Dose reduction and discontinuation of standard-dose regorafenib associated with adverse drug events in cancer patients: a systematic review and meta-analysis

Abstract

Background:

Regorafenib (REG) is an oral multikinase inhibitor used in colorectal cancer, gastrointestinal stromal tumour and hepatocellular carcinoma. Several adverse events (AEs) are commonly reported during REG administration, and strategies for managing AEs in everyday clinical practice include supportive care, dose modifications and, when necessary, treatment withdrawal. We performed a systematic review and meta-analysis to assess the schedule treatment modifications of REG associated with AEs across randomized controlled clinical trials (RCTs).

Methods:

Eligible studies included RCTs assessing standard dose REG versus placebo. Outcomes of interest included: AE-related permanent discontinuation, dose interruptions and dose reductions.

Results:

We retrieved all the relevant RCTs through PubMed/Med, Cochrane library and EMBASE: 7 eligible studies involving a total of 2099 patients (Regorafenib: 1362; placebo: 737) were included in our analysis. The use of REG was associated with higher incidence and risk of all outcomes of interest when compared with placebo. The incidences of permanent discontinuation, dose interruptions and dose reductions in patients receiving REG were 9.7%, 57.2% and 47%, respectively, versus 3.3%, 16.7% and 7.7% of placebo group; compared with placebo, the summary relative risks (RRs) of permanent discontinuation, dose interruptions and dose reductions in REG arm were 2.80 (95% CI 1.85–4.22), 3.21 (95% CI 2.59–3.99) and 6.02 (95% CI 3.28–11.03), respectively.

Conclusions:

Treatment with REG at the standard dose of 160 mg is associated with a significant increase in AE-related permanent discontinuation, dose interruptions and dose reductions. Prompt identification and management of AEs seem mandatory to obtain maximal benefit from REG treatment. In the current landscape, dose personalization of REG may have the potential to improve quality of life, minimize treatment discontinuation and maximize patient outcomes.

Keywords

colorectal cancer gastrointestinal stromal tumours GIST meta-analysis regorafenib

Introduction

Regorafenib (REG) is an orally bio-available multikinase inhibitor (MKI) that blocks the activity of several protein kinases, including those associated with proliferation (KIT, BRAF, RAF-1 and RET), tumour angiogenesis (VEGFR-1, VEGFR-2, VEGFR-3 and TIE2) and tumour microenvironment signalling (PDGFR and FGFR).^1,2 Clinical benefits from the administration of REG were initially observed in metastatic colorectal cancer (CRC) and gastrointestinal stromal tumour (GIST), as stated by the three randomized controlled clinical trials (RCTs) CORRECT, GRID and CONCUR.^3–5 More recently, REG gained approval in hepatocellular carcinoma (HCC), on the basis of data from the RESORCE trial,⁶ where REG showed a survival benefit in patients affected by advanced or metastatic HCC who progressed on sorafenib treatment. Currently, REG is approved as a single agent for the treatment of CRC, GIST and HCC at a dose of 160 mg orally once daily on days 1–21 of each 28 days cycle.⁷ There are currently ongoing trials aimed to evaluate the efficacy of REG as monotherapy or in combination with other anticancer agents and the number of indications and patients receiving REG is supposed to further increase in the near future.^8,9 REG has undoubtedly modified clinical practice for patients affected by several malignancies, however various drug-related adverse events (AEs), such as fatigue, hypertension, hand–foot skin reaction (HFSR), rash and diarrhoea have been reported.^10–12 Moreover, REG-related AEs frequently require treatment modifications and may also result in early discontinuation of treatment.^13,14 As consequence, this management may interfere with the efficacy and long-term outcomes of patients. Prompt identification of AEs is fundamental to guarantee that patients can be treated as safely as possible and, in order to ensure that anticancer treatment is effective, maintaining the optimal dose levels represents a major issue.^15,16

In the current study, we performed a systematic review and meta-analysis to examine AE-related permanent discontinuation of treatment, AE-related dose interruptions and AE-related dose reductions in patients receiving REG, across the seven available RCTs.

Materials and methods

Search strategies

All phase II and III clinical trials published from 15 June 2008 to 29 January 2020 regarding the clinical role of REG therapy in advanced malignancies were retrieved. Keywords used for searching on PubMed/ Medline, Cochrane Library and EMBASE were: “Regorafenib” OR “Stivarga” OR “BAY 73-4506” AND “phase 2 trial” OR “phase 3 trial”; only articles published in peer-reviewed journals and written in English language were considered. Furthermore, proceedings of the main international oncological meetings (American Society of Clinical Oncology, European Society of Medical Oncology, European Council of Clinical Oncology and American Association for Cancer Research) were also searched from 2005 onward for relevant abstracts.

