Activity of Sorafenib Plus Capecitabine in Previously Treated Metastatic Colorectal Cancer.

Thomas J George, Alison M Ivey, Azka Ali, Ji-Hyun Lee, Yu Wang, Karen C Daily, Brian H Ramnaraign, Sanda A Tan, Krista P Terracina, Thomas E Read, Long H Dang, Atif Iqbal

Journal: The oncologist 2021;26(5):362-e724

PMID: 33512054

Abstract

LESSONS LEARNED

Treatment for patients with metastatic colorectal cancer (mCRC) typically involves multiple lines of therapy with eventual development of treatment resistance. In this single-arm, phase II study involving heavily pretreated patients, the combination of sorafenib and capecitabine yielded a clinically meaningful progression-free survival of 6.2 months with an acceptable toxicity profile. This oral doublet therapy is worthy of continued investigation for clinical use in patients with mCRC.

BACKGROUND

Capecitabine (Cape) is an oral prodrug of the antimetabolite 5-fluorouracil. Sorafenib (Sor) inhibits multiple signaling pathways involved in angiogenesis and tumor proliferation. SorCape has been previously studied in metastatic breast cancer.

METHODS

This single-arm, phase II study was designed to evaluate the activity of SorCape in refractory metastatic colorectal cancer (mCRC). Patients received Sor (200 mg p.o. b.i.d. max daily) and Cape (1,000 mg/m p.o. b.i.d. on days 1-14) on a 21-day treatment cycle. Primary endpoint was progression-free survival (PFS) with preplanned comparison with historical controls.

RESULTS

Forty-two patients were treated for a median number of 3.5 cycles (range 1-39). Median PFS was 6.2 (95% confidence interval [CI], 4.3-7.9) months, and overall survival (OS) was 8.8 (95% CI, 4.3-12.2) months. One patient (2.4%) had partial response (PR), and 22 patients (52.4%) had stable disease (SD) for a clinical benefit rate of 54.8% (95% CI, 38.7%-70.2%). Hand-foot syndrome was the most common adverse event seen in 36 patients (85.7%) and was grade ≥ 3 in 16 patients (38.1%). One patient (2.4%) had a grade 4 sepsis, and one patient (2.4%) died while on treatment.

CONCLUSION

SorCape in this heavily pretreated population yielded a reasonable PFS with manageable but notable toxicity. The combination should be investigated further.

© AlphaMed Press; the data published online to support this summary are the property of the authors.

Address: Division of Hematology Oncology, Department of Medicine, University of Florida Cancer Center, Gainesville, Florida, USA.; University of Florida Health Cancer Center, Gainesville, Florida, USA.; University of Florida Health Cancer Center, Gainesville, Florida, USA.; Department of Biostatistics, University of Florida, Gainesville, Florida, USA.; Division of Quantitative Sciences, UF Health Cancer Center, Gainesville, Florida, USA.; Division of Quantitative Sciences, UF Health Cancer Center, Gainesville, Florida, USA.; Department of Surgery, University of Florida, Gainesville, Florida, USA.; Department of Surgery, University of Florida, Gainesville, Florida, USA.; Department of Oncology, Ochsner Health, Baton Rouge, Louisiana, Texas, USA.; Department of Surgery, Baylor University, Houston, Texas, USA.
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