Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Identification of chemotherapeutic refractory cases based on human chorionic gonadotropin values among patients with low-risk persistent trophoblastic disease treated with 8-day methotrexate-folinic acid
1Department of Obstetrics and Gynecology, Graduate School of Medical Sciences, Japan
2Department of Medical Information Science, Kyushu University Hospital, Fukuoka, Japan
*Corresponding Author(s): T. Shigematsu E-mail:
Purpose: The aim of the present study was to establish the accurate cutoff points of post-treatment serum beta-hCG values in identifying chemotherapeutic refractory cases among patients with low-risk persistent trophoblastic disease (PTD) treated with 8-day methotrexate-folinic acid as the primary therapy.
Materials and methods: The values of serum beta-hCG measured before initiating treatment and weekly thereafter in 26 patients with low-risk PTD undergoing 8-day methotrexate-folinic acid treatment were analyzed. Thereafter, we determined the weekly cutoff points to identify the patient refractory for treatment by means of receiver-operating characteristic (ROC) plots analysis.
Results: The values of cutoff points in the pretreatment, the post-treatment 1st, 2nd, 3rd, and 4th week were 18.6, 15.0, 5.4, 3.4, and 2.0 ng/ml, respectively, and the value of accuracy during these weeks was appropriate (> 80%). When using the cutoff points of one and two weeks after initiating treatment, the accuracy in identifying chemotherapeutic refractory patients was 87.5% and 88.0%, respectively, with the highest values exceeding 85%. The sensitivity and specificity at one week were 92.9 and 80.0%, respectively. Similarly, the sensitivity and specificity at two weeks were 93.3 and 80.0%, respectively.
Conclusion: These results suggest that the cutoff points of one and two weeks after initiating treatment are useful in identifying chemotherapeutic refractory patients among low-risk PTD patients, receiving 8-day methotrexate-folinic acid treatment.
Persistent Trophoblastic disease; Low-risk PTD; Methotrexate; Human Chorionic Gonadotropin
T. Shigematsu,T. Hirakawa,H. Yahata,T. Sonoda,N. Kinukawa,H. Nakano. Identification of chemotherapeutic refractory cases based on human chorionic gonadotropin values among patients with low-risk persistent trophoblastic disease treated with 8-day methotrexate-folinic acid. European Journal of Gynaecological Oncology. 2003. 24(2);113-116.
[1] Matsui H., Iitsuka Y., Seki K., Sekiya S.: "Comparison of chemotherapies with methotrexate,V P-16 and actinomycin-D in lowrisk gestational trophoblastic disease: remission rates and drug toxicities". Gynecol. Obstet. Invest., 1998, 46, 5.
[2] Roberts J.P.,L urain J. R.: "Treatment of low-risk metastatic gestational trophoblastic tumors with single-agent chemotherapy". Am. J. Obstet. Gynecol., 1996, 174, 1917.
[3] Hoffman M. S., Fiorica J. V., Gleeson N. C., Roberts W. S., Cavanagh D.: "A single institution experience with weekly intramuscuJar methotrexate for nonmetastatic gestational trophoblastic disease". Gynecol. Oneal., 1996, 60, 292.
[4] Soper J. T., Clarke-Pearson D. L., Berchuck A.. Rodriguez G., Hammond C.B.: "5-day methotrexate for women with metastatic gestational trophoblastic disease". Gynecol. Oneal., 1994, 54, 76
[5] Homesley H. D.: "Development of single-agent chemotherapy regimens for gestational disease". J. Reprod. Med., 1994, 39, 185.
[6] Gleeson N. C., Finan M.A., Fiorica J. V., Robert W. S., Hoffman M. S., Wilson J.: "Nonmetastatic gestational trophoblastic disease weekly methotrexate compared with 8-day methotrexate-folinic acid". Eur. J. Gynaecol. Oncol., I 993, 14, 461.
[7] Kohorn E. I.: "Single-agent chemotherapy for nonmetastatic gestational trophoblastic neoplasia: perspective for the 21st century after three decades of use". J. Reprod. Med., 1991, 36, 49.
[8] Homesley H. D., Blessing J. A., Schlaerth J., Rettenmaier M., Major F. J.: "Rapid escalation of weekly intramuscular methotrexate for nonmetastatic gestational trophoblastic disease: a gynecologic oncology group study", 1990, 39, 305.
[9] Barter J. F., Soong S. J., Hatch K. D., Orr J. W., Partridge E. C., Austion J. M. et al.: "Treatment of nonmetastatic gestational trophoblastic disease with sequential intramuscular and oral methotrexate". Gynecol. Oncol., 1989, 33, 82.
[10] Homesley H. D., Blessing J. A., Rettenmaier M., Capizzi R. L., Major F. J., Twiggs L. B.: "Weekly intramuscular methotrexate for nonmetastatic gestational trophoblastic disease". Ob stet. Gynecol., 1988, 72, 413.
[11] Rotmensh J., Rosenshein N. B., Block B. S.: "Comparison of human chorionic gonadotropin regression in molar pregnancies and post-molar nonmetastatic gestational trophoblastic neoplasia". Gynecol. Oneal., 1988, 29, 82.
