Randomised study of systematic lymphadenectomy in patients with epithelial ovarian cancer macroscopically confined to the pelvis

A Maggioni, P Benedetti Panici, T Dell'Anna, F Landoni, A Lissoni, A Pellegrino, R S Rossi, S Chiari, E Campagnutta, S Greggi, R Angioli, N Manci, M Calcagno, G Scambia, R Fossati, I Floriani, V Torri, R Grassi, C Mangioni, A Maggioni, P Benedetti Panici, T Dell'Anna, F Landoni, A Lissoni, A Pellegrino, R S Rossi, S Chiari, E Campagnutta, S Greggi, R Angioli, N Manci, M Calcagno, G Scambia, R Fossati, I Floriani, V Torri, R Grassi, C Mangioni

Abstract

No randomised trials have addressed the value of systematic aortic and pelvic lymphadenectomy (SL) in ovarian cancer macroscopically confined to the pelvis. This study was conducted to investigate the role of SL compared with lymph nodes sampling (CONTROL) in the management of early stage ovarian cancer. A total of 268 eligible patients with macroscopically intrapelvic ovarian carcinoma were randomised to SL (N=138) or CONTROL (N=130). The primary objective was to compare the proportion of patients with retroperitoneal nodal involvement between the two groups. Median operating time was longer and more patients required blood transfusions in the SL arm than the CONTROL arm (240 vs 150 min, P<0.001, and 36 vs 22%, P=0.012, respectively). More patients in the SL group had positive nodes at histologic examination than patients on CONTROL (9 vs 22%, P=0.007). Postoperative chemotherapy was delivered in 66% and 51% of patients with negative nodes on CONTROL and SL, respectively (P=0.03). At a median follow-up of 87.8 months, the adjusted risks for progression (hazard ratio [HR]=0.72, 95%CI=0.46-1.21, P=0.16) and death (HR=0.85, 95%CI=0.49-1.47, P=0.56) were lower, but not statistically significant, in the SL than the CONTROL arm. Five-year progression-free survival was 71.3 and 78.3% (difference=7.0%, 95% CI=-3.4-14.3%) and 5-year overall survival was 81.3 and 84.2% (difference=2.9%, 95% CI=-7.0-9.2%) respectively for CONTROL and SL. SL detects a higher proportion of patients with metastatic lymph nodes. This trial may have lacked power to exclude clinically important effects of SL on progression free and overall survival.

Figures

Figure 1
Figure 1
CONSORT trial flow diagram for patients with early stage ovarian cancer who were accrued into the trial.
Figure 2
Figure 2
Overall survival (OS) for patients with optimally debulked early ovarian carcinoma undergoing systematic aortic and pelvic lymphadenectomy (Lymphad.) vs lymph nodes sampling only (No lymphad). Five-year overall survival was 81.6 and 84.0% (difference=2.4%, 95% CI=−8.3 to 8.9%) respectively for lymph nodes sampling only and lymphadenectomy.
Figure 3
Figure 3
Progression-free survival (PFS) for patients with optimally debulked early ovarian carcinoma undergoing systematic aortic and pelvic lymphadenectomy (Lymphad.) vs lymph nodes sampling only (No lymphad.). Five-year progression-free survival was 73.4 and 78.3% (difference=4.9%, 95% CI=−5.9 to 12.5%) respectively, for lymph nodes sampling only and lymphadenectomy.

