Overview
This phase III trial compares the effect of stereotactic radiosurgery and whole brain radiation therapy that avoids the hippocampus (the memory zone of the brain) for the treatment of small cell lung cancer that has spread to the brain.
Description
Small cell lung cancer (SCLC) is the most aggressive histologic subtype of lung cancer, with a predilection for early metastases. Brain metastases (BM) are a significant threat to quality of life in patients with SCLC. Stereotactic radiosurgery (SRS)/ Stereotactic Radiotherapy (SRT) is a specialized radiation therapy that delivers a single, high dose of radiation directly to the tumor and may cause less damage to the surrounding normal tissue. Thus SRS/SRT has now emerged as the preferred treatment modality, either alone or in combination with other modalities for BM. However, given the propensity for dissemination of SCLC, SRS/SRT does not appear to be a rational approach to this pathology. Recently, in selected patients, whole brain radiotherapy (WBRT) has been omitted from the initial management for BM with the aim of reducing the potential risk of delayed neurological toxicity[1-3]. Thus, the role of upfront focal treatment by means of SRS for BM from SCLC has yet to be determined
This phase III trial compares the effect of upfront local treatment (including SRS/SRT and hypofractionated radiotherapy [Hypo-RT]) and WBRT that avoids the hippocampus (the memory zone of the brain) for the treatment of no more than 10 BM in SCLC patients. The expectation is that SRS/SRT/Hypo-RT will be one of standard upfront local treatments in SCLC patients with no more than 10 BM.
Eligible patients will be 1:1 randomized to receive ether local treatment (SRS/SRT/Hypo-RT), or hippocampal-voidance WBRT. The prescription dose of SRS/SRT is 18-22Gy in 1 fraction, 27Gy in 3 fractions and 30Gy in 5 fractions. The prescription dose of Hypo-RT is 40Gy in 8 fraction. The prescription dose of HA-WBRT is 30Gy in 10 fraction. The prescription dose could be adjusted if lesions are located in brain stem when treat with SRS/SRT/Hypo-RT.
Eligibility
Inclusion Criteria:
Investigators should consider these factors when selecting patients for this trial.
Investigators also should consider all other relevant factors (medical and non-medical), as
well as the risks and benefits of the study therapy, when deciding if a patient is an
appropriate candidate for this trial.
1. Adult patients (18-80 years of age) with Eastern Cooperative Oncology Group
performance status 0-2 or Karnofsky performance score ≥ 70, expected life time more
than 6 months;
2. Pathologically (histologically or cytologically) proven diagnosis of small cell lung
cancer within 5 years of registration. If the original histologic proof of malignancy
is greater than 5 years, then pathological (i.e., more recent) confirmation is
required (e.g., from a systemic or brain metastasis). Patients with de novo or
recurrent small cell lung cancer are permitted;
3. No more than 10 metastatic brain lesions with ≤5 cm in largest diameter and ≤150 ml in
treated volume, confirmed by a high-resolution (thickness ≤2mm) , 3-dimensional
T1-weighted postgadolinium magnetic resonance imaging (MRI) brain scan within 2 weeks
of study initiation. All brain metastases must be outside a 5-mm margin around either
hippocampus or optic pathways.
4. Not all metastatic brain lesions are recommended or suitable for surgical resection
after multidisciplinary team discussion. If part of metastatic brain lesions are
resected, the patient is permitted for enrollment evaluation at least two weeks after
resection; 5 Patients must have the psychological ability and general health that
permits completion of the study requirements, all assessment (HVLT-R, MoCA, EORTC
QLQ-C30) and required follow up (at least 6 months);
6. At least one measurable BM according to the Response Evaluation Criteria in Solid Tumors
Version 1.1 (RECIST 1.1) criteria; 7. Women of childbearing potential and men who are
sexually active should be willing and able to use medically acceptable forms of
contraception during treatment on this study and for up to 180 days after completion of all
treatment to prevent pregnancy or fathering a child; 8. Written informed consent (must be
available before enrolment in the trial).
Exclusion Criteria:
1. Clinical or radiologic evidence of new, untreated, and/or progressive brain metastases
prior to registration;
2. Previous radiotherapy of the brain;
3. Patients can not tolerate immobilization or are with MRI contraindication (i.e.,
cardiac pacemaker, implanted defibrillator, certain cardiac valve replacements,
certain metal implants);
4. Radiographic evidence of hydrocephalus or other architectural distortion of the
ventricular system, leptomeningeal metastases, increased intracranial pressure
requiring immediate depression surgery.
5. Patients who have not yet recovered from acute high-grade (≥Grade 3) toxicities of
prior therapies according Common Terminology Criteria for Adverse EventsVersion5.0
(CTC 5.0);
6. Presence of other serious illnesses such as acute myocardial infarction, severe
arrhythmia, or psychiatric disorders within the past 6 months;
7. Known carcinoma < 5 years ago (excluding carcinoma in situ of the cervix, basal cell
carcinoma, squamous cell carcinoma of the skin) requiring immediate treatment
interfering with study therapy;
8. Pregnant or lactating women;
9. Participation in another clinical study or observation period of competing trials,
respectively;