Mid-course thoracic radiotherapy with cisplatin-etoposide chemotherapy in limited-stage small-cell lung cancer

AKYÜREK S., Onal C., Cagar A., Hicsonmez A., Andrieu M. N., Kurtman C.

MEDICAL ONCOLOGY, cilt.23, sa.4, ss.499-505, 2006 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 23 Sayı: 4
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1385/mo:23:4:499
  • Dergi Adı: MEDICAL ONCOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.499-505
  • Anahtar Kelimeler: small-cell lung carcinoma, radiotherapy, chemotherapy, treatment time, HYPERFRACTIONATED RADIATION-THERAPY, PROPHYLACTIC CRANIAL IRRADIATION, CONCURRENT CHEMOTHERAPY, LOCAL-CONTROL, CARCINOMA, COMBINATION, METASTASES, SURVIVAL, TRIAL, GY
  • Ankara Üniversitesi Adresli: Evet

Özet

Combination chemoradiotherapy is a standard treatment for limited-stage small-cell lung cancer (LSSCLQ. However, there is still controversery about the optimal timing of thoracic radiotherapy (TRT). In this study, the outcome of 70 patients who had received TRT at a dose of median 50 Gy (range, 46-60 Gy) with a second or third cycle of chemotherapy (CHT) either concurrently (n = 41) or sequentially (n = 29) were analyzed retrospectively. All patients were administered a median of five cycles (range, four to six cycles) cisplatin plus etoposide (EP) CHT. Prophylactic cranial radiotherapy was delivered to 30 (43%) patients. The median follow-up for all patients was 15 mo (range, 6-60 mo). The median overall survival was 19 mo in the concurrent arm vs 15 mo in the sequential arm. The 2-yr local control, disease-free survival, and overall survival rates were 60%, 19%, and 36%, respectively. The most common toxicity was esophagitis. However, there were no grade 3-4 esophagitis in either arm. Grade 3-4 hematologic toxicity, on the other hand, appeared significantly more in the concurrent arm (p < 0.001). Mid-course of once-daily TRT at a moderate total dose with CHT failed to show any improvement in survival. Additionally, there were no differences between concurrent and sequential CHT with TRT. However, acceptable toxicity rates support the use of once-daily fractionation to higher total dose of TRT.