 and 3 after chemotherapy initiation.
Patients and methods
Study design
This was a phase III, randomized, open-label, parallel-group, active-comparator, non-inferiority trial (EudraCT number 2006-000644-13). Patients were enrolled in 15 centers in Italy coordinated by the Italian Trials in Medical Oncology (I.T.M.O.) Group. This was an unsponsored, investigator-initiated trial. Design and methodology of this trial, with the exception of blinding, were similar to those of the two phase III registration studies that assessed the efficacy of palonosetron alone in patients receiving MEC [11, 12]. The institutional review board at each study site approved the study protocol, and patients provided written informed consent prior to participation.
Eligibility criteria
Patients eligible for the study were adults with a histologically or cytologically confirmed solid tumor receiving chemotherapy for the first time with intravenous agents classified as moderately emetogenic according to the modified Hesketh chemotherapy classification given as single doses on study day 1 [5]. Patients were required to have acceptable hematologic, hepatic, and renal functions for administration of chemotherapy, and an adequate Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2. Patients could not receive any drug with potential anti-emetic efficacy other than the study drug given immediately before or during the study period, and could not receive radiotherapy within 30 days before chemotherapy initiation or during the study period. Patients were considered ineligible if they had known central nervous system malignancy or another organic cause for nausea or vomiting unrelated to chemotherapy administration. Nausea or vomiting within 24 h prior to initiation of chemotherapy also led to exclusion. Patients were ineligible if they had active infection or were unable to understand or cooperate with study procedures. Pregnant or nursing women were ineligible.
Treatment plan and random assignment
Regardless of assignment to either study arm, all patients received a single, fixed, intravenous dose of palonosetron (0.25 mg) as a bolus over 30 s given 30 min before chemotherapy initiation on day 1. Administration of prophylactic dexamethasone (8 mg intravenously) within 15 min before chemotherapy initiation on day 1 was also required. Patients were randomly assigned to one of two delayed anti-emetic regimens: (1) no additional dexamethasone, or (2) dexamethasone (8 mg orally) on days 2 and 3. After chemotherapy, rescue medication including dexamethasone and/or metoclopramide for the treatment of nausea and vomiting was permitted on an as-needed basis. Patients who met eligibility criteria were randomly assigned to either treatment arm using an allocation schedule with a block-size of four that had been generated before the trial by an independent statistician.
Study endpoints and assessments
The primary efficacy endpoint of this study was CR (defined as no emetic episodes, and no rescue medication use) during the overall study period (days 1 through 5 after chemotherapy initiation). Secondary endpoints were the proportion of patients who achieved the following during the overall, acute (0–24 h post-chemotherapy), and delayed phase (24–120 h post-chemotherapy): CR (not including overall phase), complete control (CC; defined as no emetic episodes, no use of rescue medication, and no more than mild nausea), no emesis (defined as no vomiting or retching), no nausea, and no use of rescue medication. An additional endpoint was severity of nausea that was recorded on a four-point categorical Likert scale (0, none; 1, mild; 2, moderate; 3, severe), according to subjective assessment by each patient.
Patients were instructed to record the relevant study information in a diary provided by the investigators. To assess efficacy, patients made daily entries in the diary for 5 days after chemotherapy initiation to record the number and time of any emetic events in the previous 24 h, use of rescue medication, and maximum nausea experienced in the previous 24 h assessed by a Likert scale. Patients made daily entries in the diary noting any adverse event or use of concomitant medication. When patient returned to the clinic for the second course of chemotherapy, the patient diary was collected and reviewed to ensure adherence to the required diary documentation and the prescribed study medication at home. Adverse events judged by the investigator to be possibly, probably, or definitely related to the study treatment were regarded as a treatment-related adverse event.
Statistical analysis
The intention-to-treat (ITT) cohort included patients who received at least one dose of the study medication and MEC chemotherapy. The per-protocol (PP) cohort included all patients who received study medication and completed the follow-up period (days 1–5 after chemotherapy initiation) without any major protocol deviation. The safety cohort included all patients who received at least one dose of the study medication after randomization. The primary efficacy hypothesis was that palonosetron plus a single-dose of dexamethasone was non-inferior to palonosetron plus dexamethasone for 3 days during the overall study period (0–120 h post-chemotherapy) using a non-inferiority margin of a 15% difference between groups in the proportion of patients who had a CR. Considering previous pivotal studies, the number of patients needed in the study was estimated to be 330, who were distributed into two groups (i.e., 165 patient/group) based on the assumption of a CR rate of 70% in the two treatment groups and a difference of −15% in the CR rate [11, 12]. To obtain 80% statistical power with a one-sided α level of 0.025, a sample size of 150 evaluable patients per group was needed. Assuming a 10% drop-out rate, 165 patients per group needed to be enrolled. To assess non-inferiority for the primary endpoint of a CR rate at 120 h, the lower boundary of the two-sided 95% confidence interval (CI) for the difference (1-day dexamethasone minus 3-day dexamethasone) between the CR rates in the two treatment arms was compared with the preset threshold.