The search and review of the articles were evaluated by two authors (AR and MN) independently.

Aims of the systematic review and meta-analysis

The aims of the systematic review and meta-analysis were:

to evaluate incidence and risk of AE-related permanent discontinuation in RCTs comparing REG treatment versus placebo;

to evaluate incidence and risk of AE-related dose interruptions in RCTs comparing REG treatment versus placebo;

to evaluate incidence and risk of AE-related dose reductions in RCTs comparing REG treatment versus placebo.

Selection criteria

Studies selected from first analysis were then restricted to: (a) prospective phase II or III RCTs in advanced malignancies; (b) participants enrolled in REG treatment or placebo; (c) studies with available data about AE-related dose reductions and/or AE-related dose interruptions and/or AE-related permanent discontinuation of treatment.

Data extraction and quality assessment

The following data were extracted for each publication: (a) study general information (author, year, phase, carry out country, inclusion criteria); (b) primary site; (c) interventions; (d) formulation of REG therapy; (e) number of patients; (f) available outcomes in terms of AE-related dose reductions, dose interruptions and/or permanent discontinuation. Two separate authors (AR and MN) conducted the search and identification independently.

We assessed the methodological quality of the included trials using Cochrane Collaboration tool. Studies examined were graded as having a ‘low risk’, ‘high risk’, or ‘unclear risk’ of bias across the seven specified domains. This meta-analysis was conducted according to Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) guidelines.¹⁷

Assessment of risk of bias

Risk of bias in the seven selected studies was assessed independently by two authors (AR and MN) using the tool of The Cochrane Collaboration for assessing risk of bias and therefore including selection, performance, detection, attrition and reporting bias.¹⁸ The lists of outcomes reported in the published paper were compared with those from study protocols or trials registries. The results were summarized in a risk of bias graph ( Figure 1 ).

Figure 1.

Risk of bias graph: authors’ judgements on each risk of bias item presented as percentages across all included studies.

Types of outcome measures

We examined three outcomes: AE-related dose reductions, AE-related dose interruptions and AE-related permanent discontinuation. Dose interruptions were defined as AE-related transitory discontinuation of treatment. All data were obtained from full text or supplementary material of each study.

Statistical design

All statistical analyses were performed using R studio. For the calculation of incidence rate (IR), the number of patients with AE-related dose reductions, AE-related dose interruptions and AE-related permanent discontinuation and the total number of patients being treated with REG and placebo were determined from each trial. The proportions of patients and 95% CIs were derived.

Relative risks (RRs) were used to analyse dichotomous variables, including AE-related dose reductions, dose interruptions and permanent discontinuation: RRs were combined with the Mantel–Haenszel method. Statistical heterogeneity between studies was examined using the chi-squared test and the I² statistic: substantial heterogeneity was considered to exist when the I² value was greater than 50% or there was a low p value (<0.10) in the chi-squared test.

Results

Studies selected

In our search, we identified 792 potentially relevant reports, which were subsequently restricted to seven.^19–25 We excluded 785 records as non-pertinent reports (meta-analysis and systematic reviews, review articles, editorials, case reports, pre-clinical studies, retrospective studies, non-randomized studies, no placebo-controlled arm trials, ongoing trials/trials in progress), as shown in Figure 2 . All studies included in our analysis were published in full manuscript.

Figure 2.

Study flow diagram.

Of the seven eligible studies, two trials compared REG treatment versus placebo in pretreated patients affected by advanced or metastatic CRC.^19–21 The same comparison was made in the other five trials, comparing REG versus placebo in advanced or metastatic GIST,²⁰ gastric cancer/gastroesophageal junction (GC/GEJ),²² HCC,²⁴ osteosarcoma²⁵ and soft tissue sarcoma (STS).²³ Four trials were phase III studies,^19–21,24 whereas three studies were phase II trials.^22,23,25

The seven studies shared several characteristics: they were all randomized, double-blind, multicentre, placebo-controlled trials including patients whose disease had progressed after treatment with one to two previous lines of chemotherapy for advanced or metastatic disease. In all these RCTs only patients with an Eastern Cooperative Oncology Group performance status (ECOG-PS) of 0 or 1 were enrolled.^19–25

A total of 2099 patients were available for the meta-analysis (REG: 1362; placebo: 737); REG dosage and schedule was as follows: 160 mg orally on days 1 to 21 of each 28-day cycle. A summary of the included RCTs is presented in the Table 1 .

