Impact of nutritional status in the era of FOLFOX/FIRI-based chemotherapy

The study group comprised patients who received chemotherapy (FOLFOX/FOLFIRI with or without an anti-vascular endothelial growth factor antibody or an anti-epidermal growth factor receptor agent) for initially unresectable or recurrent colorectal cancer. All patients were able to have perioral food intake. When ileus was observed, transient colostomy was made to have perioral food intake as much as possible. Patients were excluded if they had received adjuvant chemotherapy, double primary cancers, and severe comorbidity requiring a reduction in the dose of chemotherapy. The data was retrospectively collected after the chemotherapy.

The indication for liver resection was the presence of entire tumors of colorectal origin, which if removed would be curative in the absence of any medical contraindications. Neither the number of tumors nor the tumor diameter limited the indication for liver resection [10]. The upper limit of the liver volume to be resected was assessed by the indocyanine green retention rate at 15 min. If the estimated remnant liver volume was considered insufficient, portal vein embolization was performed before the liver resection [11]. The presence of extrahepatic metastases did not contraindicate liver resection if the lesion was estimated to be curable by metachronous resection.

The patients were divided into two groups according to whether the nutritional status was well or bad-nourished, assessed before chemotherapy and 2 months (after initial 4 cycles) and 6 months after the chemotherapy. Well-nourished was defined as a serum albumin level of ≥ 3.8 g/dL or an increase in the serum albumin level of ≥ 1.0 g/dL as compared with the baseline value before chemotherapy (3.8 g/dL: lower limit of normal value at our institution). The control group was defined as a serum albumin level of < 3.8 g/dL or a decrease in the serum albumin level of < 1.0 g/dL when the baseline serum albumin level was ≥ 3.8 g/dL.

Chemotherapy-related adverse events (hematotoxic AE, non-hematotoxic AE, discontinue or dose reduction of scheduled chemotherapy) were evaluated 2- and 6 months after the chemotherapy. Based on the nutritional status at 6 months after the start of chemotherapy, the response of chemotherapy, progression-free survival (PFS), and overall survival (OS) were evaluated.

Hematotoxicity was assessed according to the Common Terminology Criteria for Adverse Events (CTC-AE), version 5.0. [12] Complications were assessed and graded by a single observer (S.O.) who was not involved in the administration of chemotherapy. This study was confirmed by the institutional review board of our hospital.

Data are expressed as median values and ranges or as absolute values and percentages. p values of < 0.05 were considered to indicate statistical significance. Student’s t test, the χ2 test, the Mann-Whitney U test, and the Fisher’s exact test were used for univariate analysis as required. Survival rates were calculated using a Cox proportional-hazards model, survival curves were obtained using the Kaplan-Meier method, and comparisons were made using the log-rank test. All statistical analyses were performed with the use of a statistical software package (JMP version 9.0, SAS Institute Inc., Cary, NC, USA).

Between May 2010 and January 2013, FOLFOX/FOLFIRI-based chemotherapy was given to 157 consecutive patients with colorectal cancer. A total of 49 patients were excluded: 31 patients had no target lesions (adjuvant chemotherapy), 9 had double primary cancers, 9 had serious concurrent illnesses requiring reduced doses of anticancer agents, and 1 received cetuximab. Data on the remaining 108 consecutive patients were analyzed.

There was a total of 108 patients and the median age was 65 years (range 34–83) (Table 1).

There were 75 patients with colon cancer and 33 patients with rectal cancer. The 17 patients had a primary unresectable cancer with metastasis. The rate of KRAS gene mutation is 38.0% (41/108 patients). There were 30 patients (27.8%) of FOLFOX and 78 patients (32.2%) of FOLFIRI at first line chemotherapy. The 41 patients (38.0%) received anti-vascular endothelial growth factor (VEGFR) antibody, and the 38 patients (35.1%) received an anti-epidermal growth factor receptor antibody. The serum carcinoembryonic antigen (CEA) value (median 18.0 ng/mL [interquartile range (IQR): 4.7–65.3]) and the carbohydrate antigen (CA) 19-9 level (35.7 U/mL [6.-329.4]).

The nutritional status was estimated and divided into the two groups according to the nutritional status after the 4 cycles (2 month) of FOLFOX/FIRI therapy. There were 69 patients in the well-nourished group and 39 patients in the control group (Table 2). The proportion of age, gender, WHO performance status, BMI, site of primary tumor, and residual of the tumor did not differ significantly between the well-nourished and control. There was no significant difference of the first line chemotherapy regimen and additional targeting agent between the two groups.

As for the chemotherapy-induced AE, the hematotoxic AE tended to less frequent in well-nourished (grade 2 18.8 vs. 30.8%, p = 0.11). The non-hematotoxic AE was significantly less frequent in well-nourished (grade 2 15.9 vs. 38.5%, < 0.01). There was no significant difference in the median tumor marker value in 2 months after initial chemotherapy (CEA 16.8 vs. 6.9 mg/L, p = 0.39; CA19-9 19.6 vs. 15.6, p = 0.19).

Six months after the start of chemotherapy, there were 67 patients in the well-nourished and 41 in the control group (Table 3). There were significant difference in the proportion of bad WHO performance status (> 2) [6 (9.0%) patients vs. 16 (39.0%) patients, p < 0.01] and who were able to have perioral intake [67 (100%) patients vs. 36 (87.9%) patients, p = 0.02]. The median number of cycles of performing FOLFOX/FIRI therapy during 6 months was significantly longer in the well-nourished group than that in the bad-nourished group [21 cycles, (6–24) vs. 11 (4–24), p < 0.01]. As for the AE of the chemotherapy, the hematotoxic AE was significantly less frequent in well-nourished (grade 3, 9.0 vs. 19.5%, p = 0.03). The non-hematotoxic AE was also significantly less frequent in patients with well-nourished (grade 2, 31.3 vs. 51.2%, p = 0.04, grade 3, 6.0 vs. 24.4%, p < 0.01). The rate of discontinue of chemotherapy (6.0 vs. 34.1%, p < 0.01) and dose reduction (6.0 vs. 24.4%, p < 0.01) was significantly smaller in patients in the well-nourished group. The rate of conversion surgery is significantly frequent in the well-nourished (9.0 vs. 2.4%, p = 0.18). The median serum CEA level was significantly lower in the well-nourished than in the control group (5.3 U/mL [2.85–15.05] vs. 27.75 U/mL [7.98–78.9], p < 0.01), while the CA19-9 value did not differ significantly (p = 0.25).

The median follow-up time in this study is 3 years. The median PFS is significantly better in the well-nourished than that in the control (364 vs. 233 days, p < 0.01) (Fig. 1). Also, the OS is significantly better in the well-nourished (1 year, 96.9 vs. 92.7%; 3 years, 38.2 vs. 18.4%; 5 years, 26.5 vs. 11.1%, p = 0.01) (Fig. 2).