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- Publisher Website: 10.1200/JCO.2011.35.6923
- Scopus: eid_2-s2.0-81755172139
- PMID: 21969504
- WOS: WOS:000297257400022
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Article: Cisplatin, irinotecan, and bevacizumab for untreated extensive-stage small-cell lung cancer: CALGB 30306, a phase II study
Title | Cisplatin, irinotecan, and bevacizumab for untreated extensive-stage small-cell lung cancer: CALGB 30306, a phase II study |
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Authors | |
Issue Date | 2011 |
Citation | Journal of Clinical Oncology, 2011, v. 29 n. 33, p. 4436-4441 How to Cite? |
Abstract | Purpose: The efficacy of cisplatin, irinotecan, and bevacizumab was evaluated in patients with extensive-stage small-cell lung cancer (ES-SCLC). Patients and Methods: Patients with ES-SCLC received cisplatin 30 mg/m 2 and irinotecan 65 mg/m 2 on days 1 and 8 plus bevacizumab 15 mg/kg on day 1 every 21 days for six cycles on this phase II study. The primary end point was to differentiate between 50% and 65% 12-month survival rates. Results: Seventy-two patients were enrolled between March 2005 and April 2006; four patients canceled, and four were ineligible. Grade 3 or 4 toxicities included neutropenia (25%), all electrolyte (23%), diarrhea (16%), thrombocytopenia (10%), fatigue (10%), nausea (10%), hypertension (9%), anemia (9%), infection (7%), vascular access thrombosis (2%), stroke (2%), and bowel perforation (1%). Three deaths (5%) occurred on therapy as a result of pneumonitis (n = 1), stroke (n = 1), and heart failure (n = 1). Complete response, partial response, and stable disease occurred in three (5%), 45 (70%), and 11 patients (17%), respectively. Progressive disease occurred in one patient (2%). Overall response rate was 75%. Median progression-free survival (PFS) was 7.0 months (95% CI, 6.4 to 8.4 months). Median overall survival (OS) was 11.6 months (95% CI, 10.5 to 15.1 months). Hypertension ≥ grade 1 was associated with improved OS after adjusting for performance status (PS) and age (hazard ratio [HR], 0.55; 95% CI, 0.31 to 0.97; P = .04). Lower vascular endothelial growth factor levels correlated with worse PFS after adjusting for age and PS (HR, 0.90; 95% CI, 0.83 to 0.99; P = .03). Conclusion: PFS and OS times were higher compared with US trials in ES-SCLC with the same chemotherapy. However, the primary end point of the trial was not met. Hypertension was associated with improved survival after adjusting for age and PS. © 2011 by American Society of Clinical Oncology. |
Persistent Identifier | http://hdl.handle.net/10722/194336 |
ISSN | 2023 Impact Factor: 42.1 2023 SCImago Journal Rankings: 10.639 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Ready, NE | - |
dc.contributor.author | Dudek, AZ | - |
dc.contributor.author | Pang, HH | - |
dc.contributor.author | Hodgson, LD | - |
dc.contributor.author | Graziano, SL | - |
dc.contributor.author | Green, MR | - |
dc.contributor.author | Vokes, EE | - |
dc.date.accessioned | 2014-01-30T03:32:28Z | - |
dc.date.available | 2014-01-30T03:32:28Z | - |
dc.date.issued | 2011 | - |
dc.identifier.citation | Journal of Clinical Oncology, 2011, v. 29 n. 33, p. 4436-4441 | - |
dc.identifier.issn | 0732-183X | - |
dc.identifier.uri | http://hdl.handle.net/10722/194336 | - |
dc.description.abstract | Purpose: The efficacy of cisplatin, irinotecan, and bevacizumab was evaluated in patients with extensive-stage small-cell lung cancer (ES-SCLC). Patients and Methods: Patients with ES-SCLC received cisplatin 30 mg/m 2 and irinotecan 65 mg/m 2 on days 1 and 8 plus bevacizumab 15 mg/kg on day 1 every 21 days for six cycles on this phase II study. The primary end point was to differentiate between 50% and 65% 12-month survival rates. Results: Seventy-two patients were enrolled between March 2005 and April 2006; four patients canceled, and four were ineligible. Grade 3 or 4 toxicities included neutropenia (25%), all electrolyte (23%), diarrhea (16%), thrombocytopenia (10%), fatigue (10%), nausea (10%), hypertension (9%), anemia (9%), infection (7%), vascular access thrombosis (2%), stroke (2%), and bowel perforation (1%). Three deaths (5%) occurred on therapy as a result of pneumonitis (n = 1), stroke (n = 1), and heart failure (n = 1). Complete response, partial response, and stable disease occurred in three (5%), 45 (70%), and 11 patients (17%), respectively. Progressive disease occurred in one patient (2%). Overall response rate was 75%. Median progression-free survival (PFS) was 7.0 months (95% CI, 6.4 to 8.4 months). Median overall survival (OS) was 11.6 months (95% CI, 10.5 to 15.1 months). Hypertension ≥ grade 1 was associated with improved OS after adjusting for performance status (PS) and age (hazard ratio [HR], 0.55; 95% CI, 0.31 to 0.97; P = .04). Lower vascular endothelial growth factor levels correlated with worse PFS after adjusting for age and PS (HR, 0.90; 95% CI, 0.83 to 0.99; P = .03). Conclusion: PFS and OS times were higher compared with US trials in ES-SCLC with the same chemotherapy. However, the primary end point of the trial was not met. Hypertension was associated with improved survival after adjusting for age and PS. © 2011 by American Society of Clinical Oncology. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Clinical Oncology | - |
dc.title | Cisplatin, irinotecan, and bevacizumab for untreated extensive-stage small-cell lung cancer: CALGB 30306, a phase II study | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1200/JCO.2011.35.6923 | - |
dc.identifier.pmid | 21969504 | - |
dc.identifier.scopus | eid_2-s2.0-81755172139 | - |
dc.identifier.volume | 29 | - |
dc.identifier.issue | 33 | - |
dc.identifier.spage | 4436 | - |
dc.identifier.epage | 4441 | - |
dc.identifier.isi | WOS:000297257400022 | - |
dc.identifier.issnl | 0732-183X | - |