A Phase I/II Trial of Stereotactic Body Radiation Therapy (SBRT) Dose Escalation in the Treatment of Patients With Inoperable Stage I/II Non-Small Cell Lung Cancer Arising Within the Zone of the Proximal Bronchial Tree
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 74
- 试验地点
- 1
- 主要终点
- Phase I Portion Only: Determine the Maximum Tolerated Dose of SBRT
研究概览
简要总结
The purpose of this study is to use SBRT in patients with early stage lung cancer and find out what effects (good and bad) SBRT has on their cancer. This research is being done because SBRT has not been used very often in patients with early stage lung cancer or in patients with other serious health problems. In addition, this study also will gather information about patient's health and hospitalization history. This information will be used to find out if there are any factors that can help predict recovery or outcome of patients with lung cancer.
详细描述
Stage I Non-small Cell Lung Cancer Lung cancer is the most frequent cause of cancer death in both men and women in North America, accounting for approximately 13% of all cancers diagnosed and 28% of all cancer deaths. There will be an estimated 173,770 new lung cancer cases in the United States in the year 2004 with an estimated 160,440 deaths due to lung cancer.1 Seventy-five percent of patients with bronchogenic carcinoma will be diagnosed with non-small cell lung cancer (NSCLC). The number of patients with early or localized disease (currently an estimated 15-20% of NSCLC patients)2 is expected to rise over the next several years due to widespread screening with CT scanning.
The treatment of choice for stage I (T1-T2N0) NSCLC is surgical resection which results in 5-year survival rates of approximately 60 to 70%.3-5 Occasionally, however, there are patients with early-stage NSCLC that are unable to tolerate surgical resection or the postoperative recovery period due to various comorbidities.
While conventionally fractionated radiation therapy has been utilized as nonsurgical therapy for these medically inoperable patients, close observation with no specific cancer therapy has also been advocated in highly selected cases. McGarry, et. al., reviewed outcomes in 75 patients who had received no specific cancer therapy for stage I NSCLC, and the cause of death was progressive cancer in 53% of cases with a median survival time of 14.2 ± 2.4 months.6
Definitive conventionally fractionated RT for early-stage NSCLC is considered reasonable non-surgical therapy but yields poor 5-year survival rates ranging from 10 to 30%.7-11 Several studies have suggested a dose-response relationship reporting a benefit to dose escalation above the standard conventionally fractionated 4,500 to 6,600 cGy. This benefit was evident in both survival and local control in these patients.10-14 Sibley, et. al., reviewed 156 medically inoperable patients with stage I NSCLC treated with primary RT at Duke University between 1980 and 1995. They reported a 5-year, cause-specific survival rate of 32%. There was a trend toward improved survival in those patients achieving local control which approached significance for higher RT doses (p = 0.07).13 At this institution, we have published a series treating 56 patients with medically inoperable NSCLC with a median dose of 70 Gy using conformal radiotherapy techniques.15 Actuarial local control rates were 69% and 63% at two- and three years of follow up, respectively. These data serve as the estimate for statistical power calculations for this trial.
Radiation fields have historically encompassed the primary tumor as well as the regional lymphatics in the ipsilateral hilum and mediastinum. This elective treatment was based on the identified risk of occult lymph node involvement ranging up to 20% in some surgical series.16 In recent years, elimination of elective nodal irradiation, which is potentially poorly tolerated in this population,17 has been validated by several retrospective studies permitting treatment of the primary tumor alone with limited fields.18-21 Slotman, et. al., in a study from the Netherlands, reported the use of limited "postage-stamp" fields to treat early stage lung cancer patients using hypofractionated RT (i.e., 4,800 cGy in 400-cGy fractions). Reported 3-year overall and disease-specific survival rates were 42% and 76%, respectively.20
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Sequential
- 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
- •ELIGIBILITY:
- •Inclusion Criteria
- •Histologically confirmed non-small cell cancer by biopsy or cytology. Squamous cell carcinoma, adenocarcinoma, large cell carcinoma, bronchioalveolar carcinoma, or non-small cell carcinoma (not otherwise specified) are allowed.
- •Staging studies must identify patient as AJCC Stage I or II based on only 1 of following combinations of TNM staging:
- •T1, N0, M0
- •T2 (<=7cm), N0, M0
- •T3 (<=7cm), N0, M0
- •Primary tumor must be arising in one of the following central chest locations:
- •Within or touching the zone of the proximal bronchial tree (a volume 2cm in all directions around the proximal bronchial tree [carina, R & L main bronchi, R & L upper lobe bronchi, intermedius bronchus, R middle lobe bronchus, lingular bronchus, R & L lower lobe bronchi])
- •Adjacent to (within 5 mm) or invading the mediastinal pleura
- •Adjacent to (within 5 mm) or invading the parietal pericardium
- •To differentiate T3 lesions involving the mediastinal pleura from T4 lesions involving major vessels or organs, a chest MRI will be obtained. If any uncertainty remains, the patient will have four-dimensional CT scans (4DCT) in an effort to determine the degree of tumor motion. A freely mobile tumor during ventilation will be judged to be T3 disease.
- •Patients with hilar or mediastinal lymph nodes <=1cm and no abnormal hilar or mediastinal uptake on PET will be considered N
- •Patients with >1cm hilar or mediastinal lymph nodes on CT or abnormal PET (including suspicious but non-diagnostic uptake) may be eligible if directed tissue biopsy of all abnormally identified areas are negative for cancer.