The primary endpoint was analyzed for both the ITT and PP cohort, and the results were interpreted in a confirmatory manner to demonstrate the non-inferiority hypothesis. The PP cohort was used for all secondary efficacy analyses including the primary endpoint analyzed in the multivariable context. The data analyses were carried out by an independent statistician who was blinded to study treatments.
Comparisons of CR during the acute phase (0–24 h), and delayed phase (24–120 h) were preplanned secondary analyses for either cohort. Consistency of treatment effect (CR in the overall study period) across gender (female versus male) and type of chemotherapy (anthracycline plus cyclophosphamide (AC)-based versus non-AC-based) were assessed by evaluating the first-order interactions between treatment and either risk factor, included one by one into a generalized linear model implemented with binomial distribution and identity link function. This non-canonical link function was adopted to estimate risk differences (RD) instead of the usual odds ratios. RD allowed a straightforward comparison between the unadjusted (univariable analysis) and adjusted (multivariable analysis) two-sided 95% CI of between-group difference in CR to anti-emetic treatment for testing the non-inferiority.
A chi-square test was used to analyze the following: CC rates; proportion of patients with no emetic episodes, no nausea, or no rescue medication; and proportion of patients with nausea (worst severity as assessed by the Likert scale). Treatment-related adverse events occurring in at least 2% of patients were summarized descriptively by treatment group.
The analyses of all secondary endpoints were evaluated in an explorative or descriptive manner, and therefore no adjustment for multiplicity was performed. All P values were two-sided, and a P value <0.05 was considered statistically significant. All statistical analyses were performed using SAS software (version 9.1; SAS Institute, Cary, NC).
Results
Patient characteristics
From October 13, 2006 to June 6, 2008, 334 patients were randomized to receive palonosetron in combination with dexamethasone as either a single dose or for 3 days. Two patients did not receive study treatment (Fig. 1); thus, a total of 332 patients were included in the ITT cohort for efficacy analyses. Five patients were lost to follow-up (two patients in the study arm and three in the reference arm) and an additional three had a major protocol deviation (one patient in the study arm and two in the reference arm). Therefore, a total of 324 patients were evaluable for efficacy analysis in the PP cohort.
Fig. 1.
Study flow chart. ITT intention-to-treat, PP per-protocol
Demographic and clinical characteristics for the ITT cohort were similar between treatment groups (Table 1). The majority of the study population (225 of 332 patients (67.8%)) was less than 65 years of age, and most patients (216 of 332 patients (65.1%)) were women. The majority of patients were diagnosed with either breast (143 of 332 patients (43.1%)) or colorectal (121 of 332 patients (36.4%)) cancers. Of the chemotherapeutic treatments received on day 1 in the efficacy analyses, most patients received either oxaliplatin-based regimens (119 of 332 patients (35.8%)) or AC-containing regimens (35.2% of the study population).
Table 1.
