Influence of UGT1A1 *6/*28 Polymorphisms on Irinotecan-Related Toxicity and Survival in Pediatric Patients with Relapsed/Refractory Solid Tumors Treated with the VIT Regimen

Abstract

Objective

The association between UGT1A1*6/*28 polymorphisms and treatment outcomes of irinotecan in children remains unknown. This retrospective study investigated the influence of UGT1A1*6/*28 polymorphisms on irinotecan toxicity and survival of pediatric patients with relapsed/refractory solid tumors.

Methods

The present study enrolled a total of 44 patients aged younger than 18 years at Sun Yat-sen University Cancer Center between 2014 and 2017.

Results

There were 26 boys and 18 girls; the median age at first VIT course was six years (range: 1–18 years). The tumor types included neuroblastoma (n = 25), rhabdomyosarcoma (n = 11), Wilm’s tumor (n = 4), medulloblastoma (n = 2), and desmoplastic small round cell tumor (n = 2). Overall, 203 courses of VIT regimens were prescribed. Neither UGT1A1*6 nor *28 polymorphisms were associated with the incidence rates of severe (grade III–IV) irinotecan-related toxicities, but tended to reduce the patient overall survival (UGT1A1*6, P = 0.146; UGT1A1*28, P = 0.195). Moreover, patients with mutant UGT1A1*6 genotypes were more likely to develop grade I–IV irinotecan-related diarrhea (P = 0.043) and anemia (P = 0.002). Overall, the UGT1A1*28 polymorphism may play a protective role against irinotecan-related diarrhea and abdominal pain.

Conclusion

In relapsed/refractory pediatric solid tumors, the UGT1A1*6 polymorphism was a risk factor of irinotecan-related diarrhea and anemia. The UGT1A1*28 polymorphism may serve a protective role in irinotecan-related abdominal pain and diarrhea. Both mutations had a tendency to be risk factors for survival. Nevertheless, prospective studies are required to verify such conclusions.

Keywords:

• UGT1A1 *6/*28 polymorphism
• irinotecan toxicity
• pediatric
• relapsed/refractory solid tumors

Introduction

Irinotecan, a semisynthetic water-soluble analog of camptothecin, is a prodrug activated by carboxylesterases to produce SN-38 in the human liver, intestinal mucosa, and plasma.^1–3 Irinotecan has been used clinically as a single agent or in combination with other chemotherapeutic agents for the treatment of lung, colorectal (CRC), esophageal, gastric, cervical, ovarian, and gynecological cancers.^2,4–6 Irinotecan has also shown notable antitumor activity in many recurrent and newly diagnosed pediatric solid tumors, including neuroblastoma (NB), rhabdomyosarcoma (RMS), brain tumors, non-Hodgkin lymphoma, and hepatoblastoma.^5,7 Moreover, a variety of schedules have been used in phase I^7–10 or phase II^1,3,11 studies of irinotecan in children; however, up to 36% of patients experience severe, potentially life-threatening toxicities (ie, diarrhea) following irinotecan treatment, depending on the irinotecan dosage and regimen.^2,4,7,10,12 These toxicities can cause unexpected reductions in the dosage or treatment withdrawal,⁴ which has been shown to be associated with increased disease progression and lower survival in patients with colorectal cancer.¹³

Both irinotecan and SN-38 have inhibitory effects on topoisomerase I, which breaks DNA strands during the replicative phase in main toxicity-targeted tissues and tumors,¹⁴ which leads to gastrointestinal (ie, diarrhea) or hematological toxicities (ie, neutropenia and leucopenia). SN-38 has a substantially greater potency to produce such lesions compared to that of irinotecan.^14–16 However, the accumulation of SN-38 in the intestine can result in direct enteric injury, which has been shown to be responsible for the diarrhea attributed to irinotecan administration.^2,6,15 A large body of evidence suggests that genetic differences may play a key role in drug pharmacokinetics and pharmacodynamics, which is particularly crucial when a drug is metabolized by a specific predominant route, without many other alternative pathways. This is the case of irinotecan, for which SN-38 metabolism is largely reliant on the uridine diphosphate glucuronosyltransferase (UGT) enzyme family.^6,12 In the liver, SN-38 is conjugated to glucuronic acid by UDP-glycosyltransferase 1 polypeptide A1 (UGT1A1) to form SN-38G,^2,5,14 which represents the major elimination pathway of SN-38.¹⁵ Therefore, the UGT1A1-mediated glucuronidation of SN-38 to SN-38G may play a key role in protection against irinotecan-related toxicities;² however, UGT1A1 genetic polymorphisms have been reported to be related with decreased SN-38 glucuronidation,^2,17 and will therefore be likely to play a significant role in the pharmacokinetic variability of irinotecan.¹⁸ The pharmacogenetics of irinotecan has been subjected to considerable study to optimize therapy through personalized medicine and to reduce any adverse events.⁴ The relevance of the decreased glucuronidation of SN-38 for irinotecan toxicity was first shown in patients with Gilbert syndrome,¹⁹ leading to the identification of UGT1A1 polymorphisms as the main predictors of irinotecan toxicity in cancer patients.^4,14,19

