Neoadjuvant capecitabine and oxaliplatin (XELOX) with bevacizumab for locally advanced rectal cancer.

Authors

null

Junichi Hasegawa

Department of Surgery, Osaka Rosai Hospital

Junichi Hasegawa , Tsunekazu Mizushima , Ho Min Kim , Yasuhiro Miyake , Hiroyoshi Takemoto , Hiroshi Tamagawa , Shingo Noura , Masayuki Ohue , Makoto Fujii , Yuichiro Fujie , Hirofumi Ota , Takeshi Kato , Mutsumi Fukunaga , Ichiro Takemasa , Masataka Ikeda , Hirofumi Yamamoto , Mistugu Sekimoto , Riichiro Nezu , Yuichiro Doki , Masaki Mori

Organizations

Department of Surgery, Osaka Rosai Hospital, Department of Gastroenterological Surgery, Osaka U, Department of Surgery, Minou Municipal Hospital, Department of Surgery, Kinki Central Hospital of t, Department of Surgery, Osaka General Medical Cente, Department of Surgery, Osaka Medical Center for Ca, Department of Surgery, Osaka Koseinenkin Hospital, Department of Surgery, Osaka Saiseikai Senri Hospi, Department of Surgery, Kansai Rosai Hospital, Sakai City Hospital, Department of Surgery, National Hospital Organizat

Research Funding

Other

Background: Chemoradiotherapy (CRT) followed by surgery is a standard treatment for locally advanced rectal cancer. Although preoperative CRT decreases local recurrence (LR), pelvic radiation is associated with long-term morbidity. We conducted this study to evaluate the feasibility of neoadjuvant XELOX with bevacizumab (Bmab) in patients (pts) with locally advanced rectal cancer. Methods: Pts with T4 or lymph node (LN) positive rectal cancer were treated with 3 cycles of XELOX with Bmab and one additional cycle of XELOX. Total mesorectal excision was performed 3-8 weeks after the last chemotherapy. The primary endpoint was to assess feasibility and secondary endpoints were R0 resection rate, down staging rate, pathological complete response (pCR) rate and pathological effect over grade 2 (tumor cell death in more than two-thirds of the entire lesion). Results: Twenty five pts were recruited between December 2009 and November 2011. Characteristics of pts were as the following: male/female, 18/7; median age, 63 years (range, 37-75); median diameter of tumor, 52.8mm (range, 38.3-110); T2-T3/T4a/T4b, 7/8/10 and N0/N1/N2, 3/14/8. In 4% of the pts (7 pts), following grade 3-4 adverse events occurred; neutropenia, hypertension, bleeding, rectal obstruction, pelvic infection, anorexia and nausea. The down staging rate of T2-T3/T4a/T4b and N1/N2 were 29/63/50 % and 86/63 %, respectively. Seven pts (28%) discontinued the treatment after 2-3 cycles of XELOX with Bmab (13% in T2-T4a, 50% in T4b). The rate of conducting surgery was 92% and all of them had R0 resections. Postoperative complications were found in 9 pts (39%). The pCR rate was 4%, and the rate of pathological effect over grade 2 was 61%. Two LR (LN positive) and two distant recurrences (1 lung, 1 liver) were reported. Conclusions: XELOX with Bmab followed by surgery was safely performed for locally advanced rectal cancer. The down staging rate was 50% even in T4b pts although half of T4b pts discontinued the study treatment. Based on these preliminary results, we are planning a phase II trial of perioperative XELOX and surgery in locally advanced rectal cancer. Clinical trial information: 000003219.

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Abstract Details

Meeting

2013 Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

General Poster Session C: Cancers of the Colon and Rectum

Track

Cancers of the Colon, Rectum, and Anus

Sub Track

Multidisciplinary Treatment

Clinical Trial Registration Number

000003219

Citation

J Clin Oncol 31, 2013 (suppl 4; abstr566)

DOI

10.1200/jco.2013.31.4_suppl.566

Abstract #

566

Poster Bd #

E14

Abstract Disclosures