Baseline demographic and clinical characteristics in the intention-to-treat cohort
| Variable | Palo plus 1-day Dexa (n = 166) | Palo plus 3-day Dex (n = 166) |
|---|---|---|
| Age categories (n (%)) | ||
| <65 years | 114 (68.7) | 111 (66.9) |
| ≥65 years | 52 (31.3) | 55 (33.1) |
| Mean (±SD) | 56.9 (±11.8) | 57.2 (±11.3) |
| Body weight (kg) | ||
| Mean (±SD) | 68.8 (±14.7) | 66.6 (±12.6) |
| Height (cm) | ||
| Mean (±SD) | 163.7 (±8.9) | 163.1 (±7.8) |
| Gender (n (%)) | ||
| Female | 103 (62) | 113 (68.1) |
| Male | 63 (38) | 53 (31.9) |
| ECOG scoreb (n (%)) | ||
| 0 | 152 (91.6) | 152 (91.6) |
| 1 | 14 (8.4) | 13 (7.8) |
| 2 | 0 | 1 (0.6) |
| Tumor type (n (%)) | ||
| Breast | 65 (39.2) | 78 (47) |
| Colorectal | 65 (39.2) | 56 (33.7) |
| Lung | 15 (9.0) | 13 (7.8) |
| Other | 21 (12.6) | 19 (11.5) |
| Alcohol consumption (n (%)) | ||
| No | 101 (60.8) | 99 (59.6) |
| Everydayc | 65 (39.2) | 67 (40.4) |
| Tumor stage (n (%)) | ||
| Early | 98 (59) | 115 (69.3) |
| Metastatic | 68 (41) | 51 (30.7) |
| Chemotherapy (n (%)) | ||
| AC-basedd | 54 (32.5) | 63 (38) |
| Oxaliplatin-based | 64 (38.6) | 55 (33.1) |
| Carboplatin-based | 21 (12.7) | 16 (9.6) |
| Irinotecan-based | 14 (8.4) | 15 (9.1) |
| Other | 13 (7.8) | 17 (10.2) |
aPalonosetron plus dexamethasone
bEastern Cooperative Oncology Group
c1–2 glasses of wine
dAnthracycline plus cyclophosphamide
Efficacy
The proportion of patients in either the ITT or PP cohort achieving CR during the overall study period (0–120 h) after MEC is presented in Table 2. Non-inferiority of the 1-day regimen was demonstrated, as the lower boundaries of the 95% CI of the difference with the 3-day regimen were greater than the preset threshold of −15% difference. For the acute (0–24 h) and delayed (24–120 h) phases, palonosetron plus 1-day dexamethasone was non-inferior to the 3-day regimen. Secondary efficacy analyses are presented in Table 3. During the delayed phase, significantly fewer patients receiving the 1-day dexamethasone regimen required no rescue medication compared with those who received the 3-day regimen. When the proportion of patients with no emesis or nausea was assessed daily, there were also no statistically significant differences between groups at any time point after chemotherapy initiation (data not shown).
Table 2.
Complete response (defined as no emetic episodes and no use of rescue medication) rates in the study cohorts
| Complete responses | ||||
|---|---|---|---|---|
| Palo plus 1-day Dexa (n (%)) | Palo plus 3-day Dex (n (%)) | Difference between groupsb (95% CI), % | P c | |
| ITT cohortd, n = 332 | n = 166 | n = 166 | ||
| Acute phase (0–24 h) | 147 (88.6) | 140 (84.3) | 4.2 (−3.1 to 11.6) | 0.262 |
| 95% CI | 82.7 to 92.9 | 77.9 to 89.5 | ||
| Delayed phase (24–120 h) | 114 (68.7) | 129 (77.7) | −9.0 (−18.5 to 0.4) | 0.116 |
| 95% CI | 61.0 to 75.6 | 70.6 to 83.8 | ||
| Overall phasee (0–120 h) | 112 (67.5) | 118 (71.1) | −3.6 (−13.5 to 6.3) | ND |
| 95% CI | 59.8 to 74.5 | 63.6 to 77.9 | ||
| PP cohortf, n = 324 | (n = 163) | (n = 161) | ||
| Acute phase (0–24 h) | 144 (88.3) | 135 (83.9) | 4.5 (−3 to 12) | 0.242 |
| 95% CI | 82.4 to 92.8 | 77.2 to 89.2 | ||
| Delayed phase (24–120 h) | 112 (68.7) | 124 (77.0) | −8.3 (−17.9 to 1.3) | 0.093 |
| 95% CI | 60.9 to 75.7 | 69.7 to 83.3 | ||
| Overall phasee (0–120 h) | 109 (66.9) | 113 (70.2) | −3.3 (−13.4 to 6.8) | ND |
| 95% CI | 59.1 to 74.0 | 62.5 to 77.1 | ||
ND not done
aPalonosetron plus dexamethasone
b1-day minus 3-day regimen with 95% confidence interval obtained using normal approximation of binomial data
cTwo-sided chi-square test (1-day vs. 3-day)
dIntention-to-treat
eNon-inferiority hypothesis in primary analysis was proven as the lower boundaries of the 95% CI of between-group difference were greater than the preset threshold (−15%)
fPer-protocol cohort
Table 3.
