共 72 条
Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials
被引:26
作者:

Bailey, Christopher H.
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机构:
Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA

Jameson, Gayle
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Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA

Sima, Chao
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机构:
Translat Genom Res Inst TGen, Phoenix, AZ USA Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA

Fleck, Sharon
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h-index: 0
机构:
Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA

White, Erica
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机构:
Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA

Von Hoff, Daniel D.
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Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA
Translat Genom Res Inst TGen, Phoenix, AZ USA Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA

Weiss, Glen J.
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机构:
Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA
Translat Genom Res Inst TGen, Phoenix, AZ USA Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA
机构:
[1] Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA
[2] Translat Genom Res Inst TGen, Phoenix, AZ USA
来源:
关键词:
Progression-free survival;
chemotherapy;
advanced cancer;
systemic therapy;
phase I clinical trials;
CELL LUNG-CANCER;
METASTATIC COLORECTAL-CANCER;
OXALIPLATIN-BASED CHEMOTHERAPY;
ADVANCED PANCREATIC-CANCER;
ADVANCED GASTRIC-CANCER;
III TRIAL;
1ST-LINE TREATMENT;
2ND-LINE TREATMENT;
GASTROESOPHAGEAL ADENOCARCINOMA;
CARBOPLATIN-PACLITAXEL;
D O I:
10.7150/jca.3.7
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: There is often a finite progression-free interval of time between one systemic therapy and the next when treating patients with advanced cancer. While it appears that progression-free survival (PFS) between systemic therapies tends to get shorter for a number of factors, there has not been a formal evaluation of diverse tumor types in an advanced cancer population treated with commercially-available systemic therapies. Methods: In an attempt to clarify the relationship between PFS between subsequent systemic therapies, we analyzed the records of 165 advanced cancer patients coming to our clinic for consideration for participation in six different phase I clinical trials requiring detailed and extensive past medical treatment history documentation. Results: There were 77 men and 65 women meeting inclusion criteria with a median age at diagnosis of 55.3 years (range 9.4-81.6). The most common cancer types were colorectal (13.9%), other gastrointestinal (11.8%), prostate (11.8%). A median of 3 (range 1-11) systemic therapies were received prior to phase I evaluation. There was a significant decrease in PFS in systemic therapy for advanced disease from treatment 1 to treatment 2 to treatment 3 (p = 0.002), as well as, from treatment 1 through treatment 5 (p < 0.001). Conclusions: In an advanced cancer population of diverse tumor types, we observe a statistically significant decrease in PFS with each successive standard therapy. Identification of new therapies that reverse this trend of decreasing PFS may lead to improved clinical outcomes.
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页码:7 / 13
页数:7
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