Wenyang Liu1, Yu Tang1, Jing Jin1, Haizeng Zhang2, Lin Yang3, Hua Ren1, Hui Fang1, Weihu Wang1, Yongwen Song1, Yueping Liu1, Shulian Wang1, Yexiong Li1
1Radiation Oncology, Cancer Hospital, Chinese Academy of Medical Science, Beijing, China, 2Abdominal Surgery, Cancer Hospital, Chinese Academy of Medical Science, Beijing, China, 3Medical Oncology, Cancer Hospital, Chinese Academy of Medical Science, Beijing, China
Objective:To evaluate the maximum tolerated dose (MTD)
of concurrent capecitabine with preoperative radiation (RT) in elderly patients
with rectal cancer, as well as safety and efficacy. Method: Surgical
candidates aged ≥ 75 years with stage II/III (AJCC 7th) rectal adenocarcinoma
were enrolled to receive preoperative concurrent chemoradiation (CRT) with
capecitabine. Capecitabine was administered for two cycles of 14 days separated
by a 7-day rest, with the dose escalating from 1,000 mg/m2/day as
far as no more than 1/3 of patients in a level developing dose limiting
toxicities (DLT), to the upper limit at 1,650 mg/m2/d. The academic
multidisciplinary team (MDT) then re-evaluated the patients and decided the
following treatment within 6-8 weeks after the completion of RT. Result: In
the 24 patients enrolled, 17 (70.8%) patients developed grade 2 acute
toxicities, while 3 (12.5%) developed grade 3. Radiation dermatitis,
gastrointestinal side effects, leukopenia and fatigue were the most common
observed acute toxicities. DLTs were seen in one of six patients at each dose
level of 1200 mg/m2/d, 1350 mg/m2/d and 1650 mg/m2/d.
The MTD was not reached. Only 11 patients underwent surgery, three (27.3%) had
pathologic complete response (pCR), and the remaining eight (72.7%) were
overall downstaged. No treatment-related death occurred. Three patients (27.3%)
had grade 2 or 3 postoperative complications. With a median follow-up of 23
months, the 2-year overall survival rate and 2-year cancer-specific survival
rate was 67.4% and 74.9%, respectively. No significant differences were found
between the outcomes of patients with or without surgery. Conclusion: In
selected elderly patients aged ≥ 75 years with locally advanced rectal cancer,
preoperative CRT with capecitabine at the dose of 1650 mg/m2/d was
acceptable. Although the pathologic results appeared encouraging, only half of
patients received the subsequent surgery, individualized strategy is needed for
this fairly old group of patients. (ClinicalTrials.gov number, NCT01584544.).
Key
Words: rectal cancer preoperative concurrent chemoradiotherapy
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