Chemotherapy Plus Radiation Therapy in Treating Patients With Limited-Stage Small Cell Lung Cancer
Topotecan/Paclitaxel Induction Followed by Consolidation Chemoradiotherapy for Limited Stage Small Cell Lung Cancer: A Phase II Study
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining more than one drug and giving them before and with radiation therapy may be an effective treatment for limited-stage small cell lung cancer.
PURPOSE: Phase II trial to study the effectiveness of chemotherapy plus radiation therapy in treating patients who have limited-stage small cell lung cancer.
調査の概要
詳細な説明
OBJECTIVES: I. Determine the complete response rate to 2 courses of paclitaxel and topotecan followed by consolidation chemoradiotherapy in patients with limited stage small cell lung cancer. II. Determine the toxic effects of this regimen in this patient population. III. Describe the pattern of relapse, documenting carefully the location of relapse with respect to the original disease volume and the radiation treatment field in these patients. IV. Determine the overall and failure free survival of these patients.
OUTLINE: Patients receive topotecan IV on days 1-5 and paclitaxel IV over 3 hours on day 1. Filgrastim (G-CSF) is administered subcutaneously every day starting on day 6 until blood counts recover. The course is repeated once beginning on day 22. After restaging, patients begin thoracic radiotherapy daily, five days per week, for 6-7 weeks. On the same day that radiotherapy begins, patients receive carboplatin IV over 1 hour (day 43) and etoposide IV over 1 hour daily for 3 days (days 43-45). The consolidation chemotherapy is repeated every 21 days for a total of 3 courses. Patients with stable or responding disease undergo prophylactic cranial irradiation. Patients are followed at least every 3 months for 2 years, every 6 months for 3 years, and then at least every year.
PROJECTED ACCRUAL: A total of 70 patients will be accrued for this study within 15-18 months.
研究の種類
入学 (実際)
段階
- フェーズ2
連絡先と場所
研究場所
-
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Alabama
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Birmingham、Alabama、アメリカ、35233
- Veterans Affairs Medical Center - Birmingham
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California
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La Jolla、California、アメリカ、92093-0658
- University of California San Diego Cancer Center
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San Francisco、California、アメリカ、94121
- Veterans Affairs Medical Center - San Francisco
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San Francisco、California、アメリカ、94115-0128
- UCSF Cancer Center and Cancer Research Institute
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Delaware
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Wilmington、Delaware、アメリカ、19899
- CCOP - Christiana Care Health Services
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District of Columbia
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Washington、District of Columbia、アメリカ、20307-5000
- Walter Reed Army Medical Center
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Washington、District of Columbia、アメリカ、20007
- Vincent T. Lombardi Cancer Research Center, Georgetown University
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Florida
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Miami Beach、Florida、アメリカ、33140
- CCOP - Mount Sinai Medical Center
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Illinois
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Chicago、Illinois、アメリカ、60612
- Veterans Affairs Medical Center - Chicago (Westside Hospital)
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Chicago、Illinois、アメリカ、60637
- University of Chicago Cancer Research Center
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Chicago、Illinois、アメリカ、60612
- University of Illinois at Chicago Health Sciences Center
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Iowa
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Iowa City、Iowa、アメリカ、52242
- University of Iowa Hospitals and Clinics
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Maine
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Togus、Maine、アメリカ、04330
- Veterans Affairs Medical Center - Togus
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Maryland
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Baltimore、Maryland、アメリカ、21201
- Marlene & Stewart Greenebaum Cancer Center, University of Maryland
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Massachusetts
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Boston、Massachusetts、アメリカ、02115
- Dana-Farber Cancer Institute
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Worcester、Massachusetts、アメリカ、01655
- University of Massachusetts Memorial Medical Center
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Minnesota
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Minneapolis、Minnesota、アメリカ、55417
- Veterans Affairs Medical Center - Minneapolis
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Missouri
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Columbia、Missouri、アメリカ、65201
- Veterans Affairs Medical Center - Columbia (Truman Memorial)
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Columbia、Missouri、アメリカ、65203
- Ellis Fischel Cancer Center - Columbia
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Saint Louis、Missouri、アメリカ、63110
- Barnes-Jewish Hospital
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Saint Louis、Missouri、アメリカ、63131
- Missouri Baptist Cancer Center
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Nebraska
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Omaha、Nebraska、アメリカ、68198-3330
