Long-Term Follow-Up of a Phase I/II Trial of Dose Escalating Three-Dimensional Conformal Thoracic Radiation Therapy with Induction and Concurrent Carboplatin and Paclitaxel in Unresectable Stage IIIA/B Non-small Cell Lung Cancer

We conducted a modified phase I/II trial investigating the incorporation of three-dimensional conformal thoracic radiation therapy (TCRT) into the treatment paradigm of induction and concurrent carboplatin and paclitaxel in patients with unresectable stage IIIA/B non-small cell lung cancer. Patients...

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Veröffentlicht in:Journal of thoracic oncology 2008-11, Vol.3 (11), p.1279-1285
Hauptverfasser: Stinchcombe, Thomas E., Lee, Carrie B., Moore, Dominic T., Rivera, M Patricia, Halle, Jan, Limentani, Steven, Rosenman, Julian G., Socinski, Mark A.
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container_end_page 1285
container_issue 11
container_start_page 1279
container_title Journal of thoracic oncology
container_volume 3
creator Stinchcombe, Thomas E.
Lee, Carrie B.
Moore, Dominic T.
Rivera, M Patricia
Halle, Jan
Limentani, Steven
Rosenman, Julian G.
Socinski, Mark A.
description We conducted a modified phase I/II trial investigating the incorporation of three-dimensional conformal thoracic radiation therapy (TCRT) into the treatment paradigm of induction and concurrent carboplatin and paclitaxel in patients with unresectable stage IIIA/B non-small cell lung cancer. Patients received 2 cycles of induction carboplatin (area under the curve of 6) and paclitaxel (225 mg/m2) on days 1, and 22. On day 43 concurrent TCRT and weekly ×6 of carboplatin (area under the curve = 2) and paclitaxel (45 mg/m2) was initiated. The TCRT dose was escalated from 60 to 74 Gy in 4 cohorts (60, 66, 70, and 74 Gy), and the 74 Gy cohort was expanded into a phase II trial. Sixty-two patients were enrolled; the median age 57 years (range, 36–82), 39 were male (63%), 61 (98%) had a performance status of 0 or 1, 28 (45%) had stage IIIA disease, 21 (34%) had >5% weight loss, and the median forced expiratory volume 1 = 2.10 liters (range, 1.02–3.75). With a median follow-up for survivors of approximately 9 years (range, 7–11 years) the median progression-free survival, time to tumor progression, and overall survival (OS) (with 95% confidence intervals) were 10 (8.5–17), 15 (9–50), and 25 months (18–37), respectively. The 5-year progression-free survival and OS rates were 21% (12–32%) and 27% (17–39%), respectively. The 10-year OS rate was 14% (7–25%). The long term survival rate compares favorably to other treatment approaches for stage III non-small cell lung cancer.
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The 5-year progression-free survival and OS rates were 21% (12–32%) and 27% (17–39%), respectively. The 10-year OS rate was 14% (7–25%). 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The 5-year progression-free survival and OS rates were 21% (12–32%) and 27% (17–39%), respectively. The 10-year OS rate was 14% (7–25%). The long term survival rate compares favorably to other treatment approaches for stage III non-small cell lung cancer.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18978563</pmid><doi>10.1097/JTO.0b013e31818b1971</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Carboplatin
Carboplatin - administration & dosage
Carcinoma, Non-Small-Cell Lung - drug therapy
Carcinoma, Non-Small-Cell Lung - pathology
Carcinoma, Non-Small-Cell Lung - radiotherapy
Carcinoma, Non-Small-Cell Lung - therapy
Combined Modality Therapy
Conformal thoracic therapy
Feasibility Studies
Female
Follow-Up Studies
High dose
Humans
Locally advanced non-small cell lung cancer
Lung Neoplasms - drug therapy
Lung Neoplasms - pathology
Lung Neoplasms - radiotherapy
Lung Neoplasms - therapy
Male
Maximum Tolerated Dose
Middle Aged
Neoplasm Staging
Paclitaxel
Paclitaxel - administration & dosage
Prognosis
Radiotherapy, Conformal
Remission Induction
Survival Rate
Time Factors
title Long-Term Follow-Up of a Phase I/II Trial of Dose Escalating Three-Dimensional Conformal Thoracic Radiation Therapy with Induction and Concurrent Carboplatin and Paclitaxel in Unresectable Stage IIIA/B Non-small Cell Lung Cancer
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