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Virtual Journal Club

Volume 3, Number 1 – January, 2004

The following articles appeared in this month's issues of the surveyed journals. Articles that seem to be of most interest to the practicing gynecologic oncologist are included. The journals that are surveyed are New England Journal of Medicine, Journal of Clinical Oncology, Gynecologic Oncology, Cancer, American Journal of Obstetrics and Gynecology, Lancet, Cancer Research, Obstetrics and Gynecology, Journal of the National Cancer Institute, Journal of the American Medical Association and American Journal of Surgical Pathology. The participants in this program are the active clinical fellows at Memorial Hospital: Mario Leitao, Christopher Awtrey, Sarah Ferguson, Alan Schlaerth, Destin Black and Margrit Juretzka. The managing editor is Douglas Levine. Comments, questions, complaints and suggestions are always welcome, please E-mail us at: VJC@smgo.org or click here.  To subscribe or unsubscribe to the VJC, click here.

Gynecologic Oncology – Christopher Awtrey

Title: Phase II trial of alternating courses of megestrol acetate and tamoxifen in advanced endometrial carcinoma: a Gynecologic Oncology Group study

Authors: James V. Fiorica, Virginia L. Brunetto, Parviz Hanjani, Samuel S. Lentz, Robert Mannel and Willie Andersen

Source: Gynecologic Oncology, Volume 92, Issue 1, January 2004, Pages 10-14

Summary:  This is one of two articles in this month’s Gynecologic Oncology that looks at the clinical value of adding tamoxifen to progestins in the treatment of advanced or recurrent endometrial cancer. This article describes GOG # 153 in which megestrol acetate (MA) 80 mg given BID for 3 weeks was alternated with tamoxifen (T) citrate 20 mg PO BID for 3 weeks. This sequence was given until disease progression or until adverse effects prohibited further therapy. Of 56 evaluable patients who had not received prior cytotoxic or hormonal therapy, there were 15 responses for a response rate of 27%. There were 12 CR’s and 3 PR’s. Responses were seen in 31% of patients with extra-pelvic disease as opposed to 14% for those with vaginal or pelvic disease only. The median PFS was 2.7 months for the group and the most serious adverse effect noted were thromboembolic events. There were 2 DVT’s and 3 PE's. The authors conclude that this regimen of alternating MA and T is active in treating endometrial cancer and may result in a prolonged CR in some patients.

Click here for abstract from Gynecologic Oncology

Title: Phase II study of medroxyprogesterone acetate plus tamoxifen in advanced endometrial carcinoma: a Gynecologic Oncology Group study

Authors: Charles W. Whitney, Virginia L. Brunetto, Richard J. Zaino, Samuel S. Lentz, Joel Sorosky, Deborah K. Armstrong and Roger B. Lee

Source: Gynecologic Oncology, Volume 92, Issue 1, January 2004, Pages 4-9

Summary:  This paper examines the use of the combination of progestin and tamoxifen in the treatment of patients with advanced or recurrent endometrial cancer. This study is GOG # 119 and patients received a 20 mg BID of tamoxifen given continuously. On alternating even numbered weeks they also received 100 mg PO BID of MPA.  In this study of 58 evaluable patients medication was administered until disease progression or an adverse event. There were 6 complete and 13 partial responses for a total response rate of 33%. The median PFS was 3 months and the median overall survival was 13 months. This response rate is similar to that seen for active single agent cytotoxic chemotherapy suggesting that this treatment should be studied further as these initial results are promising.

Click here for abstract from Gynecologic Oncology

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Journal of Clinical Oncology - Mario Leitao

Nothing of interest this month

Journal of the National Cancer Institute – Alan Schlaerth

[Ed note:  There were two articles in the January 7, 2004 issue of JNCI that investigated the risk of colorectal cancer in Jewish BRCA mutations carriers. Both studies were unable to demonstrate any increased risk of colorectal cancer associated with BRCA founder mutations.  This is noteworthy information when counseling BRCA heterozygotes for prophylactic oophorectomy and other related issues.  Links to these abstracts can be found here: article 1 and article 2.]