Secondary efficacy analyses in the per-protocol cohort
| Variable | Palo plus 1-day Dexa (n = 163), n (%) | Palo plus 3-day Dex (n = 161), n (%) | Differenceb, 95% CI (%) |
|---|---|---|---|
| Complete controlc | |||
| Acute phase (0–24 h) | 142 (87.1) | 132 (82.0) | 5.1 (−2.7 to 13) |
| Delayed phase (24–120 h) | 108 (66.3) | 122 (75.8) | −9.5 (−19.3 to 0.3) |
| Overall phase (0–120 h) | 105 (64.4) | 109 (67.7) | −3.3 (−13.6 to 7) |
| No emetic episodes | |||
| Acute phase (0–24 h) | 153 (93.9) | 148 (91.9) | 1.9 (−3.7 to 7.5) |
| Delayed phase (24–120 h) | 140 (85.9) | 145 (90.1) | −4.2 (−11.2 to 2.9) |
| Overall phase (0–120 h) | 134 (82.2) | 135 (83.9) | −1.6 (−9.8 to 6.5) |
| No nausea | |||
| Acute phase (0–24 h) | 128 (78.5) | 117 (72.7) | 5.9 (−3.5 to 15.2) |
| Delayed phase (24–120 h) | 93 (57.1) | 100 (62.1) | −5.1 (−15.7 to 5.6) |
| Overall phase (0–120 h) | 85 (52.1) | 91 (56.5) | −4.4 (−15.2 to 6.5) |
| No use of rescue medication | |||
| Acute phase (0–24 h) | 148 (90.8) | 144 (89.4) | 1.4 (−5.1 to 7.9) |
| Delayed phase (24–120 h) | 119 (73.0) | 134 (83.2)* | −10.2 (−19.2 to −1.3) |
| Overall phase (0–120 h) | 116 (71.2) | 129 (80.1) | −9 (−18.3 to 0.3) |
*P = 0.026 (two-sided Chi-square test (1-day vs. 3-day))
apalonosetron plus dexamethasone
b1-day minus 3-day regimen with 95% confidence interval obtained using normal approximation of binomial data
cNo emetic episodes, no use of rescue medication, and no more than mild nausea
Subset analyses of each treatment group by gender and type of chemotherapy administered were done for CR during the acute and delayed phases (Table 4). Lower rates of CR were observed for palonosetron plus single-dose dexamethasone compared with palonosetron plus 3-day dexamethasone in women during the delayed phase (24–120 h). CR rates in the subgroup of patients receiving non-AC MEC regimens showed no difference between treatment groups in the acute and delayed phases. Fewer patients receiving AC-containing regimens achieved CR in the 1-day regimen with respect to those in the 3-day regimen during the delayed phase. It should be noted that half of the female patients (1-day regimen, 49.5%; 3-day regimen, 52%) in either arm received AC-containing chemotherapy. There were no significant interactions between treatment and either gender (P = 0.512) or type of chemotherapy (P = 0.672) in the overall study period for the primary endpoint of CR. On univariable analysis only female gender (RD 14.7%; 95% CI, 4.7 to 24.7%; P = 0.004) and AC-containing chemotherapy (RD 12.8%; 95% CI, 2.0 to 23.6%; P = 0.020) were associated with worse outcome in terms of overall CR to anti-emetic treatment. Nevertheless such associations were no longer statistically significant in a multivariable analysis. On both univariable and multivariable analysis the lower boundaries of the 95% CI of between-group difference were greater than the preset threshold of −15% (univariable: RD −3.3%; 95% CI, −13.4 to 6.8%; P = 0.520; multivariable: RD −4.4%; 95% CI, −14.1 to 5.4%; P = 0.381). Therefore, the non-inferiority hypothesis of the 1-day regimen was proven also after adjusting for the model covariates.
Table 4.