The two most extensively reported single-nucleotide polymorphisms (SNPs) of UGT1A1 concerning irinotecan toxicity are the *6 variant (rs4148323)¹⁷ and *28 variant (rs8175347),^6,12 focusing on adult solid tumors;^{16,17,20–22} however, little is known about the relationship between UGT1A1*6/*28 polymorphisms and irinotecan treatment outcomes in pediatric solid tumors. Therefore, this retrospective study aimed to evaluate the influence of UGT1A1 *6/*28 polymorphisms on irinotecan-related toxicities and survival in children with relapsed/refractory solid tumors who received irinotecan-containing VIT regimens.

Methods

Patients and Treatment

We searched the Sun Yat-sen University Cancer Center (SYSUCC) database for patient data that met the requisite inclusion criteria”. The inclusion criteria consisted of 1) age ≤18 years; 2) diagnosis of relapsed/refractory solid tumor; 3) genotype for the UGT1A1 *6/*28 polymorphism; and 4) administration of VIT chemotherapeutic regimes as the salvage therapy between 2014 and 2017. Each cycle consisted of irinotecan (50 mg/m²/day intravenously for 90 mins) on days 1–5 and temozolomide (100 mg/m²/day orally 1 h before irinotecan) on days 1–5, and vincristine (1.5 mg/m²/day intravenously) on day 1. The schedule is described in Table S1. Atropine (0.01 mg/kg) was administered 0.5 h prior to irinotecan as a prophylactic treatment for adverse gastrointestinal effects. Loperamide was administered orally at a dosage of 0.08–0.24 mg/kg body weight daily in two or three doses when the patients experienced diarrhea following an infusion with irinotecan.²³ Patients who experienced severe diarrhea (grade III/IV) during the first course of VIT therapy would receive cefixime (1.5–6 mg/kg) orally as prophylactic treatment prior to each course of following VIT therapies. This study was approved by the SYSUCC Institutional Review Board and the Research Ethics Committee (IRB: B2020-313-01). The confidentiality and compliance of the patient data were conducted in accordance with the World Medical Association Declaration of Helsinki. Since this was a retrospective study and the exemption of informed consent does not harm the rights and health of the subjects, informed consent was waived by SYSUCC Institutional Review Board and the Research Ethics Committee.

Irinotecan-Related Toxicities

Irinotecan-related toxicities (eg, vomiting, diarrhea, abdominal pain, and hematological suppression) were recorded in detail following irinotecan treatment until the subsequent course of chemotherapy. Adverse events were assessed using the NCI Common Terminology Criteria for Adverse Events version (CTCAE) 3.0.

Detection of UGT1A1 Polymorphisms

A 3 mL EDTA peripheral blood sample was collected from each patient. Genomic DNA was isolated from the blood samples using a Qiagen DNA Blood Mini Kit (# 51104, Qiagen, Germany) according to the manufacturer’s protocol. Genotyping of the TATAA box sequence repeat (UGT1A1*28) in the UGT1A1 promoter region and UGT1A1*6 (rs4148323), a SNP also known as 211G > A or G71R, at exon 1 were determined by sequencing polymerase chain reaction (PCR) amplicons. PCR was performed according to the following conditions: 94°C for 5 min, followed by 94°C for 30 s, 58°C for 50 s, 72°C for 30 s for 30 cycles, and finally, 72°C 5 for min. The PCR amplicons were used for Sanger sequencing. The primers used in this study are listed in Table S2. For the *28 site, the subjects were categorized as three different genotypes depending on the number of TA repeats in the promoter region of the UGT1A1 gene: 6/6 wild type, 6/7 heterozygote, and 7/7 homozygote. For the *6 site, the subjects were grouped into three genotypes: G/G wild type, G/A heterozygote, and A/A homozygote.

