Partial response after transcatheter arterial infusion chemotherapy in a patient with systemic chemotherapy-resistant unresectable colon cancer and hepatic metastasis: (case report)
© Sawai et al.; licensee BioMed Central Ltd. 2013
Received: 6 March 2013
Accepted: 5 August 2013
Published: 17 August 2013
We report here a case of partial response to hepatic arterial infusion chemotherapy in a patient who developed serious hepatic failure due to unresectable colorectal cancer and hepatic metastasis and showed resistance to systemic chemotherapy with molecular targeted drugs, mFOLFOX6, and FOLFIRI. The patient was a 60-year-old woman who underwent sigmoidectomy for sigmoid colon cancer, lateral posterior hepatic segmentectomy for metastatic liver cancer, and postoperative radiation therapy for metastatic lung cancer. As first-line systemic chemotherapy, mFOLFOX6 (oxaliplatin, 5-fluorouracil, and leucovorin), bevacizumab + FOLFIRI (irinotecan, 5-fluorouracil, leucovorin), and anti-epidermal growth factor receptor antibody + irinotecan were administered, in that order. However, recurrent hepatic metastasis was exacerbated, which induced serious hepatic failure manifested by general malaise, jaundice, abnormal hepatic function, difficulty in walking due to bilateral lower extremity edema, and decreased appetite. The patient was admitted in a serious condition. After hospitalization, the patient received hepatic arterial infusion chemotherapy with 5-fluorouracil and l-leucovorin. After two complete courses, the symptoms improved. The patient’s performance status also improved, and she was discharged from the hospital. Four months after discharge, the patient had continued outpatient chemotherapy and maintained excellent performance status. Although HAIC is not presently considered an alternative to systemic chemotherapy, it is sometimes effective in patients who show resistance to molecular targeted drug therapy, FOLFOX, and FOLFIRI, and in whom hepatic metastasis is a key factor in determining prognosis and serious hepatic failure. Further studies should be performed in the future to verify these findings.
KeywordsHepatic arterial infusion chemotherapy Resistance to systemic chemotherapy Unresectable colon cancer
Epidermal growth factor receptor
Irinotecan, 5-fluorouracil, leucovorin
Hepatic arterial infusion chemotherapy
Oxaliplatin, 5-fluorouracil, and leucovorin
National comprehensive cancer network.
The Japanese guidelines for colorectal cancer treatment and the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines in Oncology for Colon and Rectal Cancers recommend systemic administration of l-leucovorin, 5-fluorouracil, irinotecan, oxaliplatin, bevacizumab, and anti-epidermal growth factor receptor (EGFR) antibody for unresectable or recurrent colon cancer . However, there is no effective therapy for patients who have developed resistance to this therapy. We report here a case of colorectal cancer with hepatic metastasis, which was resistant to systemic therapy, and serious hepatic failure, for which hepatic arterial infusion chemotherapy (HAIC) was effective.
The patient was a 60-year-old woman with chief complaints of general malaise, jaundice, bilateral lower extremity edema, and decreased appetite. At admission, she presented with conjunctival anemia and jaundice, mild tenderness in the right upper abdomen, a palpable liver 3 cm below the right costal margin, and bilateral lower extremity edema. Her body temperature was 37.8°C, and her performance status was 3 . Routine admission serum chemistry showed a white blood cell count of 17,200/μl (normal range = 3400 to 9600/μl), and the following concentrations: hemoglobin, 8.1 g/dl (normal range = 13.4 to 17.6 g/dl); total bilirubin, 9.5 mg/dl (normal range = 0.2 to 1.2 mg/dl); aspartate transaminase, 105 IU/l (normal range = 13 to 34 IU/l), γ-glutamyl transpeptidase, 643 IU/l (normal range = 12 to 60 IU/l), lactate dehydrogenase, 1,414 IU/l (normal range = 119 to 214 IU/l), and alkaline phosphatase, 4,558 IU/l (normal range = 107 to 340 IU/l). These results indicated a hepatic function disorder. The concentrations of tumor markers CEA and CA19-9 were significantly increased to 197 ng/ml (normal range = 0 to 5.0 ng/ml) and 42.9 U/ml (normal range = 0 to 37 U/ml) respectively.
Illness and course
Sigmoidectomy, lateral and posterior hepatic segmentectomy, and postoperative radiation therapy were performed in February 2008 to treat sigmoid colon cancer, metastatic liver cancer, and metastatic lung cancer, respectively. The final diagnosis was of sigmoid colon cancer (6 × 4 cm), type 2, invasion depth SE, lymph node metastasis N2, hepatic metastasis H2, P0, M1 stage IV .
The Japanese guidelines for colorectal cancer treatment and the NCCN clinical practice guidelines in oncology for colon and rectal cancers recommend FOLFOX as the optimal treatment for patients with unresectable recurrent colon cancer with hepatic metastasis, and systemic chemotherapy with a combination of FOLFIRI and anti-VEGF antibody or anti-EGFR antibody. The median survival of patients with unresectable or advanced recurrent colon cancer who do not undergo chemotherapy has been reported as approximately 8 months. However, owing to recent developments in chemotherapy, median survival has been extended to approximately 2 years [1, 5]. At the initial examination, the patient had stage IV colorectal cancer with hepatic metastasis and lung metastasis, and had a risk of digestive tract ileus due to the primary focus. Therefore, the primary focus and the hepatic metastasis were removed. Radiotherapy was performed to treat the single lung metastasis. At that time, all lesions disappeared on the images. However, 11 months after the operation, unresectable recurrent hepatic metastasis developed, and systemic chemotherapy was performed in accordance with the clinical practice guidelines for colon and rectal cancers. The patient’s condition was maintained for 2 years and 8 months after the therapy; however, she then developed serious hepatic failure manifested by abnormal hepatic function, decreased appetite, general malaise, and difficulty in walking due to bilateral lower extremity edema due to exacerbation of hepatic metastasis. Discontinuation of the chemotherapy was considered, since the standard therapy was not indicated, but the patient’s condition would not be life threatening, regardless of multiple metastases to other organs. Control of hepatic metastasis could prolong her life. There are no reports of the use of HAIC to treat patients showing resistance to systemic chemotherapy with anti-EGFR antibody, anti-EGFR antibody, mFOLFOX6, and FOLFIRI. However, some reports have shown that HAIC was effective for size regression and local control of hepatic metastasis [6, 7]. Therefore, HAIC was performed after obtaining informed consent from the patient and her family members. No adverse reactions occurred, and serious hepatic failure was improved. After the patient was discharged, her quality of life improved and she could do household chores, while currently receiving outpatient treatment. Therefore, HAIC was effective in this case. Recently, some studies have reported that HAIC or a combination of HAIC and systemic chemotherapy was effective for patients who showed resistance to systemic chemotherapy [8–11]. HAIC has again received attention in patients in whom hepatic metastasis is a key factor determining prognosis. In recent years, systemic chemotherapy has seen remarkable progress.
Although HAIC is not presently considered an alternative to systemic chemotherapy, it is sometimes effective in patients who show resistance to molecular targeted drug therapy, FOLFOX, and FOLFIRI, and in whom hepatic metastasis is a key factor in determining prognosis and serious hepatic failure. Further studies should be performed in the future to verify these findings.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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- NCCN Clinical Practice Guidelines in Oncology. Antiemesis: V.2.2010. http://www.nccn.org/professionals/physician-gls/PDF/antiemesis
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