Table 1.

Summary of the included studies.

Author/ year^reference	Phase of CT	Primary site	Carry out country	Number in intervention/control group	ECOG-PS	Type of treatment	ADE-related outcomes included in analysis
Grothey / 2013 ¹⁹	III	CRC	16 countries in North America, Europe, Asia, and Australia	500/253	0,1	Oral regorafenib 160 mg once daily on days 1–21 each 28-day cycle + BSC versus placebo + BSC	Dose reductions Dose interruptions Permanent discontinuation
Demetri / 2013 ²⁰	III	GIST	17 countries in North America, Europe, and Asia	132/66	0,1	Oral regorafenib 160 mg once daily on days 1–21 each 28-day cycle + BSC versus placebo + BSC	Dose reductions Permanent discontinuation
Li / 2015 ²¹	III	CRC	China, Hong Kong, South Korea, Taiwan, and Vietnam	136/68	0,1	Oral regorafenib 160 mg once daily on days 1–21 each 28-day cycle + BSC versus placebo + BSC	Dose reductions Dose interruptions Permanent discontinuation
Pavlakis / 2016 ²²	II	GC / GEJ	Australia, New Zealand, Canada, Korea	56/29	0,1	Oral regorafenib 160 mg daily on days 1–21 each 28-day cycle + BSC versus oral placebo + BSC	Permanent discontinuation
Mir / 2016 ²³	II	STS	France, Austria	26/12	0,1	Oral regorafenib 160 mg once daily on days 1–21 each 28-day cycle versus placebo	Dose reductions Dose interruptions Permanent discontinuation
Bruix / 2017 ²⁴	III	HCC	21 countries in North America, South America, Europe, Asia, and Australia	379/194	0,1	Oral regorafenib 160 mg once daily on days 1–21 each 28-day cycle + BSC versus placebo + BSC	Dose reductions Permanent discontinuation
Duffaud / 2019 ²⁵	II	Osteosarcoma	France	89/92	0,1	Oral regorafenib 160 mg once daily on days 1–21 each 28-day cycle + BSC versus placebo + BSC	Dose reductions Dose interruptions Permanent discontinuation

ADE, adverse drug event; BSC, best supportive care; CRC, colorectal cancer; CT, clinical trial; ECOG-PS, Eastern Cooperative Oncology Group performance status; GC, gastric cancer; GEJ, gastroesophageal junction; GIST, gastrointestinal stromal tumour; HCC, hepatocellular carcinoma; STS, soft tissue sarcoma.

All seven RCTs reported data on AE-related permanent discontinuation;^19–25 four trials reported data on AE-related dose interruption^19,21,23,25 whereas six studies reported data on AE-related dose reductions during treatment.^{19–21,23–25}

Incidence and RR of AE-related permanent discontinuation

Table 2 shows the pooled IRs of all outcomes included in our analysis. In order to evaluate AE-related permanent discontinuation, data were extracted from all seven RCTs comprising 2099 patients.^19–25 The incidence of AE-related permanent discontinuation during REG treatment and placebo were 9.7% and 3.3%, respectively. Patients treated with REG showed higher risk of permanent discontinuation (RR = 2.80; 95% CI 1.85–4.22) ( Figure 3 ); results were associated with low heterogeneity (I² = 32%), therefore a fixed effects model was used.

Table 2.

Incidence rate of drug-related AE outcomes resulting from regorafenib treatment and placebo.

Drug-related AE outcomes	Number of events/sample size		Incidence rate % (95% CI)
Drug-related AE outcomes	Regorafenib	Placebo	Regorafenib	Placebo
Permanent discontinuation	132/1362	25/737	9.7% (8.1–11.2)	3.3% (2.1–4.6)
Transient interruptions	430/751	71/425	57.2% (53.7–60.8)	16.7% (13.1-20.2)
Dose reductions	593/1262	53/685	47% (44.2–49.7)	7.7% (5.7–9.7)

AE, adverse event.

Figure 3.

Forest plot of comparison between regorafenib treatment and placebo: the outcome was risk ratio of permanent discontinuation.

Incidence and RR of AE-related dose interruption

Four RCTs^19,21,23,25 provided data on AE-related dose interruption in 501 patients. REG treatment was associated with a pooled IR of dose interruption of 57.2% versus 16.7% in the placebo group ( Table 2 ). Patients receiving REG showed an increased RR of AE-related dose interruption (RR = 3.21; 95% CI 2.59–3.99) ( Figure 4 ); results were associated to low heterogeneity (I² = 36%), therefore a fixed effects model was used.

