Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Results of a Phase I trial of concurrent chemotherapy and escalating doses of radiation for unresectable non-small-cell lung cancer

Journal Article · · International Journal of Radiation Oncology, Biology and Physics
 [1];  [2];  [3];  [1];  [4];  [4];  [1];  [5];  [6];  [7];  [1];  [1]
  1. Mayo Clinic and Mayo Foundation, Rochester, MN (United States)
  2. Iowa Oncology Research Association Community Clinical Oncology Program (CCOP), Des Moines, IA (United States)
  3. Carle Cancer Center Community Clinical Oncology Program (CCOP), Urbana, IL (United States)
  4. Scottsdale Community Clinical Oncology Program (CCOP), Scottsdale, AZ (United States)
  5. Meritcare Hospital Community Clinical Oncology Program (CCOP), Fargo, ND (United States)
  6. Sioux Community Cancer Consortium, Sioux Falls, SD (United States)
  7. Toledo Community Hospital Oncology Program Community Clinical Oncology Program (CCOP), Toledo, OH (United States)
Purpose: This trial was performed to determine the maximum tolerated dose (MTD) of radiation that can be administered with carboplatin and paclitaxel. Methods and Materials: This trial included 15 patients with unresectable non-small-cell lung cancer. Paclitaxel (50 mg/m{sup 2}) and carboplatin (area under the curve = 2) were given weekly during radiation therapy (RT). The RT included 2 Gy daily to an initial dose of 70 Gy, and the dose was increased in 4 Gy increments until determining the MTD. The MTD was defined as the highest safely tolerated dose where at most 1 patient of 6 experienced dose-limiting toxicity (DLT) with the next higher dose having at least 2 of 6 patients experiencing DLT. Three-dimensional treatment planning techniques were used without prophylactic nodal RT. Results: Two patients were not evaluable because they did not receive therapy according to the protocol. No DLTs occurred in the 3 patients who received 70 Gy, 1 DLT occurred in the 6 patients who received 74 Gy, and 2 DLTs occurred in the 4 patients who received 78 Gy. The DLTs included Grade 3 pneumonitis (n = 2) and Grade 4 pneumonitis (n = 1). There have been 3 deaths during follow-up ranging from 14 to 38 months (median, 28 months). Conclusions: The MTD of the RT was 74 Gy with weekly carboplatin and paclitaxel. The Phase II portion of this trial is currently under way. The goal is to improve local control and survival with higher doses of RT delivered with this combined modality approach.
OSTI ID:
20849984
Journal Information:
International Journal of Radiation Oncology, Biology and Physics, Journal Name: International Journal of Radiation Oncology, Biology and Physics Journal Issue: 4 Vol. 65; ISSN IOBPD3; ISSN 0360-3016
Country of Publication:
United States
Language:
English

Similar Records

A Phase I/II Radiation Dose Escalation Study With Concurrent Chemotherapy for Patients With Inoperable Stages I to III Non-Small-Cell Lung Cancer: Phase I Results of RTOG 0117
Journal Article · Tue Jun 01 00:00:00 EDT 2010 · International Journal of Radiation Oncology, Biology and Physics · OSTI ID:21372281

A Phase I study of capecitabine, carboplatin, and paclitaxel with external beam radiation therapy for esophageal carcinoma
Journal Article · Thu Mar 15 00:00:00 EDT 2007 · International Journal of Radiation Oncology, Biology and Physics · OSTI ID:20944756

Phase 1 Dose Escalation Study of Accelerated Radiation Therapy With Concurrent Chemotherapy for Locally Advanced Lung Cancer
Journal Article · Mon Nov 30 23:00:00 EST 2015 · International Journal of Radiation Oncology, Biology and Physics · OSTI ID:22645027