Modified RECIST criteria for assessment of response in malignant pleural mesothelioma

被引:506
作者
Byrne, MJ [1 ]
Nowak, AK
机构
[1] Sir Charles Gairdner Hosp, Dept Med Oncol, Nedlands, WA 6009, Australia
[2] Univ Western Australia, Dept Med, Nedlands, WA 6009, Australia
关键词
chemotherapy; clinical trials; mesothelioma; RECIST; response criteria; validation;
D O I
10.1093/annonc/mdh059
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The growth pattern of malignant pleural mesothelioma makes the use of RECIST (response evaluation criteria in solid tumours) response criteria difficult. We have developed and validated Modified RECIST criteria adapted to the growth pattern of malignant pleural mesothelioma. Patients and methods: We evaluated 73 patients from two clinical trials of cisplatin/gemcitabine chemotherapy in malignant pleural mesothelioma. Tumour thickness perpendicular to the chest wall or mediastinum was measured in two positions at three separate levels on thoracic CT scans. The sum of the six measurements defined a pleural unidimensional measure. Bidimensionally measureable lesions were measured unidimensionally as for RECIST. All measurements were added to obtain the total turnout measurement. A reduction of at least 30% on two occasions 4 weeks apart defined a partial response; an increase of 20% over the nadir measurement, progressive disease. The validity of the modified criteria was gauged by evaluating survival and pulmonary function. Results: Response according to these criteria predicted for superior survival (15.1 versus 8.9 months; P = 0.03) and forced vital capacity (FVC) increase during treatment (P <0.0001). A significant correlation between change in linear turnout measurement and FVC was seen (R = 0.63; P = 0.0001). Conclusion: These Modified RECIST criteria for turnout response correlate with survival and lung function and can be used to measure outcome in pleural mesothelioma.
引用
收藏
页码:257 / 260
页数:4
相关论文
共 8 条
  • [1] ARMATO SG, 2003, P AN M AM SOC CLIN, V22, P668
  • [2] Cisplatin and gemcitabine treatment for malignant mesothelioma: A phase II study
    Byrne, MJ
    Davidson, JA
    Musk, AW
    Dewar, J
    van Hazel, G
    Buck, M
    de Klerk, NH
    Robinson, BWS
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (01) : 25 - 30
  • [3] Interobserver and intraobserver variability in measurement of non-small-cell carcinoma lung lesions: Implications for assessment of tumor response
    Erasmus, JJ
    Gladish, GW
    Broemeling, L
    Sabloff, BS
    Truong, MT
    Herbst, RS
    Munden, RF
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (13) : 2574 - 2582
  • [4] MILLER AB, 1981, CANCER, V47, P207, DOI 10.1002/1097-0142(19810101)47:1<207::AID-CNCR2820470134>3.0.CO
  • [5] 2-6
  • [6] A multicentre phase II study of cisplatin and gemcitabine for malignant mesothelioma
    Nowak, AK
    Byrne, MJ
    Williamson, R
    Ryan, G
    Segal, A
    Fielding, D
    Mitchell, P
    Musk, AW
    Robinson, BWS
    [J]. BRITISH JOURNAL OF CANCER, 2002, 87 (05) : 491 - 496
  • [7] Therasse P, 2000, J NATL CANCER I, V92, P205, DOI 10.1093/jnci/92.3.205
  • [8] VANKLAVEREN RJ, 2002, P AN M AM SOC CLIN, V21, pA310