Follow-Up

Progression disease (PD), relapse, and death due to any cause were evaluated as events. The overall survival (OS) time was calculated from the date of first VIT therapy to the date of death. The event-free survival (EFS) time was from the date of first VIT therapy to the date of the occurrence of any event, including death, disease progression, second tumor development, or lethal or intolerable side effects. Patients who had not died or experienced other events at the final analysis were censored at the last follow-up in September 2020.

Statistical Analyses

Statistical analyses were performed using IBM SPSS Statistics 25.0 software (SPSS Inc. Headquarters, Chicago, IL, USA). Deviations from the Hardy–Weinberg (H–W) equilibrium of the UGT1A1 *6/*28 polymorphism genotypes and the association between categorical variables were tested using a chi-squared test. EFS and OS were analyzed in accordance with the Kaplan–Meier (K–M) method using the patient follow-up; differences were compared using a log-rank (Mantel Cox) test. The K–M survival curves were plotted using GraphPad Prism 8.0 (GraphPad Software, San Diego, CA, USA). P values <0.05 were considered to be significant. All data in our study have been recorded at SYSUCC for future reference (RDDA2020001730, https://www.researchdata.org.cn).

Results

Patient Clinical Characteristics

The characteristics of the 44 eligible patients who received 203 courses of VIT therapy (median, 4 courses; range: 1–11 courses) are summarized in Table 1. There were 26 (59.1%) boys and 18 (40.9%) girls, and the median age at the initial diagnosis was five years (range: 1–15 years). The median age at the time of the first VIT therapy was six years (range: 1–18years). The most common diagnosis was NB (n = 25; 56.8%), and a quarter of the patients were diagnosed as RMS (n = 11). The remaining patients were diagnosed with Wilm’s tumor (WM) (n = 4; 9.1%), medulloblastoma (MB) (n = 2; 4.5%), and desmoplastic small round cell tumor (DSRCT) (n = 2; 4.5%). Both the UGT1A1*6 and *28 alleles exhibited H–W equilibrium in the studied population (UGT1A1 *6 variant: χ² = 0.0164, P = 0.8981; UGT1A1*28 variant: χ² = 0.1855, P = 0.6667). The frequency of the UGT1A1*6 wild (G/G), heterozygous (G/A), and homozygous (A/A) genotypes was 31 (70.4%), 12 (27.3%), and 1 (2.3%), respectively. The majority of patients (n = 34; 77.3%) carried the UGT1A1*28 wild (6/6) genotype, whereas there were 9 (20.3%) and 1 (2.3%) patients who carried the heterozygous (6/7), and homozygous (7/7) genotypes, respectively.

Table 1 Clinical Characteristics of the Investigated Pediatric Patients with Relapsed/Refractory Solid Tumors (n = 44)

Characteristics	No. of Patients (%)	No. of VIT Courses (%)
Age at initial diagnosis, y
Median	5
Range	1–15
Age at first VIT therapy, y
Median	6
Range	1–18
Sex
Boys	26 (59.1)	136 (67.0)
Girls	18 (40.9)	67 (33.0)
Diagnosis
NB	25 (56.8)	144 (70.9)
RMS	11 (25.0)	39 (19.2)
WM	4 (9.1)	10 (4.9)
MB	2 (4.5)	4 (2.0)
DSRCT	2 (4.5)	6 (3.0)
UGT1A1 *6
71Gly/Gly	31 (70.4)	150 (73.9)
71Gly/Arg	12 (27.3)	48 (23.6)
71Arg/Arg	1 (2.3)	5 (2.5)
MT	13 (29.6)	53 (26.1)
UGT1A1 *28
(TA)6/(TA)6	34 (77.3)	157 (77.3)
(TA)6/(TA)7	9 (20.3)	38 (18.7)
(TA)7/(TA)7	1 (2.3)	8 (3.9)
MT	10 (22.6)	46 (22.6)
First event
None	8 (18.2)
PD	17 (38.6)
Relapse	9 (20.5)
Death	10 (22.7)
Follow-up status
Alive	15 (34.1)
Death	29 (65.9)
Follow-up time, m
Median	35
Range	1–78

Abbreviations: NB, neuroblastoma; RMS, rhabdomyosarcoma; WM, Wilm’s tumor; MB, medulloblastoma; PD, progression disease; DSRCT, desmoplastic small round cell tumor; MT, mutant type.

