Literature DB >> 2825357

The importance of dose and dose intensity in lung cancer chemotherapy.

N Murray1.   

Abstract

The concepts of dose-response and intensity-response are distinguished via analysis of chemotherapeutic regimens for small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC) with methodology previously described. Using the data base for CAV (cyclophosphamide, doxorubicin, vincristine), and CAE (cyclophosphamide, doxorubicin, etoposide) chemotherapy, there was no consistent correlation between cyclophosphamide dose intensity and outcome; however, doxorubicin dose intensity in extensive stage disease was highly significantly associated with response rates for both regimens and median survival time for the CAE combination. Analysis of cyclophosphamide results for NSCLC do not support its use at any dose. While waiting for the development of new and more active drugs for lung cancer chemotherapy, the innovative investigation of the best drugs currently available provides the best chance for improved results.

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Year:  1987        PMID: 2825357

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  8 in total

1.  Tolerability and efficacy of GM-CSF [Leucomax] in patients with small cell lung cancer treated with intensive chemotherapy.

Authors:  J Walewski; J Romejko-Jarosińska; J Zwoliński; S Falkowski; P Siedlecki
Journal:  Med Oncol       Date:  1996-12       Impact factor: 3.064

2.  Economic analysis of lenograstim in the correction of neutropenia following chemotherapy for non-Hodgkin's lymphoma.

Authors:  E Souêtre; W Qing
Journal:  Pharmacoeconomics       Date:  1994       Impact factor: 4.981

3.  A phase II trial of dose-dense chemotherapy, followed by surgical resection and/or thoracic radiotherapy, in locally advanced thymoma: report of a Japan Clinical Oncology Group trial (JCOG 9606).

Authors:  H Kunitoh; T Tamura; T Shibata; K Takeda; N Katakami; K Nakagawa; A Yokoyama; Y Nishiwaki; K Noda; K Watanabe; N Saijo
Journal:  Br J Cancer       Date:  2010-06-15       Impact factor: 7.640

4.  Doxorubicin plus ifosfamide with rhGM-CSF in the treatment of advanced adult soft-tissue sarcomas: preliminary results of a phase II study from the EORTC Soft-Tissue and Bone Sarcoma Group.

Authors:  W P Steward; J Verweij; R Somers; G Blackledge; M Clavel; A T Van Oosterom; B Greifenberg; J Soedirman; D Thomas; M Van Glabbeke
Journal:  J Cancer Res Clin Oncol       Date:  1991       Impact factor: 4.553

5.  Economic study of neutropenia induced by myelotoxic chemotherapy.

Authors:  M C Montero; M L Valdivia; E Carvajal; A Montaño; C Buenestado; A Lluch; M Atienza
Journal:  Pharm World Sci       Date:  1994-08-05

6.  A phase-II trial of dose-dense chemotherapy in patients with disseminated thymoma: report of a Japan Clinical Oncology Group trial (JCOG 9605).

Authors:  H Kunitoh; T Tamura; T Shibata; K Nakagawa; K Takeda; Y Nishiwaki; Y Osaki; K Noda; A Yokoyama; N Saijo
Journal:  Br J Cancer       Date:  2009-10-06       Impact factor: 7.640

7.  Effects of interleukin-3 on myelosuppression induced by chemotherapy for ovarian cancer and small cell undifferentiated tumours.

Authors:  M W Dercksen; K Hoekman; W W ten Bokkel Huinink; E M Rankin; R Dubbelman; H van Tinteren; J Wagstaff; H M Pinedo
Journal:  Br J Cancer       Date:  1993-11       Impact factor: 7.640

8.  Intensification of chemotherapy for the treatment of solid tumours: feasibility of a 3-fold increase in dose intensity with peripheral blood progenitor cells and granulocyte colony-stimulating factor.

Authors:  S Leyvraz; N Ketterer; L Perey; J Bauer; P Vuichard; J P Grob; P Schneider; V von Fliedner; F Lejeune; F Bachmann
Journal:  Br J Cancer       Date:  1995-07       Impact factor: 7.640

  8 in total

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