A Retrospective Analysis of the Effect of Irinotecan-Based Regimens in Patients With Metastatic Breast Cancer Previously Treated With Anthracyclines and Taxanes

Abstract

Background:

At present, patients with metastatic breast cancer (MBC) have few treatment options after receiving anthracyclines and taxanes. Studies have shown that irinotecan has modest systemic activity in some patients previously treated with anthracyclines and taxanes. This study aimed to evaluate the efficacy of irinotecan-based chemotherapy for breast cancer patients in a metastatic setting.

Methods:

We retrospectively collected the clinical information and survival data of 51 patients with MBC who received irinotecan at West China Hospital of Sichuan University. The primary endpoints were the progression free survival (PFS) and overall survival (OS), and the secondary endpoint was the objective response rate (ORR). To minimize potential confounding factors, we matched 51 patients who received third-line chemotherapy without irinotecan through propensity score matching (PSM) based on age, hormone receptor (HR), and human epidermal growth factor receptor 2 (HER2), compared their OS and PFS rates to those treated with irinotecan.

Results:

From July 2012 to October 2020, 51 patients were treated with an irinotecan-containing regimen. The median number of previous treatment lines was 4, and a median of two previous chemotherapy cycles (ranging from 1–14 cycles) were given in a salvage line setting. The ORR was 15.7%, and the disease control rate (DCR) was 37.3%. For the irinotecan group, the median PFS was 3.2 months (95% CI 2.7–3.7), while the median OS was 33.1 months (95% CI 27.9–38.3). Univariate analysis results suggested that irinotecan could improve PFS in patients with visceral metastasis (P=0.031), which was 0.7 months longer than patients without visceral metastasis (3.5 months vs. 2.8 months). Compared to the patients who received third-line non-irinotecan chemotherapy, the irinotecan group showed a longer trend of PFS without statistical significance (3.2 months vs 2.1 months, P = 0.052). Similarly, the OS of the irinotecan group was longer than the third-line survival without irinotecan, but it was not statistically significant (33.1 months vs 18.0 months, P = 0.072).

Conclusions:

For MBC patients who were previously treated with anthracyclines and/or taxanes, an irinotecan-containing regimen achieved moderate objective response and showed a trend of survival benefit, which deserves further study.

Introduction

Globally, breast cancer is the most common cancer and the leading cause of cancer death in women (1). The incidence of breast cancer has been rising, and this trend is expected to continue. Long-term survival mainly depends on tumor stage and molecular subtype. Early detection and early treatment are important strategies for improving prognosis. The 5-year survival rate of those diagnosed with early breast cancer is 99%, while that of those diagnosed with metastatic breast cancer (MBC) is 25% (2, 3). In the past few decades, significant progress has been made in improving the survival rate of patients with MBC, but most cannot be cured by existing treatment methods (4, 5). In patients with rapid tumor progression or life-threatening visceral metastasis, or those who need to quickly control tumor progression or relieve symptoms, combination chemotherapy is usually appropriate (6).There is currently no standard chemotherapy regimen for MBC (7). The available treatment options include anthracyclines, taxanes, 5-fluorouracil, vinorelbine, gemcitabine (5, 8). Those breast cancer patients with relatively long survival time often face the dilemma that no effective drugs are available. Irinotecan is a topoisomerase I inhibitor, which is widely used in clinical treatment of advanced colorectal cancer, lung cancer, gastric cancer (9–11). A few clinical trials have shown that irinotecan had modest systemic activity in some patients previously treated with anthracyclines and taxanes. The objective response rate (ORR) of patients with MBC who received irinotecan monotherapy was 5%–23%, while the ORR of patients with MBC who received a combination of irinotecan and various chemotherapy drugs ranged from 14%–64%, usually including patients who had been heavily pretreated (5, 12, 13). Irinotecan has not been regarded as a routine treatment option for patients with MBC, and the outcome of subsequent therapy with irinotecan in patients with MBC was not clear. The aim of the present study was to evaluate the efficacy of irinotecan as a salvage line therapy for patients with MBC.

