Computed tomography response, but not positron emission tomography scan response, predicts survival after neoadjuvant chemotherapy for resectable non-small-cell lung cancer

被引:54
作者
Tanvetyanon, Tawee [1 ]
Eikman, Edward A. [1 ]
Sommers, Eric [1 ]
Robinson, Lary [1 ]
Boulware, David [1 ]
Bepler, Gerold [1 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Div Thorac Oncol, Tampa, FL USA
关键词
D O I
10.1200/JCO.2008.16.9383
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Tumor response is considered a surrogate marker of survival. We investigated whether tumor response based on computed tomography (CT) scan or whole-body [F-18] fluorodeoxyglucose positron emission tomography (PET) scan after neoadjuvant chemotherapy for resectable non-small-cell lung cancer (NSCLC) is prognostic of survival. Patients and Methods Two consecutive phase II clinical trials were jointly analyzed. Patients underwent CT and PET scans before and after completion of neoadjuvant chemotherapy, followed by surgery. Results Eighty-nine patients were included. Patients with a partial or complete response based on Response Evaluation Criteria in Solid Tumors categories (n = 33) had a better overall survival than those with stable or progressive disease (n = 56; median survival time, not reached v 36 months, respectively; P = .04). Of all patients, those with response in the highest quartile had 1-and 2-year survival rates of 100% and 81%, respectively, compared with 77% and 61%, respectively, among patients in the lowest quartile. However, on the basis of visual analysis of PET scan, patients with a metabolic response (n = 28) had no significant difference in survival compared with patients without response (n = 61; median survival time, 35.6 months v not reached, respectively; P = .94). In addition, on the basis of a semiquantitative analysis of PET scan, using at least 30% reduction in tumor metabolism as a response (n = 59), we also found no significant difference in survival among those with or without response. Conclusion Among patients with resectable NSCLC treated with neoadjuvant chemotherapy, we found no evidence that tumor response by PET scan after chemotherapy is prognostic of survival; however, response by CT scan was associated with better survival.
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页码:4610 / 4616
页数:7
相关论文
共 24 条
  • [1] An initial experience with FDG-PET in the imaging of residual disease after induction therapy for lung cancer
    Akhurst, T
    Downey, RJ
    Ginsberg, MS
    Gonen, M
    Bains, M
    Korst, R
    Ginsberg, RJ
    Rusch, VW
    Larson, SM
    [J]. ANNALS OF THORACIC SURGERY, 2002, 73 (01) : 259 - 264
  • [2] BEPLER G, J THORAC ON IN PRESS
  • [3] Relation between tumour response to first-line chemotherapy and survival in advanced colorectal cancer: a meta-analysis
    Buyse, M
    Thirion, P
    Carlson, RW
    Burzykowski, T
    Molenberghs, G
    Piedbois, P
    [J]. LANCET, 2000, 356 (9227) : 373 - 378
  • [4] Repeat FDG-PET after neoadjuvant therapy is a predictor of pathologic response in patients with non-small cell lung cancer
    Cerfolio, RJ
    Bryant, AS
    Winokur, TS
    Ohja, B
    Bartolucci, AA
    [J]. ANNALS OF THORACIC SURGERY, 2004, 78 (06) : 1903 - 1909
  • [5] Chemotherapy response evaluation with 18F-FDG PET in patients with non-small cell lung cancer
    de Geus-Oei, Lioe-Fee
    van der Heijden, Henricus F. M.
    Visser, Eric P.
    Hermsen, Rick
    van Hoorn, Bas A.
    Timmer-Bonte, Johanna N. H.
    Willemsen, Antoon T.
    Pruim, Jan
    Corstens, Frans H. M.
    Krabbe, Paul F. M.
    Oyen, Wim J. G.
    [J]. JOURNAL OF NUCLEAR MEDICINE, 2007, 48 (10) : 1592 - 1598
  • [6] Preoperative chemotherapy followed by surgery compared with primary surgery in resectable stage I (except T1N0), II, and IIIa non-small-cell lung cancer
    Depierre, A
    Milleron, B
    Moro-Sibilot, D
    Chevret, S
    Quoix, E
    Lebeau, B
    Braun, D
    Breton, JL
    Lemarié, E
    Gouva, S
    Paillot, N
    Bréchot, JM
    Janicot, H
    Lebas, FX
    Terrioux, P
    Clavier, J
    Foucher, P
    Monchâtre, M
    Coëtmeur, D
    Level, MC
    Leclerc, P
    Blanchon, F
    Rodier, JM
    Thiberville, L
    Villeneuve, A
    Westeel, V
    Chastang, C
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (01) : 247 - 253
  • [7] 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
  • [8] Repeat 18F-FDG PET for monitoring neoadjuvant chemotherapy in patients with stage III non-small cell lung cancer
    Eschmann, S. M.
    Friedel, G.
    Paulsen, F.
    Reimold, M.
    Hehr, T.
    Budach, W.
    Dittmann, H.
    Langen, H. -J.
    Bares, R.
    [J]. LUNG CANCER, 2007, 55 (02) : 165 - 171
  • [9] GILLIGAN D, PREOPERATIVE CHEMOTH
  • [10] A problem in diagnosing N3 disease using FDG-PET in patients with lung cancer - High false positive rate with visual assessment
    Hara, M
    Shiraki, N
    Itoh, M
    Shibamoto, Y
    Iida, A
    Nishio, M
    Tamaki, T
    [J]. ANNALS OF NUCLEAR MEDICINE, 2004, 18 (06) : 483 - 488