Association Between Genetic Polymorphisms and Irinotecan-Related Toxicities

The prevalence of irinotecan-related toxicities in children with relapsed/refractory solid tumors is presented in Tables 2 and 3. Grade III–IV diarrhea, abdominal pain, and vomiting were observed in 18.2%, (n = 37), 3.4% (n = 7), and 4.9% (n = 10) courses of VIT therapy, respectively. Diarrhea and abdominal pain that lasted ≥4 days were observed in 18.2% (n = 37) and 10.3% (n = 21) of courses of VIT therapy, respectively. For hematological suppression, grade III–IV leucopenia (n = 49, 24.1%) and neutropenia (n = 58, 28.6%) occurred more frequently than anemia (n = 23, 11.3%) and thrombocytopenia (n = 13, 6.4%). The frequency of grade III–IV toxicities was not significantly different between wild and mutant UGT1A1 *6/*28 genotypes. However, the duration of diarrhea and abdominal pain were correlated with the UGT1A1 *28 polymorphism. The incidence rates of ≥4 days of diarrhea (22.9% vs 2.2%; P = 0.001) and ≥4 days of abdominal pain (12.7% vs 2.2%; P = 0.039) were significantly higher in patients with the UGT1A1 *28 wild-type genotype (Table 4).

Table 2 Prevalence of CPT-11-Related Toxicities in Children with Relapsed/Refractory Solid Tumors (n = 203)

Toxicity	Number of Courses (%)
	Grade 0	Grade I–II	Grade III–IV
Diarrhea	97 (47.8)	69 (34.0)	37 (18.2)
Abdominal pain	138 (68.0)	56 (27.6)	7 (3.4)
Vomiting	171 (84.2)	22 (10.8)	10 (4.9)
Leucopenia	68 (33.5)	86 (42.4)	49 (24.1)
Neutropenia	82 (44.4)	63 (31.0)	58 (28.6)
Anemia	41 (20.2)	139 (68.5)	23 (11.3)
Thrombocytopenia	171 (84.2)	19 (9.4)	13 (6.4)

Table 3 Duration of Diarrhea and Abdominal Pain in Children with Relapsed/Refractory Solid Tumors (n = 203)

Duration (Day)	Number of Courses (%)
	0	1–3	≥4
Diarrhea	97 (47.8)	69 (34.0)	37 (18.2)
Abdominal pain	138 (68.0)	44 (21.7)	21 (10.3)

Table 4 Association Between the UGT1A1 *6/*28 Polymorphism and Irinotecan-Related Toxicities (G0-II vs GIII-IV)

Toxicity (GIII-IV)	UGT1A1 *6		χ^2	P	UGT1A1 *28		χ^2	P
	WT	MT			WT	MT
Diarrhea	29 (19.3)	8 (15.1)	0.472	0.492	29 (18.5)	8 (17.4)	0.028	0.867
Abdominal pain	7 (4.7)	0 (0)	2.562	0.109	7 (4.5)	0 (0)	2.124	0.145
Vomiting	6 (4.0)	4 (7.5)	1.052	0.305	9 (5.7)	1 (2.2)	0.962	0.327
Leucopenia	35 (23.3)	14 (26.4)	0.203	0.652	41 (26.1)	8 (17.4)	1.478	0.224
Neutropenia	41 (27.3)	17 (32.1)	0.432	0.511	44 (28.0)	14 (28.6)	0.101	0.750
Anemia	16 (10.7)	7 (13.2)	0.252	0.616	15 (9.6)	8 (17.4)	2.175	0.140
Thrombocytopenia	7 (4.7)	6 (11.3)	2.893	0.089	11 (7.0)	2 (4.3)	0.420	0.517
Duration of diarrhea (≥4d)	29 (19.3)	8 (15.1)	0.472	0.492	36 (22.9)	1 (2.2)	10.281	0.001
Duration of abdominal pain (≥4d)	16 (10.7)	5 (9.4)	0.064	0.800	20 (12.7)	1 (2.2)	4.282	0.039