Title: Risk of Malignant Mixed Mullerian Tumors After Tamoxifen Therapy for Breast Cancer

Authors: Rochelle E. Curtis, D. Michal Freedman, Mark E. Sherman, and Joseph F. Fraumeni, Jr

Source: J Natl Cancer Inst 2004; 96: 70-74

Summary:  Recent studies have indicated that the tamoxifen-related risk of uterine corpus cancer may be especially high for some uncommon cell types. Data from 39 451 breast cancer patients diagnosed from 1980 through 2000 who were initially treated with tamoxifen were evaluated and found that the overall risk of subsequent uterine corpus cancer was increased more than twofold (observed-to-expected ratio [O/E] = 2.17, 95% confidence interval [CI] = 1.95 to 2.41) relative to the general SEER population. The relative risk was substantially higher for malignant mixed mullerian tumors (MMMTs) (O/E = 4.62, O = 34, 95% CI = 3.20 to 6.46) than for endometrial adenocarcinomas (O/E = 2.07, O = 306, 95% CI = 1.85 to 2.32), although the excess absolute risk was smaller—an additional 1.4 versus 8.4 cancers per 10 000 women per year, respectively. Among those who survived for 5 years or longer, there was an eightfold relative risk for MMMTs and a 2.3-fold risk for endometrial adenocarcinomas, with patients developing MMMTs having a worse prognosis. These findings indicate that tamoxifen may have delayed effects, such as the increased risk of MMMTs, rare but aggressive tumors of unclear pathogenesis.

Click here for abstract from JNCI

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Obstetrics and Gynecology – Margrit Juretzka

Nothing of interest this month

American Journal of Obstetrics and Gynecology – Sarah Ferguson

Title: Glassy cell adenocarcinoma of the uterine cervix

Authors: Michael P. Hopkins and George W. Morley

Source: American Journal of Obstetrics and Gynecology, Volume 190, Issue 1, January 2004, Pages 67-70

Summary:  Due to the controversy over whether glassy cell adenocarcinoma has a worse outcome then other variants of cervical adenocarcinoma, the authors report a case series of 21 women with glassy cell adenocarcinoma of the cervix treated at a single institution from 1970 to 1985. The mean age of diagnosis was44 years (range 12-69. The patients were distributed by stage as follows: stage I = 10; stage II = 8; stage III = 1; and stage IV = 2.  The cumulative 5 years survival for all stage I glassy cell adenocarcinomas was not significantly different when compared with stage I non-glassy cell adenocarcinomas (61% vs 48%). In comparisons to previously published series this is a similar survival excluding the original report by Glucksman and Cherry (1956) which did not specify stage.  The authors conclude that stage I glassy cell adenocarcinoma of the cervix has a 5-year overall survival approaching 60%, which is similar to other subtypes of cervical adenocarcinoma. Unfortunately, advanced stage disease has a uniformly poor prognosis.

Click here for abstract from Am J Ob/Gyn

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New England Journal of Medicine – Mario Leitao

Nothing of interest this month

Journal of the American Medical Association – Margrit Juretzka

Nothing of interest this month

Cancer – Destin Black

Title:  Surgical treatment of recurrent endometrial carcinoma

Authors:  Elio Campagnutta, M.D., Giorgio Giorda, M.D., Giovanni De Piero, M.D., Francesco Sopracordevole, M.D., M. Caterina Visentin, M.D., Luca Martella, M.D., Carlo Scarabelli, M.D.

Source: Cancer, Volume 100, Issue 1, Pages 89-96

Summary:  This retrospective analysis included 75 patients who underwent secondary cytoreductive surgery for pelvic or abdominal endometrial cancer recurrence.  Inclusion criteria were as follows: 1) pelvic or abdominal recurrence with or without liver, abdominal wall, inguinal, or vulvar involvement; 2) central pelvic-vaginal recurrence measuring > 4 cm or with lateral pelvic side-wall extension; 3) Gynecologic Oncology Group performance status < 4; and 4) absence of lung, bone, or brain metastases.  Patients with < 1cm residual tumor were classified as optimally debulked.  Postoperative salvage therapy after secondary surgery was undertaken at the discretion of the medical oncologist.  Fifty-six patients (74.7%) were optimally debulked and the mortality rate for surgical complications after the postoperative period was 8%.   Patients who were secondarily optimally debulked had a significantly better cumulative survival than patients who had residual disease (36% vs. 0% at 60 months P<0.05).  In addition to residual disease, the authors found that chemotherapy use after secondary surgery and central pelvis-vagina as the only site of recurrence were also associated with better survival. The authors conclude that this approach has a high mortality rate, yet can useful in improving overall survival.  Careful selection of patients is key.

Click here for abstract from Cancer

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Lancet – Sarah Ferguson

Nothing of interest this month

Cancer Research – Destin Black

Nothing of interest this month

American Journal of Surgical Pathology Alan Schlaerth

Nothing of interest this month

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