Patients and Methods

We enrolled patients with MBC who were admitted to West China Hospital from July 1, 2012 to October 30, 2020 and were registered in the Breast Cancer Information Management System (BCIMS). The BCIMS prospectively records patient clinical and pathological characteristics, medical history, diagnoses, laboratory results, treatments, and follow-up data (14).

Eligibility criteria included (1) Patients with MBC, that is pathologically diagnosed breast cancer with metastasis sites, including skin, lymph node (non-breast lymphatic drainage area),bone and other visceral metastasis and (2) Patients received systemic chemotherapy with or without irinotecan in a salvage line. The prior treatment regimens and lines for metastatic disease were not limited. Of the 1607 patients in the database, fifty-one patients treated with irinotecan met the inclusion criteria of the irinotecan group. Patients with no irinotecan medication record (1556 cases) in the database were matched through propensity score matching (PSM) in a 1:1 ratio as the control group, and the matching factor was age ( ± 5years), hormone receptor (HR), human epidermal growth factor receptor 2 (HER2) and the number of treatment lines was three lines or above. Then, two matched cohorts of 51 patients were created. Their data, including basic information, diagnosis, molecular subtypes, chemotherapy regimens, evaluation of efficacy, were exported from BCIMS.

Therapeutic Schedule

Patients were treated with intravenous irinotecan 125 mg/m² weekly for 4 weeks followed by a 2-week break. This regime was based on one randomized Phase II trial with irinotecan in MBC, which showed that weekly treatment schedules, compared with every 3 weeks, had better response rates (15). Irinotecan was combined with a variety of other chemotherapeutics, including 5-FU analogs, vinorelbine, gemcitabine, and platinum, as well as being combined with various biologic agents, such as trastuzumab, apatinib (Table 1).

Efficacy Evaluation

The ORR was defined as the objective response rate—that is, the ratio of patients with complete response (CR) plus partial response (PR) to all patients. The disease control rate (DCR) was defined as the ratio of CR+PR+SD (stable disease) patients to all patients. Progression free survival (PFS) was defined as the time from initiation of irinotecan to the presence of objective evidence of disease progression (or death for any reason). Overall survival (OS) was defined as the time from initiation of irinotecan until death, or loss of follow-up or reaching the study observation deadline. Follow-up was conducted via telephone or medical visit until death. Lost to follow-up was defined as failure to make contact with the patient on > 2 consecutive occasions (16). The longest follow-up time was 40 months. According to response evaluation criteria in solid tumors 1.1 (RECIST 1.1), the therapeutic effect should be evaluated through imaging examination about 2 cycles. The primary endpoints were PFS and OS, and the secondary endpoint was ORR.

Analysis Methods

Survival analysis was performed using SPSS version 25.0. A survival curve was created using the Kaplan–Meier method. A log-rank test was used for univariate analysis of PFS and OS. Categorical variables were compared with the χ2 test or Fisher’s exact test. PSM was conducted using R software (version 4.0.3), employing a 1:1 nearest neighbor with a caliper of 0.02. Subgroup analysis was performed with R software (version 4.0.3). P < 0.05 was considered statistically significant.

Results

Baseline Characteristics of Subjects

A total of 51 patients with MBC entered the irinotecan group and the control group, respectively. The characteristics of the two groups were roughly similar. Almost all patients in both groups were female. The median patient age was 43 years, and premenopausal patients accounted for more than 60% of the patients. The biological subtype included estrogen receptor (ER)-positive and/or progesterone receptor (PR)-positive (74.5%), HER2-positive (35.3%), and triple negative (13.7%). Visceral metastasis had occurred in more than 85% of the patients, more than 85% of the patients had previously received anthracyclines, and more than 95% had been treated with taxanes. The median number of previous treatment lines was 4, and a median of two previous chemotherapy cycles (ranging from 1–14 cycles) were given in a salvage line setting. Demographic and clinical characteristics between the irinotecan and control groups are shown in Table 2.