Next, we dichotomized the toxicity grades as grade 0 versus grade I–IV, and performed a chi-squared test to further evaluate the influence of the UGT1A1 *6/*28 polymorphism on the irinotecan-related toxicities. As shown in Table 5, the results indicated that the UGT1A1*6 polymorphism was correlated with diarrhea and anemia. Patients with the mutant genotype were more pronounced to experience diarrhea (48.0% vs 64.2%; P = 0.043) and anemia (74.7% vs 94.3%); P = 0.002). The UGT1A1*28 polymorphism was correlated with abdominal pain, and the patients with a mutant genotype had a significantly lower risk of abdominal pain (38.2% vs 10.9%; P < 0.001) and tended to have a lower risk of diarrhea (55.4% vs 41.3%).

Table 5 Association Between the UGT1A1 *6/*28 Polymorphism and Irinotecan-Related Toxicities (G0 vs GI-IV)

Toxicity (GI-IV)	UGT1A1 *6		χ^2	P	UGT1A1 *28		χ^2	P
	WT	MT			WT	MT
Diarrhea	72 (48.0)	34 (64.2)	4.094	0.043	87 (55.4)	19 (41.3)	2.839	0.092
Abdominal pain	48 (32.0)	17 (32.1)	<0.001	0.992	60 (38.2)	5 (10.9)	12.228	<0.001
Vomiting	23 (15.3)	9 (17.0)	0.080	0.777	26 (16.6)	6 (13.0)	0.331	0.565
Leucopenia	100 (66.7)	35 (66.0)	0.007	0.934	109 (69.4)	26 (56.5)	2.660	0.103
Neutropenia	91 (60.7)	31 (58.5)	0.077	0.781	95 (60.5)	27 (58.7)	0.049	0.825
Anemia	112 (74.7)	50 (94.3)	9.404	0.002	121 (77.1)	41 (89.1)	3.221	0.073
Thrombocytopenia	21 (14.0)	11 (20.8)	1.346	0.246	21 (13.4)	11 (23.9)	2.975	0.085

Influence of UGT1A1 *6/*28 on the Survival of Pediatric Patients with Relapsed/Refractory Solid Tumors

The median follow-up time was 35 months (range: 1–78 months) for all patients. The first events were observed as PD in 8 patients (18.2%), relapse in 9 patients (20.5%), and death in 10 patients (22/7%). As of the last follow-up on September 2020, 29 patients (65.9%) died of cancer. The one- to five-year EFS and OS are listed in Table S3. The K–M survival analysis revealed that both UGT1A1*6 and *28 polymorphisms were not significantly associated with the EFS and OS (Figure 1A–D); however, patients with the UGT1A1*6 (P = 0.146) or *28 (P = 0.195) mutant genotypes tended to have an inferior OS compared to those with the wild-type genotype.

Figure 1 Kaplan–Meier analysis of event-free survival (EFS) and overall survival (OS) in the pediatric relapsed/refractory solid tumors with genotype of the UGT1A1*6/*28 polymorphisms (n = 44); No significant difference was found in EFS/OS among the different genotypes; WT, wild genotype; MT, mutant genotype. (A) The three-year EFS rate for UGT1A1*6 WT and MT was 25.8% and 16.7%, Respectively. (B) Patients carrying UGT1A1*6 MT had a non-significantly higher three-year OS rate than those with WT (54.8% vs 41.7%). (C) The three-year EFS rate for UGT1A1*28 WT and MT was 27.3% and 20.0%, respectively. (D) Patients carrying UGT1A1*28 MT had a non-significantly higher three-year OS rate than those with WT (54.5% vs 40.0%).