References

    1. Baiocchi G, Grosso G, Di Re E, Fontanelli R, Raspagliesi F, Di Re F (1998) Systematic pelvic and paraaortic lymphadenectomy at second look laparotomy for ovarian cancer. Gynecol Oncol 69: 151–156
    1. Benedetti Panici P, Greggi S, Maneschi F, Scambia G, Amoroso M, Rabitti C, Mancuso S (1993) Anatomical and pathological study of retroperitoneal nodes in epithelial ovarian cancer. Gynecol Oncol 51: 150–154
    1. Benedetti Panici P, Maggioni A, Hacker N, Landoni F, Ackermann S, Campagnutta E, Tamussino K, Winter R, Pellegrino A, Greggi S, Angioli R, Manci N, Scambia G, Dell'Anna T, Fossati R, Floriani I, Rossi RS, Grassi R, Favalli G, Raspagliesi F, Giannarelli D, Martella L, Mangioni C. (2005) Systematic aortic and pelvic lymphadenectomy vs resection of bulky nodes only in optimally debulked advanced ovarian cancer: a randomised clinical trial. J Natl Cancer Inst 97: 560–566
    1. Burghadt E, Girardi F, Lahousen M, Tamussino K (1991) Patterns of pelvic and paraaortic lymph node involvement in ovarian cancer. Gynecol Oncol 40: 103–106
    1. Carnino F, Fuda G, Ciccone G, Iskra L, Guercio E, Dadone D, Conte PF (1997) Significance of lymph nodes sampling in epithelial carcinoma of the ovary. Gynecol Oncol 65: 467–472
    1. Chen SS, Lee L (1983) Incidence of para-aortic and pelvic lymph-node metastases in epithelial carcinoma of the ovary. Gynecol Oncol 16: 95–100
    1. Di Re F, Baiocchi G (2000) Value of lymph node assessment in ovarian cancer: status of the art at the end of second millenium. Int J Gynecol Cancer 10: 435–442
    1. Di Re F, Fontanelli R, Raspagliesi F, Di Re E (1989) Pelvic and paraaortic lymphadenectomy in cancer of the ovary. Bailliere's Clin Obstet Gynaecol 13: 131–142
    1. FIGO Committee on Gynecologic Oncology (2000) FIGO staging classifications and clinical practice guidelines in the management of gynecologic cancers. Int J Gynaecol Obstet 70: 209–262
    1. International Collaborative Ovarian Neoplasm (ICON1) Collaborators (2003) International collaborative Ovarian Neoplasm Trial 1: a randomised trial of adjuvant chemotherapy in women with early-stage ovarian cancer. J Natl Cancer Inst 95: 125–132
    1. Jemal A, Murray T, Ward E, Samuels A, Tiwari RC, Ghafoor A, Feuer EJ, Thun MJ (2005) Cancer statistics, 2005. CA Cancer J Clin 55: 10–30
    1. Kaplan EL, Meier P (1958) Nonparametric estimation from incomplete observations. J Am Stat Assoc 53: 457–481
    1. Lanza A, D'Addato F, Valli M, Bussone R, Caldarola B, Re A, Olivero F, Ferraris G (1988) Pelvic and para-aortic lymph nodal positivity in the ovarian carcinoma. Its prognostic significance. Eur J Gynaecol Oncol 1: 36–39
    1. Liotta LA, Kohn EC, Petricoin EF (2001) Clinical proteomics: personalized molecular medicine. JAMA 286: 2211–2214
    1. Musumeci R, Banfi A, Bolis G, Candiani GB, De Palo G, Di Re F, Lucina L, Lattuada A, Mangioni C, Mattioli G, Natale N (1977) Lymphangiography in patients with ovarian epithelial cancer. Cancer 40: 1444–1449
    1. Parkin DM, Laara E, Muir CS (1988) Estimates of the worldwide frequency of sixteen major cancers in 1980. Int J Cancer 41: 184–197
    1. Parmar MKB, Machin D (1995) Survival analysis: a practical approach. Chichester: John Wiley
    1. Piver S, Barlow J, Lele S (1978) Incidence of subclinical metastasis in stage I and II ovarian carcinoma. Obstet Gynecol 52: 100–104
    1. Skates SJ, Menon U, MacDonald N, Rosenthal AN, Oram DH, Knapp RC, Jacobs IJ (2003) Calculation of the risk of ovarian cancer from serial CA –125 values for preclinical detection in postmenopausal women. J Clin Oncol 21(suppl): 206s–210s
    1. Trimbos JB, Vergote I, Bolis G, Vermorken JB, Mangioni C, Madronal C, Franchi M, Tateo S, Zanetta G, Scarfone G, Giurgea L, Timmers P, Coens C, Pecorelli S; EORTC-ACTION collaborators (2003) European Organisation for Research and Treatment of Cancer-Adjuvant ChemoTherapy in Ovarian Neoplasm. Impact of adjuvant chemotherapy and surgical staging in early-stage ovarian carcinoma: European Organisation for Research and Treatment of Cancer-Adjuvant ChemoTherapy in Ovarian Neoplasm trial. J Natl Cancer Inst 95: 113–125
    1. Tsuruchi N, Kamura T, Tsukamoto N, Akazawa K, Saito T, Kaku T, To N, Nakano H (1993) Relationship between paraaortic lymph node involvement and intraperitoneal spread in patients with ovarian cancer-a multivariate analysis. Gynecol Oncol 49: 51–55

Source: PubMed

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