Esophageal Cancer, GastroEsophageal Cancer, Oesophageal Cancer
Conditions
Keywords
Pulsed Low-Dose-Rate Radiation, Chemoradiation, esophagitis, Esophagectomy, Esophageal Cancer, Oesophageal Cancer, GastroEsophageal Cancer, Pulsed reduced dose rate radiation, Pulsed radiation
Brief summary
This is a prospective, randomized, open-label, two-arm phase 2 trial that will evaluate whether the use of Pulsed Low-Dose-Rate radiation technique, as compared to standard radiation, is associated with reduced rates of clinically significant esophagitis during and following chemoradiation.
Detailed description
PLDR radiation technique has been shown to kill cancer cells while limiting normal tissue toxicity. In PLDR, subjects receive the same total dose of radiation for each treatment, but the treatment is delivered in a series of low-dose pulses which are separated by timed pauses. Radiation given with this approach may be less toxic but appears to be equally effective. This trial will evaluate the PLDR technique in combination with standard chemotherapy as part of definitive or curative treatment for locally advanced esophageal cancer.
Interventions
DRUGInduction Chemotherapy (modified FLOT or modified FOLFOX-6)
Subjects are expected to receive 2-4 months of induction chemotherapy; the interval and dosages will be determined and can be modified at the discretion of their medical oncologist. The preferred induction chemotherapies are modified FLOT or FOLFOX-6. Subjects can enroll if they receive less than 2 months of induction chemotherapy as long as they are deemed to be a candidate for concurrent chemoradiation therapy.
DRUGChemotherapy
The preferred concurrent chemoradiation is carboplatin/paclitaxel weekly.
RADIATIONConventional Radiation
For both standard conventional radiation therapy and PLDR radiation therapy, the standard dose (5000cGy/25fx default, 4140-5040 in 23-28 fractions) should be given. Fractions should consist of 180-200 cGy per treatment.
RADIATIONPulsed Low-Dose-Rate (PLDR) Radiation
For both standard conventional radiation therapy and PLDR radiation therapy, the standard dose (5000cGy/25fx default, 4140-5040 in 23-28 fractions) should be given. Fractions should consist of 180-200 cGy per treatment. For PLDR radiation therapy, each fraction will be delivered as a series of 20 cGy (or 0.2 Gy) pulses that are separated by 3-minute time intervals.
PROCEDURESurgery
Esophagectomy is not required for trial and will be administered per medical judgement of the treating physicians. Surgery will take place at the time directed by the surgeon. This typically will take place approximately 6-13 weeks after chemoradiation therapy.
Sponsors
Medical College of Wisconsin
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
A potential study subject who meets all of the following inclusion criteria is eligible to participate in the study. 1. Age ≥ 18 years. 2. Stage II-IVb adenocarcinoma of the esophagus (if IVb, oligometastatic only, felt to be eligible for definitive dose CRT treatment by treating physician). 3. Currently receiving or have received induction chemotherapy and planned for definitive dose chemoradiation (+/- esophagectomy). 4. Eastern Cooperative Oncology Group (ECOG) performance status 0-2. 5. Adequate hematologic function within 30 days prior to registration defined as follows: 1. Absolute Neutrophil Count ≥ 1,500/mcg 2. Hemoglobin ≥ 8 gm/dL 3. Platelets ≥ 100,000/mcL. 6. Adequate renal function within 30 days prior to registration, defined as a creatinine clearance of ≥ 50 ml/min as calculated by the Cockcroft-Gault equation. 7. Adequate hepatic function within 30 days prior to registration, defined as total bilirubin ≤ 1.5 x ULN a. Note: patients with known Gilbert Syndrome can have a total bilirubin \< 2.5 x upper limit of normal (ULN). 8. Female patients \<65 years of age and of childbearing potential must have a negative serum/urine pregnancy test within 14 days prior to study entry. A female not of childbearing potential is one who has undergone a hysterectomy, bilateral oophorectomy, tubal ligation, or who has had no menses for 12 consecutive months. 9. Patients of reproductive potential must agree to use effective contraception for the duration of study treatment. Effective contraception includes oral contraceptives, implantable hormonal contraception, double-barrier method, or intrauterine device. 10. Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial. 11. Ability to understand a written informed consent document, and the willingness to sign it.
Exclusion criteria
A potential study subject who meets any of the following
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| New prescription for narcotics | Up to 6 weeks after radiation treatment | The number of subjects requiring a new prescription for narcotics. |
| Increasing existing narcotics | Up to 6 weeks after radiation treatment | The number of subjects increasing existing narcotics by 25%. |
| Oral intake | Up to 6 weeks after radiation therapy | The number of subjects transitioning from solid to liquid or liquid to no oral intake. |
Countries
United States
Contacts
CONTACTMedical College of Wisconsin Cancer Center Clinical Trials Office
PRINCIPAL_INVESTIGATORLindsay Puckett, MD
Medical College of Wisconsin
Outcome results
None listed