Efficacy

At the cutoff of October 30, 2020, the best overall response of the irinotecan group was: CR (n =1), PR (n =7), SD (n = 11), progression disease (PD) (n = 32), an ORR of 15.7%, and a DCR of 37.3%. The median PFS for the irinotecan group was 3.2 months (95% CI 2.7–3.7) (Figure 1), the median OS was 33.1 months (95% CI 27.9–38.3), and the 2-year OS rate was 70.0% (Figure 2).

Figure 1

Figure 2

Results of the univariate analysis indicated that the PFS of the irinotecan group was significantly prolonged in patients with visceral metastasis (P = 0.031) compared with those without visceral metastases. Age (< 45 years, ≥ 45 years), menopausal status (pre-menopause, post-menopause), triple negative (positive/negative), HER2 status (positive/negative), HR status (positive/negative), and number of previous chemotherapy lines (≤ 3, >3) were not associated with the PFS of irinotecan (Table 3). With regard to OS, the univariate analysis found no clinicopathological factors affecting OS (Table 3).

After PSM, the baseline characteristics were relatively comparable. The PFS of the irinotecan group showed a longer trend of PFS without statistical significance at 3.2 months (95% CI 2.7–3.7) vs 2.1 months (95% CI 1.4–2.8), (P = 0.052) (Figure 1). Similarly, the OS of the irinotecan group was longer than the third-line survival without irinotecan, but it was not statistically significant at 33.1 months (95% CI 27.4–38.8) vs 18.0 months (95% CI 3.2–32.8), (P = 0.072) (Figure 2).

Subgroup analysis found that patients younger than 45 years (P=0.039), premenopausal (P=0.004), HR positive (P=0.021), non-triple negative (P=0.039), with visceral metastases (P=0,028), and prior anthracycline therapy (P=0.025) had a longer PFS in patients treated with irinotecan. Premenopausal patients (P=0.029) with irinotecan had a longer OS. Other factors were not found to be significantly associated with patients’ PFS and OS (Figures 3, 4).

Figure 3

Figure 4

Subsequent Treatment

The large majority of patients received further therapy after irinotecan progression: 52 patients (86.7%) received systemic treatment (see specific treatment status in Table 4). As the higher proportion of patients receiving subsequent treatment would have inevitably affected OS, indicators such as the 2-year OS rate may more reliably reflect the efficacy of irinotecan in treating patients with MBC.

Discussion

This study retrospectively analyzed the efficacy of irinotecan in patients with MBC who had been heavily pretreated in the real world. Based on the limited available data in our database, we found that after failure of multi-line treatment of MBC patients, an irinotecan-containing regimen achieved an ORR of 15.7%, a DCR of 37.3%, and a median PFS of 3.2 months, achieving a median OS of 33.1 months.

The efficacy of irinotecan varies greatly among previous studies. A systemic analysis that enrolled 217 patients with refractory MBC in 5 irinotecan-based clinical studies confirmed a pooled RR of 48.8% (17). Other Phase I/II studies enrolled patients (n = 18–64) with MBC previously exposed to anthracycline and/or taxane-containing therapy using an irinotecan combination with other drugs such as cetuximab, temozolomide, docetaxel, gemcitabine, or etoposide. Those studies demonstrated an ORR of 5.6%–58.3%, a clinical benefit rate of 16%–97%, a median time to progression (TTP) of 1.4–14 months, and a median OS of 4.9–26 months (3, 18–27). There are few findings from large-scale, prospective, randomized studies on the use of irinotecan for MBC. We found only one Phase III randomized controlled trial comparing capecitabine with or without irinotecan in patients with MBC previously treated with anthracycline and taxane. The results suggest that for PFS, OS, and ORR, capecitabine plus irinotecan therapy is not significantly better than capecitabine. Until now, irinotecan’s position in breast cancer treatment regimens has not been established.

