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E u r o p e a n C o n g r e s s o n

Vaccines & Vaccination

and Gynecologic Oncology

Vaccines & Vaccination and Gynecologic Oncology 2018

O c t o b e r 2 6 - 2 7 , 2 0 1 8

B u d a p e s t , H u n g a r y

Critical Care Obstetrics and Gynecology

ISSN: 2471-9803

Objective:

A Randomized phase III trial was conducted to determine if neoadjuvant chemotherapy (NACT) prior to radical hysterectomy

and pelvic/para-aortic lymphadenectomy (RHPPL) could improve progression-free survival (PFS) and overall survival (OS), as well as

operability, with acceptable levels of toxicity. Adjuvant radiation therapy was prescribed for specific surgical/pathological risk factors

for both regimens.

Methods:

Eligible patients were required to have bulky FIGO stage IB cervical cancer, tumor diameter ≥4 cm, adequate bone marrow,

renal and hepatic function, and performance status ≤2. Prospective random allocation was to either NACT (vincristine-cisplatin chemo-

therapy every 10 days for 3 cycles) before exploratory laparotomy and planned RHPPL (NACT+RHPPL), or RHPPL only.

Results:

The study was closed prematurely, because of slow accrual, after 291 patients were enrolled, three were ineligible; thus 288

were eligible and randomly allocated to RHPPL (N=143) or NACT+RHPPL (N=145). There were no notable differences between regi-

mens regarding patients’ age, race, performance status, or tumour size. The median follow-up time is 62months among living patients.

The NACT+RHPPL group had very similar recurrence rates (relative risk: 0.998) and death rates (relative risk: 1.008) when compared to

the RHPPL group. There were 79% that had surgery in the RHPPL group compared to 78% in the NACT RHPPL group. There were 52%

who received post-operative RT in the RHPPL group compared to 45% in the NACT+RHPPL group (not statistically significant).

Conclusion:

There is no evidence from this trial that NACT offered any additional objective benefit to patients undergoing RHPPL for

suboptimal stage IB cervical cancer

.

zalousta217@gmail.com

Treatment of (“bulky”) stage IB cervical cancer with

or without neoadjuvant vincristine and cisplatin

prior to radical hysterectomy and pelvic/para-aortic

lymphadenectomy: A phase III trial of the gynaecologic

oncology group

Zeyad Esmael Alousta

Misurata medical centre, Libiya

Crit Care Obst & Gyne 2018, Volume: 4

DOI:10.21767/2471-9803-C1-003