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Randomized Phase II Study of Once Daily Accelerated Fractionation With Concomitant Boost to the Gross Tumor Volume Compared With Twice Daily Hyperfractionation in Concurrent Chemoradiation in Patients With Limited Disease Small Cell Lung Cancer


Phase 2
18 Years
N/A
Open (Enrolling)
Both
Limited Disease Small Cell Lung Cancer

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Trial Information

Randomized Phase II Study of Once Daily Accelerated Fractionation With Concomitant Boost to the Gross Tumor Volume Compared With Twice Daily Hyperfractionation in Concurrent Chemoradiation in Patients With Limited Disease Small Cell Lung Cancer


Inclusion Criteria:



- Histologically or cytologically (if cannot be proven histologically, at least twice
positive findings on fine needle aspiration or sputum cytology) confirmed SCLC

- Limited stage (Clinical stage I-IIIb, lesion limited to one side of thorax, e.g.
Excluding T4 disease with malignant pleural effusion or N3 disease with contralateral
hilum/supraclavicular lymph node invasion).

- Measurable or assessable lesion

- Age over 18 years old

- Performance status (ECOG scale): 0~2

- Adequate organ functions: ANC ≥ 1500/ul, PLT ≥ 100 x 103/u, Total Bilirubin ≤ 1.5
mg/dl, Creatinine ≤ 1.5 mg/dl

- Inclusion of tumor within the limited radiation field without significant loss of
pulmonary function (confirmed by radiation oncologist)

- Sexually active fertile men and women using a contraceptive method

- Patients should sign a written informed consest before study entry

Exclusion Criteria:

- T4 disease with malignant pleural effusion; N3 disease with contralateral
hilum/supraclavicular lymph node invasion

- Lesion with mixed small cell nonsmall cell feature (pathologically)

- prior chemotherapy or radiation therapy.

- Pericardial or pleural effusion on chest X-ray image regardless of cytological
finding

- T4 disease with tumor invasion to great vessels, heart, trachea, or esophagus;
Concerns about possible perforation by tumor necrosis

- Severe comorbidities such as cardiac disease with symptom, myocardiac infarction
within 6 months, chronic obstructive pulmonary disease with FEV1 less than 1.0ℓ, or
uncontrolled bronchospasm of unaffected lung

- With atelectasis that makes GTV unidentifiable

- Other primary malignancy (except in situ carcinoma of the cervix or adequately
treated basal cell carcinoma of the skin or prior malignancy treated more than 3
years ago without recurrence)

- Uncontrolled psychiatric disorder, serious head injury, chronic alcoholism, drug
addiction and central nervous system disease

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

progression free survival

Outcome Time Frame:

5years after chemoradiotherapy

Safety Issue:

No

Principal Investigator

Kwan Ho Cho, M.D.

Investigator Role:

Principal Investigator

Investigator Affiliation:

National Cancer Center, Korea

Authority:

Korea: Food and Drug Administration

Study ID:

NCCCTS-11-531

NCT ID:

NCT01710956

Start Date:

March 2011

Completion Date:

December 2014

Related Keywords:

  • Limited Disease Small Cell Lung Cancer
  • concurrent chemoradiation in patients with limited disease small cell lung cancer
  • Lung Neoplasms
  • Small Cell Lung Carcinoma

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