Efficacy of nanoparticle albumin-bound paclitaxel regimens for relapsed small cell lung cancer

نویسندگان

  • Yujiro Naito
  • Akihiro Tamiya
  • Motohiro Tamiya
  • Yohei Kimura
  • Masanari Hamaguchi
  • Nobuhiko Saijo
  • Masaki Kanazu
  • Sayoko Tokura
  • Takayuki Shiroyama
  • Naoko Morisita
  • Naoki Omachi
  • Hidekazu Suzuki
  • Norio Okamoto
  • Kyoichi Okishio
  • Tomonori Hirashima
  • Shinji Atagi
چکیده

Although small cell lung cancer (SCLC) is initially sensitive to chemotherapy, it recurs in most cases. Standard regimens for salvage chemotherapy have not been established, and the prognosis of relapsed SCLC remains poor. In the present study, we investigated the clinical efficacy and safety of nanoparticle albumin-bound paclitaxel (nab-paclitaxel) regimens for the treatment of relapsed SCLC.In this retrospective multicenter analysis, 14 patients (3 women and 11 men; median age 71 years) with relapsed SCLC received nab-paclitaxel alone or in combination with carboplatin between February 2013 and July 2014. The safety and efficacy of the regimens were evaluated.The response rates, disease control rates, and median overall survival for the total patient population were 36%, 64%, and 7.8 months, respectively. Response rates, disease control rates, and the median overall survival were 11%, 44%, and 4 months, respectively, in the monotherapy group; and 80%, 100%, and 10.6 months, respectively, in the combination therapy group. The most common adverse events were hematological toxicities such as neutropenia and anemia. Severe neutropenia appeared in some patients, although it was resolved by treatment in all. The most common nonhematological toxicity was anorexia (64%), followed by neurotoxicity and constipation. All nonhematological toxicities were mild and manageable.Our results suggest that chemotherapy with nab-paclitaxel regimens for relapsed SCLC exhibits moderate clinical efficacy and is well-tolerated. Further clinical trials in relapsed SCLC patients are warranted.

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عنوان ژورنال:

دوره 96  شماره 

صفحات  -

تاریخ انتشار 2017