Figure 4.

Forest plot of comparison between regorafenib treatment and placebo: the outcome was risk ratio of dose interruption.

Incidence and RR of AE-related dose reduction

Data were available in six RCTs^{19–21,23–25} comprising 646 patients. The incidence of AE-related dose reduction in REG arm and placebo arm was 47% and 7.7%, respectively ( Table 2 ). REG was associated with higher RR of dose reduction when compared with placebo (RR = 6.02; 95% CI 3.28–11.03) ( Figure 5 ). The analysis was associated with significant heterogeneity between trials (I² = 74%), so a random-effects model was used for the OS analysis.

Figure 5.

Forest plot of comparison between regorafenib treatment and placebo; the outcome was risk ratio of dose reduction.

Discussion

In recent years, the use of MKIs as a standard of care in several solid tumours has notably changed the landscape of cancer management.^26,27 All MKIs, including REG at the recommended standard dose of 160 mg, are associated with various drug-related AEs that mainly occur within the first cycles of therapy and which can result in a relevant impact on the quality of life of patients and frequently lead to treatment dose reduction and drug discontinuation.²⁸ A plethora of recent meta-analyses evidenced that standard-dose REG leads to a significant risk of developing several all-grade and grade 3–4 AEs in patients with advanced cancer.^29–31

To the best of the authors’ knowledge, this is the first meta-analysis to investigate the incidence and risk of AE-related permanent discontinuation of treatment, dose interruptions and dose reductions associated with standard-dose REG in cancer patients. The meta-analysis was based on seven RCTs^19–25 with a total of 2099 patients, 1362 of which received standard-dose REG. We noted that AE-related dose reductions, dose interruptions and permanent treatment interruptions were, as expected, more common in the REG group than in the placebo group (reductions: 47% versus 7.7%; dose interruptions: 57.2% versus 16.7%; permanent discontinuation: 9.7% versus 3.3%, respectively).

As stated previously, in placebo-controlled RCTs regarding REG, a large proportion of patients experienced either an AE-related dose reduction or interruption when receiving the standard schedule; moreover, a small but non-negligible proportion of participants (9.7%) had to permanently discontinue the treatment and withdrew from the trial as AE-related result. This data has even more relevance considering that all patients enrolled into RCTs must have good performance status (ECOG = 0, 1) and no significant comorbidities.³² To address this relevant source of bias, the European REBECCA trial recently evaluated the role of REG in metastatic CRC with a focus on efficacy and optimal safety in a real-world setting and revealing that progression-free survival, overall survival and safety profile were similar to those of CORRECT and CONCUR trial.³³

Despite a steadily increased use of REG in advanced malignancies over the last years, real-world data on the role of non-standard schedules are scarce, often resulting from small study populations with short follow-up.³⁴ In this scenario, balancing between treatment efficacy, tolerability and quality of life is of major interest. A German study by Mross et al., revealed that REG presented similar pharmacokinetic and pharmacodynamic effects for dose levels from 120 to 220 mg; moreover, no significant pharmacologic activity was shown at doses of less than 120 mg.³⁵ As regards current clinical practice, the use of REG seems heterogeneous, with several authors which recommend REG at the starting dose of 80 or 120 mg and subsequent dose-escalation, and others which prefer shorter cycles at standard doses of 160 mg.^36,37 In our recent retrospective Italian multicentre experience, we identified approximately 20 different strategies of treatment personalization in patients affected by advanced or metastatic GIST, including dose reduction from 160 to 120 mg, 120 mg as starting dose, the initial dose of 80 mg and several others.³⁸ Of note, whatever was the strategy adopted, REG treatment personalization has led not only to a clinical benefit defined as complete or partial resolution of side effects in almost all patients, but especially positively affected the duration of REG treatment. In particular, a median duration of 9.9 months was observed, significantly greater than the 22.9 weeks of the GRID trial, with 23% of patients who exceeded 20 months and a mean duration of 32.14 months (range 20.50–53.67 months).

