We have heard a lot about a handful of patients on IFN in CCR who have
managed to stay off Interferon without relapse.  It is always good to
go back into the Interferon studies to see what the relapse risk is in
IFN patients on CCR.  I give an article below and this shows that with
IFN CCRs, there can be significant relapse risk so one has to factor
that into account in any future Gleevec trials where IFN is added in
CCR with the idea of going off meds.  While IFN does act in a different
way from Gleevec, by eliciting immune responses, it is to be seen with
the help of trials how much IFN can do in the way of a cure in Gleevec
CCR patients, especially as pitted against those who take CML vaccines
after Gleevec CCR.  Such a trial is soon going to be under way at the
Sidney Kimmel Cancer Center.

While looking at IFN and vaccines as possible vehicles after Gleevec
CCR to a short or long-term cure, one also must not discount ways other
than immunotherapy, like killing of the quiescent cells by drug therapy
as a possible way to a cure.  Last ASH also reported such a drug from
Bristol-Myers-Squibb.

  I was happy to see Dorothy's feedback, funding of CML research indeed
does depend on institutions like NIH and steps taken to advocacy in
this area is indeed very welcome for the future of a CML drug cure.

Best Wishes,
Anjana
caregiver to Roy


J Clin Oncol. 2002 Jan 1;20(1):214-20. Links

Follow-up of complete cytogenetic remission in patients with chronic
myeloid
leukemia after cessation of interferon alfa.
a.. Mahon FX,
b.. Delbrel X,
c.. Cony-Makhoul P,
d.. Faberes C,
e.. Boiron JM,
f.. Barthe C,
g.. Bilhou-Nabera C,
h.. Pigneux A,
i.. Marit G,
j.. Reiffers J.
Service des Maladies du Sang, Centre Hospitalier Universitaire de
Bordeaux,
Bordeaux 2, France.

PURPOSE: A small proportion of patients with chronic myeloid leukemia
(CML)
achieve a complete cytogenetic response (CCR), defined as the
disappearance of
Philadelphia (Ph) chromosome-positive metaphases, after treatment with
interferon alfa (IFN). In this population of patients, the question of
whether
treatment should then be withdrawn is not yet resolved. PATIENTS AND
METHODS: In
the present study, we followed 15 patients who stopped IFN after
achieving CCR.
In nine patients IFN was stopped in view of adverse reactions (n = 8)
or
patient's choice (n = 1). For the remaining six patients, the treatment
was
stopped because no BCR/ABL rearrangement could be detected by reverse
transcriptase polymerase chain reaction (RT-PCR) in four successive
analyses
using peripheral-blood samples. RESULTS: Loss of CCR and survival were
not
statistically different (P =.48; P =.7) for the 15 patients who stopped
IFN
compared with 41 other CCR patients who continued IFN therapy in our
institution. The median follow-up after discontinuation of IFN
treatment was 36
months (range, 6 to 108 months). Seven patients (47%) (females, or CCR
> 24
months and RT-PCR negative before IFN cessation; P <.0001) did not
relapse.
Eight other patients (53%) relapsed (lost CCR) within 3 to 33 months of
treatment discontinuation. One of them relapsed in major cytogenetic
remission
(MCR) and was still in MCR 87 months after stopping therapy without any
treatment. CONCLUSION: It is possible to stop IFN treatment at least in
some
patients with CML who achieve a prolonged period of CCR. This study
also
illustrates the hypothesis that persistence of low numbers of
Ph-positive cells
does not necessarily imply hematologic relapse.


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