- University of Nebraska Medical Center
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Nevada
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Las Vegas、Nevada、アメリカ、89106
- CCOP - Southern Nevada Cancer Research Foundation
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New Hampshire
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Lebanon、New Hampshire、アメリカ、03756
- Norris Cotton Cancer Center
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New York
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Buffalo、New York、アメリカ、14263-0001
- Roswell Park Cancer Institute
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Buffalo、New York、アメリカ、14215
- Veterans Affairs Medical Center - Buffalo
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Manhasset、New York、アメリカ、11030
- CCOP - North Shore University Hospital
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Manhasset、New York、アメリカ、11030
- North Shore University Hospital
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New York、New York、アメリカ、10021
- Memorial Sloan-Kettering Cancer Center
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New York、New York、アメリカ、10021
- New York Presbyterian Hospital - Cornell Campus
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New York、New York、アメリカ、10029
- Mount Sinai Medical Center, NY
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Syracuse、New York、アメリカ、13210
- State University of New York - Upstate Medical University
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Syracuse、New York、アメリカ、13210
- Veterans Affairs Medical Center - Syracuse
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Syracuse、New York、アメリカ、13210
- CCOP - Syracuse Hematology-Oncology Associates of Central New York, P.C.
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North Carolina
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Chapel Hill、North Carolina、アメリカ、27599-7295
- Lineberger Comprehensive Cancer Center, UNC
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Durham、North Carolina、アメリカ、27705
- Veterans Affairs Medical Center - Durham
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Durham、North Carolina、アメリカ、27710
- Duke Comprehensive Cancer Center
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Winston-Salem、North Carolina、アメリカ、27104-4241
- CCOP - Southeast Cancer Control Consortium
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Winston-Salem、North Carolina、アメリカ、27157-1082
- Comprehensive Cancer Center of Wake Forest University Baptist Medical Center
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Ohio
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Columbus、Ohio、アメリカ、43210
- Arthur G. James Cancer Hospital - Ohio State University
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Rhode Island
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Providence、Rhode Island、アメリカ、02903
- Rhode Island Hospital
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South Carolina
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Charleston、South Carolina、アメリカ、29425-0721
- Medical University of South Carolina
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Tennessee
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Memphis、Tennessee、アメリカ、38104
- Veterans Affairs Medical Center - Memphis
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Memphis、Tennessee、アメリカ、38163
- University of Tennessee, Memphis Cancer Center
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Vermont
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Burlington、Vermont、アメリカ、05401-3498
- Vermont Cancer Center
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White River Junction、Vermont、アメリカ、05009
- Veterans Affairs Medical Center - White River Junction
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Virginia
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Richmond、Virginia、アメリカ、23298-0037
- MBCCOP - Massey Cancer Center
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Richmond、Virginia、アメリカ、23249
- Veterans Affairs Medical Center - Richmond
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed limited stage small cell lung cancer Includes disease restricted to one hemithorax with regional lymph node metastases, including hilar, ipsilateral and contralateral mediastinal lymph nodes Clinically suspected or confirmed supraclavicular lymph node metastases and pleural effusions that are visible on plain chest radiographs, whether cytologically positive or not, are not eligible Unidimensionally or bidimensionally measurable disease
PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Life expectancy: Not specified Hematopoietic: Granulocyte count at least 1,500/mm3 Platelet count at least 100,000/mm3 Hepatic: Bilirubin less than 1.5 mg/dL SGOT less than 2 times upper limit of normal (ULN) Renal: Creatinine no greater than ULN Other: Not pregnant or nursing Fertile patients must use effective contraception No concurrent active second malignancy except nonmelanoma skin cancer (i.e., completed therapy and considered to be at less than 30% risk of relapse)
PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No prior chemotherapy for small cell lung cancer No other concurrent chemotherapy Endocrine therapy: No concurrent steroids except for adrenal failure No concurrent hormones except for nondisease related conditions (e.g., insulin for diabetes) No concurrent dexamethasone except for intermittent use as an antiemetic or as an adjunct to prophylactic cranial irradiation Radiotherapy: No prior mediastinal radiotherapy Surgery: Not specified
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
---|---|
実験的:chemotherapy + radiation therapy
Patients receive topotecan IV on days 1-5 and paclitaxel IV over 3 hours on day 1.
