Comparison of two different carboplatin and weekly paclitaxel schedule in elderly advanced non-small cell lung cancer patients


Salim D. K., Telli T. A., TATLI A. M., Kilickap S., Yumuk P. F.

CANCER CHEMOTHERAPY AND PHARMACOLOGY, cilt.83, sa.6, ss.1137-1145, 2019 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 83 Sayı: 6
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1007/s00280-019-03839-w
  • Dergi Adı: CANCER CHEMOTHERAPY AND PHARMACOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1137-1145
  • Anahtar Kelimeler: NSCLC, Elderly, Carboplatin, Paclitaxel, GEMCITABINE PLUS VINORELBINE, SINGLE-AGENT, PHASE-III, DOUBLET CHEMOTHERAPY, RANDOMIZED-TRIAL, MULTICENTER, COMBINATION, MONOTHERAPY, SOCIETY
  • Akdeniz Üniversitesi Adresli: Evet

Özet

PurposeIn this study our aim was to compare efficacy and toxicity profiles of two different schedule of carboplatin-paclitaxel regimen in elderly advanced non-small cell lung cancer (NSCLC) patients.MethodsData from the charts of 59 elderly patients with metastatic NSCLC, treated with weekly paclitaxel combined with two different schedule of carboplatinwere collected retrospectively from three medical oncology centers in Turkeybetween September 2002 to March 2018. No prior systemic therapy or radiotherapy was allowed. Brain metastases were not considered as exclusion criteria unless symptomatic. Patients were analyzed in two treatment groups; CP3 (who received 3 weekly carboplatin and weekly paclitaxel), and CP1 (weekly carboplatin and weekly paclitaxel). Overall survival (OS) was the primary endpoint of the study. Secondary end points were as follows: progression free survival (PFS), response rates (RR), grade 3-4 toxicities, skipped cycles, dose reductions, and treatment discontinuation rates.ResultsTwenty-four patients received 3 weekly carboplatin and weekly paclitaxel schedule (CP3) while weekly carboplatin and weekly paclitaxel schedule (CP1) was performed in 35 patients. CP3 had a median OSof 14months whereas CP1 had 9months of median OS (p=0.084). Both treatments (CP3 vs CP1) had similar median PFS (7months vs 4months, p=0.109) and objective RR (20.9% vs 29.4%, p=0.465). There was an increased incidence of grade 3-4 anemia and grade 3-4 neutropenia in CP3 compared to CP1 (p=0.003 in both), but no major differences in febrile neutropenia and infection toxicity profiles (p=0.289 and p=0.770, respectively). Weekly schedule (CP1) had a tendency of increased grade 3-4 neurotoxicity (33.3% vs 42.9%, p=0.461).ConclusionWeekly carboplatin and paclitaxel might be more tolerable and is as effective as 3 weekly carboplatin and weekly paclitaxel schedule in metastatic elderly NSCLC patients.