Discussion

The SNP UGT1A1*6 is a missense polymorphism that leads to a single amino acid change from glycine to arginine (Gly71Arg) at site 71 of the UGT1A1 gene. Such substitution alters the hydrophobicity and secondary structure of the protein.^17,24 The in vitro studies revealed that the enzymatic activity of the UGT1A1*6 variant is approximately one-third of that of the *1 allele.¹² The UGT1A1*28 polymorphism results from a change in the number of TA repeats in the TATA box of the UGT1A1 promoter from six wild-type repeats to seven variant repeats. The overall number of TA repeats varies from 5 to 8. UGT1A1 expression in individuals with the variant TA7 allele, especially homozygotes, could be decreased by as much as 70%.^5,6,12 Therefore, UGT1A1*6 and *28 polymorphisms are theoretically expected to reduce the glucuronidation of SN-38 and could increase the risk of irinotecan-induced toxicities. The association between irinotecan-related toxicities and UGT1A1 genetic polymorphisms in a variety of malignancies have been widely acknowledged and considered for therapeutic recommendations in many countries.²⁵ In 2005, UGT1A1*28 polymorphism genotyping before prescribing irinotecan was recommended by the Food and Drug Administration to reduce irinotecan related toxicities, due to the increased incidence of neutropenia in adult patients with the 7/7 genotype after each 21-day dosage of irinotecan.^9,14,26 Reduced initial irinotecan dosages should be considered in patients with the UGT1A1*28 genotype.^5,16 However, controversial results concerning the relevance of this test for predicting irinotecan toxicity have been reported in several studies.^16,27 The study by Cecchin et al proposed that genotyping a few markers in the UGT1A genes, rather than a single UGT1A1*28 polymorphism, can significantly improve the predicted outcome of CRC patients, and indicates that the optimal dose reduction in *28/*28 patients, which would not compromise its efficacy.¹⁶

Numerous studies have investigated the association between UGT1A1*6/*28 polymorphisms and irinotecan toxicities in adult solid tumors, focusing on CRC, lung cancer, and gastric cancer, with inconsistent results. Thus, a series of meta-analyses have been conducted to investigate this topic. Consistent conclusions were made regarding the UGT1A1*6 polymorphism, which could be regarded as a biomarker of irinotecan-related neutropenia and diarrhea, and can particularly benefit Asian cancer patients.^4,24,28–33 Several of the most recent studies in Asia have experienced similar results.^17,34–36 The UGT1A1*28 polymorphism has also been reported to be correlated with irinotecan-related diarrhea; however, the conclusions were controversial for neutropenia. The majority of meta-analyses^4,24,28–33 and two recent studies performed in Asia^35,36 concluded that the UGT1A1*28 polymorphism could increase the risk of neutropenia. Campbell et al revealed that such an effect was greater than that of neutropenia in both Asian and Caucasian patients.²⁸ Other studies have showed that the UGT1A1*28 polymorphism was not associated with neutropenia or diarrhea and may not be a suitable predictor of irinotecan toxicity.^5,30 Moreover, a recent Japanese study, which included a total of 651 patients with a wide-range of adult solid tumors and hematopoietic malignancies concluded that UGT1A1 testing could be useful to predict irinotecan-induced adverse reactions, and that UTG1A1*6 rather than UGT1A1*28 contributed to the occurrence of adverse drug reactions.²⁵ Another recent study from Guangxi Zhuang in China also indicated that UGT1A1*28 was not correlated with irinotecan-related neutropenia in metastatic CRC patients.³⁴

Compared to adult solid tumors, data is limited regarding the influence of UGT1A1*6/*28 on irinotecan toxicity in pediatric malignancies. Two clinical trials have suggested that the UGT1A1 genotype was not associated with irinotecan-related neutropenia and diarrhea in pediatric refractory solid tumors treated with a low-dose protracted schedule of irinotecan.^3,7 Many clinical and pharmacogenetic factors, including gender, age, drug administration schedule, and metabolic enzymes, have been reported to be associated with irinotecan toxicity.^12,14 Therefore, our analysis only enrolled pediatric patients with relapsed/refractory solid tumors who received VIT regimens with irinotecan administrated at a dose of 50 mg/m² to minimize the impact of co-founding factors on irinotecan toxicity. Previous studies have reported that the frequency of the UGT1A1*28 polymorphism is 39% in the white population, whereas that in Asians was only 16%,³⁷ which is similar to the 10% reported in our study. The mutation rates of UGT1A1*6 and *28 are similar in the present study. Our findings suggest that both UGT1A1*6 and *28 polymorphisms were associated with irinotecan-related toxicity. Consistent with previous reports of adult malignancies, pediatric patients with relapsed/refractory solid tumors who carried mutant UGT1A1*6 genotypes were found to be more likely to experience diarrhea (P = 0.043) in our study; however, the UGT1A1*6 polymorphism increased the risk of anemia (P = 0.002) rather than neutropenia. In contrast, the UGT1A1*28 polymorphism was not related to bone marrow suppression and interestingly, may play a protective role against diarrhea and abdominal pain. Patients with the mutant UGT1A1*28 genotype were less likely to experience abdominal pain (P < 0.001) and tended to have lower risk of diarrhea (P = 0.092). Moreover, mutant UGT1A1*28 genotypes were correlated with a shorter duration of diarrhea (P = 0.001) and abdominal pain (P = 0.039). All of the irinotecan-related toxicities in our study were manageable with medication. Previous research showed that the influence of UGT1A1*6/*28 polymorphisms on irinotecan toxicity varied by race, region, cancer type, irinotecan dose, and duration of treatment.^28,29 In addition, the adult dose and schedule of irinotecan varies significantly compared to that of children. This may partially account for the discrepancy between our study and previous research, especially the data pertaining to adults. Also, the sample number in our study was relatively small compared to studies in adult; younger patients (preschool-aged children) added to the difficulty to record the grade of subjective toxicities in the current study. Moreover, the prophylactic treatment of cefixime in patients with previous severe diarrhea may have disguised the influence of UGT1A1 polymorphisms in irinotecan-related diarrhea.

