ONCAlert | 2018 ASCO Annual Meeting
Colorectal Cancer Case Studies

Tanios Bekaii-Saab, MD: Impact of Third-Line Therapy

Tanios Bekaii-Saab, MD
Published Online:Apr 26, 2016
Scott is a 62-year-old male from Montgomery County, Arkansas who works as a teacher and football coach at a local high school. He was diagnosed with metastatic colon adenocarcinoma in December of 2012.

mCRC with Tanios Bekaii-Saab, MD and Tara Seery, MD: Case 2



How might the choice of third-line treatment in this patient impact subsequent lines of therapy?

In the RAS mutated patients, we have 2 options now. We have regorafenib and TAS-102. We have a third and fourth line, and the question is now how do you sequence those agents. We have used regorafenib in the third-line setting for our patients until TAS-102 was approved and TAS-102 found its natural placement in the fourth line, although you can argue for some patients you may use TAS-102 in the third line first. Those are the patients who may have liver dysfunction, although they're not severe, and patients with hand-and-foot syndrome, although those are rare.

If a patient has had a lot of chemotherapy and issues with maintaining their blood counts, and platelet counts, white counts, and anemia, then TAS-102 can induce neutropenia in some patients. So TAS-102 may not be favored in that setting. There are certain groups of patients where you can think about sequencing, but naturally right now the way the studies worked out and the natural way it has worked out in the clinic is two lines of chemotherapy plus bevacizumab for the RAS mutated patients, regorafenib, and then TAS-102.

Case 2: mCRC

Scott T. is a 62-year-old male from Montgomery County, Arkansas who works as a teacher and football coach at a local high school. He was diagnosed with metastatic colon adenocarcinoma in December of 2012.

  • Medical history is notable for well-controlled hypertension, and hypercholesterolemia, managed with diet and statin therapy
  • Patient underwent a right hemicolectomy in January 2013, which showed stage IIIC disease with several visceral metastases noted and 5 of 14 positive lymph nodes; biopsy showed well-differentiated adenocarcinoma that was KRAS-mutation and BRAF-mutation negative on molecular testing
  • He received initial therapy with FOLFOX and bevacizumab and showed a good response after 6 cycles, with a reduction in several target lesions on CT scan

In October of 2013, the patient returned for a follow-up with increasing fatigue, intermittent dyspnea, and chest pain.

  •  
  • Follow-up CT showed marked progression of target lesions, and multiple lung nodules consistent with metastatic disease; performance status at time of recurrence was 0. His chemotherapy was switched to FOLFIRI, and bevacizumab was continued
  • After 5 cycles, the patient’s condition improved and CT scan was consistent with stable disease
  • After 7 cycles, the patient requested to discontinue chemotherapy while traveling, but maintenance bevacizumab was continued

In July of 2014, the patient returned for follow-up with marked fatigue, declining performance status (PS 1), increasing dyspnea and chest pain; CT scan at that time showed marked progression of lung and peritoneal target lesions.

  • Liver and kidney function were within normal limits, and he began treatment with regorafenib at a dose of 160 mg.
  • After 2 weeks, treatment had to be interrupted due to grade 2 hypertension with fatigue and lightheadedness
  • The patient’s condition improved with antihypertensive therapy, and after 10 days treatment was reinitiated at a dose of 120 mg
  • Patient was able to tolerate the reduced dose, with some mild fatigue and diarrhea
  • After 5 cycles at 120 mg, the patient showed a good response, with a reduction in both lung and peritoneal metastases on CT scan; his performance status also improved (PS 0)

The patient’s disease remained stable until August of 2015, at which time his CT scan showed marked progression of the peritoneal lesions, and his CEA levels had increased to 33.5 ng/mL. He was initiated on trifluridine-tipiracil (TAS-102) in September of 2015 and his disease again stabilized. He remains on treatment at last follow-up.

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