Primary fallopian tube cancer (PFTC), often just tubal cancer, is a malignant neoplasm that originates from the fallopian tube.[1]

Signs and symptoms

The internal location of the fallopian tubes makes it difficult to reach an early diagnosis. Symptoms are nonspecific, and may consist of pain and vaginal discharge or bleeding. A pelvic mass may be detected on a routine gynecologic examination.

Vaginal discharge in fallopian tube carcinoma results from intermittent hydrosalphinx, also known as hydrops tubae profluens.[2]

Pathology

The most common cancer type within this disease is adenocarcinoma; in the largest series of 3,051 cases as reported by Stewart et al. 88% of cases fell into this category.[3] According to their study, half of the cases were poorly differentiated, 89% unilateral, and the distribution showed a third each with local disease only, with regional disease only, and with distant extensions. Rarer forms of tubal neoplasm include leiomyosarcoma, and transitional cell carcinoma.

As the tumor is often enmeshed with the adjacent ovary, it may be the pathologist and not the surgeon who determines that the lesion is indeed tubal in origin.

Secondary tubal cancer usually originates from cancer of the ovaries, the endometrium, the GI tract, the peritoneum, and the breast.

Diagnosis

A pelvic examination may detect an adnexal mass. A CA-125 blood test is a nonspecific test that tends to be elevated in patients with tubal cancer. More specific tests are a gynecologic ultrasound examination, a CT scan, or an MRI of the pelvis. Occasionally, an early fallopian tube cancer may be detected by chance during pelvic surgery.

Staging

International Federation of Gynecology and Obstetrics (FIGO) staging is done at the time of surgery:

Stage 0: Carcinoma in situ
Stage I: Growth limited to fallopian tubes
Stage II: Growth involving one or both fallopian tubes with extension to pelvis
Stage III: Tumor involving one or both fallopian tubes with spread outside pelvis
Stage IV: Growth involving one or more fallopian tubes with distant metastases

Treatment

The initial approach to tubal cancer is generally surgical, and similar to that of ovarian cancer. As the lesion will spread first to the adjacent uterus and ovary, a total abdominal hysterectomy is an essential part of this approach, removing the ovaries, the tubes, and the uterus with the cervix. Also, peritoneal washings are taken, the omentum is removed, and pelvic and paraaortic lymph nodes are sampled. Staging at the time of surgery and pathological findings will determine further steps. In advanced cases when the cancer has spread to other organs and cannot be completely removed, cytoreductive surgery is used to lessen the tumor burden for subsequent treatments. Surgical treatments are typically followed by adjuvant, usually platinum-based, chemotherapy.[4][5] Radiation therapy has been applied with some success to patients with tubal cancer for palliative or curative indications.[6]

Prognosis

Prognosis depends to a large degree on the stage of the condition. In 1991 it was reported that about half of the patients with advanced stage disease survived 5 years with a surgical approach followed by cisplatinum-based chemotherapy.[7]

Frequency

Tubal cancer is thought to be a relatively rare primary cancer among women, accounting for 1 to 2 percent of all gynecologic cancers,[8] In the US, tubal cancer had an incidence of 0.41 per 100,000 women from 1998 to 2003.[3] Demographic distribution is similar to that of ovarian cancer, and the highest incidence is found in white, non-Hispanic women aged 60–79.[3] However, recent evidence suggests tubal cancer to be much more frequent .[9]

Evidence is accumulating that individuals with mutations of BRCA1 and BRCA2 are at higher risk for the development of PFTC.[10][11]

See also

SEE-FIM Protocol

References

  1. ↑ Horng, Huann-Cheng; Teng, Sen-Wen; Huang, Ben-Shian; Sun, Hsu-Dong; Yen, Ming-Shyen; Wang, Peng-Hui; Tsui, Kuan-Hao; Wen, Kuo-Chang; Chen, Yi-Jen (September 2014). "Primary fallopian tube cancer: domestic data and up-to-date review". Taiwanese Journal of Obstetrics & Gynecology. 53 (3): 287–292. doi:10.1016/j.tjog.2014.07.003. ISSN 1875-6263. PMID 25286779.
  2. ↑ GOLDMAN JA, GANS B, ECKERLING B (November 1961). "Hydrops tubae profluens--symptom in tubal carcinoma". Obstet Gynecol. 18: 631–4. PMID 13899814.
  3. 1 2 3 Stewart SL, Wike JM, Foster SL, Michaud F (2007). "The incidence of primary fallopian tube cancer in the United States". Gynecol. Oncol. 107 (3): 392–7. doi:10.1016/j.ygyno.2007.09.018. PMID 17961642.
  4. ↑ Liapis A, Bakalianou K, Mpotsa E, Salakos N, Fotiou S, Kondi-Paffiti A (2008). "Fallopian tube malignancies: A retrospective clinical pathological study of 17 cases". J Obstet Gynaecol. 28 (1): 93–5. doi:10.1080/01443610701811894. PMID 18259909. S2CID 5351886.
  5. ↑ Takeshima N, Hasumi K (2000). "Treatment of fallopian tube cancer. Review of the literature". Arch Gynecol Obstet. 264 (1): 13–9. doi:10.1007/pl00007475. PMID 10985612. S2CID 34114333.
  6. ↑ Schray MF, Podratz KC, Malkasian GD (1987). "Fallopian tube cancer: the role of radiation therapy". Radiother. Oncol. 10 (4): 267–75. doi:10.1016/s0167-8140(87)80032-4. PMID 3444903.
  7. ↑ Barakat RR, Rubin SC, Saigo PE, et al. (1991). "Cisplatin-based combination chemotherapy in carcinoma of the fallopian tube". Gynecol Oncol. 42 (2): 156–160. doi:10.1016/0090-8258(91)90337-5. PMID 1894176.
  8. ↑ UCSF. "Gynecologic Cancer: Fallopian Tube Cancer". accessed 08-14-2008
  9. ↑ Piek JM, van Diest PJ, Verheijen RH (2008). "Ovarian carcinogenesis: an alternative hypothesis". Adv. Exp. Med. Biol. Advances in Experimental Medicine and Biology. 622: 79–87. doi:10.1007/978-0-387-68969-2_7. ISBN 978-0-387-68966-1. PMID 18546620.
  10. ↑ BRCA mutations link to tubal cancer, accessed 08-14-2008
  11. ↑ Piek, J. M. J. (2004). Hereditary serous ovarian carcinogenesis, a hypothesis (PhD thesis). Vrije Universiteit Amsterdam. hdl:1871/9013. ISBN 9064646406.
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