Filgrastim (G-CSF) is administered subcutaneously every day starting on day 6 until blood counts recover.
The course is repeated once beginning on day 22.
After restaging, patients begin thoracic radiotherapy daily, five days per week, for 6-7 weeks.
On the same day that radiotherapy begins, patients receive carboplatin IV over 1 hour (day 43) and etoposide IV over 1 hour daily for 3 days (days 43-45).
The consolidation chemotherapy is repeated every 21 days for a total of 3 courses.
Patients with stable or responding disease undergo prophylactic cranial irradiation.
Patients are followed at least every 3 months for 2 years, every 6 months for 3 years, and then at least every year.
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
---|---|
回答率
時間枠:5年まで
|
5年まで
|
全生存
時間枠:5年まで
|
5年まで
|
協力者と研究者
捜査官
- スタディチェア:Alan P. Lyss, MD、Missouri Baptist Cancer Center
出版物と役立つリンク
一般刊行物
- Bogart JA, Herndon JE 2nd, Lyss AP, Watson D, Miller AA, Lee ME, Turrisi AT, Green MR; Cancer and Leukemia Group B study 39808. 70 Gy thoracic radiotherapy is feasible concurrent with chemotherapy for limited-stage small-cell lung cancer: analysis of Cancer and Leukemia Group B study 39808. Int J Radiat Oncol Biol Phys. 2004 Jun 1;59(2):460-8. doi: 10.1016/j.ijrobp.2003.10.021.
- Cicchetti MG, Bogart J, Lyss A, et al.: Spinal cord dose in limited stage small cell lung cancer: a preliminary Quality Assurance Review Committee (QARC) report on CALGB 39808, using target thoracic radiotherapy (TRT) doses of 60 - 70 Gy. [Abstract] Int J Radiat Oncol Biol Phys 51(3 suppl 1): A-656, 356, 2001.
- Lyss AP, Herndon JE, Bogart JE, et al.: Topotecan (Topo) + paclitaxel (Tax) + G-CSF (G) induction followed by concurrent chemoradiotherapy (CCRT) for patients (pts) with limited stage small cell lung cancer (L-SCLC): preliminary analysis of CALGB 39808. [Abstract] Proceedings of the American Society of Clinical Oncology 20: A-1270, 2001.
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- CALGB-39808
- U10CA031946 (米国 NIH グラント/契約)
- CLB-39808
- CDR0000066958 (レジストリ識別子:NCI Physician Data Query)
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
肺癌の臨床試験
-
Jonsson Comprehensive Cancer CenterNational Cancer Institute (NCI); Highlight Therapeutics積極的、募集していない平滑筋肉腫 | 悪性末梢神経鞘腫瘍 | 滑膜肉腫 | 未分化多形肉腫 | 骨の未分化高悪性度多形肉腫 | 粘液線維肉腫 | II期の体幹および四肢の軟部肉腫 AJCC v8 | III期の体幹および四肢の軟部肉腫 AJCC v8 | IIIA 期の体幹および四肢の軟部肉腫 AJCC v8 | IIIB 期の体幹および四肢の軟部肉腫 AJCC v8 | 切除可能な軟部肉腫 | 多形性横紋筋肉腫 | 切除可能な脱分化型脂肪肉腫 | 切除可能な未分化多形肉腫 | 軟部組織線維肉腫 | 紡錘細胞肉腫 | ステージ I 後腹膜肉腫 AJCC (American Joint Committee on Cancer) v8 | 体幹および四肢の I 期軟部肉腫 AJCC v8 | ステージ... およびその他の条件アメリカ
カルボプラチンの臨床試験
-
Virginia Commonwealth UniversityNational Cancer Institute (NCI)引きこもったステージ IIIA 非小細胞肺がん | ステージ IIIB 非小細胞肺がん | 扁平上皮肺がん | 肺の腺癌 | 大細胞肺がん | ステージ IIA 非小細胞肺がん | ステージ IIB 非小細胞肺がん
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Children's Oncology GroupNational Cancer Institute (NCI)完了脳腫瘍 | 中枢神経系腫瘍アメリカ, カナダ, オーストラリア, スイス, オランダ, ニュージーランド