Impact of KRAS mutation on response and outcome of patients with stage III non‐squamous non‐small cell lung cancer
| العنوان: | Impact of |
|---|---|
| المؤلفون: | Tomohide Tamura, Noboru Yamamoto, Shigehiro Yagishita, Kuniko Sunami, Koji Tsuta, Kouya Shiraishi, Yuichiro Ohe, Hidehito Horinouchi, Koh Furuta, Hiroshi Nokihara, Takashi Kohno, Yutaka Fujiwara, Minako Sumi, Shintaro Kanda |
| المصدر: | Cancer Science |
| بيانات النشر: | Wiley, 2015. |
| سنة النشر: | 2015 |
| مصطلحات موضوعية: | Adult, Male, Oncology, Cancer Research, medicine.medical_specialty, Lung Neoplasms, medicine.disease_cause, Disease-Free Survival, Proto-Oncogene Proteins p21(ras), Carcinoma, Non-Small-Cell Lung, Proto-Oncogene Proteins, Internal medicine, KRAS, medicine, Humans, Lung cancer, non-small cell lung cancer, Aged, Neoplasm Staging, relapse, Brain Neoplasms, business.industry, Disease progression, Original Articles, Chemoradiotherapy, General Medicine, Middle Aged, medicine.disease, Treatment Outcome, Non squamous, Mutation, ras Proteins, Female, Non small cell, Neoplasm Recurrence, Local, business, Biomarkers, Median survival, Kras mutation |
| الوصف: | The frequency and clinical profile of patients with stage III non-small cell lung cancer harboring KRAS mutations have not yet been well documented. Here, we analyzed hotspot KRAS mutations using high-resolution melting analyses in tumor specimens from patients who received chemoradiotherapy between January 2001 and December 2010 at the National Cancer Center Hospital. The associations between the presence of KRAS mutations and the response rate, relapse-free survival, first relapse sites, survival post-progression and overall survival were investigated. A total of 274 non-squamous non-small cell lung cancer patients received chemoradiotherapy at our hospital. After excluding 121 patients for whom tumor specimens were not available and 34 patients with EGFR mutations, the remaining 119 patients were included in the analysis. KRAS mutations were found at a frequency of 13%. Patients with KRAS mutations had a shorter median relapse-free survival (6.1 vs 10.9 months) and a lower response rate (63% vs 81%). As for the first relapse site, patients with KRAS mutations had fewer local relapses (8% vs 23%) and more brain metastases (46% vs 12%). After disease progression, patients with KRAS mutations had a significantly shorter median survival post-progression (2.5 vs 7.3 months, P = 0.028) and median overall survival (15.1 vs 29.1 months, P = 0.022). Our results suggested that KRAS mutation could be associated with a reduced efficacy of chemoradiotherapy and a shortened survival time. |
| تدمد: | 1349-7006 1347-9032 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26f4e6f61cfd33e9b6a330eb948c9399Test https://doi.org/10.1111/cas.12740Test |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....26f4e6f61cfd33e9b6a330eb948c9399 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 13497006 13479032 |
|---|