Compared to the current approved drugs for anthracycline and taxane-pretreated MBC such as capecitabine or eribulin, the PFS of our study was similar to those of eribulin or capecitabine, in which eribulin showed an ORR of 14.9%–20%, a clinical benefit rate of 30%, and a PFS of 3.9–4.0 months (28), while capecitabine’s ORR ranged from 14%–29% and exhibited a median TTP range from 3.1–5.9 months (29). After balancing age and molecular subtypes through PSM, the OS and PFS of MBC patients after the progression of anthracycline and paclitaxel with irinotecan may be better than those without irinotecan in third-line treatment, but it is not statistically significant. For patients with advanced MBC after failure of multi-line therapy, despite anthracycline and taxane having been used in the prior line, irinotecan may be considered as a treatment option when no better choice is available.

A handful of reports have suggested that irinotecan showed potentially promising results in triple negative breast cancer (3, 9), but unlike those studies, we found HR positive or non-triple negative patients had longer PFS treated with irinotecan compared with hormone receptor-negative patients. Second, we noticed that patients with younger than 45 years, premenopausal, with visceral metastasis, and prior anthracycline therapy had longer PFS. In particular, we observed a certain extension in PFS in patients with visceral metastasis with irinotecan (Previous treatment line of irinotecan was 4, indicating a possible drug-resistant population), suggesting that irinotecan is a posterior option for patients with visceral metastasis. Large-sample studies are needed to further identify patients with the highest likelihood of responding to treatment with irinotecan (13).

Given the dose-limiting toxicity of irinotecan and its inactivity in a large proportion of patients, it is more desirable to identify a biomarker to predict irinotecan’s activity. Some researchers have explored whether the increased topoisomerase 1 gene copy number or UGT1A1 polymorphisms can predict the response of the topoisomerase inhibitor irinotecan (3, 12). Due to the limited number of cases, no significant correlation has been found to be related to irinotecan’s response. Similarly, Cinzia Tesauro et al. investigated the relationship between CPT efficacy and TOP1 activity (including gene and protein levels) in BC cell lines (Luminal, HER2, and TNBC) in vitro, and found that TOP1 activity was not a marker for camptothecin sensitivity in breast cancer (9). Furthermore, researchers are also exploring several delivery strategies of SN-38, an active metabolite of irinotecan, showing a 100- to 1000-fold greater potency than irinotecan (30). Some preclinical work found liposomal irinotecan preferentially accumulates in metastatic lesions and acted as a reservoir for the release of irinotecan, improving anti-tumor activity with decreased toxicity in a number of animal models of human cancer (31, 32). And in a recent study(n=30), liposomal irinotecan showed favorable antitumor activity in heavily pretreated patients with or without brain metastasis, the reported objective response rate of 30%-34.5% with single drug and disease control rate 34.5%-50% (33).

Other evidence suggests that combining the topoisomerase I inhibitor deruxtecan with HER2-targeting antibody had excellent effects in breast cancer patients with HER2-positive and low-level HER2 expression. A Phase 2 study that enrolled 184 patients who received a median of 6 previous treatments followed by DS8201, a HER2-targeting antibody drug conjugate, found an RR of 60.9%, while the median duration of PFS was 16.4 months (34). From the above, we may see that it is possible to improve the efficacy of drugs by developing novel dosage formulations such as nanoparticles, liposomes, or pegylation; using drugs in combination with targeted agents; or using novel linker payload technology (compared with TDM1) (35).

Limitations

This was a retrospective analysis of data collected at a single center. The sample size was limited. Several subtypes of breast cancers were mixed and irinotecan schedules were heterogenous.

Conclusion

Irinotecan-containing regimens may achieve moderate objective response and showed a trend of survival benefit as a salvage treatment in MBC. The role of the topoisomerase 1 inhibitors in MBC still needs to be further validated in large-sample, prospective studies.

Funding

This work was supported by the National Key Development Plan for Precision Medicine Research (grant number 2017YFC0910004), the 135 project for disciplines of excellence, West China Hospital, Sichuan University (grant number ZYGD18012), and Science and Technology Department of Sichuan Province project funding (2017FZ0062).

Publisher’s Note

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