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Feasibility Study of Adjuvant Chemotherapy with Carboplatin and Nab-Paclitaxel for Completely Resected NSCLC
PURPOSE: Adjuvant chemotherapy with cisplatin (CDDP) plus vinorelbine is the standard regimen for the treatment of non-small cell lung cancer (NSCLC). However, CDDP elicits severe toxic effects, including emesis, neurotoxicity, and renal damage; carboplatin (CBDCA) may be a feasible alternative for...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007497/ https://www.ncbi.nlm.nih.gov/pubmed/32099473 http://dx.doi.org/10.2147/CMAR.S239647 |
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author | Katsurada, Naoko Tachihara, Motoko Hatakeyama, Yukihisa Koyama, Kiyoko Yumura, Masako Kiriu, Tatsunori Dokuni, Ryota Hazama, Daisuke Tokunaga, Shuntaro Tamura, Daisuke Nakata, Kyosuke Yamamoto, Masatsugu Kamiryo, Hiroshi Kobayashi, Kazuyuki Tanaka, Yugo Maniwa, Yoshimasa Nishimura, Yoshihiro |
author_facet | Katsurada, Naoko Tachihara, Motoko Hatakeyama, Yukihisa Koyama, Kiyoko Yumura, Masako Kiriu, Tatsunori Dokuni, Ryota Hazama, Daisuke Tokunaga, Shuntaro Tamura, Daisuke Nakata, Kyosuke Yamamoto, Masatsugu Kamiryo, Hiroshi Kobayashi, Kazuyuki Tanaka, Yugo Maniwa, Yoshimasa Nishimura, Yoshihiro |
author_sort | Katsurada, Naoko |
collection | PubMed |
description | PURPOSE: Adjuvant chemotherapy with cisplatin (CDDP) plus vinorelbine is the standard regimen for the treatment of non-small cell lung cancer (NSCLC). However, CDDP elicits severe toxic effects, including emesis, neurotoxicity, and renal damage; carboplatin (CBDCA) may be a feasible alternative for CDDP-unfit patients. CBDCA plus paclitaxel (PTX) adjuvant chemotherapy showed a survival benefit for patients with stage IB tumors >4 cm in size, while CBDCA plus nanoparticle albumin-bound (nab)-PTX showed greater efficacy and lower neurotoxicity than CBDCA plus PTX in advanced NSCLC. Here, we investigated the feasibility of using CBDCA plus nab-PTX as adjuvant chemotherapy for NSCLC. PATIENTS AND METHODS: Patients with completely resected stage II or III NSCLC, with an Eastern Cooperative Oncology Group performance status of 0–1 and adequate kidney function, received four cycles of postoperative adjuvant chemotherapy with CBDCA (AUC=5 mg/mL/min, on day 1) and nab-PTX (100 mg/m(2), on days 1, 8, and 15) administered every 4 weeks within 8 weeks after surgery. The study was designed as a prospective, single-center, Phase II study. The primary endpoint was the completion rate of chemotherapy; secondary endpoints were two-year relapse-free survival (RFS) and safety. The expected completion rate was 80%, with a 50% lower limit. RESULTS: Of 21 enrolled patients, 18 (85.7%) were CDDP-unfit owing to age (≥75 years old [n=11, 52.4%]) or mild renal impairment (n=7, 33.3%). Nineteen of the 21 enrolled patients were assigned to the intervention. The most common grade 3 or 4 adverse events were neutropenia (n=15, 78.9%) and anemia (n=3, 15.8%). The completion rate for the four cycles was 63.2% (95% CI, 38.4–83.7). Two-year RFS was 56.8% (95% CI, 29.7–76.9). CONCLUSION: The completion rate for CBDCA plus nab-PTX as adjuvant chemotherapy for CDDP-unfit NSCLC patients did not reach treatment feasibility. Further dose modifications may be required in future studies. |
format | Online Article Text |
