Literature DB >> 9020492

Tumour marker concentration at the start of chemotherapy is a stronger predictor of treatment failure than marker half-life: a study in patients with disseminated non-seminomatous testicular cancer.

R de Wit1, R Sylvester, C Tsitsa, P H de Mulder, D T Sleyfer, W W ten Bokkel Huinink, S B Kaye, A T van Oosterom, E Boven, K Vermeylen, G Stoter.   

Abstract

We investigated the prognostic value of the serum half-life of human chorionic gonadotrophin (HCG) and alpha-fetoprotein (AFP) during induction chemotherapy and the relative prognostic importance of initial marker concentrations and marker half-life. Marker half-lives were calculated using two abnormal values observed between day 8 and day 22 of the first chemotherapy cycle. Moreover, analyses were carried out using day 43 as the second measurement point. Treatment failure at any time was chosen as the end point. The relative prognostic influence of marker half-lives and initial marker concentrations was tested in univariate and multivariate analyses. Half-lives were considered to be prolonged if > 3 days for HCG and > 6 days for AFP. In addition, we separated patients into those with half-lives > 6 days for HCG and those with half-lives > 10 days for AFP to examine whether these long half-lives were associated with a poor prognosis. A group of 669 patients treated with cisplatin combination chemotherapy was studied. Forty-two per cent of the patients had normal HCG and 37% had normal AFP at the start of chemotherapy. At day 22, HCG was still elevated in 138 patients and AFP in 211. At day 43, the numbers of these patients were 35 and 80 respectively. Based on the measurements obtained on day 8 and day 22, a half-life of HCG > 3 days or > 6 days and/or a half-life AFP > 6 days or > 10 days did not accurately predict treatment failure (P=0.413 and P=0.851, respectively; values obtained using tests for trend). However, initial marker concentrations of HCG and/or AFP > 1000 IU l(-1) were highly significant prognosticators for treatment failure (P=0.001 and P < 0.001 respectively), independent of half-life values. Half-lives calculated with the values obtained on day 43 did not contribute to the accuracy of the prediction of treatment failure. We conclude that half-lives of HCG and AFP during induction chemotherapy are inaccurate parameters for the prediction of treatment failure. In contrast, initial serum concentrations of HCG and AFP are highly significant in the prediction of unfavourable treatment outcome.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9020492      PMCID: PMC2063372          DOI: 10.1038/bjc.1997.71

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  17 in total

1.  Serum tumor marker half-life during chemotherapy allows early prediction of complete response and survival in nonseminomatous germ cell tumors.

Authors:  G C Toner; N L Geller; C Tan; J Nisselbaum; G J Bosl
Journal:  Cancer Res       Date:  1990-09-15       Impact factor: 12.701

2.  Prognostic factors in unselected patients with nonseminomatous metastatic testicular cancer: a multicenter experience.

Authors:  N Aass; O Klepp; E Cavallin-Stahl; O Dahl; H Wicklund; B Unsgaard; L Baldetorp; S Ahlström; S D Fosså
Journal:  J Clin Oncol       Date:  1991-05       Impact factor: 44.544

3.  Multivariate analysis of prognostic variables in patients with metastatic testicular cancer.

Authors:  G J Bosl; N L Geller; C Cirrincione; N J Vogelzang; B J Kennedy; W F Whitmore; D Vugrin; H Scher; J Nisselbaum; R B Golbey
Journal:  Cancer Res       Date:  1983-07       Impact factor: 12.701

4.  Phase II trial of high-dose carboplatin and etoposide with autologous bone marrow transplantation in first-line therapy for patients with poor-risk germ cell tumors.

Authors:  R J Motzer; M Mazumdar; S C Gulati; D F Bajorin; P Lyn; V Vlamis; G J Bosl
Journal:  J Natl Cancer Inst       Date:  1993-11-17       Impact factor: 13.506

5.  Prognostic factors for favorable outcome in disseminated germ cell tumors.

Authors:  R Birch; S Williams; A Cone; L Einhorn; P Roark; S Turner; F A Greco
Journal:  J Clin Oncol       Date:  1986-03       Impact factor: 44.544

6.  The Second Medical Research Council study of prognostic factors in nonseminomatous germ cell tumors. Medical Research Council Testicular Tumour Working Party.