Although the association between UGT1A1*6/*28 and irinotecan toxicity was extensively studied, there is a lack of evidence regarding whether UGT1A1*6/*28 genotyping is of clinical value for predicting survival following irinotecan therapy. Previous observational studies evaluating the influence of UGT1A1*6/*28 on survival have revealed contradictory results. Reviews suggest that the UGT1A1*28 polymorphism was not associated with any changes to the objective response rate, progression-free survival (PFS), or overall survival (OS) following irinotecan treatment.^4,38 A recent study also found that neither UGT1A1*6 nor *28 had an impact on treatment efficacy and PFS in metastatic CRC;³⁴ however, Matsuoka et al suggested that UGT1A1 polymorphisms were significantly related with longer PFS in uterine cervical cancer.³⁹ Similarly, the findings by Henriksen et al revealed that UGT1A1*28 improved the PFS and OS in metastatic renal cell carcinoma.⁴⁰ In contrast, the study by Yamaguchi et al confirmed that UGT1A1*6 and *28 were shown to be related to a shorter OS in advanced gastric cancer when irinotecan monotherapy was used as a third-line treatment.⁴¹ In the present study, the K–M survival analysis revealed that patients with mutant UGT1A1*6 (P = 0.146) or *28 (P = 0.195) genotypes had a non-significant inferior OS compared to those with the wild genotype.

We are aware of several limitations associated with this study. The major limitation is the retrospective nature. Since not all patients were willing to be genotyped for the UGT1A1 6*/*28 polymorphism, there was a small sample number included in this study, and this was a single center study. Additionally, irinotecan metabolism is influenced by both UGT1A1*6/*28, as well as several other genetic polymorphisms, including CYP3A4/5, DPYD, CES2, SLCO1B1, ABCB1, and ABCC2.^14,18,35 Therefore, taking only UGT1A1*6/*28 into consideration may not be sufficiently convincing to explore the relationship with irinotecan toxicities. In conclusion, UGT1A1*6 and *28 polymorphisms may represent biomarkers of irinotecan toxicities but not to the extent of severe toxicities (grade III–IV). In addition, UGT1A1*6 and *28 genotyping may have use for predicting survival following VIT regimens in pediatric patients with relapsed/refractory solid tumors. Nevertheless, further prospective multicenter studies are required to validate the predictive significance of these associations.

Abbreviations

UGT1A1, UDP-glycosyltransferase 1 polypeptide A1; VIT regimen, irinotecan, vincristine, temozolomide; CRC, colorectal cancer; NB, neuroblastoma; RMS, rhabdomyosarcoma; SNP, single-nucleotide polymorphism; SYSUCC, Sun Yat-sen University Cancer Center; CTCAE, NCI Common Terminology Criteria for Adverse Events version; PD, progression disease; OS, overall survival; EFS, event-free survival; H–W, Hardy–Weinberg; K–M, Kaplan–Meier; W-M, Wilm’s tumor; MB, medulloblastoma; DSRCT, desmoplastic small round cell tumor; PFS, progression-free survival.

Disclosure

The authors report no conflicts of interest in this work.