id | pubmed-7007497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-70074972020-02-25 Feasibility Study of Adjuvant Chemotherapy with Carboplatin and Nab-Paclitaxel for Completely Resected NSCLC Katsurada, Naoko Tachihara, Motoko Hatakeyama, Yukihisa Koyama, Kiyoko Yumura, Masako Kiriu, Tatsunori Dokuni, Ryota Hazama, Daisuke Tokunaga, Shuntaro Tamura, Daisuke Nakata, Kyosuke Yamamoto, Masatsugu Kamiryo, Hiroshi Kobayashi, Kazuyuki Tanaka, Yugo Maniwa, Yoshimasa Nishimura, Yoshihiro Cancer Manag Res Clinical Trial Report PURPOSE: Adjuvant chemotherapy with cisplatin (CDDP) plus vinorelbine is the standard regimen for the treatment of non-small cell lung cancer (NSCLC). However, CDDP elicits severe toxic effects, including emesis, neurotoxicity, and renal damage; carboplatin (CBDCA) may be a feasible alternative for CDDP-unfit patients. CBDCA plus paclitaxel (PTX) adjuvant chemotherapy showed a survival benefit for patients with stage IB tumors >4 cm in size, while CBDCA plus nanoparticle albumin-bound (nab)-PTX showed greater efficacy and lower neurotoxicity than CBDCA plus PTX in advanced NSCLC. Here, we investigated the feasibility of using CBDCA plus nab-PTX as adjuvant chemotherapy for NSCLC. PATIENTS AND METHODS: Patients with completely resected stage II or III NSCLC, with an Eastern Cooperative Oncology Group performance status of 0–1 and adequate kidney function, received four cycles of postoperative adjuvant chemotherapy with CBDCA (AUC=5 mg/mL/min, on day 1) and nab-PTX (100 mg/m(2), on days 1, 8, and 15) administered every 4 weeks within 8 weeks after surgery. The study was designed as a prospective, single-center, Phase II study. The primary endpoint was the completion rate of chemotherapy; secondary endpoints were two-year relapse-free survival (RFS) and safety. The expected completion rate was 80%, with a 50% lower limit. RESULTS: Of 21 enrolled patients, 18 (85.7%) were CDDP-unfit owing to age (≥75 years old [n=11, 52.4%]) or mild renal impairment (n=7, 33.3%). Nineteen of the 21 enrolled patients were assigned to the intervention. The most common grade 3 or 4 adverse events were neutropenia (n=15, 78.9%) and anemia (n=3, 15.8%). The completion rate for the four cycles was 63.2% (95% CI, 38.4–83.7). Two-year RFS was 56.8% (95% CI, 29.7–76.9). CONCLUSION: The completion rate for CBDCA plus nab-PTX as adjuvant chemotherapy for CDDP-unfit NSCLC patients did not reach treatment feasibility. Further dose modifications may be required in future studies. Dove 2020-02-03 /pmc/articles/PMC7007497/ /pubmed/32099473 http://dx.doi.org/10.2147/CMAR.S239647 Text en © 2020 Katsurada et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Clinical Trial Report Katsurada, Naoko Tachihara, Motoko Hatakeyama, Yukihisa Koyama, Kiyoko Yumura, Masako Kiriu, Tatsunori Dokuni, Ryota Hazama, Daisuke Tokunaga, Shuntaro Tamura, Daisuke Nakata, Kyosuke Yamamoto, Masatsugu Kamiryo, Hiroshi Kobayashi, Kazuyuki Tanaka, Yugo Maniwa, Yoshimasa Nishimura, Yoshihiro Feasibility Study of Adjuvant Chemotherapy with Carboplatin and Nab-Paclitaxel for Completely Resected NSCLC |
title | Feasibility Study of Adjuvant Chemotherapy with Carboplatin and Nab-Paclitaxel for Completely Resected NSCLC |
title_full | Feasibility Study of Adjuvant Chemotherapy with Carboplatin and Nab-Paclitaxel for Completely Resected NSCLC |
title_fullStr | Feasibility Study of Adjuvant Chemotherapy with Carboplatin and Nab-Paclitaxel for Completely Resected NSCLC |
title_full_unstemmed | Feasibility Study of Adjuvant Chemotherapy with Carboplatin and Nab-Paclitaxel for Completely Resected NSCLC |
title_short | Feasibility Study of Adjuvant Chemotherapy with Carboplatin and Nab-Paclitaxel for Completely Resected NSCLC |
title_sort | feasibility study of adjuvant chemotherapy with carboplatin and nab-paclitaxel for completely resected nsclc |
topic | Clinical Trial Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007497/ https://www.ncbi.nlm.nih.gov/pubmed/32099473 http://dx.doi.org/10.2147/CMAR.S239647 |
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