Authors:  G M Mead; S P Stenning; M C Parkinson; A Horwich; S D Fossa; P M Wilkinson; S B Kaye; E S Newlands; P A Cook
Journal:  J Clin Oncol       Date:  1992-01       Impact factor: 44.544

7.  Acute changes of alpha-fetoprotein and human chorionic gonadotropin during induction chemotherapy of germ cell tumors.

Authors:  N J Vogelzang; P H Lange; A Goldman; R H Vessela; E E Fraley; B J Kennedy
Journal:  Cancer Res       Date:  1982-11       Impact factor: 12.701

8.  Multivariate analysis of prognostic factors in patients with disseminated nonseminomatous testicular cancer: results from a European Organization for Research on Treatment of Cancer Multiinstitutional Phase III Study.

Authors:  G Stoter; R Sylvester; D T Sleijfer; W W ten Bokkel Huinink; S B Kaye; W G Jones; A T van Oosterom; C P Vendrik; P Spaander; M de Pauw
Journal:  Cancer Res       Date:  1987-05-15       Impact factor: 12.701

9.  Prognostic significance of early serum tumor marker half-life in metastatic testicular teratoma.

Authors:  M J Stevens; A R Norman; D P Dearnaley; A Horwich
Journal:  J Clin Oncol       Date:  1995-01       Impact factor: 44.544

10.  Four cycles of BEP versus an alternating regime of PVB and BEP in patients with poor-prognosis metastatic testicular non-seminoma; a randomised study of the EORTC Genitourinary Tract Cancer Cooperative Group.

Authors:  R de Wit; G Stoter; D T Sleijfer; S B Kaye; P H de Mulder; W W ten Bokkel Huinink; P J Spaander; M de Pauw; R Sylvester
Journal:  Br J Cancer       Date:  1995-06       Impact factor: 7.640

View more
  4 in total

1.  Canadian consensus guidelines for the management of testicular germ cell cancer.

Authors:  Lori Wood; Christian Kollmannsberger; Michael Jewett; Peter Chung; Sebastian Hotte; Martin O'Malley; Joan Sweet; Lynn Anson-Cartwright; Eric Winquist; Scott North; Scott Tyldesley; Jeremy Sturgeon; Mary Gospodarowicz; Roanne Segal; Tina Cheng; Peter Venner; Malcolm Moore; Peter Albers; Robert Huddart; Craig Nichols; Padraig Warde
Journal:  Can Urol Assoc J       Date:  2010-04       Impact factor: 1.862

2.  Logarithmic decrease of serum alpha-fetoprotein or human chorionic gonadotropin in response to chemotherapy can distinguish a subgroup with better prognosis among highly malignant intracranial non-germinomatous germ cell tumors.

Authors:  Tomohiro Kawaguchi; Toshihiro Kumabe; Masayuki Kanamori; Ryuta Saito; Yoji Yamashita; Yukihiko Sonoda; Mika Watanabe; Teiji Tominaga
Journal:  J Neurooncol       Date:  2011-02-26       Impact factor: 4.130

3.  Early prediction of treatment response to high-dose salvage chemotherapy in patients with relapsed germ cell cancer using [(18)F]FDG PET.

Authors:  C Bokemeyer; C Kollmannsberger; K Oechsle; B M Dohmen; A Pfannenberg; C D Claussen; R Bares; L Kanz
Journal:  Br J Cancer       Date:  2002-02-12       Impact factor: 7.640

4.  125I-labelled human chorionic gonadotrophin (hCG) as an elimination marker in the evaluation of hCG decline during chemotherapy in patients with testicular cancer.

Authors:  T B Christensen; F Engbaek; J Marqversen; S I Nielsen; C Kamby; H von der Maase
Journal:  Br J Cancer       Date:  1999-07       Impact factor: 7.640

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.