- •Primary tumor must be technically resectable by an experienced thoracic cancer clinician, with a reasonable possibility of obtaining a gross total resection with negative margins (potentially curative resection, PCR). However, patients must have underlying physiological medical problems prohibiting PCR (i.e., problems with general anesthesia, the operation, the post-op recovery period, or removal of adjacent functioning lung) or refuse surgery. Deeming a patient medically inoperable based on pulmonary function for surgical resection may include any of the following: baseline FEV1 <40% predicted; post-operative predicted FEV1 <30% predicted; severely reduced diffusion capacity; baseline hypoxemia and/or hypercapnia; exercise oxygen consumption <50% predicted; severe pulmonary hypertension; diabetes with severe end organ damage; severe cerebral, cardiac, or peripheral vascular disease; or severe chronic heart disease. Any one of these problems will qualify a patient for this trial.
- •Zubrod performance status 0-
- •Women of childbearing potential must use effective contraception.
- •No direct evidence of regional or distant metastases after appropriate staging studies. No synchronous primary or prior malignancy in past 2 years except non-melanoma skin cancer or in situ cancer.
- •No previous lung or mediastinal radiation therapy.
- •No plans for concomitant antineoplastic therapy (including standard fractionated RT, chemo, biologic, vaccine therapy, or surgery) while on this protocol except at disease progression.
- •No active systemic, pulmonary, or pericardial infection.
- •No pregnant or lactating women.
- •PRESTUDY REQUIREMENTS:
- •History and Physical Examination, Weight, Zubrod performance status (within 4 weeks pre-study entry)
- •Evaluation by thoracic cancer clinician (within 8 weeks pre-study entry)
- •Pregnancy test, if applicable (serum or urine, within 72 hours prior to treatment start.)
- •CT (preferably with contrast unless medically contraindicated; both lungs, mediastinum, liver, adrenals)
- •PET (using FDG with visualization of primary tumor and draining lymph node basins in hilar and mediastinal regions)
- •Brain MRI or head CT with contrast
- •PFTs - include routine spirometry, lung volumes, diffusion capacity
- •Signed informed consent.
排除标准
- •There is no exclusion criteria associated with this protocol. Please see the above inclusion criteria.-
研究组 & 干预措施
Phase I Dose Level A: SBRT 9Gy x 5 fractions
-Stereotactic body radiation therapy (SBRT) dose of 9Gy for 5 fractions which is 5 total radiation treatments given over the course of about a week.
干预措施: Stereotactic Body Radiation Therapy (SBRT) (Radiation)
Phase I Dose Level B: SBRT 10Gy x 5 fractions
-Stereotactic body radiation therapy (SBRT) dose of 10Gy for 5 fractions which is 5 total radiation treatments given over the course of about a week.
干预措施: Stereotactic Body Radiation Therapy (SBRT) (Radiation)
Phase I Dose Level C: SBRT 11Gy x 5 fractions
-Stereotactic body radiation therapy (SBRT) dose of 11Gy for 5 fractions which is 5 total radiation treatments given over the course of about a week.
干预措施: Stereotactic Body Radiation Therapy (SBRT) (Radiation)
Phase I Dose Level D: SBRT 12Gy x 5 fractions
-Stereotactic body radiation therapy (SBRT) dose of 12Gy for 5 fractions which is 5 total radiation treatments given over the course of about a week.
干预措施: Stereotactic Body Radiation Therapy (SBRT) (Radiation)
Phase II: SBRT 11Gy x 5 fractions
-Stereotactic body radiation therapy (SBRT) dose of 11Gy for 5 fractions which is 5 total radiation treatments given over the course of about a week. The phase II dose was determined during the phase I portion of the study.
干预措施: Stereotactic Body Radiation Therapy (SBRT) (Radiation)
结局指标
主要结局
Phase I Portion Only: Determine the Maximum Tolerated Dose of SBRT
时间窗: Completion of phase I enrollment (Phase I enrollment took 4 years)
The phase 1 portion had a "5+3" strategy with four escalating dose levels, only one of which was open for accrual at any time. Five patients were accrued to each dose level, and once closed, the next dose level could not be opened until the preceding dose was deemed acceptable. With a minimum of 90 days from the start of RT, if there were no acute grade 3 or 4 non-hematologic toxicities in the five patients, the current dose was deemed acceptable. If one such toxicity was observed, an additional 3 patients were recruited and followed for a minimum of 90 days. If 2 or more such toxicities were observed, the current dose was determined as dose limiting, and the previous dose level was used for the phase 2 portion.
Phase I Portion Only: Number of Participants With Acute Treatment Related Grade 3-5 Toxicity
时间窗: Up to 90 days
* CTCAE version 3.0 will be used to grade toxicity * Acute toxicity are adverse events that occur from start of treatment through 90 days
Phase I Portion Only: Number of Participants With Late Treatment Related Grade 3-5 Toxicity
时间窗: 91 days to 2 years
* CTCAE version 3.0 will be used to grade toxicity * Late toxicity are adverse events that occur from Day 91 through 2 years
Phase II Portion Only: Local Control Rate
时间窗: 2 years
Local control rate is defined as the absence of isolated failure (progression) within the primary tumor and involved lobe
次要结局
- Phase II Only: Disseminated Recurrence Rate(2 years)
- Phase II Only: Regional Nodal Recurrence Rate(2 years)
- Phase II Only: Overall Survival Rate(2 years)
- Phase II Only: Disease-free Survival Rate(2 years)
