Literature DB >> 10761747

Is òne cycle every three or four weeks' obsolete? A critical review of dose-dense chemotherapy in solid neoplasms.

K Fizazi1, L Zelek.   

Abstract

BACKGROUND: Shortening the interval between cycles is one means of increasing the dose intensity of chemotherapy, and can be supported by biological and mathematical rationales. Our objective was to assess the clinical relevance of the rapid repetition of regimens (so-called 'dose-dense chemotherapy') in various solid neoplasms.
DESIGN: The medical literature was reviewed in accord with Mulrow's recommendations. Randomised studies comparing frequently-repeated chemotherapy to standard regimens as well as open studies are described and critically examined.
RESULTS: Dose-dense regimens were widely found to be feasible. In small-cell lung cancer, survival of patients receiving dose-dense regimens was better than that of patients treated by standard chemotherapy in three trials, two of which reached significance, when these intensive regimens allowed better dose intensity. In poor-prognosis germ-cell tumors, a dose-dense regimen was not better than standard therapy, perhaps because of an excessively high toxicity-related death rate. However, recent phase II studies have provided encouraging results. In early breast cancer, the one published randomized study in the adjuvant setting showed only a trend towards better disease-free survival in node-positive women receiving a weekly-repeated regimen. Two randomized trials failed to show any benefit in the neoadjuvant setting with a dose-dense regimen. No evidence of a benefit was provided in metastatic breast cancer. In advanced colorectal cancer, evidence of an improvement in survival with weekly or bi-weekly 5-FU-leucovorin compared to a classic monthly schedule has recently been shown in two randomized trials, and dose-dense regimens are recognized as standard therapy in many countries. Phase II studies of dose-dense regimens have also shown high response rates and long survival in many neoplasms, including Ewing's sarcoma, gestational trophoblastic disease, ovarian carcinoma and gastric cancer.
CONCLUSIONS: A considerable amount of experience has been gained with frequently-repeated regimens. A few randomized trials have demonstrated a benefit for survival on standard chemotherapy in small-cell lung cancer and advanced colorectal cancer. However, this benefit appears to be weak. The combination of dose-dense chemotherapy regimens with new anti-cancer strategies based on our insights into the mechanisms of oncogenesis is a challenge on the eve of the millennium.

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Year:  2000        PMID: 10761747     DOI: 10.1023/a:1008344014518

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  8 in total

1.  Personalised chemotherapy based on tumour marker decline in poor prognosis germ-cell tumours (GETUG 13): a phase 3, multicentre, randomised trial.

Authors:  Karim Fizazi; Lance Pagliaro; Agnes Laplanche; Aude Fléchon; Josef Mardiak; Lionnel Geoffrois; Pierre Kerbrat; Christine Chevreau; Remy Delva; Frederic Rolland; Christine Theodore; Guilhem Roubaud; Gwenaëlle Gravis; Jean-Christophe Eymard; Jean-Pierre Malhaire; Claude Linassier; Muriel Habibian; Anne-Laure Martin; Florence Journeau; Maria Reckova; Christopher Logothetis; Stephane Culine
Journal:  Lancet Oncol       Date:  2014-11-13       Impact factor: 41.316

Review 2.  Ewing tumour: incidence, prognosis and treatment options.

Authors:  M Paulussen; B Fröhlich; H Jürgens
Journal:  Paediatr Drugs       Date:  2001       Impact factor: 3.022

3.  Efficacy and tolerability of chemotherapy with modified dose-dense TCF regimen (TCF-dd) in locally advanced or metastatic gastric cancer: final results of a phase II trial.

Authors:  Gianluca Tomasello; Wanda Liguigli; Rossana Poli; Silvia Lazzarelli; Matteo Brighenti; Federica Negri; Alessandra Curti; Mario Martinotti; Lucio Olivetti; Massimo Rovatti; Gianvito Donati; Rodolfo Passalacqua
Journal:  Gastric Cancer       Date:  2013-11-27       Impact factor: 7.370

4.  Accelerated BEP: a phase I trial of dose-dense BEP for intermediate and poor prognosis metastatic germ cell tumour.

Authors:  Y Rimmer; J Chester; J Joffe; D Stark; J Shamash; T Powles; J White; J Wason; D Parashar; G Armstrong; D Mazhar; M V Williams
Journal:  Br J Cancer       Date:  2011-08-16       Impact factor: 7.640

5.  A phase II study of sequential chemotherapy with docetaxel after the weekly PELF regimen in advanced gastric cancer. A report from the Italian group for the study of digestive tract cancer.

Authors:  S Cascinu; F Graziano; S Barni; R Labianca; G Comella; R Casaretti; L Frontini; V Catalano; A M Baldelli; G Catalano
Journal:  Br J Cancer       Date:  2001-02       Impact factor: 7.640

6.  Is CBOP/BEP an alternative to BEP for patients with poor prognosis metastatic germ cell tumours?

Authors:  A Addeo; V Fusco; J P Braybrooke
Journal:  ESMO Open       Date:  2016-08-25

7.  Alternating dose-dense chemotherapy in patients with high volume disseminated non-seminomatous germ cell tumours.

Authors:  K Fizazi; D M Prow; K-A Do; X Wang; L Finn; J Kim; D Daliani; C N Papandreou; S-M Tu; R E Millikan; L C Pagliaro; C J Logothetis; R J Amato
Journal:  Br J Cancer       Date:  2002-05-20       Impact factor: 7.640

8.  Comparing Paclitaxel-Carboplatin with Paclitaxel-Cisplatin as the Front-Line Chemotherapy for Patients with FIGO IIIC Serous-Type Tubo-Ovarian Cancer.

Authors:  Chen-Yu Huang; Min Cheng; Na-Rong Lee; Hsin-Yi Huang; Wen-Ling Lee; Wen-Hsun Chang; Peng-Hui Wang
Journal:  Int J Environ Res Public Health       Date:  2020-03-26       Impact factor: 3.390

  8 in total

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