Organ Preservation in Locally Advanced Rectal Cancer by Radiochemotherapy Followed by Consolidation Chemotherapy. A Prospective Phase II Pilot Trial of the German Rectal Cancer Study Group
试验速览
- 阶段
- 2 期
- 入组人数
- 94
- 试验地点
- 4
- 主要终点
- Clinical complete response rate
研究概览
简要总结
There is a growing body of evidence that surgery and associated morbidities can be omitted without compromising oncological safety in selected patients who have achieved a clinical complete response after radiochemotherapy. However with standard neoadjuvant treatment regimens the pathological complete response rate lies in the range between 10%-20%, the number of patients qualifying for non-operative management is even lower since the sensitivity of currently available diagnostic measures for predicting the pathological complete response hardly surpasses 50%-60%.The hereby proposed phase II trial CAO/ARO/AIO-16 aims at finding novel and innovative aspects of rectal cancer treatment. According to recently published data the radiochemotherapy regime in the present study with consolidating chemotherapy and delayed assessment of response has the potential to achieve pathological complete rates of approximately 40%. A standardized re-evaluation after consolidating chemotherapy will select patients who are candidates for organ-preservation. These patients will not undergo radical surgery and will instead be follow-up closely for tumor regrowth.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male and female patients with histologically confirmed diagnosis of rectal cancer localized 0 - 12 cm from the anocutaneous line as measured by rigid rectoscopy (i.e. lower and middle third of the rectum)
- •Any MRI staged cT3 tumor or any cT1 cN+ or cT2 cN+ with nodal staging according to "SOP MRI"
- •Staging requirements: High-resolution, thin-sliced (i.e. 3mm) magnetic resonance imaging (MRI) of the pelvis is the mandatory local staging procedure.
- •Cross-sectional imaging of the abdomen and chest to exclude distant metastases.
- •Aged at least 18 years. No upper age limit.
- •WHO/ECOG Performance Status ≤ 1
- •Adequate hematological, hepatic, renal and metabolic function parameters
- •Informed consent of the patient
排除标准
- •Lower border of the tumor localised more than 12 cm from the anocutaneous line as measured by rigid rectoscopy
- •cT4 tumors
- •Positive lateral pelvic lymph nodes
- •Distant metastases (to be excluded by CT scan of the thorax and abdomen)
- •Preexisting fecal incontinence for solid stool
- •Preexisting peripheral sensory neuropathy with functional impairment
- •Preexisting myelosuppression reflected by a neutrophil count < 2.000/mm^3 and/or platelets < 100.000/mm^3
- •Severe impairment of kidney function with a Creatinin Clearance < 30 ml/min)
- •Prior antineoplastic therapy for rectal cancer
- •Prior radiotherapy of the pelvic region
- •Major surgery within the last 4 weeks prior to inclusion
- •Subject pregnant or breast feeding, or planning to become pregnant within 6 months after the end of treatment.
- •Subject (male or female) is not willing to use highly effective methods of contraception according to the "Clinical trial fertility group"
- •On-treatment participation in an interventional clinical study in the period 30 days prior to inclusion
- •Previous or current drug abuse
- •Other concomitant antineoplastic therapy
- •Serious concurrent diseases, including neurologic or psychiatric disorders (incl. dementia and uncontrolled seizures), active, uncontrolled infections, active, disseminated coagulation disorder, severe liver function disorders
- •WHO/ECOG Performance Status > 1
- •Clinically significant cardiovascular disease (incl. myocardial infarction, unstable angina, symptomatic congestive heart failure, serious uncontrolled cardiac arrhythmia) ≤ 6 months before enrolment.
- •Chronic diarrhea (> grade 1 according NCI CTCAE) Prior or concurrent malignancy ≤ 3 years prior to enrolment in study (Exception: non-melanoma skin cancer or cervical carcinoma FIGO stage 0-1), if the patient is continuously disease-free
- •Known allergic reactions on study medication
- •Known dihydropyrimidine dehydrogenase deficiency
- •Medication inhibitors of the dihydropyrimidine dehydrogenase, such as Brivudin, Sorivudin and its analogues.
- •Pernicious anemia or other anemias caused by Vitamin B-12 deficiency.
- •Psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule (these conditions should be discussed with the patient before registration in the trial).
- •Additionally for hyperthermia cardiac pacemakers and metal implants in the proximity of the pelvis constitute a criterion for exclusion.
研究组 & 干预措施
Radiochemotherapy -> chemotherapy.
Radiochemotherapy followed by consolidation chemotherapy. Deep regional hyperthermia can additionally be performed at the centers in Tübingen and Erlangen.
干预措施: Radiotherapy (Radiation)
Radiochemotherapy -> chemotherapy.
Radiochemotherapy followed by consolidation chemotherapy. Deep regional hyperthermia can additionally be performed at the centers in Tübingen and Erlangen.
干预措施: Chemotherapy (Drug)
Radiochemotherapy -> chemotherapy.
Radiochemotherapy followed by consolidation chemotherapy. Deep regional hyperthermia can additionally be performed at the centers in Tübingen and Erlangen.
干预措施: Deep regional hyperthermia (Other)
结局指标
主要结局
Clinical complete response rate
时间窗: Day 106 after the start of treatment
Response to treatment is assessed on day 106 after the start of radiochemotherapy. A clinical complete response is defined by standardized findings in rectoscopy, MRI and digital rectal examination
次要结局
- Pathological staging, tumor downstaging (assessed by ypTNM findings in relation to initial cTNM staging), tumor regression grading according to Dworak in patients undergoing surgery(Day 123 after the start of treatment)
- Fecal incontinence according to Wexner-Vaizey Score(4 years)
- Local regrowth rate(4 years)
- Safety of the treatment (toxicity assessment according to NCI CTCAE Version 4.0)(4 years)
- Quality of life according to EORTC Quality of Life questionnaire - C30(4 years)
- Frequency of Low anterior resection syndrome (LARS-scale)(4 years)
- R0 resection rate, rate of circumferential resection margin negativity (> 1mm) in patients undergoing surgery(Day 123 after the start of treatment)
- Surgical morbidity in patients undergoing surgery(up to 30 days after surgery)
- Surgical complications in patients undergoing surgery(up to 30 days after surgery)
- Quality of life according to EORTC Quality of Life questionnaire - CR29(4 years)
- Rate of sphincter-sparing surgery in patients undergoing surgery(Day 123 after the start of treatment)
- Relapse-free survival (local / distant / overall)(4 years)
- Overall survival(4 years)