Subgroup analysis by gender and type of chemotherapy of the complete response (defined as no emetic episodes and no rescue medication) rates in the per-protocol cohort
| Complete responses | |||
|---|---|---|---|
| Palo plus 1-day Dexa (n (%)) | Palo plus 3-day Dex (n (%)) | bDifference, 95% CI (%) | |
| Acute phase (0–24 h) Gender | |||
| Women | 88/101 (87.1) | 85/109 (78) | 9.1 (−1 to 19.3) |
| Men | 54/62 (87.1) | 47/52 (90.4) | −3.3 (−14.9 to 8.3) |
| Chemotherapy | |||
| AC-basedc | 44/52 (84.6) | 45/61 (73.8) | 10.8 (−3.9 to 25.6) |
| Non-AC-based | 98/111 (88.3) | 87/100 (87.0) | 1.3 (−7.6 to 10.2) |
| Delayed phase (24–120 h) Gender | |||
| Women | 62/101 (61.4) | 81/109 (74.3)* | −12.9 (−25.5 to −0.4) |
| Men | 46/62 (74.2) | 41/52 (78.8) | −4.7 (−20.2 to 10.9) |
| Chemotherapy | |||
| AC-basedc | 29/52 (55.8) | 46/61 (75.4)** | −19.6 (−36.9 to −2.3) |
| Non-AC-based | 79/111 (71.2) | 76/100 (76.0) | −4.8 (−16.7 to 7) |
*P = 0.045 (two-sided chi-square test (1-day vs. 3-day)); **P = 0.028
aPalonosetron plus dexamethasone
b1-day minus 3-day regimen with 95% confidence interval obtained using normal approximation of binomial data
cAnthracycline plus cyclophosphamide
The severity of nausea was not significantly different between groups for each study day or during the delayed and overall phases. However, this was only an exploratory analysis due to the unblinded design of the study. The majority of nausea was mild in severity during the delayed phase (1-day regimen, 33.7%; 3-day regimen 29.2%); very few patients reported nausea of at least moderate severity on any study day in the 1-day regimen (2.4% to 4.9% of patients) or in the 3-day regimen (3.1% to 6.8% of patients). In both groups, very few patients experienced severe nausea within 24 h (0 of 163 patients in the 1-day regimen and four of 161 patients (2.5%) in the 3-day regimen). Only one patient receiving the 1-day regimen had severe nausea 120 h after chemotherapy initiation.
Tolerability
A total of 332 patients were evaluable for safety. Overall, 159 patients (47.9%) reported one or more adverse events (both related and unrelated to study treatment), 82 patients (49.4%) in the 1-day regimen and 77 patients (46.4%) in the 3-day regimen. There were no clinically relevant differences between groups with respect to the overall incidence of adverse events. The most common treatment-related adverse events in either treatment group were headache (1-day regimen, 19.9%; 3-day regimen, 13.9%) followed by constipation (9.6% and 10.8%, respectively) and fatigue (9.0% and 4.2%, respectively). No serious adverse events occurred during the study.
Discussion
In the current phase III trial, the primary hypothesis of non-inferiority of palonosetron plus single-dose dexamethasone compared with 3-day dexamethasone regimen in the prevention of CINV following a broad range of MEC regimens was shown for CR during the overall phase (0–120 h post-chemotherapy).
In patients receiving MEC, current guidelines recommend a combination of a 5-HT3-receptor antagonist and dexamethasone before chemotherapy initiation, with either agent given alone on days 2 and 3 [3]. However, the use of dexamethasone in clinical practice remains limited because of concerns about potential side effects and/or other factors [5, 8].
The second-generation 5-HT3-receptor antagonist palonosetron has been recently reported to lead to receptor alteration or internalization resulting in a extended inhibition of receptor function [16]. Two phase III trials have demonstrated that palonosetron alone is effective in preventing both acute and delayed CINV following MEC [11, 12].
Following the design and methodology of the pivotal phase III trials, we have explored the hypothesis that additional dexamethasone doses beyond day 1 of MEC administration may not be necessary in patients receiving palonosetron. In the current study, which included a heterogeneous patient population receiving commonly administered MEC regimens to reflect actual clinical practice, CR rates were 89% in the 1-day regimen arm versus 84% in the 3-day regimen arm during the acute phase. Response rates were 68% versus 71%, respectively, for complete protection against CINV during the overall study period. However, analysis of the components of CR, vomiting and use of rescue medication, showed that fewer patients taking a single dexamethasone dose reported no rescue medication use during the delayed phase. The added benefit for this secondary endpoint in patients taking additional dexamethasone doses is most likely related to the characteristics of the study population. Women accounted for the majority of patients in each treatment group, and half of the female patients in either arm received AC-containing chemotherapy. This may bias the anti-emetic protection against delayed CINV in the patient cohort receiving no additional dexamethasone less favorably than cohort taking dexamethasone on days 2 and 3. A subgroup analysis showed that the standard 3-day regimen was better than the 1-day regimen for complete protection against delayed CINV in women (61.4% versus 74.3%; P = 