p53 and Response to Preoperative Radiotherapy for T2 and T3 (PART1)

Medical University of Vienna

Status

Unknown

Conditions

Rectal Cancer

Treatments

Radiation: preoperative short course radiation

Study type

Observational

Funder types

Other

Identifiers

NCT02140723

PART1

Details and patient eligibility

About

Background:

Meta-analyses of large randomized trials proved the superiority of preoperative short course radiation and surgery, as compared with surgery alone. Short course radiation results in a 50% reduction in terms of local relapse in stage II and III rectal cancer patients. Patients with complete pathological remission additionally show a significant survival benefit. Complete pathological remission (pCR) occurs in 8% after preoperative radiation and in >16% if the interval between radiation and surgery is at least 8 weeks.

It is generally accepted that mutations in the TP53 gene represent a crucial defect in the apoptosis pathway. Radiation therapy is suggested to act via induction of apoptosis in irradiated cells. Therefore, it is expected that a defect in the TP53 gene has an effect on the success of radiation therapy.

Currently available imaging tools are hardly able to diagnose response to radiation therapy correctly, as this does not essentially correlate with tumor size.

Method:

Aim of this prospective observation study is to strengthen the hypothesis that the TP53 genotype is a promising marker to predict response to radiation therapy in rectal cancer patients. Consequently, the expected results will justify prospective, randomized intervention trials to obtain level of evidence I for the p53 marker hypothesis. Trial endpoint is downstaging and pCR rate. Tumor stage and pathological remission will be evaluated by MRT and pathohistology and correlated to the TP53 genotype of the diagnostic biopsy. Additionally, we will investigate the applicability of novel imaging modalities in magnet resonance tomography to monitor response to radiotherapy.

The objective of this study is

to evaluate the effect of a genetic tumor marker (TP53 genotype) on the response to preoperative short course radiation (in terms of downstaging and pCR rate)
to evaluate the applicability of novel magnet resonance tomography imaging modalities to monitor response to preoperative short time radiation.

Conclusion:

The prospective evaluation of the potential predictive marker TP53 may bring us one-step closer to an individualized therapy regimen, which allows the restriction of preoperative radiation in rectal cancer to those patients who will benefit.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients who are eligible for this observational study will be treated according to current standards with preoperative short course radiation (5x5 Gy) and a subsequent interval to surgery of at least 8 to maximum 16 weeks.

According to standards of rectal cancer therapy, eligible patients will meet the following criteria:

Histologically confirmed adenocarcinoma of the rectum
Tumor staging with MRI
Inferior margin of the tumor located not farther than 15 cm from anal verge and below the level of S1-2
Tumor stage T2 and T3
No evidence of metastatic disease
No prior tumor therapy for rectal or pelvic cancers (surgery, radio-, chemo-, immunotherapy, molecular target therapy, or any other type of tumor therapy)
Medical fitness of the patient for treatment (decided by the involved physician)
Patient compliance
Signed informed consent from the patient or a legal representative, for the analysis of the tumor including genetic analyses of the tumor DNA.

Exclusion criteria

Patients will be excluded from the study for any of the following reasons

Clinical stage T1 (appropriate for local excision),
Clinical stage T4 (Radio/Chemotherapy)
Clinical stage M+ (distant metastases)
No tumor staging with MRI
Inoperability (technical or functional)
Prior tumor therapy of the pelvis
Concurrent administration of any other tumor therapy
Second primary malignancy that is clinically detectable at the time of consideration for study enrollment
Serious concomitant disorders or attitudes of the patient that would compromise the safety of the patient or his/her ability to complete the study.