[12] Bolis G., Colombo N., Epis A., Mangili G., Vassena L., Vergadoro F. et al.: "Methotrexate with citrovorum factor in low-risk gestational trophoblastic tumor". Tumori, 1987, 73, 309.
[13] Berkowitz R. S., Goldstein D. P., Bernstein M. R.: "Ten years'experience with methotrexate and folinic acid as primary therapy for gestational trophoblastic disease". Gynecol. Oncol., 1986, 23, 111.
[14] Berkowitz R. S., Goldstein D. P., Bernstein M. R.: "Methotrexate with citrovorum factor rescue as primary therapy for gestational trophoblastic disease". Cancer, 1982, 50, 2024.
[15] Berkowitz R. S., Goldstein D. P., Jones M. A., Marean A. R., Bernstein M. R.: "Methotrexate with citrovorum rescue: reduced chemotherapy toxicity in the management of gestational trophoblastic neoplasms". Cancer, 1980, 45, 423.
[16] Goldstein D. P., Saracco P. Osathanondh R., Goldstein P. R., Marean A. R., Bernstein M. R.: "Methotrexate with citrovorum factor rescue for gestational trophoblastic neoplasms". Obstet. Gynecol., 1978, 51, 93.
[17] Lewis J. L. Jr.: "Current status of treatment of gestational trophoblastic disease". Cancer, 1976, 38, 620.
[18] Kim S. J., Bae S. N., Kim J. H., Kim C. T., Han K. T., Lee J. M. et al.: "Effects of multiagent chemotherapy and independent risk factors in the treatment of high-risk GTT: 25 years experience of KRI-TRD". Int. J. Gynaecol. Obstet., 1998, 60, 85.
[19] Newlands E. S., Bagshawe K. D.: "Anti-tumor activity of the epipodophyllin derivative VP 16-213 (etoposide: NSC-141540) in gestational choriocarcinoma". Eur. J. Cancer, 1980, 16, 401.
[20] Elit L., Covens A., Osborne R., Gerulath A., Murphy J., Rosen B. et al.: "High-dose methotrexate for gestational trophoblastic disease". Gynecol. Oncol., 1994, 54, 282.
[21] Soper J. T., Evans A. C., Clarke-Pearson D. L., Berchuck A., Rodriguez G., Hammond C. B.: "Alternating weekly chemotherapy with etoposide-methotrexate-dactinomycin/cyclophosphamide-vincristine for high-risk gestational trophoblastic disease". Obstet. Gynecol., 1994, 83, 113.
[22) Schink J. C., Singh D. K., Rademaker A. W., Miller D. S., Lurain J. R.: "Etoposide, methotrexate, actinomycin D, cyclophosphamide, and vincristine for the treatment of metastatic, high-risk gestational trophoblastic disease". Obstet. Gynecol., 1992, 80, 817.
[23] Soper J. T., Clarke-Pearson D., Hammond C. B.: "Metastatic gestational trophoblastic disease: prognostic factors in previously untreated patients". Obstet. Gynecol., 1988, 71, 338.
[24] McDonald T. W., Ruffolo E. H.: "Modern management of gestational trophoblastic disease". Obstet. Gynecol. Surv., 1983, 38, 67.
[25] Lurain J. R., Brewer J. I., Torok E. E., Halpern B.: "Gestational trophoblastic disease: treatment results at the Brewer Trophoblastic Disease Center". Obstet. Gynecol., 1982, 60, 354.
[26] World Health Organization Scientific Group on Gestational trophoblastic diseases. Technical Report Series 692. World Health Organization, Geneva, 1983.
[27] Japan Society for Cancer Therapy: "Criteria for the evaluation of the clinical effects of solid cancer chemotherapy". J. Jpn. Soc. Cancer, 1986, 21, 929.
[28] Zweig M. H., Campbell G.: "Receiver-operating characteristic (ROC) plots: a fundamental evaluation tool in clinical medicine". Clin. Chem., 1993, 39, 561.
[29] Bagshawe K. D., Wilde C. E.: "Infusion therapy for pelvic trophoblastic tumors". J. Obstet. Gynecol. Br. Commnnw., 1964, 72, 565.
[30] Chen L. P., Cai S. M., F an J.X., Li Z. T.: "PEBA regimen (cisplatin, etoposide, bleomycin, and adriamycin) in the treatment of drug-resistant choriocarcinoma". Gynecol. Oneal., 1995, 56, 231.
[31] Garris P. D., Gallup D. G., Melton K.: "Long -term remission of previously resistant choriocarcinoma with a combination of etoposide, ifosfamide, and cisplatin". Gynecol. Oneal., 1995, 57, 254.
[32] Willemse P. H., Aalders J. G., Bouma J., Sleijfer D. T.: "Chemotherapy-resistant gestanonal tr9phoblastic neoplasia treated successfully with cisplatin, etoposide, and bleomycin". Obstet. Gynecol., 1988, 71, 438.
Top