0.045). It is well known that women who receive AC-containing chemotherapy have a particularly high risk of developing CINV, but at the time the current trial was planned, the AC-based regimens were considered as MEC [17]. Within the AC subgroup, the standard regimen appeared to be more efficacious in the delayed phase in comparison with the 1-day regimen (CR, 55.8% versus 75.4%; P = 0.028). A recently reported double-blind, phase III trial evaluated the efficacy of palonosetron plus 1- versus 3-day dexamethasone in chemotherapy-naïve female breast cancer patients (n = 300) receiving anthracycline and/or cyclophosphamide-containing chemotherapy [18]. Non-inferiority between the two treatments was demonstrated by similar CR rates in the overall period (study primary endpoint) but, interestingly, patients receiving the 3-day dexamethasone regimen experienced on day 3 less emesis than the group receiving a single dose of dexamethasone (89% versus 97%, P = 0.004). In the current study, on univariable analysis female gender and AC-containing chemotherapy were significantly associated with worse outcome. Such associations were no longer statistically significant in a multivariable analysis, but the trial was not powered to enable careful assessment of whether there is any difference in efficacy from gender and the type of chemotherapy. In patients with breast cancer receiving AC-containing chemotherapy, the MASCC/ESMO anti-emetic guidelines, recently updated in 2010, recommend a 5-HT3-receptor antagonist in combination with dexamethasone and an neurokinin-1 receptor antagonist (aprepitant or fosaprepitant) to prevent acute CINV, with aprepitant given alone on days 2 and 3 for prevention of delayed symptoms [19]. In a phase II trial evaluating the efficacy of palonosetron plus 3-day dexamethasone and aprepitant in 58 patients receiving MEC (including AC-containing chemotherapy in 41% of cases), 78% of patients achieved CR during the delayed and overall phases [20]. More recently, results from a phase II study that included 41 patients (40 were female) receiving MEC (including AC-containing chemotherapy in 90% of cases) indicated that a single-day regimen of palonosetron, dexamethasone and aprepitant is feasible and effective for protection against acute and delayed vomiting [21]. In the light of this, a single-day three-drug anti-emetic regimen should be formally compared with the standard multi-day regimen in female patients for the prevention of CINV following AC-containing chemotherapy.
We acknowledge that as the present trial was unblinded this could have potentially influenced the results. However, the consistency of the efficacy results observed in the 1-day regimen arm with those previously reported on palonosetron supports the validity of the current study [13, 15, 22].
In conclusion, we provide evidence that the combination of palonosetron and dexamethasone given on day 1 of common MEC regimens is non-inferior to the same regimen with dexamethasone also administered on days 2 and 3 for the complete protection against acute and delayed CINV. It is important to remember that the current study was not designed to address whether the 1-day regimen should be pursued or not according to the type of MEC chemotherapy. An unplanned subgroup analysis suggested that the major benefit of the 1-day regimen occurs in patients receiving non-AC-containing chemotherapy (65% of the study population). Therefore, in patients receiving MEC other than AC-based regimens, this dexamethasone sparing regimen minimizes medication administration that patients must remember at home and provides the potential to improve both adherence with anti-emetic prophylaxis and quality of life.
Acknowledgements
The authors thank the following clinicians who participated in the study:
Federica Villa, Ospedale San Gerardo, Monza, Italy; Maria Teresa Cattaneo, Ospedale L. Sacco, Milan, Italy; Michelangelo Russillo, Istituto Regina Elena, Rome, Italy; Raffaele Venezia, Ospedale Serbelloni, Gorgonzola, Italy; Claudia Biasini, Ospedale Guglielmo da Saliceto, Piacenza, Italy; Fabio Malugani, Ospedale di Sondrio, Sondrio, Italy; Rodolfo Passalacqua, Silvia Lazzarelli, Istituti Ospitalieri, Cremona, Italy; Luigi Dogliotti, Lucianna Russo, Ospedale San Luigi Gonzaga, Orbassano, Italy; Alessandra Galetto, David Rondonotti, Ospedale Maggiore della Carità, Novara, Italy; Enrico Aitini, Maria Antonietta Perrone, Ospedale C. Poma, Mantova, Italy; Graziella Pinotti, Giovanni Giardina, Ospedale di Circolo, Varese, Italy; Ignazio Carreca, Dario Piazza, Policlinico P. Giaccone, Palermo, Italy.
The authors thank the patients, nurses, and data managers who participated in this trial. We also thank Italfarmaco S.p.A., Milan, Italy for the generous gift of palonosetron.
Presented in part at the 10th Annual Meeting of the Italian Association of Medical Oncology, Verona, Italy, October 2008.
Conflict of interest
The study was not funded. There were no financial disclosures from any authors.
Open Access
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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