In a recent retrospective large study on 2376 Japanese patients affected by metastatic CRC, the initial dose of 80 mg or 120 mg REG had lower grade 3–4 AEs but similar efficacy when compared with recommended standard dose of 160 mg.³⁹ Moreover, the results of the phase II REDOS RCT comparing a dose-escalation approach with the standard REG dosing strategy of 160 mg daily in 123 patients affected by metastatic CRC, are currently available.⁴⁰ The study reported that the dose-escalation strategy starting from 80 to 160 mg daily via 40 mg increases over 3 weeks represents a safe and effective alternative to the standard dose, confirming the results from previous field-practice studies. There are currently ongoing trials, including the phase II trial REGOCC21, aimed to compare different schedules of REG treatment and which finals results will help to shed light on different dose-escalation approaches.⁴¹

In patients receiving 160 mg, an important number of AEs occur within the first cycles of therapy, suggesting that treatment adjustment during REG is not only a common event but also an early one.⁴² In REBECCA study, for example, the median time between the start of 160 mg treatment and first dose adjustment was 0.7 months;³³ thus, early monitoring and effective management of AEs seems mandatory to reduce treatment discontinuation and to optimize clinical benefit. In addition, the risks associated with REG therapy may be increased by other underlying factors, including prior oncologic and non-oncologic therapies, concomitant medications and other comorbidities.^43–46

From our point of view, modifications of REG dose and schedule should be more valorized and spread into everyday clinical practice, because it may positively affect patient’s compliance and enhance adherence to treatment. This inevitably leads to an undoubtful optimization of treatment duration, that clearly affects disease long-term outcome. Since the chronic and continuative MKI intake is crucial according to their mechanism of action, therapy optimization takes part for the treatment.

Our meta-analysis holds its own strengths and limitations. The strengths of our work regard the inclusions of only placebo-controlled RCTs, the total number of patients and the high quality of statistical analysis. However, the results of this meta-analysis should be interpreted with caution for some limitations. First, despite random-effects modelling was used in order to address heterogeneity, AE-related dose reduction analysis was burdened by substantial heterogeneity (I² = 74%). Second, data were extracted from published clinical trial results and were not gathered from individual patient data; moreover, the seven RCTs included were industry funded. Third, no subgroup analysis has been performed. The selection of patients represents another key element. In fact, all these studies compared REG versus placebo in participants with ECOG-PS grade 0 or 1 and which can only partly be representative of all patients receiving REG for advanced malignancies in everyday clinical practice. Patients with comorbidities, including uncontrolled hypertension, impaired hepatic or renal function and/or history of venous thromboembolic events, were excluded from the RCTs as well as subjects with ECOG-PS ⩾2. Finally, geographical elements [single country (n = 1 RCT), two European countries (n = 1), multinational (n = 4), single continent (n = 1)], the impact of previous treatments and primary cancer site [GIST (n = 1), CRC (n = 2), GC/GEJ (n = 1), STS (n = 1), HCC (n = 1) and osteosarcoma (n = 1)] may represent other possible sources of heterogeneity.

Conclusion

To the best of the authors’ knowledge, this is the first meta-analysis addressing this issue, providing evidence that REG 160 mg is associated with a significant increased incidence and risk of AE-related permanent discontinuation, dose interruptions and dose reductions. Therefore, despite the several limitations owing to the substantial heterogeneity, our findings may assist and help clinicians to optimize REG treatment, since early recognition and management of AEs are mandatory in clinical practice. Ongoing trials on REG are focused on the identification of effective and personalized strategies helping clinicians to maximize treatment benefits and to minimize the need for therapy discontinuation in the fragile population of pretreated patients affected by advanced cancer.

Supplemental Material

Rizzo_et_al_Revised_Supplementary_material – Supplemental material for Dose reduction and discontinuation of standard-dose regorafenib associated with adverse drug events in cancer patients: a systematic review and meta-analysis

Supplemental material, Rizzo_et_al_Revised_Supplementary_material for Dose reduction and discontinuation of standard-dose regorafenib associated with adverse drug events in cancer patients: a systematic review and meta-analysis by Alessandro Rizzo, Margherita Nannini, Marco Novelli, Angela Dalia Ricci, Valerio Di Scioscio and Maria Abbondanza Pantaleo in Therapeutic Advances in Medical Oncology

Footnotes

Author contributions

Study concept and design: Alessandro Rizzo, Margherita Nannini and Maria Abbondanza Pantaleo; acquisition of data: Angela Dalia Ricci; statistical analysis: Alessandro Rizzo and Marco Novelli; analysis and interpretation of data: Alessandro Rizzo and Marco Novelli; drafting of the manuscript: Alessandro Rizzo, Angela Dalia Ricci and Valerio Di Scioscio; critical revision of the manuscript for important intellectual content: Margherita Nannini and Maria Abbondanza Pantaleo.

Funding

The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by Department of Experimental, Diagnostic and Specialty Medicine, DIMES, Sant’Orsola-Malpighi University Hospital, Bologna, Italy.

Conflict of interest statement

The authors declare that there is no conflict of interest.

ORCID iD

Alessandro Rizzo

Supplemental material

Supplemental material for this article is available online.

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